{"id":19,"date":"2015-08-31T05:27:24","date_gmt":"2015-08-31T05:27:24","guid":{"rendered":"http:\/\/biophotonics.bccrc.ca\/?page_id=19"},"modified":"2025-10-05T11:10:41","modified_gmt":"2025-10-05T18:10:41","slug":"publications","status":"publish","type":"page","link":"https:\/\/biophotonics.bccrc.ca\/index.php\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\" id=\"journal-articles\">Journal Articles<\/h2>\n\n\n<div class=\"teachpress_pub_list\"><form name=\"tppublistform\" method=\"get\"><a name=\"tppubs\" id=\"tppubs\"><\/a><\/form><div class=\"teachpress_publication_list\"><h3 class=\"tp_h3\" id=\"tp_h3_2025\">2025<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Segmental airway adenocarcinoma-simulating phantom for endoscopic near-infrared optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/JBO_30_10_105002_f004.png\" width=\"128\" alt=\"Segmental airway adenocarcinoma-simulating phantom for endoscopic near-infrared optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Brace, Eric;  Fung, Alicia;  Tanskanen, Adrian;  Jeanie Malone, Calum E. MacAulay;  Lane, Pierre M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.30.10.105002\" title=\"DOI\" target=\"blank\">Segmental airway adenocarcinoma-simulating phantom for endoscopic near-infrared optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 30, <\/span><span class=\"tp_pub_additional_issue\">iss. 10, <\/span><span class=\"tp_pub_additional_pages\">pp. 105002 , <\/span><span class=\"tp_pub_additional_year\">2025<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_192\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('192','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_192\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('192','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_192\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('192','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_192\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Brace2025,<br \/>\r\ntitle = {Segmental airway adenocarcinoma-simulating phantom for endoscopic near-infrared optical coherence tomography},<br \/>\r\nauthor = {Eric Brace AND Alicia Fung AND Adrian Tanskanen AND Jeanie Malone, Calum E. MacAulay AND Pierre M. Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.1117\/1.JBO.30.10.105002, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brace-2025.pdf, PDF},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-10-07},<br \/>\r\nurldate = {2025-10-07},<br \/>\r\njournal = {Journal of Biomedical Optics},<br \/>\r\nvolume = {30},<br \/>\r\nissue = {10},<br \/>\r\npages = {105002 },<br \/>\r\nabstract = {Significance: There is an unmet need for readily accessible imaging targets to verify whether devices can discriminate lesions from healthy tissue and identify sub-surface vasculature in the small airways.<br \/>\r\n<br \/>\r\nAim: Our aim is to develop a phantom that mimics human segmental airway adenocarcinoma in vivo for 1310 nm endoscopic optical coherence tomography (OCT) and angiography characterization.<br \/>\r\n<br \/>\r\nApproach: We develop phantoms using a mixture of agar, intralipid, and coconut oil cured in a 3D printed mold with embedded tubing to mimic vasculature. The parenchyma optical attenuation coefficient (OAC) is calibrated using optical transmission measurements from an agar and intralipid dilution series. Depth-resolved OAC histogram distributions, analysis of variance, and image quality are used to assess repeatability and biofidelity of these phantoms.<br \/>\r\n<br \/>\r\nResults: Transmission measurements show large increases in OAC when intralipid is cured with agar compared with water-intralipid dilutions. Representative phantom OACs show repeatability within 2.7% and match normal in vivo tissue measurements within 16%. Embedded lesion phantoms achieve imaging characteristics of in vivo adenocarcinoma. Fluid flow within embedded tubing is visualized with Doppler OCT.<br \/>\r\n<br \/>\r\nConclusions: The segmental airway phantoms demonstrate in vivo human imaging characteristics, including structural and optical markers of pathological progression\u2014providing a platform for imaging system characterization and optimization.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('192','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_192\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Significance: There is an unmet need for readily accessible imaging targets to verify whether devices can discriminate lesions from healthy tissue and identify sub-surface vasculature in the small airways.<br \/>\r\n<br \/>\r\nAim: Our aim is to develop a phantom that mimics human segmental airway adenocarcinoma in vivo for 1310 nm endoscopic optical coherence tomography (OCT) and angiography characterization.<br \/>\r\n<br \/>\r\nApproach: We develop phantoms using a mixture of agar, intralipid, and coconut oil cured in a 3D printed mold with embedded tubing to mimic vasculature. The parenchyma optical attenuation coefficient (OAC) is calibrated using optical transmission measurements from an agar and intralipid dilution series. Depth-resolved OAC histogram distributions, analysis of variance, and image quality are used to assess repeatability and biofidelity of these phantoms.<br \/>\r\n<br \/>\r\nResults: Transmission measurements show large increases in OAC when intralipid is cured with agar compared with water-intralipid dilutions. Representative phantom OACs show repeatability within 2.7% and match normal in vivo tissue measurements within 16%. Embedded lesion phantoms achieve imaging characteristics of in vivo adenocarcinoma. Fluid flow within embedded tubing is visualized with Doppler OCT.<br \/>\r\n<br \/>\r\nConclusions: The segmental airway phantoms demonstrate in vivo human imaging characteristics, including structural and optical markers of pathological progression\u2014providing a platform for imaging system characterization and optimization.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('192','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_192\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.30.10.105002\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brace-2025.pdf\" title=\"PDF\" target=\"_blank\">PDF<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('192','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2024\">2024<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Machine Learning and Computed Tomography Radiomics to Predict Disease Progression to Upfront Pembrolizumab Monotherapy in Advanced Non-Small-Cell Lung Cancer: A Pilot Study\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/01\/ianpaper-e1736799511103.png\" width=\"128\" alt=\"Machine Learning and Computed Tomography Radiomics to Predict Disease Progression to Upfront Pembrolizumab Monotherapy in Advanced Non-Small-Cell Lung Cancer: A Pilot Study\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Janzen, Ian;  Ho, Cheryl;  Melosky, Barbara;  Ye, Qian;  Li, Jessica;  Wang, Gang;  Lam, Stephen;  MacAulay, Calum;  Yuan, Ren<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/cancers17010058\" title=\"DOI\" target=\"blank\">Machine Learning and Computed Tomography Radiomics to Predict Disease Progression to Upfront Pembrolizumab Monotherapy in Advanced Non-Small-Cell Lung Cancer: A Pilot Study<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">MDPI Cancers, <\/span><span class=\"tp_pub_additional_volume\">vol. 17, <\/span><span class=\"tp_pub_additional_issue\">iss. 1, <\/span><span class=\"tp_pub_additional_number\">no. 58, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_175\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('175','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_175\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('175','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_175\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('175','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_175\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Janzen2024,<br \/>\r\ntitle = {Machine Learning and Computed Tomography Radiomics to Predict Disease Progression to Upfront Pembrolizumab Monotherapy in Advanced Non-Small-Cell Lung Cancer: A Pilot Study},<br \/>\r\nauthor = {Ian Janzen AND Cheryl Ho AND Barbara Melosky AND Qian Ye AND Jessica Li AND Gang Wang AND Stephen Lam AND Calum MacAulay AND Ren Yuan},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/cancers17010058, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/01\/cancers-17-00058-v2.pdf, PDF},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-12-28},<br \/>\r\nurldate = {2024-12-28},<br \/>\r\njournal = {MDPI Cancers},<br \/>\r\nvolume = {17},<br \/>\r\nnumber = {58},<br \/>\r\nissue = {1},<br \/>\r\nabstract = {Background\/Objectives: Pembrolizumab monotherapy is approved in Canada for first-line treatment of advanced NSCLC with PD-L1 \u2265 50% and no EGFR\/ALK aberrations. However, approximately 55% of these patients do not respond to pembrolizumab, underscoring the need for the early intervention of non-responders to optimize treatment strategies. Distinguishing the 55% sub-cohort prior to treatment is a real-world dilemma. Methods: In this retrospective study, we analyzed two patient cohorts treated with pembrolizumab monotherapy (training set: n = 97; test set: n = 17). The treatment response was assessed using baseline and follow-up CT scans via RECIST 1.1 criteria. Results: A logistic regression model, incorporating pre-treatment CT radiomic features of lung tumors and clinical variables, achieved high predictive accuracy (AUC: 0.85 in training; 0.81 in testing, 95% CI: 0.63\u20130.99). Notably, radiomic features from the peritumoral region were found to be independent predictors, complementing the standard CT evaluations and other clinical characteristics. Conclusions: This pragmatic model offers a valuable tool to guide first-line treatment decisions in NSCLC patients with high PD-L1 expression and has the potential to advance personalized oncology and improve timely disease management.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('175','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_175\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Background\/Objectives: Pembrolizumab monotherapy is approved in Canada for first-line treatment of advanced NSCLC with PD-L1 \u2265 50% and no EGFR\/ALK aberrations. However, approximately 55% of these patients do not respond to pembrolizumab, underscoring the need for the early intervention of non-responders to optimize treatment strategies. Distinguishing the 55% sub-cohort prior to treatment is a real-world dilemma. Methods: In this retrospective study, we analyzed two patient cohorts treated with pembrolizumab monotherapy (training set: n = 97; test set: n = 17). The treatment response was assessed using baseline and follow-up CT scans via RECIST 1.1 criteria. Results: A logistic regression model, incorporating pre-treatment CT radiomic features of lung tumors and clinical variables, achieved high predictive accuracy (AUC: 0.85 in training; 0.81 in testing, 95% CI: 0.63\u20130.99). Notably, radiomic features from the peritumoral region were found to be independent predictors, complementing the standard CT evaluations and other clinical characteristics. Conclusions: This pragmatic model offers a valuable tool to guide first-line treatment decisions in NSCLC patients with high PD-L1 expression and has the potential to advance personalized oncology and improve timely disease management.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('175','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_175\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/cancers17010058\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/01\/cancers-17-00058-v2.pdf\" title=\"PDF\" target=\"_blank\">PDF<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('175','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Multimodal Optical Imaging of Ex Vivo Fallopian Tubes to Distinguish Early and Occult Tubo-Ovarian Cancers\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/10\/Capture.png\" width=\"128\" alt=\"Multimodal Optical Imaging of Ex Vivo Fallopian Tubes to Distinguish Early and Occult Tubo-Ovarian Cancers\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Malone, Jeanie;  Tanskanen, Adrian;  Hill, Chloe;  Cynamon, Allan Zuckermann;  Hoang, Lien;  MacAulay, Calum;  McAlpine, Jessica N.;  Lane, Pierre M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/cancers16213618\" title=\"DOI\" target=\"blank\">Multimodal Optical Imaging of Ex Vivo Fallopian Tubes to Distinguish Early and Occult Tubo-Ovarian Cancers<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">MDPI Cancers, <\/span><span class=\"tp_pub_additional_volume\">vol. 16, <\/span><span class=\"tp_pub_additional_issue\">iss. 21, <\/span><span class=\"tp_pub_additional_number\">no. 3618, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_174\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('174','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_174\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('174','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_174\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('174','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_174\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{MaloneFallopian2024,<br \/>\r\ntitle = {Multimodal Optical Imaging of Ex Vivo Fallopian Tubes to Distinguish Early and Occult Tubo-Ovarian Cancers},<br \/>\r\nauthor = {Jeanie Malone AND Adrian Tanskanen AND Chloe Hill AND Allan Zuckermann Cynamon AND Lien Hoang AND Calum MacAulay AND Jessica N. McAlpine AND Pierre M. Lane<br \/>\r\n},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/cancers16213618, DOI, <br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/10\/cancers-16-03618.pdf, PDF},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-10-26},<br \/>\r\nurldate = {2024-10-26},<br \/>\r\njournal = {MDPI Cancers},<br \/>\r\nvolume = {16},<br \/>\r\nnumber = {3618},<br \/>\r\nissue = {21},<br \/>\r\nabstract = {Tubo-ovarian cancers are associated with high mortality as they are often not detected until a late stage. Early diagnosis is associated with better patient outcomes, but there are currently no effective screening measures. We explore whether an optical imaging catheter can detect early or occult lesions in the fallopian tubes. This device collects three-dimensional structural images of tissue through optical coherence tomography (OCT) simultaneously with functional imaging through autofluorescence imaging (AFI). We image ex vivo fallopian tubes from n = 28 patients (n = 7 cancer patients) and explore eleven imaging biomarkers for their ability to distinguish early or occult disease. We find that high-grade serous ovarian carcinomas can be visually distinguished through this approach, and that there are several quantitative changes within the area of lesion and throughout the specimen that can be measured through these imaging biomarkers. We conclude that this approach shows promise and merits further investigation of its diagnostic potential.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('174','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_174\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Tubo-ovarian cancers are associated with high mortality as they are often not detected until a late stage. Early diagnosis is associated with better patient outcomes, but there are currently no effective screening measures. We explore whether an optical imaging catheter can detect early or occult lesions in the fallopian tubes. This device collects three-dimensional structural images of tissue through optical coherence tomography (OCT) simultaneously with functional imaging through autofluorescence imaging (AFI). We image ex vivo fallopian tubes from n = 28 patients (n = 7 cancer patients) and explore eleven imaging biomarkers for their ability to distinguish early or occult disease. We find that high-grade serous ovarian carcinomas can be visually distinguished through this approach, and that there are several quantitative changes within the area of lesion and throughout the specimen that can be measured through these imaging biomarkers. We conclude that this approach shows promise and merits further investigation of its diagnostic potential.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('174','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_174\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/cancers16213618\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/10\/cancers-16-03618.pdf\" title=\"PDF\" target=\"_blank\">PDF<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('174','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Imaging Biomarkers of Oral Dysplasia and Carcinoma Measured with In Vivo Endoscopic Optical Coherence Tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/08\/cancers-16-02751-g006-SMALL.png\" width=\"128\" alt=\"Imaging Biomarkers of Oral Dysplasia and Carcinoma Measured with In Vivo Endoscopic Optical Coherence Tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Malone, Jeanie;  Hill, Chloe;  Tanskanen, Adrian;  Liu, Kelly;  Ng, Samson;  MacAulay, Calum;  Poh, Catherine F.;  Lane, Pierre M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/cancers16152751\" title=\"DOI\" target=\"blank\">Imaging Biomarkers of Oral Dysplasia and Carcinoma Measured with In Vivo Endoscopic Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">MDPI Cancers, <\/span><span class=\"tp_pub_additional_volume\">vol. 16, <\/span><span class=\"tp_pub_additional_issue\">iss. 15, <\/span><span class=\"tp_pub_additional_number\">no. 15, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_173\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('173','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_173\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('173','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_173\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('173','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_173\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{MaloneOral2024,<br \/>\r\ntitle = {Imaging Biomarkers of Oral Dysplasia and Carcinoma Measured with In Vivo Endoscopic Optical Coherence Tomography},<br \/>\r\nauthor = {Jeanie Malone AND Chloe Hill AND Adrian Tanskanen AND Kelly Liu AND Samson Ng AND Calum MacAulay AND Catherine F. Poh AND Pierre M. Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/cancers16152751, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/08\/cancers-16-02751.pdf, PDF},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-08-02},<br \/>\r\nurldate = {2024-08-02},<br \/>\r\njournal = {MDPI Cancers},<br \/>\r\nvolume = {16},<br \/>\r\nnumber = {15},<br \/>\r\nissue = {15},<br \/>\r\nabstract = {Oral cancers are associated with high mortality in advanced stages. Early diagnosis is associated with better patient outcomes, but this is challenging to achieve as benign lesions look similar to lesions of concern, and multiple biopsies may be required to ensure the most pathologic tissue is sampled. This work leverages a previously developed endoscopic imaging system and deep learning segmentation tool to provide measurements of subsurface changes in the first few millimeters of oral tissue. We present seven quantitative features that allow for rapid examination of tissue, which we propose may be useful for biopsy site or treatment margin selection.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('173','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_173\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Oral cancers are associated with high mortality in advanced stages. Early diagnosis is associated with better patient outcomes, but this is challenging to achieve as benign lesions look similar to lesions of concern, and multiple biopsies may be required to ensure the most pathologic tissue is sampled. This work leverages a previously developed endoscopic imaging system and deep learning segmentation tool to provide measurements of subsurface changes in the first few millimeters of oral tissue. We present seven quantitative features that allow for rapid examination of tissue, which we propose may be useful for biopsy site or treatment margin selection.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('173','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_173\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/cancers16152751\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/08\/cancers-16-02751.pdf\" title=\"PDF\" target=\"_blank\">PDF<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('173','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Three-Dimension Epithelial Segmentation in Optical Coherence Tomography of the Oral Cavity Using Deep Learning\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/06\/Graphical-Abstract.png\" width=\"128\" alt=\"Three-Dimension Epithelial Segmentation in Optical Coherence Tomography of the Oral Cavity Using Deep Learning\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Hill, Chloe;  Malone, Jeanie;  Liu, Kelly;  Ng, Samson Pak-Yan;  MacAulay, Calum;  Poh, Catherine;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/cancers16112144\" title=\"DOI\" target=\"blank\">Three-Dimension Epithelial Segmentation in Optical Coherence Tomography of the Oral Cavity Using Deep Learning<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">MDPI Cancers, <\/span><span class=\"tp_pub_additional_volume\">vol. 16, <\/span><span class=\"tp_pub_additional_issue\">iss. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 2144, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_172\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('172','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_172\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('172','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_172\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('172','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_172\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Hill2024,<br \/>\r\ntitle = {Three-Dimension Epithelial Segmentation in Optical Coherence Tomography of the Oral Cavity Using Deep Learning},<br \/>\r\nauthor = {Chloe Hill and Jeanie Malone and Kelly Liu and Samson Pak-Yan Ng and Calum MacAulay and Catherine Poh and Pierre Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/cancers16112144, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/06\/Hill-2024.pdf, PDF},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-06-05},<br \/>\r\nurldate = {2024-06-05},<br \/>\r\njournal = {MDPI Cancers},<br \/>\r\nvolume = {16},<br \/>\r\nissue = {11},<br \/>\r\npages = {2144},<br \/>\r\nabstract = {This paper aims to simplify the application of optical coherence tomography (OCT) for the examination of subsurface morphology in the oral cavity and reduce barriers towards the adoption of OCT as a biopsy guidance device. The aim of this work was to develop automated software tools for the simplified analysis of the large volume of data collected during OCT. Imaging and corresponding histopathology were acquired in-clinic using a wide-field endoscopic OCT system. An annotated dataset (n = 294 images) from 60 patients (34 male and 26 female) was assembled to train four unique neural networks. A deep learning pipeline was built using convolutional and modified u-net models to detect the imaging field of view (network 1), detect artifacts (network 2), identify the tissue surface (network 3), and identify the presence and location of the epithelial\u2013stromal boundary (network 4). The area under the curve of the image and artifact detection networks was 1.00 and 0.94, respectively. The Dice similarity score for the surface and epithelial\u2013stromal boundary segmentation networks was 0.98 and 0.83, respectively. Deep learning (DL) techniques can identify the location and variations in the epithelial surface and epithelial\u2013stromal boundary in OCT images of the oral mucosa. Segmentation results can be synthesized into accessible en face maps to allow easier visualization of changes.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('172','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_172\" style=\"display:none;\"><div class=\"tp_abstract_entry\">This paper aims to simplify the application of optical coherence tomography (OCT) for the examination of subsurface morphology in the oral cavity and reduce barriers towards the adoption of OCT as a biopsy guidance device. The aim of this work was to develop automated software tools for the simplified analysis of the large volume of data collected during OCT. Imaging and corresponding histopathology were acquired in-clinic using a wide-field endoscopic OCT system. An annotated dataset (n = 294 images) from 60 patients (34 male and 26 female) was assembled to train four unique neural networks. A deep learning pipeline was built using convolutional and modified u-net models to detect the imaging field of view (network 1), detect artifacts (network 2), identify the tissue surface (network 3), and identify the presence and location of the epithelial\u2013stromal boundary (network 4). The area under the curve of the image and artifact detection networks was 1.00 and 0.94, respectively. The Dice similarity score for the surface and epithelial\u2013stromal boundary segmentation networks was 0.98 and 0.83, respectively. Deep learning (DL) techniques can identify the location and variations in the epithelial surface and epithelial\u2013stromal boundary in OCT images of the oral mucosa. Segmentation results can be synthesized into accessible en face maps to allow easier visualization of changes.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('172','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_172\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/cancers16112144\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/06\/Hill-2024.pdf\" title=\"PDF\" target=\"_blank\">PDF<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('172','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Distal planar rotary scanner for endoscopic optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/02\/SearlesFig1.png\" width=\"128\" alt=\"Distal planar rotary scanner for endoscopic optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Searles, Kyle;  Shalabi, Nabil;  Hohert, Geoffrey;  Gharib, Nirvana;  Jayhooni, Sayed Mohammad Hashem; andKenichi Takahata, Pierre M. Lane<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1007\/s13534-024-00353-8\" title=\"DOI\" target=\"blank\">Distal planar rotary scanner for endoscopic optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomedical Engineering Letters, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_171\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('171','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_171\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('171','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_171\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('171','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_171\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Searles2024,<br \/>\r\ntitle = {Distal planar rotary scanner for endoscopic optical coherence tomography},<br \/>\r\nauthor = {Kyle Searles and Nabil Shalabi and Geoffrey Hohert and Nirvana Gharib and Sayed Mohammad Hashem Jayhooni and Pierre M. Lane andKenichi Takahata},<br \/>\r\nurl = {https:\/\/doi.org\/10.1007\/s13534-024-00353-8, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/02\/s13534-024-00353-8.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-02-19},<br \/>\r\nurldate = {2024-02-19},<br \/>\r\njournal = {Biomedical Engineering Letters},<br \/>\r\nabstract = {Optical coherence tomography (OCT) is becoming a more common endoscopic imaging modality for detecting and treating disease given its high resolution and image quality. To use OCT for 3-dimensional imaging of small lumen, embedding an optical scanner at the distal end of an endoscopic probe for circumferential scanning the probing light is a promising way to implement high-quality imaging unachievable with the conventional method of revolving an entire probe. To this end, the present work proposes a hollow and planar micro rotary actuator for its use as an endoscopic distal scanner. A miniaturized design of this ferrofluid-assisted electromagnetic actuator is prototyped to act as a full 360\u00b0 optical scanner, which is integrated at the tip of a fiber-optic probe together with a gradient-index lens for use with OCT. The scanner is revealed to achieve a notably improved dynamic performance that shows a maximum speed of 6500 rpm, representing 325% of the same reported with the preceding design, while staying below the thermal limit for safe in-vivo use. The scanner is demonstrated to perform real-time OCT using human fingers as live tissue samples for the imaging tests. The acquired images display no shadows from the electrical wires to the scanner, given its hollow architecture that allows the probing light to pass through the actuator body, as well as the quality high enough to differentiate the dermis from the epidermis while resolving individual sweat glands, proving the effectiveness of the prototyped scanner design for endoscopic OCT application.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('171','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_171\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Optical coherence tomography (OCT) is becoming a more common endoscopic imaging modality for detecting and treating disease given its high resolution and image quality. To use OCT for 3-dimensional imaging of small lumen, embedding an optical scanner at the distal end of an endoscopic probe for circumferential scanning the probing light is a promising way to implement high-quality imaging unachievable with the conventional method of revolving an entire probe. To this end, the present work proposes a hollow and planar micro rotary actuator for its use as an endoscopic distal scanner. A miniaturized design of this ferrofluid-assisted electromagnetic actuator is prototyped to act as a full 360\u00b0 optical scanner, which is integrated at the tip of a fiber-optic probe together with a gradient-index lens for use with OCT. The scanner is revealed to achieve a notably improved dynamic performance that shows a maximum speed of 6500 rpm, representing 325% of the same reported with the preceding design, while staying below the thermal limit for safe in-vivo use. The scanner is demonstrated to perform real-time OCT using human fingers as live tissue samples for the imaging tests. The acquired images display no shadows from the electrical wires to the scanner, given its hollow architecture that allows the probing light to pass through the actuator body, as well as the quality high enough to differentiate the dermis from the epidermis while resolving individual sweat glands, proving the effectiveness of the prototyped scanner design for endoscopic OCT application.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('171','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_171\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1007\/s13534-024-00353-8\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2024\/02\/s13534-024-00353-8.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('171','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2023\">2023<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Multipath artifacts enable angular contrast in multimodal endoscopic optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/12\/Capture2.png\" width=\"128\" alt=\"Multipath artifacts enable angular contrast in multimodal endoscopic optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Tanskanen, Adrian;  Malone, Jeanie;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1364\/OE.504854\" title=\"DOI\" target=\"blank\">Multipath artifacts enable angular contrast in multimodal endoscopic optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Express Vol. 31, Issue 26, <\/span><span class=\"tp_pub_additional_volume\">vol. 31, <\/span><span class=\"tp_pub_additional_issue\">iss. 26, <\/span><span class=\"tp_pub_additional_pages\">pp. 44224-44245, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_170\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('170','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_170\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('170','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_170\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('170','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_170\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{TanskanenMalone2023,<br \/>\r\ntitle = {Multipath artifacts enable angular contrast in multimodal endoscopic optical coherence tomography},<br \/>\r\nauthor = {Adrian Tanskanen and Jeanie Malone and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.1364\/OE.504854, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/12\/oe-31-26-44224.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-12-12},<br \/>\r\nurldate = {2023-12-12},<br \/>\r\njournal = {Optics Express Vol. 31, Issue 26},<br \/>\r\nvolume = {31},<br \/>\r\nissue = {26},<br \/>\r\npages = {44224-44245},<br \/>\r\nabstract = {Multipath artifacts are inherent to double-clad fiber based optical coherence tomography (OCT), appearing as ghost images blurred in the A-line direction. They result from the excitation of higher-order inner-cladding modes in the OCT sample arm which cross-couple into the fundamental mode at discontinuities and thus are detected in single-mode fiber-based interferometers. Historically, multipath artifacts have been regarded as a drawback in single fiber endoscopic multimodal OCT systems as they degrade OCT quality. In this work, we reveal that multipath artifacts can be projected into high-quality two-dimensional en face images which encode high angle backscattering features. Using a combination of experiment and simulation, we characterize the coupling of Mie-range scatterers into the fundamental image (LP01 mode) and higher-order image (multipath artifact). This is validated experimentally through imaging of microspheres with an endoscopic multimodal OCT system. The angular dependence of the fundamental image and higher order image generated by the multipath artifact lays the basis for multipath contrast, a ratiometric measurement of differential coupling which provides information regarding the angular diversity of a sample. Multipath contrast images can be generated from OCT data where multipath artifacts are present, meaning that a wealth of clinical data can be retrospectively examined.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('170','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_170\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Multipath artifacts are inherent to double-clad fiber based optical coherence tomography (OCT), appearing as ghost images blurred in the A-line direction. They result from the excitation of higher-order inner-cladding modes in the OCT sample arm which cross-couple into the fundamental mode at discontinuities and thus are detected in single-mode fiber-based interferometers. Historically, multipath artifacts have been regarded as a drawback in single fiber endoscopic multimodal OCT systems as they degrade OCT quality. In this work, we reveal that multipath artifacts can be projected into high-quality two-dimensional en face images which encode high angle backscattering features. Using a combination of experiment and simulation, we characterize the coupling of Mie-range scatterers into the fundamental image (LP01 mode) and higher-order image (multipath artifact). This is validated experimentally through imaging of microspheres with an endoscopic multimodal OCT system. The angular dependence of the fundamental image and higher order image generated by the multipath artifact lays the basis for multipath contrast, a ratiometric measurement of differential coupling which provides information regarding the angular diversity of a sample. Multipath contrast images can be generated from OCT data where multipath artifacts are present, meaning that a wealth of clinical data can be retrospectively examined.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('170','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_170\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1364\/OE.504854\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/12\/oe-31-26-44224.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('170','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Triple-clad W-type fiber mitigates multipath artifacts in multimodal optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/Screenshot-2023-01-25-at-9.34.06-AM-300x290.png\" width=\"128\" alt=\"Triple-clad W-type fiber mitigates multipath artifacts in multimodal optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Tanskanen, Adrian;  Malone, Jeanie;  Hohert, Geoffrey;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1364\/OE.476768\" title=\"DOI\" target=\"blank\">Triple-clad W-type fiber mitigates multipath artifacts in multimodal optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 31, <\/span><span class=\"tp_pub_additional_pages\">pp. 4465-4481, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_169\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('169','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_169\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('169','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_169\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('169','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_169\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Tanskanen2023,<br \/>\r\ntitle = {Triple-clad W-type fiber mitigates multipath artifacts in multimodal optical coherence tomography},<br \/>\r\nauthor = {Adrian Tanskanen and Jeanie Malone and Geoffrey Hohert and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.1364\/OE.476768, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/oe-31-3-4465.pdf, Full Text (PDF)<br \/>\r\n},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-01-24},<br \/>\r\nurldate = {2023-01-24},<br \/>\r\njournal = {Optics Express},<br \/>\r\nvolume = {31},<br \/>\r\npages = {4465-4481},<br \/>\r\nabstract = {Multimodal endoscopic optical coherence tomography (OCT) can be implemented with double-clad fiber by using the presumed single-mode core for OCT and the higher numerical aperture cladding for a secondary modality. However, the quality of OCT in double-clad fiber (DCF) based systems is compromised by the introduction of multipath artifacts that aren't present in single-mode fiber OCT systems. Herein, the mechanisms for multipath artifacts in DCF are linked to its modal contents using a commercial software package and experimental measurement. A triple-clad W-type fiber is proposed as a method for achieving multimodal imaging with single-mode quality OCT in an endoscopic system. Simulations of the modal contents of a W-type fiber are compared to DCF and single-mode fiber. Finally, a W-Type fiber rotary catheter is used in a DCF-based endoscopic OCT and autofluorescence imaging (AFI) system to demonstrate multipath artifact free OCT and AFI of a human fingertip.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('169','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_169\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Multimodal endoscopic optical coherence tomography (OCT) can be implemented with double-clad fiber by using the presumed single-mode core for OCT and the higher numerical aperture cladding for a secondary modality. However, the quality of OCT in double-clad fiber (DCF) based systems is compromised by the introduction of multipath artifacts that aren't present in single-mode fiber OCT systems. Herein, the mechanisms for multipath artifacts in DCF are linked to its modal contents using a commercial software package and experimental measurement. A triple-clad W-type fiber is proposed as a method for achieving multimodal imaging with single-mode quality OCT in an endoscopic system. Simulations of the modal contents of a W-type fiber are compared to DCF and single-mode fiber. Finally, a W-Type fiber rotary catheter is used in a DCF-based endoscopic OCT and autofluorescence imaging (AFI) system to demonstrate multipath artifact free OCT and AFI of a human fingertip.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('169','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_169\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1364\/OE.476768\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/oe-31-3-4465.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('169','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2022\">2022<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Software development to optimize the minimal detectable difference in human airway images captured using optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/Screenshot-2023-01-04-at-10.00.57-AM-300x262.png\" width=\"128\" alt=\"Software development to optimize the minimal detectable difference in human airway images captured using optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Peters, Carli M.;  Peters, Robert C.;  Lee, Anthony D.;  Lane, Pierre;  Lam, Stephen;  Sin, Don D.;  McKenzie, Donald C.;  Sheel, A. William<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1111\/cpf.12762\" title=\"DOI\" target=\"blank\">Software development to optimize the minimal detectable difference in human airway images captured using optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Clinical Physiology and Functional Imaging, <\/span><span class=\"tp_pub_additional_issue\">iss. 42, <\/span><span class=\"tp_pub_additional_pages\">pp. 308\u2013319, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_168\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('168','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_168\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('168','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_168\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('168','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_168\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Peters2022,<br \/>\r\ntitle = {Software development to optimize the minimal detectable difference in human airway images captured using optical coherence tomography},<br \/>\r\nauthor = {Carli M. Peters and Robert C. Peters and Anthony D. Lee and Pierre Lane and Stephen Lam and Don D. Sin and Donald C. McKenzie and A. William Sheel},<br \/>\r\nurl = {https:\/\/doi.org\/10.1111\/cpf.12762, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/Clin-Physio-Funct-Imaging-2022-Peters-Software-development-to-optimize-the-minimal-detectable-difference-in-human.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-05-04},<br \/>\r\nurldate = {2022-05-04},<br \/>\r\njournal = {Clinical Physiology and Functional Imaging},<br \/>\r\nissue = {42},<br \/>\r\npages = {308\u2013319},<br \/>\r\nabstract = {Optical coherence tomography (OCT) is an imaging methodology that can be used to assess human airways. OCT avoids the harmful effects of ionizing radiation and has a high spatial resolution making it well suited for imaging the structure of small airways. Analysis of OCT airway images has typically been performed manually by tracing the airway with a relatively high coefficient of variation. The purpose of this study was to develop an analysis tool to reduce the inter\u2010 and intra\u2010observer reproducibility of OCT and improve the ability to detect differences in airways. OCT images from healthy, young human volunteers were used to develop and test the OCT software. Measurement software was developed to allow the conversion of the original image into a grayscale image and was followed by an enhancement operation to brighten the image, and contour measurement. A total of 140 OCT images, 70 small (&lt;2 mm) and 70 medium (2\u20134 mm) sized airways were analyzed. The inter\u2010 and intraobserver reproducibility of airway measurements ranged for strong to very strong in the small\u2010sized airways. For medium\u2010sized airways the reproducibility was considered moderate. Bland\u2010Altman bias was low between observers and observations for all measures. The minimal detectable differences in the airway measurements with our semi\u2010automated software were lower relative to manual tracing in medium\u2010sized airways. Our software improves the ability to perform quantitative OCT analysis and may help to quantify the extent of airway remodelling in respiratory disease or elite athletes in future studies.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('168','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_168\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Optical coherence tomography (OCT) is an imaging methodology that can be used to assess human airways. OCT avoids the harmful effects of ionizing radiation and has a high spatial resolution making it well suited for imaging the structure of small airways. Analysis of OCT airway images has typically been performed manually by tracing the airway with a relatively high coefficient of variation. The purpose of this study was to develop an analysis tool to reduce the inter\u2010 and intra\u2010observer reproducibility of OCT and improve the ability to detect differences in airways. OCT images from healthy, young human volunteers were used to develop and test the OCT software. Measurement software was developed to allow the conversion of the original image into a grayscale image and was followed by an enhancement operation to brighten the image, and contour measurement. A total of 140 OCT images, 70 small (&lt;2 mm) and 70 medium (2\u20134 mm) sized airways were analyzed. The inter\u2010 and intraobserver reproducibility of airway measurements ranged for strong to very strong in the small\u2010sized airways. For medium\u2010sized airways the reproducibility was considered moderate. Bland\u2010Altman bias was low between observers and observations for all measures. The minimal detectable differences in the airway measurements with our semi\u2010automated software were lower relative to manual tracing in medium\u2010sized airways. Our software improves the ability to perform quantitative OCT analysis and may help to quantify the extent of airway remodelling in respiratory disease or elite athletes in future studies.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('168','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_168\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1111\/cpf.12762\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2023\/01\/Clin-Physio-Funct-Imaging-2022-Peters-Software-development-to-optimize-the-minimal-detectable-difference-in-human.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('168','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2021\">2021<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fabrication of a stepped optical fiber tip for miniaturized scanners\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-10.37.24-AM.png\" width=\"128\" alt=\"Fabrication of a stepped optical fiber tip for miniaturized scanners\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kaur, Mandeep;  Hohert, Geoffrey;  Lane, Pierre M.;  Menon, Carlo<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1016\/j.yofte.2020.102436\" title=\"DOI\" target=\"blank\">Fabrication of a stepped optical fiber tip for miniaturized scanners<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optical Fiber Technology, <\/span><span class=\"tp_pub_additional_volume\">vol. 61, <\/span><span class=\"tp_pub_additional_number\">no. 102436, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_160\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('160','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_160\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('160','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_160\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('160','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_160\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kaur2021,<br \/>\r\ntitle = {Fabrication of a stepped optical fiber tip for miniaturized scanners},<br \/>\r\nauthor = {Mandeep Kaur and Geoffrey Hohert and Pierre M. Lane and Carlo Menon},<br \/>\r\nurl = {https:\/\/doi.org\/10.1016\/j.yofte.2020.102436, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/1-s2.0-S1068520020304260-main.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-12-30},<br \/>\r\nurldate = {2021-12-30},<br \/>\r\njournal = {Optical Fiber Technology},<br \/>\r\nvolume = {61},<br \/>\r\nnumber = {102436},<br \/>\r\nabstract = {Advancements in fabrication of miniaturized optical scanners would benefit from micrometer sized optical fiber tips. The change in the cross section of an optical fiber tip is often accompanied with the presence of a longer tapered area. The reduction of the cross section of double clad optical fibers (DCFs) with a flat interface surface at the region where a change in the cross section takes place (with an abrupt change in the cross section) is considered in this paper. Various methods such as heating and pulling, wet etching using hydrofluoric acid (HF), and etching in a vaporous state were explored. The optical etching rate and its dependence on the temperature of the etchant solution were also determined. Optical fibers etch linearly with time, and the etching speed is dependent on the temperature of the etchant solution which shows a parabolic trend. The flatness of the surface at the cross section change is an interesting parameter in the fabrication of submillimeter sized scanners where the light is transmitted through the core of the DCF, and reflected light is collected through the inner cladding of the same fiber, or vice versa. The surface flatness at the interface was compared among different fiber samples developed using the aforementioned techniques. This research illustrates that the wet chemical etching performed by blocking the capillary rising of etchant solution along the fiber provided advantages over the heating and pulling technique in terms of light intensity transmitted to the target sample and the reflected light collected through the interface of etched cladding.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('160','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_160\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Advancements in fabrication of miniaturized optical scanners would benefit from micrometer sized optical fiber tips. The change in the cross section of an optical fiber tip is often accompanied with the presence of a longer tapered area. The reduction of the cross section of double clad optical fibers (DCFs) with a flat interface surface at the region where a change in the cross section takes place (with an abrupt change in the cross section) is considered in this paper. Various methods such as heating and pulling, wet etching using hydrofluoric acid (HF), and etching in a vaporous state were explored. The optical etching rate and its dependence on the temperature of the etchant solution were also determined. Optical fibers etch linearly with time, and the etching speed is dependent on the temperature of the etchant solution which shows a parabolic trend. The flatness of the surface at the cross section change is an interesting parameter in the fabrication of submillimeter sized scanners where the light is transmitted through the core of the DCF, and reflected light is collected through the inner cladding of the same fiber, or vice versa. The surface flatness at the interface was compared among different fiber samples developed using the aforementioned techniques. This research illustrates that the wet chemical etching performed by blocking the capillary rising of etchant solution along the fiber provided advantages over the heating and pulling technique in terms of light intensity transmitted to the target sample and the reflected light collected through the interface of etched cladding.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('160','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_160\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1016\/j.yofte.2020.102436\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/1-s2.0-S1068520020304260-main.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('160','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Airway luminal area and the resistive work of breathing during exercise in healthy young females and males\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-10.11.57-AM.png\" width=\"128\" alt=\"Airway luminal area and the resistive work of breathing during exercise in healthy young females and males\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Peters, Carli M.;  Leahy, Michael G.;  Hohert, Geoffrey;  Lane, Pierre;  Lam, Stephen;  Sin, Don D.;  McKenzie, Donald C.;  Sheel, Andrew William<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1152\/japplphysiol.00418.2021\" title=\"DOI\" target=\"blank\">Airway luminal area and the resistive work of breathing during exercise in healthy young females and males<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">J Appl Physiol, <\/span><span class=\"tp_pub_additional_volume\">vol. 131, <\/span><span class=\"tp_pub_additional_issue\">iss. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. 1750-1761, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_157\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('157','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_157\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('157','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_157\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('157','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_157\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Peters2021,<br \/>\r\ntitle = {Airway luminal area and the resistive work of breathing during exercise in healthy young females and males},<br \/>\r\nauthor = {Carli M. Peters and Michael G. Leahy and Geoffrey Hohert and Pierre Lane and Stephen Lam and Don D. Sin and Donald C. McKenzie and Andrew William Sheel },<br \/>\r\nurl = {https:\/\/doi.org\/10.1152\/japplphysiol.00418.2021, DOI},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-12-01},<br \/>\r\nurldate = {2021-12-01},<br \/>\r\njournal = {J Appl Physiol},<br \/>\r\nvolume = {131},<br \/>\r\nissue = {6},<br \/>\r\npages = {1750-1761},<br \/>\r\nabstract = {We examined the relationship between the work of breathing (Wb) during exercise and in vivo measures of airway size in healthy females and males. We hypothesized that sex differences in airway luminal area would explain the larger resistive Wb during exercise in females. Healthy participants (n = 11 females and n = 11 males; 19-30 yr) completed a cycle exercise test to exhaustion where Wb was assessed using an esophageal balloon catheter. On a separate day, each participant underwent a bronchoscopy procedure for optical coherence tomography measures of seven airways. In vivo measures of luminal area were made for the fourth to eighth airway generations. A composite index of airway size was calculated as the sum of the luminal area for each generation, and the total area was calculated based on Weibel's model. We found that index of airway size (males: 37.4 \u00b1 6.3 mm2 vs. females: 27.5 \u00b1 7.4 mm2) and airway area calculated based on Weibel's model (males: 2,274 \u00b1 557 mm2 vs. females: 1,594 \u00b1 389 mm2) were significantly larger in males (both P = 0.003). When minute ventilation was greater than \u223c60 L\u00b7min-1, the resistive Wb was higher in females. At the highest equivalent flow achieved by all subjects, resistance to inspired flow was larger in females and significantly associated with two measures of airway size in all subjects: index of airway size (r = 0.524, P = 0.012) and Weibel area (r = 0.525, P = 0.012). Our findings suggest that innate sex differences in luminal area result in a greater resistive Wb during exercise in females compared with males.NEW & NOTEWORTHY We hypothesized that the higher resistive work of breathing in females compared with males during high-intensity exercise is due to smaller airways. In vivo measures of the fourth to eighth airway generations made using optical coherence tomography show that females tend to have smaller airway luminal areas of the fourth to sixth airway generations. Sex differences in airway luminal area result in a greater resistive work of breathing during exercise in females compared with males.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('157','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_157\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We examined the relationship between the work of breathing (Wb) during exercise and in vivo measures of airway size in healthy females and males. We hypothesized that sex differences in airway luminal area would explain the larger resistive Wb during exercise in females. Healthy participants (n = 11 females and n = 11 males; 19-30 yr) completed a cycle exercise test to exhaustion where Wb was assessed using an esophageal balloon catheter. On a separate day, each participant underwent a bronchoscopy procedure for optical coherence tomography measures of seven airways. In vivo measures of luminal area were made for the fourth to eighth airway generations. A composite index of airway size was calculated as the sum of the luminal area for each generation, and the total area was calculated based on Weibel's model. We found that index of airway size (males: 37.4 \u00b1 6.3 mm2 vs. females: 27.5 \u00b1 7.4 mm2) and airway area calculated based on Weibel's model (males: 2,274 \u00b1 557 mm2 vs. females: 1,594 \u00b1 389 mm2) were significantly larger in males (both P = 0.003). When minute ventilation was greater than \u223c60 L\u00b7min-1, the resistive Wb was higher in females. At the highest equivalent flow achieved by all subjects, resistance to inspired flow was larger in females and significantly associated with two measures of airway size in all subjects: index of airway size (r = 0.524, P = 0.012) and Weibel area (r = 0.525, P = 0.012). Our findings suggest that innate sex differences in luminal area result in a greater resistive Wb during exercise in females compared with males.NEW &amp; NOTEWORTHY We hypothesized that the higher resistive work of breathing in females compared with males during high-intensity exercise is due to smaller airways. In vivo measures of the fourth to eighth airway generations made using optical coherence tomography show that females tend to have smaller airway luminal areas of the fourth to sixth airway generations. Sex differences in airway luminal area result in a greater resistive work of breathing during exercise in females compared with males.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('157','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_157\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1152\/japplphysiol.00418.2021\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('157','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Higher-Order Core-Like Modes in Double-Clad Fiber Contribute to Multipath Artifacts in Optical Coherence Tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-10.41.56-AM.png\" width=\"128\" alt=\"Higher-Order Core-Like Modes in Double-Clad Fiber Contribute to Multipath Artifacts in Optical Coherence Tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Tanskanen, Adrian;  Hohert, Geoffrey;  Lee, Anthony;  Lane, Pierre M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1109\/JLT.2021.3088055\" title=\"DOI\" target=\"blank\">Higher-Order Core-Like Modes in Double-Clad Fiber Contribute to Multipath Artifacts in Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Lightwave Technology, <\/span><span class=\"tp_pub_additional_volume\">vol. 39, <\/span><span class=\"tp_pub_additional_number\">no. 17, <\/span><span class=\"tp_pub_additional_pages\">pp. 5573-5581, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_161\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('161','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_161\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('161','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_161\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('161','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_161\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Tanskanen2021,<br \/>\r\ntitle = {Higher-Order Core-Like Modes in Double-Clad Fiber Contribute to Multipath Artifacts in Optical Coherence Tomography},<br \/>\r\nauthor = {Adrian Tanskanen and Geoffrey Hohert and Anthony Lee and Pierre M. Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.1109\/JLT.2021.3088055, DOI},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-09-01},<br \/>\r\nurldate = {2021-09-01},<br \/>\r\njournal = {Journal of Lightwave Technology},<br \/>\r\nvolume = {39},<br \/>\r\nnumber = {17},<br \/>\r\npages = {5573-5581},<br \/>\r\nabstract = {Double-clad fiber (DCF) has enabled the combination of endoscopic optical coherence tomography (OCT) with secondary optical modalities. While DCF offers an additional optical channel, it is widely understood that its use reduces the quality of OCT owing to the introduction of multipath artifacts. We show here that an unexpected higher-order mode (HOM) with its energy confined to the DCF core can contribute to these artifacts. The existence of this HOM is confirmed using the spatially and spectrally (S 2 ) resolved imaging method. The group delay difference of the HOM is shown to be consistent with the delay of the diffuse ghost artifact in DCF-acquired OCT images.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('161','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_161\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Double-clad fiber (DCF) has enabled the combination of endoscopic optical coherence tomography (OCT) with secondary optical modalities. While DCF offers an additional optical channel, it is widely understood that its use reduces the quality of OCT owing to the introduction of multipath artifacts. We show here that an unexpected higher-order mode (HOM) with its energy confined to the DCF core can contribute to these artifacts. The existence of this HOM is confirmed using the spatially and spectrally (S 2 ) resolved imaging method. The group delay difference of the HOM is shown to be consistent with the delay of the diffuse ghost artifact in DCF-acquired OCT images.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('161','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_161\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1109\/JLT.2021.3088055\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('161','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Small airway dilation measured by endoscopic optical coherence tomography correlates with chronic lung allograft dysfunction\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-11.20.32-AM.png\" width=\"128\" alt=\"Small airway dilation measured by endoscopic optical coherence tomography correlates with chronic lung allograft dysfunction\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Malone, Jeanie;  Lee, Anthony M. D.;  Hohert, Geoffrey;  Nador, Roland G.;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.26.7.076005\" title=\"DOI\" target=\"blank\">Small airway dilation measured by endoscopic optical coherence tomography correlates with chronic lung allograft dysfunction<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics , <\/span><span class=\"tp_pub_additional_volume\">vol. 26, <\/span><span class=\"tp_pub_additional_issue\">iss. 7, <\/span><span class=\"tp_pub_additional_number\">no. 076005, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_162\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('162','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_162\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('162','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_162\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('162','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_162\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Malone2021,<br \/>\r\ntitle = {Small airway dilation measured by endoscopic optical coherence tomography correlates with chronic lung allograft dysfunction},<br \/>\r\nauthor = {Jeanie Malone and Anthony M. D. Lee and Geoffrey Hohert and Roland G. Nador and Pierre Lane<br \/>\r\n},<br \/>\r\nurl = {https:\/\/doi.org\/10.1117\/1.JBO.26.7.076005, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/076005_1.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-07-14},<br \/>\r\njournal = {Journal of Biomedical Optics },<br \/>\r\nvolume = {26},<br \/>\r\nnumber = {076005},<br \/>\r\nissue = {7},<br \/>\r\nabstract = {Significance: Chronic lung allograft dysfunction (CLAD) is the leading cause of death in transplant patients who survive past the first year post-transplant. Current diagnosis is based on sustained decline in lung function; there is a need for tools that can identify CLAD onset.<br \/>\r\n<br \/>\r\nAim: Endoscopic optical coherence tomography (OCT) can visualize structural changes in the small airways, which are of interest in CLAD progression. We aim to identify OCT features in the small airways of lung allografts that correlate with CLAD status.<br \/>\r\n<br \/>\r\nApproach: Imaging was conducted with an endoscopic rotary pullback OCT catheter during routine bronchoscopy procedures (n\u2009\u2009=\u2009\u200954), collecting volumetric scans of three segmental airways per patient. Six features of interest were identified, and four blinded raters scored the dataset on the presence and intensity of each feature.<br \/>\r\n<br \/>\r\nResults: Airway dilation (AD) was the only feature found to significantly (p\u2009\u2009&lt;\u2009\u20090.003) correlate with CLAD diagnosis (R\u2009\u2009=\u2009\u20090.40 to 0.61). AD could also be fairly consistently scored between raters (\u03bainter-rater\u2009\u2009=\u2009\u20090.48, \u03baintra-rater\u2009\u2009=\u2009\u20090.64). There is a stronger relationship between AD and the combined obstructive and restrictive (BOS + RAS) phenotypes than the obstructive-only (BOS) phenotype for two raters (R\u2009\u2009=\u2009\u20090.92\u2009\u2009,\u2009\u20090.94).<br \/>\r\n<br \/>\r\nConclusions: OCT examination of small AD shows potential as a diagnostic indicator for CLAD and CLAD phenotype and merits further exploration.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('162','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_162\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Significance: Chronic lung allograft dysfunction (CLAD) is the leading cause of death in transplant patients who survive past the first year post-transplant. Current diagnosis is based on sustained decline in lung function; there is a need for tools that can identify CLAD onset.<br \/>\r\n<br \/>\r\nAim: Endoscopic optical coherence tomography (OCT) can visualize structural changes in the small airways, which are of interest in CLAD progression. We aim to identify OCT features in the small airways of lung allografts that correlate with CLAD status.<br \/>\r\n<br \/>\r\nApproach: Imaging was conducted with an endoscopic rotary pullback OCT catheter during routine bronchoscopy procedures (n\u2009\u2009=\u2009\u200954), collecting volumetric scans of three segmental airways per patient. Six features of interest were identified, and four blinded raters scored the dataset on the presence and intensity of each feature.<br \/>\r\n<br \/>\r\nResults: Airway dilation (AD) was the only feature found to significantly (p\u2009\u2009&lt;\u2009\u20090.003) correlate with CLAD diagnosis (R\u2009\u2009=\u2009\u20090.40 to 0.61). AD could also be fairly consistently scored between raters (\u03bainter-rater\u2009\u2009=\u2009\u20090.48, \u03baintra-rater\u2009\u2009=\u2009\u20090.64). There is a stronger relationship between AD and the combined obstructive and restrictive (BOS + RAS) phenotypes than the obstructive-only (BOS) phenotype for two raters (R\u2009\u2009=\u2009\u20090.92\u2009\u2009,\u2009\u20090.94).<br \/>\r\n<br \/>\r\nConclusions: OCT examination of small AD shows potential as a diagnostic indicator for CLAD and CLAD phenotype and merits further exploration.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('162','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_162\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.26.7.076005\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/076005_1.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('162','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"A Side-Viewing Endoscopic Probe With Distal Micro Rotary Scanner for Multimodal Luminal Imaging and Analysis\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-10.27.11-AM.png\" width=\"128\" alt=\"A Side-Viewing Endoscopic Probe With Distal Micro Rotary Scanner for Multimodal Luminal Imaging and Analysis\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Jayhooni, Sayed Mohammad Hashem;  Hohert, Geoffrey;  Assadsangabi, Babak;  Lane, Pierre M.;  Zeng, Haishan;  Takahata, Kenichi<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1109\/JMEMS.2021.3072617\" title=\"DOI\" target=\"blank\">A Side-Viewing Endoscopic Probe With Distal Micro Rotary Scanner for Multimodal Luminal Imaging and Analysis<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Microelectromechanical Systems, <\/span><span class=\"tp_pub_additional_volume\">vol. 30, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 433-441, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_159\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('159','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_159\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('159','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_159\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('159','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_159\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Jayhooni2021,<br \/>\r\ntitle = {A Side-Viewing Endoscopic Probe With Distal Micro Rotary Scanner for Multimodal Luminal Imaging and Analysis},<br \/>\r\nauthor = {Sayed Mohammad Hashem Jayhooni and Geoffrey Hohert and Babak Assadsangabi and Pierre M. Lane and Haishan Zeng and Kenichi Takahata},<br \/>\r\nurl = {https:\/\/doi.org\/10.1109\/JMEMS.2021.3072617, DOI},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-06-01},<br \/>\r\nurldate = {2021-06-01},<br \/>\r\njournal = {Journal of Microelectromechanical Systems},<br \/>\r\nvolume = {30},<br \/>\r\nnumber = {3},<br \/>\r\npages = {433-441},<br \/>\r\nabstract = {This paper reports a novel micro electromagnetic actuator serving as the distal rotary scanner of an endoscopic probe developed for side-viewing luminal tissue screening and analysis enabled through different endoscopic modalities. The micro rotary optical scanner, for the first time, offers stepwise, low-speed, and high-speed rotational motions to be compatible with endoscopic optical coherence tomography (OCT) and Raman spectroscopy. In comparison with preceding designs, this rotary scanner is shown to provide up to 125\u00d7 higher revolution speeds per power via a ~50% narrower body while limiting its operation temperature within a biologically safe level for in-vivo scanning purposes. A preliminary experiment on human skin tissues is performed using the prototyped side-viewing OCT endoscopic probe equipped with the developed distal scanner. The results demonstrate the probe's ability for real-time 360\u00b0 imaging of live tissue with both high speed and high resolution. These results pave the path for further testing on human internal lumens.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('159','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_159\" style=\"display:none;\"><div class=\"tp_abstract_entry\">This paper reports a novel micro electromagnetic actuator serving as the distal rotary scanner of an endoscopic probe developed for side-viewing luminal tissue screening and analysis enabled through different endoscopic modalities. The micro rotary optical scanner, for the first time, offers stepwise, low-speed, and high-speed rotational motions to be compatible with endoscopic optical coherence tomography (OCT) and Raman spectroscopy. In comparison with preceding designs, this rotary scanner is shown to provide up to 125\u00d7 higher revolution speeds per power via a ~50% narrower body while limiting its operation temperature within a biologically safe level for in-vivo scanning purposes. A preliminary experiment on human skin tissues is performed using the prototyped side-viewing OCT endoscopic probe equipped with the developed distal scanner. The results demonstrate the probe's ability for real-time 360\u00b0 imaging of live tissue with both high speed and high resolution. These results pave the path for further testing on human internal lumens.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('159','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_159\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1109\/JMEMS.2021.3072617\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('159','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Scanning and Actuation Techniques for Cantilever-Based Fiber Optic Endoscopic Scanners\u2014A Review\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-11.29.36-AM.png\" width=\"128\" alt=\"Scanning and Actuation Techniques for Cantilever-Based Fiber Optic Endoscopic Scanners\u2014A Review\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kaur, Mandeep;  Lane, Pierre M.;  Menon, Carlo<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/s21010251\" title=\"DOI\" target=\"blank\">Scanning and Actuation Techniques for Cantilever-Based Fiber Optic Endoscopic Scanners\u2014A Review<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Sensors, <\/span><span class=\"tp_pub_additional_volume\">vol. 21, <\/span><span class=\"tp_pub_additional_issue\">iss. 1, <\/span><span class=\"tp_pub_additional_number\">no. 251, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_163\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('163','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_163\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('163','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_163\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('163','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_163\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kaur2021b,<br \/>\r\ntitle = {Scanning and Actuation Techniques for Cantilever-Based Fiber Optic Endoscopic Scanners\u2014A Review},<br \/>\r\nauthor = {Mandeep Kaur and Pierre M. Lane and Carlo Menon},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/s21010251, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/sensors-21-00251-v2.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-01-02},<br \/>\r\nurldate = {2021-01-02},<br \/>\r\njournal = {Sensors},<br \/>\r\nvolume = {21},<br \/>\r\nnumber = {251},<br \/>\r\nissue = {1},<br \/>\r\nabstract = {Endoscopes are used routinely in modern medicine for in-vivo imaging of luminal organs. Technical advances in the micro-electro-mechanical system (MEMS) and optical fields have enabled the further miniaturization of endoscopes, resulting in the ability to image previously inaccessible small-caliber luminal organs, enabling the early detection of lesions and other abnormalities in these tissues. The development of scanning fiber endoscopes supports the fabrication of small cantilever-based imaging devices without compromising the image resolution. The size of an endoscope is highly dependent on the actuation and scanning method used to illuminate the target image area. Different actuation methods used in the design of small-sized cantilever-based endoscopes are reviewed in this paper along with their working principles, advantages and disadvantages, generated scanning patterns, and applications.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('163','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_163\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Endoscopes are used routinely in modern medicine for in-vivo imaging of luminal organs. Technical advances in the micro-electro-mechanical system (MEMS) and optical fields have enabled the further miniaturization of endoscopes, resulting in the ability to image previously inaccessible small-caliber luminal organs, enabling the early detection of lesions and other abnormalities in these tissues. The development of scanning fiber endoscopes supports the fabrication of small cantilever-based imaging devices without compromising the image resolution. The size of an endoscope is highly dependent on the actuation and scanning method used to illuminate the target image area. Different actuation methods used in the design of small-sized cantilever-based endoscopes are reviewed in this paper along with their working principles, advantages and disadvantages, generated scanning patterns, and applications.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('163','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_163\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/s21010251\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/sensors-21-00251-v2.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('163','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2020\">2020<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fiber optic endoscopic optical coherence tomography (OCT) to assess human airways: The relationship between anatomy and physiological function during dynamic exercise\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-10.24.43-AM-1.png\" width=\"128\" alt=\"Fiber optic endoscopic optical coherence tomography (OCT) to assess human airways: The relationship between anatomy and physiological function during dynamic exercise\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Peters, Carli M.;  Molgat-Seon, Yannick;  Dominelli, Paolo B.;  Lee, Anthony M. D.;  Lane, Pierre;  Lam, Stephen;  Sheel, Andrew W.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Physiological-Reports-2021-Peters-Fiber-optic-endoscopic-optical-coherence-tomography-OCT-to-assess-human-airways-.pdf\" title=\"Full Text (PDF)\" target=\"blank\">Fiber optic endoscopic optical coherence tomography (OCT) to assess human airways: The relationship between anatomy and physiological function during dynamic exercise<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Physiological Reports, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_issue\">iss. 1, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_158\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('158','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_158\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('158','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_158\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('158','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_158\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Peters2020,<br \/>\r\ntitle = {Fiber optic endoscopic optical coherence tomography (OCT) to assess human airways: The relationship between anatomy and physiological function during dynamic exercise},<br \/>\r\nauthor = {Carli M. Peters and Yannick Molgat-Seon and Paolo B. Dominelli and Anthony M. D. Lee and Pierre Lane and Stephen Lam and Andrew W. Sheel},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Physiological-Reports-2021-Peters-Fiber-optic-endoscopic-optical-coherence-tomography-OCT-to-assess-human-airways-.pdf, Full Text (PDF)<br \/>\r\nhttps:\/\/doi.org\/10.14814\/phy2.14657, DOI},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-12-28},<br \/>\r\nurldate = {2020-12-28},<br \/>\r\njournal = {Physiological Reports},<br \/>\r\nvolume = {9},<br \/>\r\nissue = {1},<br \/>\r\nabstract = {Airway luminal area (Ai) influences respiratory mechanics during dynamic exercise; however, previous studies have investigated the relationship between airway anatomy and physiological function in different groups of individuals. The purpose of this study was to determine the effect of Ai on respiratory mechanics by making in vivo measures of airway dimensions and work of breathing (Wb) in the same individuals. Healthy participants (3F\/2M; 23\u201345 years) completed a cycle exercise test to exhaustion. During exercise, Wb was assessed using an esophageal balloon catheter, while simultaneously assessing minute ventilation (urn:x-wiley:2051817X:media:phy214657:phy214657-math-0001E). On a separate day, subjects underwent a bronchoscopy procedure to capture optical coherence tomography (OCT) measures of three airways in the right lung. Each participant's Wb-urn:x-wiley:2051817X:media:phy214657:phy214657-math-0002E data were fit to a non-linear regression equation (Wb = aurn:x-wiley:2051817X:media:phy214657:phy214657-math-0003E3 + burn:x-wiley:2051817X:media:phy214657:phy214657-math-0004E2) that partitions Wb into its turbulent resistive (a) and viscoelastic (b) components. Measures of Ai and luminal diameter were made for the 4th\u20136th airway generations. A composite index of airway size was calculated as the sum of the Ai for each generation and the total area of the 4th\u20136th generation was calculated based on Weibel's model. Constant a was significantly correlated to the Weibel model total airway area (r = \u22120.94, p = 0.017) and index of airway size (r = \u22120.929, p = 0.023), whereas constant b was not associated with either measure (both p &gt; 0.05). We found that individuals who had the smallest Ai had the highest resistive Wb and our findings provide the basis for further study of the relationship between airway size and respiratory mechanics during exercise.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('158','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_158\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Airway luminal area (Ai) influences respiratory mechanics during dynamic exercise; however, previous studies have investigated the relationship between airway anatomy and physiological function in different groups of individuals. The purpose of this study was to determine the effect of Ai on respiratory mechanics by making in vivo measures of airway dimensions and work of breathing (Wb) in the same individuals. Healthy participants (3F\/2M; 23\u201345 years) completed a cycle exercise test to exhaustion. During exercise, Wb was assessed using an esophageal balloon catheter, while simultaneously assessing minute ventilation (urn:x-wiley:2051817X:media:phy214657:phy214657-math-0001E). On a separate day, subjects underwent a bronchoscopy procedure to capture optical coherence tomography (OCT) measures of three airways in the right lung. Each participant's Wb-urn:x-wiley:2051817X:media:phy214657:phy214657-math-0002E data were fit to a non-linear regression equation (Wb = aurn:x-wiley:2051817X:media:phy214657:phy214657-math-0003E3 + burn:x-wiley:2051817X:media:phy214657:phy214657-math-0004E2) that partitions Wb into its turbulent resistive (a) and viscoelastic (b) components. Measures of Ai and luminal diameter were made for the 4th\u20136th airway generations. A composite index of airway size was calculated as the sum of the Ai for each generation and the total area of the 4th\u20136th generation was calculated based on Weibel's model. Constant a was significantly correlated to the Weibel model total airway area (r = \u22120.94, p = 0.017) and index of airway size (r = \u22120.929, p = 0.023), whereas constant b was not associated with either measure (both p &gt; 0.05). We found that individuals who had the smallest Ai had the highest resistive Wb and our findings provide the basis for further study of the relationship between airway size and respiratory mechanics during exercise.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('158','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_158\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Physiological-Reports-2021-Peters-Fiber-optic-endoscopic-optical-coherence-tomography-OCT-to-assess-human-airways-.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.14814\/phy2.14657\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('158','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Feasibility of combined optical coherence tomography and autofluorescence imaging for visualization of needle biopsy placement\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-12.20.04-PM.png\" width=\"128\" alt=\"Feasibility of combined optical coherence tomography and autofluorescence imaging for visualization of needle biopsy placement\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Hohert, Geoffrey;  Myers, Renelle;  Lam, Sylvia;  Vertikov, Andrei;  Lee, Anthony;  Lam, Stephen;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1117\/1.jbo.25.10.106003\" title=\"DOI\" target=\"blank\">Feasibility of combined optical coherence tomography and autofluorescence imaging for visualization of needle biopsy placement<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics , <\/span><span class=\"tp_pub_additional_volume\">vol. 25, <\/span><span class=\"tp_pub_additional_issue\">iss. 10, <\/span><span class=\"tp_pub_additional_number\">no. 106003, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_164\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('164','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_164\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('164','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_164\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('164','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_164\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Hohert2020,<br \/>\r\ntitle = {Feasibility of combined optical coherence tomography and autofluorescence imaging for visualization of needle biopsy placement},<br \/>\r\nauthor = {Geoffrey Hohert and Renelle Myers and Sylvia Lam and Andrei Vertikov and Anthony Lee and Stephen Lam and Pierre Lane},<br \/>\r\nurl = {https:\/\/doi.org\/10.1117\/1.jbo.25.10.106003, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/106003_1.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-10-20},<br \/>\r\njournal = {Journal of Biomedical Optics },<br \/>\r\nvolume = {25},<br \/>\r\nnumber = {106003},<br \/>\r\nissue = {10},<br \/>\r\nabstract = {Significance: Diagnosis of suspicious lung nodules requires precise collection of relevant biopsies for histopathological analysis. Using optical coherence tomography and autofluorescence imaging (OCT-AFI) to improve diagnostic yield in parts of the lung inaccessible to larger imaging methods may allow for reducing complications related to the alternative of computed tomography-guided biopsy.<br \/>\r\n<br \/>\r\nAim: Feasibility of OCT-AFI combined with a commercially available lung biopsy needle was demonstrated for visualization of needle puncture sites in airways with diameters as small as 1.9 mm.<br \/>\r\n<br \/>\r\nApproach: A miniaturized OCT-AFI imaging stylet was developed to be inserted through an 18G biopsy needle. We present design considerations and procedure development for image-guided biopsy. Ex vivo and in vivo porcine studies were performed to demonstrate the feasibility of the procedure and the device.<br \/>\r\n<br \/>\r\nResults: OCT-AFI scans were obtained ex vivo and in vivo. Discrimination of pullback site is clear.<br \/>\r\n<br \/>\r\nConclusions: Use of the device is shown to be feasible in vivo. Images obtained show the stylet is effective at providing structural information at the puncture site that can be used to assess the diagnostic potential of the sample prior to collection.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('164','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_164\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Significance: Diagnosis of suspicious lung nodules requires precise collection of relevant biopsies for histopathological analysis. Using optical coherence tomography and autofluorescence imaging (OCT-AFI) to improve diagnostic yield in parts of the lung inaccessible to larger imaging methods may allow for reducing complications related to the alternative of computed tomography-guided biopsy.<br \/>\r\n<br \/>\r\nAim: Feasibility of OCT-AFI combined with a commercially available lung biopsy needle was demonstrated for visualization of needle puncture sites in airways with diameters as small as 1.9 mm.<br \/>\r\n<br \/>\r\nApproach: A miniaturized OCT-AFI imaging stylet was developed to be inserted through an 18G biopsy needle. We present design considerations and procedure development for image-guided biopsy. Ex vivo and in vivo porcine studies were performed to demonstrate the feasibility of the procedure and the device.<br \/>\r\n<br \/>\r\nResults: OCT-AFI scans were obtained ex vivo and in vivo. Discrimination of pullback site is clear.<br \/>\r\n<br \/>\r\nConclusions: Use of the device is shown to be feasible in vivo. Images obtained show the stylet is effective at providing structural information at the puncture site that can be used to assess the diagnostic potential of the sample prior to collection.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('164','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_164\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1117\/1.jbo.25.10.106003\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/106003_1.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('164','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Endoscopic Optical Imaging Technologies and Devices for Medical Purposes: State of the Art\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-12.29.06-PM.png\" width=\"128\" alt=\"Endoscopic Optical Imaging Technologies and Devices for Medical Purposes: State of the Art\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kaur, Mandeep;  Lane, Pierre M.;  Menon, Carlo<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.3390\/app10196865\" title=\"DOI\" target=\"blank\">Endoscopic Optical Imaging Technologies and Devices for Medical Purposes: State of the Art<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Applied Science, <\/span><span class=\"tp_pub_additional_volume\">vol. 10, <\/span><span class=\"tp_pub_additional_issue\">iss. 19, <\/span><span class=\"tp_pub_additional_number\">no. 6865, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_166\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('166','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_166\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('166','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_166\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('166','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_166\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kaur2020b,<br \/>\r\ntitle = {Endoscopic Optical Imaging Technologies and Devices for Medical Purposes: State of the Art},<br \/>\r\nauthor = {Mandeep Kaur and Pierre M. Lane and Carlo Menon},<br \/>\r\nurl = {https:\/\/doi.org\/10.3390\/app10196865, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/applsci-10-06865-v2.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-09-29},<br \/>\r\njournal = {Applied Science},<br \/>\r\nvolume = {10},<br \/>\r\nnumber = {6865},<br \/>\r\nissue = {19},<br \/>\r\nabstract = {The growth and development of optical components and, in particular, the miniaturization of micro-electro-mechanical systems (MEMSs), has motivated and enabled researchers to design smaller and smaller endoscopes. The overarching goal of this work has been to image smaller previously inaccessible luminal organs in real time, at high resolution, in a minimally invasive manner that does not compromise the comfort of the subject, nor introduce additional risk. Thus, an initial diagnosis can be made, or a small precancerous lesion may be detected, in a small-diameter luminal organ that would not have otherwise been possible. Continuous advancement in the field has enabled a wide range of optical scanners. Different scanning techniques, working principles, and the applications of endoscopic scanners are summarized in this review. },<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('166','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_166\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The growth and development of optical components and, in particular, the miniaturization of micro-electro-mechanical systems (MEMSs), has motivated and enabled researchers to design smaller and smaller endoscopes. The overarching goal of this work has been to image smaller previously inaccessible luminal organs in real time, at high resolution, in a minimally invasive manner that does not compromise the comfort of the subject, nor introduce additional risk. Thus, an initial diagnosis can be made, or a small precancerous lesion may be detected, in a small-diameter luminal organ that would not have otherwise been possible. Continuous advancement in the field has enabled a wide range of optical scanners. Different scanning techniques, working principles, and the applications of endoscopic scanners are summarized in this review. <\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('166','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_166\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/app10196865\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/applsci-10-06865-v2.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('166','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"An Electro-Thermally Actuated Micro-Cantilever-Based Fiber Optic Scanner\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-12.25.11-PM.png\" width=\"128\" alt=\"An Electro-Thermally Actuated Micro-Cantilever-Based Fiber Optic Scanner\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kaur, Mandeep;  Brown, Malcolm;  Lane, Pierre M.;  Menon, Carlo<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1109\/JSEN.2020.2992371\" title=\"DOI\" target=\"blank\">An Electro-Thermally Actuated Micro-Cantilever-Based Fiber Optic Scanner<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">IEEE Sensors Journal , <\/span><span class=\"tp_pub_additional_volume\">vol. 20, <\/span><span class=\"tp_pub_additional_issue\">iss. 17, <\/span><span class=\"tp_pub_additional_pages\">pp. 9877-9885, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_165\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('165','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_165\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('165','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_165\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('165','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_165\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kaur2020,<br \/>\r\ntitle = {An Electro-Thermally Actuated Micro-Cantilever-Based Fiber Optic Scanner},<br \/>\r\nauthor = {Mandeep Kaur and Malcolm Brown and Pierre M. Lane and Carlo Menon},<br \/>\r\nurl = {https:\/\/doi.org\/10.1109\/JSEN.2020.2992371, DOI},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-09-01},<br \/>\r\nurldate = {2020-09-01},<br \/>\r\njournal = {IEEE Sensors Journal },<br \/>\r\nvolume = {20},<br \/>\r\nissue = {17},<br \/>\r\npages = {9877-9885},<br \/>\r\nabstract = {A sub-millimeter sized optical scanner driven by electro-thermal actuation is presented. The scanner is composed of a single-mode optical fiber (SMF) with a cantilevered section at its distal tip. The fiber cantilever is electrothermally actuated near its base in a single direction and excited at resonance to obtain large deflectionsat the tip of the fiber. Two-dimensional imaging of an object is demonstrated by simultaneously rotating the object while scanning across its diameter. Illumination light from the optical core of the fiber cantilever is projected through a lens onto the object. Reflected light is collected by the same lens and projected onto a photodetector. An image of the object is reconstructed by interpolation of the detected signal. The resolution of the system was measured to be 16\u03bcm by imaging a resolution target. The electro-thermal fiber actuator may provide a new technique for scanning in sub-millimeter sized forward-viewing endoscopic catheters.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('165','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_165\" style=\"display:none;\"><div class=\"tp_abstract_entry\">A sub-millimeter sized optical scanner driven by electro-thermal actuation is presented. The scanner is composed of a single-mode optical fiber (SMF) with a cantilevered section at its distal tip. The fiber cantilever is electrothermally actuated near its base in a single direction and excited at resonance to obtain large deflectionsat the tip of the fiber. Two-dimensional imaging of an object is demonstrated by simultaneously rotating the object while scanning across its diameter. Illumination light from the optical core of the fiber cantilever is projected through a lens onto the object. Reflected light is collected by the same lens and projected onto a photodetector. An image of the object is reconstructed by interpolation of the detected signal. The resolution of the system was measured to be 16\u03bcm by imaging a resolution target. The electro-thermal fiber actuator may provide a new technique for scanning in sub-millimeter sized forward-viewing endoscopic catheters.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('165','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_165\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1109\/JSEN.2020.2992371\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('165','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2019\">2019<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Submillimeter diameter rotary-pullback fiber-optic endoscope for narrowband red-green-blue reflectance, optical coherence tomography, and autofluorescence in vivo imaging\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Screen-Shot-2022-02-11-at-12.32.19-PM.png\" width=\"128\" alt=\"Submillimeter diameter rotary-pullback fiber-optic endoscope for narrowband red-green-blue reflectance, optical coherence tomography, and autofluorescence in vivo imaging\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Buenconsejo, Andrea Louise;  Hohert, Geoffrey;  Manning, Max;  Abouei, Elham;  Tingley, Reid;  Janzen, Ian;  McAlpine, Jessica;  Miller, Dianne;  Lee, Anthony;  Lane, Pierre;  MacAulay, Calum<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.25.3.032005\" title=\"DOI\" target=\"blank\">Submillimeter diameter rotary-pullback fiber-optic endoscope for narrowband red-green-blue reflectance, optical coherence tomography, and autofluorescence in vivo imaging<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics , <\/span><span class=\"tp_pub_additional_volume\">vol. 25, <\/span><span class=\"tp_pub_additional_issue\">iss. 3, <\/span><span class=\"tp_pub_additional_number\">no. 032005, <\/span><span class=\"tp_pub_additional_year\">2019<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_167\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('167','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_167\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('167','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_167\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('167','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_167\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Buenconsejo2019,<br \/>\r\ntitle = {Submillimeter diameter rotary-pullback fiber-optic endoscope for narrowband red-green-blue reflectance, optical coherence tomography, and autofluorescence in vivo imaging},<br \/>\r\nauthor = {Andrea Louise Buenconsejo and Geoffrey Hohert and Max Manning and Elham Abouei and Reid Tingley and Ian Janzen and Jessica McAlpine and Dianne Miller and Anthony Lee and Pierre Lane and Calum MacAulay},<br \/>\r\nurl = {https:\/\/doi.org\/10.1117\/1.JBO.25.3.032005, DOI<br \/>\r\nhttps:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/032005_1.pdf, Full Text (PDF)},<br \/>\r\nyear  = {2019},<br \/>\r\ndate = {2019-10-24},<br \/>\r\nurldate = {2019-10-24},<br \/>\r\njournal = {Journal of Biomedical Optics },<br \/>\r\nvolume = {25},<br \/>\r\nnumber = {032005},<br \/>\r\nissue = {3},<br \/>\r\nabstract = {A fiber-based endoscopic imaging system combining narrowband red-green-blue (RGB) reflectance with optical coherence tomography (OCT) and autofluorescence imaging (AFI) has been developed. The system uses a submillimeter diameter rotary-pullback double-clad fiber imaging catheter for sample illumination and detection. The imaging capabilities of each modality are presented and demonstrated with images of a multicolored card, fingerprints, and tongue mucosa. Broadband imaging, which was done to compare with narrowband sources, revealed better contrast but worse color consistency compared with narrowband RGB reflectance. The measured resolution of the endoscopic system is 25\u2009\u2009\u03bcm in both the rotary direction and the pullback direction. OCT can be performed simultaneously with either narrowband RGB reflectance imaging or AFI.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('167','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_167\" style=\"display:none;\"><div class=\"tp_abstract_entry\">A fiber-based endoscopic imaging system combining narrowband red-green-blue (RGB) reflectance with optical coherence tomography (OCT) and autofluorescence imaging (AFI) has been developed. The system uses a submillimeter diameter rotary-pullback double-clad fiber imaging catheter for sample illumination and detection. The imaging capabilities of each modality are presented and demonstrated with images of a multicolored card, fingerprints, and tongue mucosa. Broadband imaging, which was done to compare with narrowband sources, revealed better contrast but worse color consistency compared with narrowband RGB reflectance. The measured resolution of the endoscopic system is 25\u2009\u2009\u03bcm in both the rotary direction and the pullback direction. OCT can be performed simultaneously with either narrowband RGB reflectance imaging or AFI.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('167','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_167\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1117\/1.JBO.25.3.032005\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/032005_1.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('167','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"An Electro-Thermal Actuation Method for Resonance Vibration of a Miniaturized Optical-Fiber Scanner for Future Scanning Fiber Endoscope Design\" src=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2019\/03\/Ahrabi-2019-e1551909151829.jpg\" width=\"128\" alt=\"An Electro-Thermal Actuation Method for Resonance Vibration of a Miniaturized Optical-Fiber Scanner for Future Scanning Fiber Endoscope Design\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Ahrabi, Aydin Aghajanzadeh;  Kaur, Mandeep;  Li, Yasong;  Lane, Pierre;  Menon, Carlo<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2019\/03\/Ahrabi-2019.pdf\" title=\"Full Text (PDF)\" target=\"blank\">An Electro-Thermal Actuation Method for Resonance Vibration of a Miniaturized Optical-Fiber Scanner for Future Scanning Fiber Endoscope Design<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Actuators, <\/span><span class=\"tp_pub_additional_volume\">vol. 8, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_year\">2019<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_156\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('156','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_156\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('156','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_156\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('156','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_156\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Ahrabi2019,<br \/>\r\ntitle = {An Electro-Thermal Actuation Method for Resonance Vibration of a Miniaturized Optical-Fiber Scanner for Future Scanning Fiber Endoscope Design},<br \/>\r\nauthor = {Aydin Aghajanzadeh Ahrabi and Mandeep Kaur and Yasong Li and Pierre Lane and Carlo Menon},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2019\/03\/Ahrabi-2019.pdf, Full Text (PDF)<br \/>\r\nhttps:\/\/doi.org\/10.3390\/act8010021, DOI},<br \/>\r\nyear  = {2019},<br \/>\r\ndate = {2019-03-01},<br \/>\r\njournal = {Actuators},<br \/>\r\nvolume = {8},<br \/>\r\nnumber = {1},<br \/>\r\nabstract = {Medical professionals increasingly rely on endoscopes to carry out many minimally invasive procedures on patients to safely examine, diagnose, and treat a large variety of conditions. However, their insertion tube diameter dictates which passages of the body they can be inserted into and, consequently, what organs they can access. For inaccessible areas and organs, patients often undergo invasive and risky procedures\u2014diagnostic confirmation of peripheral lung nodules via transthoracic needle biopsy is one example from oncology. Hence, this work sets out to present an optical-fiber scanner for a scanning fiber endoscope design that has an insertion tube diameter of about 0.5 mm, small enough to be inserted into the smallest airways of the lung. To attain this goal, a novel approach based on resonance thermal excitation of a single-mode 0.01-mm-diameter fiber-optic cantilever oscillating at 2\u20134 kHz is proposed. The small size of the electro-thermal actuator enables miniaturization of the insertion tube. Lateral free-end deflection of the cantilever is used as a benchmark for evaluating performance. Experimental results show that the cantilever can achieve over 0.2 mm of displacement at its free end. The experimental results also support finite element simulation models which can be used for future design iterations of the endoscope.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('156','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_156\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Medical professionals increasingly rely on endoscopes to carry out many minimally invasive procedures on patients to safely examine, diagnose, and treat a large variety of conditions. However, their insertion tube diameter dictates which passages of the body they can be inserted into and, consequently, what organs they can access. For inaccessible areas and organs, patients often undergo invasive and risky procedures\u2014diagnostic confirmation of peripheral lung nodules via transthoracic needle biopsy is one example from oncology. Hence, this work sets out to present an optical-fiber scanner for a scanning fiber endoscope design that has an insertion tube diameter of about 0.5 mm, small enough to be inserted into the smallest airways of the lung. To attain this goal, a novel approach based on resonance thermal excitation of a single-mode 0.01-mm-diameter fiber-optic cantilever oscillating at 2\u20134 kHz is proposed. The small size of the electro-thermal actuator enables miniaturization of the insertion tube. Lateral free-end deflection of the cantilever is used as a benchmark for evaluating performance. Experimental results show that the cantilever can achieve over 0.2 mm of displacement at its free end. The experimental results also support finite element simulation models which can be used for future design iterations of the endoscope.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('156','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_156\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2019\/03\/Ahrabi-2019.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.3390\/act8010021\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('156','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2018\">2018<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Depth-multiplexed optical coherence  tomography dual-beam manually-actuated  distortion-corrected imaging (DMDI) with a  micromotor catheter\" src=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Lee-2018.jpg\" width=\"128\" alt=\"Depth-multiplexed optical coherence  tomography dual-beam manually-actuated  distortion-corrected imaging (DMDI) with a  micromotor catheter\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony M. D.;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Lee-2018.pdf\" title=\"Full Text (PDF)\" target=\"blank\">Depth-multiplexed optical coherence  tomography dual-beam manually-actuated  distortion-corrected imaging (DMDI) with a  micromotor catheter<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 5678-5690, <\/span><span class=\"tp_pub_additional_year\">2018<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_155\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('155','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_155\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('155','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_155\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('155','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_155\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Lee2018,<br \/>\r\ntitle = {Depth-multiplexed optical coherence  tomography dual-beam manually-actuated  distortion-corrected imaging (DMDI) with a  micromotor catheter},<br \/>\r\nauthor = { Anthony M.D. Lee and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Lee-2018.pdf, Full Text (PDF)<br \/>\r\nhttps:\/\/doi.org\/10.1364\/BOE.9.005678, DOI},<br \/>\r\nyear  = {2018},<br \/>\r\ndate = {2018-11-01},<br \/>\r\njournal = {Optics Express},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {11},<br \/>\r\npages = {5678-5690},<br \/>\r\nabstract = {We present a new micromotor catheter implementation of dual-beam manuallyactuated distortion-corrected imaging (DMDI). The new catheter, called a depth-multiplexed dual-beam micromotor catheter, or mDBMC, maintains the primary advantage of unlimited field-of-view distortion-corrected imaging along the catheter axis. The mDBMC uses a polarization beam splitter and cube mirror to create two beams that scan circularly with approximately constant separation at the catheter surface. This arrangement also multiplexes both imaging channels into a single optical coherence tomography channel by offsetting them in depth, requiring half the data bandwidth compared to previous DMDI demonstrations that used two parallel image acquisition systems. Furthermore, the relatively simple scanning pattern of the two beams enables a straightforward automated distortion correction algorithm. We demonstrate the imaging capabilities of this catheter with a printed paper phantom and in a section of dragon fruit.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('155','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_155\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a new micromotor catheter implementation of dual-beam manuallyactuated distortion-corrected imaging (DMDI). The new catheter, called a depth-multiplexed dual-beam micromotor catheter, or mDBMC, maintains the primary advantage of unlimited field-of-view distortion-corrected imaging along the catheter axis. The mDBMC uses a polarization beam splitter and cube mirror to create two beams that scan circularly with approximately constant separation at the catheter surface. This arrangement also multiplexes both imaging channels into a single optical coherence tomography channel by offsetting them in depth, requiring half the data bandwidth compared to previous DMDI demonstrations that used two parallel image acquisition systems. Furthermore, the relatively simple scanning pattern of the two beams enables a straightforward automated distortion correction algorithm. We demonstrate the imaging capabilities of this catheter with a printed paper phantom and in a section of dragon fruit.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('155','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_155\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Lee-2018.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1364\/BOE.9.005678\" title=\"DOI\" target=\"_blank\">DOI<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('155','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Dual-beam manually actuated distortion corrected imaging (DMDI): two dimensional scanning with a single-axis galvanometer\" src=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Harlow-2018.jpg\" width=\"128\" alt=\"Dual-beam manually actuated distortion corrected imaging (DMDI): two dimensional scanning with a single-axis galvanometer\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Harlow, Madeline;  MacAulay, Calum;  Lane, Pierre;  Lee, Anthony M. D.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.26.018758\" title=\"Dual-beam manually actuated distortion corrected imaging (DMDI): two dimensional scanning with a single-axis galvanometer\" target=\"blank\">Dual-beam manually actuated distortion corrected imaging (DMDI): two dimensional scanning with a single-axis galvanometer<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 26, <\/span><span class=\"tp_pub_additional_number\">no. 14, <\/span><span class=\"tp_pub_additional_pages\">pp. 18758-18772, <\/span><span class=\"tp_pub_additional_year\">2018<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_154\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('154','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_154\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('154','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_154\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('154','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_154\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Harlow2018,<br \/>\r\ntitle = {Dual-beam manually actuated distortion corrected imaging (DMDI): two dimensional scanning with a single-axis galvanometer},<br \/>\r\nauthor = {Madeline Harlow and Calum MacAulay and Pierre Lane and Anthony M.D. Lee<br \/>\r\n},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Harlow-2018.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1364\/OE.26.018758},<br \/>\r\nyear  = {2018},<br \/>\r\ndate = {2018-07-09},<br \/>\r\njournal = {Optics Express},<br \/>\r\nvolume = {26},<br \/>\r\nnumber = {14},<br \/>\r\npages = {18758-18772},<br \/>\r\nabstract = {We recently demonstrated a new two-dimensional imaging paradigm called dual-beam manually actuated distortion-corrected imaging (DMDI). This technique uses a single mechanical scanner and two spatially separated beams to determine relative sample velocity and simultaneously corrects image distortions due to manual actuation. DMDI was first demonstrated using a rotating dual-beam micromotor catheter. Here, we present a new<br \/>\r\nimplementation of DMDI using a single axis galvanometer to scan a pair of beams in approximately parallel lines onto a sample. Furthermore, we present a method for automated distortion correction based on frame co-registration between images acquired by the two beams. Distortion correction is possible for manually actuated motion both perpendicular and parallel to the galvanometer-scanned lines. Using en face OCT as the imaging modality, we demonstrate DMDI and the automated distortion correction algorithm for imaging a printed<br \/>\r\npaper phantom, a dragon fruit, and a fingerprint.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('154','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_154\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We recently demonstrated a new two-dimensional imaging paradigm called dual-beam manually actuated distortion-corrected imaging (DMDI). This technique uses a single mechanical scanner and two spatially separated beams to determine relative sample velocity and simultaneously corrects image distortions due to manual actuation. DMDI was first demonstrated using a rotating dual-beam micromotor catheter. Here, we present a new<br \/>\r\nimplementation of DMDI using a single axis galvanometer to scan a pair of beams in approximately parallel lines onto a sample. Furthermore, we present a method for automated distortion correction based on frame co-registration between images acquired by the two beams. Distortion correction is possible for manually actuated motion both perpendicular and parallel to the galvanometer-scanned lines. Using en face OCT as the imaging modality, we demonstrate DMDI and the automated distortion correction algorithm for imaging a printed<br \/>\r\npaper phantom, a dragon fruit, and a fingerprint.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('154','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_154\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Harlow-2018.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.26.018758\" title=\"Follow DOI:10.1364\/OE.26.018758\" target=\"_blank\">doi:10.1364\/OE.26.018758<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('154','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Correction of motion artifacts in endoscopic optical coherence tomography and autofluorescence images based on azimuthal en face image registration\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Abouei-2018.jpg\" width=\"128\" alt=\"Correction of motion artifacts in endoscopic optical coherence tomography and autofluorescence images based on azimuthal en face image registration\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Abouei, Elham;  Lee, Anthony M. D.;  Pahlevaninezhad, Hamid;  Hohert, Geoffrey;  Cua, Michelle;  Lane, Pierre;  Lam, Stephen;  MacAulay, Calum<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.23.1.016004\" title=\"Correction of motion artifacts in endoscopic optical coherence tomography and autofluorescence images based on azimuthal en face image registration\" target=\"blank\">Correction of motion artifacts in endoscopic optical coherence tomography and autofluorescence images based on azimuthal en face image registration<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 23, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. 016004, <\/span><span class=\"tp_pub_additional_year\">2018<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_153\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('153','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_153\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('153','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_153\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('153','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_153\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Abouei2018,<br \/>\r\ntitle = {Correction of motion artifacts in endoscopic optical coherence tomography and autofluorescence images based on azimuthal en face image registration},<br \/>\r\nauthor = {Elham Abouei and Anthony M. D. Lee and Hamid Pahlevaninezhad and Geoffrey Hohert and Michelle Cua and Pierre Lane and Stephen Lam and Calum MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Abouei-2018.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1117\/1.JBO.23.1.016004},<br \/>\r\nyear  = {2018},<br \/>\r\ndate = {2018-01-04},<br \/>\r\njournal = {Journal of Biomedical Optics},<br \/>\r\nvolume = {23},<br \/>\r\nnumber = {1},<br \/>\r\npages = {016004},<br \/>\r\nabstract = {We present a method for the correction of motion artifacts present in two- and three-dimensional in vivo endoscopic images produced by rotary-pullback catheters. This method can correct for cardiac \/ breathing based motion artifacts and catheter-based motion artifacts such as nonuniform rotational distortion (NURD). This method assumes that en face tissue imaging contains slowly varying structures that are roughly parallel to the pullback axis. The method reduces motion artifacts using a dynamic time warping solution through a cost matrix that measures similarities between adjacent frames in en face images. We optimize and demonstrate the suitability of this method using a real and simulated NURD phantom and in vivo endoscopic pulmonary optical coherence tomography and autofluorescence images. Qualitative and quantitative evaluations of the method show an enhancement of the image quality.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('153','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_153\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a method for the correction of motion artifacts present in two- and three-dimensional in vivo endoscopic images produced by rotary-pullback catheters. This method can correct for cardiac \/ breathing based motion artifacts and catheter-based motion artifacts such as nonuniform rotational distortion (NURD). This method assumes that en face tissue imaging contains slowly varying structures that are roughly parallel to the pullback axis. The method reduces motion artifacts using a dynamic time warping solution through a cost matrix that measures similarities between adjacent frames in en face images. We optimize and demonstrate the suitability of this method using a real and simulated NURD phantom and in vivo endoscopic pulmonary optical coherence tomography and autofluorescence images. Qualitative and quantitative evaluations of the method show an enhancement of the image quality.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('153','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_153\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Abouei-2018.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.23.1.016004\" title=\"Follow DOI:10.1117\/1.JBO.23.1.016004\" target=\"_blank\">doi:10.1117\/1.JBO.23.1.016004<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('153','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2017\">2017<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Established and Emerging Optical Technologies for the Real-Time Detection of Cervical Neoplasia: A Review\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Hill-2017.jpg\" width=\"128\" alt=\"Established and Emerging Optical Technologies for the Real-Time Detection of Cervical Neoplasia: A Review\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Hill, Breana;  Lam, Sylvia F;  Lane, Pierre;  MacAulay, Calum;  Fradkin, Leonid;  Follen, Michele<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.4236\/jct.2017.813105\" title=\"Established and Emerging Optical Technologies for the Real-Time Detection of Cervical Neoplasia: A Review\" target=\"blank\">Established and Emerging Optical Technologies for the Real-Time Detection of Cervical Neoplasia: A Review<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Cancer Therapy, <\/span><span class=\"tp_pub_additional_volume\">vol. 8, <\/span><span class=\"tp_pub_additional_pages\">pp. 1241-1278, <\/span><span class=\"tp_pub_additional_year\">2017<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_152\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('152','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_152\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('152','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_152\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('152','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_152\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Hill12017,<br \/>\r\ntitle = {Established and Emerging Optical Technologies for the Real-Time Detection of Cervical Neoplasia: A Review},<br \/>\r\nauthor = {Breana Hill and Sylvia F Lam and Pierre Lane and Calum MacAulay and Leonid Fradkin and<br \/>\r\nMichele Follen},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Hill-2017.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.4236\/jct.2017.813105},<br \/>\r\nyear  = {2017},<br \/>\r\ndate = {2017-12-21},<br \/>\r\njournal = {Journal of Cancer Therapy},<br \/>\r\nvolume = {8},<br \/>\r\npages = {1241-1278},<br \/>\r\nabstract = {Cervical cancer remains a critically important problem for women, especially those women in the developing world where the case-fatality rate is high. There are an estimated 528,000 cases and 266,000 deaths worldwide. Established screening and detection programs in the developed world have lowered the mortality from 40\/100,000 to 2\/100,000 over the last 60 years. The standard of care has been and continues to be: a screening Papanicolaou smear with or without Human Papilloma Virus (HPV) testing; followed by colposcopy and biopsies and if the smear is abnormal; and followed by treatment if the biopsies show high grade disease (cervical intraepithelial neoplasia (CIN) grades 2 and 3 and Carcinoma-in-situ). Low grade lesions (Pap smears with Atypical Cells of Uncertain Significance (ASCUS), Low Grade Squamous Intraepithelial Lesions (LGSIL), biopsies showing HPV changes or showing CIN 1); are usually followed for two years and then treated if persistent. Treatment can be performed with loop excision, LASER, or cryotherapy. Loop excision yields a specimen which can be reviewed to establish the diagnosis more accurately. LASER vaporizes the lesion and cryotherapy leads to tissue destruction. Under long term study; loop excision, LASER, and cryotherapy have the same rate of cure. The standard of care is expensive and takes 6 - 12 weeks for the individual patient. During the last twenty years, new technologies that can view the cervix and even image the cervix with cellular resolution have been developed. These technologies could lead to a new paradigm in which diagnosis and treatment occurs at a single visit. These technologies include fluorescence and reflectance spectroscopy (probe or wide-field, whole cervix scanning approaches) and fluorescence confocal endomicroscopy or high resolution micro-endoscopy. Both technologies have received Federal Drug Administration (FDA) and have been commercialized. Research trials continue to show their remarkable performance. These technologies are reviewed and clinical trials are summarized. Emerging technologies are coming along that may compete with those already approved and include optical coherence tomography, optical coherence tomography with autofluorescence, diffuse optical microscopy, and dual mode micro-endoscopy. These technologies are also reviewed and where available, clinical data is reported. Optical technologies are ready to diffuse into clinical practice because they will save money and 3 or 4 visits in the developed world and offer the same standard of care to the developing world where more cervical cancer exists. },<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('152','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_152\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Cervical cancer remains a critically important problem for women, especially those women in the developing world where the case-fatality rate is high. There are an estimated 528,000 cases and 266,000 deaths worldwide. Established screening and detection programs in the developed world have lowered the mortality from 40\/100,000 to 2\/100,000 over the last 60 years. The standard of care has been and continues to be: a screening Papanicolaou smear with or without Human Papilloma Virus (HPV) testing; followed by colposcopy and biopsies and if the smear is abnormal; and followed by treatment if the biopsies show high grade disease (cervical intraepithelial neoplasia (CIN) grades 2 and 3 and Carcinoma-in-situ). Low grade lesions (Pap smears with Atypical Cells of Uncertain Significance (ASCUS), Low Grade Squamous Intraepithelial Lesions (LGSIL), biopsies showing HPV changes or showing CIN 1); are usually followed for two years and then treated if persistent. Treatment can be performed with loop excision, LASER, or cryotherapy. Loop excision yields a specimen which can be reviewed to establish the diagnosis more accurately. LASER vaporizes the lesion and cryotherapy leads to tissue destruction. Under long term study; loop excision, LASER, and cryotherapy have the same rate of cure. The standard of care is expensive and takes 6 - 12 weeks for the individual patient. During the last twenty years, new technologies that can view the cervix and even image the cervix with cellular resolution have been developed. These technologies could lead to a new paradigm in which diagnosis and treatment occurs at a single visit. These technologies include fluorescence and reflectance spectroscopy (probe or wide-field, whole cervix scanning approaches) and fluorescence confocal endomicroscopy or high resolution micro-endoscopy. Both technologies have received Federal Drug Administration (FDA) and have been commercialized. Research trials continue to show their remarkable performance. These technologies are reviewed and clinical trials are summarized. Emerging technologies are coming along that may compete with those already approved and include optical coherence tomography, optical coherence tomography with autofluorescence, diffuse optical microscopy, and dual mode micro-endoscopy. These technologies are also reviewed and where available, clinical data is reported. Optical technologies are ready to diffuse into clinical practice because they will save money and 3 or 4 visits in the developed world and offer the same standard of care to the developing world where more cervical cancer exists. <\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('152','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_152\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Hill-2017.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.4236\/jct.2017.813105\" title=\"Follow DOI:10.4236\/jct.2017.813105\" target=\"_blank\">doi:10.4236\/jct.2017.813105<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('152','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Dual-beam manually-actuated distortion-corrected imaging (DMDI) with micromotor catheters\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2017.jpg\" width=\"128\" alt=\"Dual-beam manually-actuated distortion-corrected imaging (DMDI) with micromotor catheters\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony M. D.;  Hohert, Geoffrey;  Angkiriwang, Patricia T.;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.25.022164\" title=\"Dual-beam manually-actuated distortion-corrected imaging (DMDI) with micromotor catheters\" target=\"blank\">Dual-beam manually-actuated distortion-corrected imaging (DMDI) with micromotor catheters<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 25, <\/span><span class=\"tp_pub_additional_number\">no. 18, <\/span><span class=\"tp_pub_additional_pages\">pp. 22164-22177, <\/span><span class=\"tp_pub_additional_year\">2017<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_151\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('151','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_151\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('151','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_151\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('151','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_151\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Lee2017,<br \/>\r\ntitle = {Dual-beam manually-actuated distortion-corrected imaging (DMDI) with micromotor catheters},<br \/>\r\nauthor = {Anthony M. D. Lee and Geoffrey Hohert and Patricia T. Angkiriwang and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2017.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1364\/OE.25.022164},<br \/>\r\nyear  = {2017},<br \/>\r\ndate = {2017-09-01},<br \/>\r\njournal = {Optics Express},<br \/>\r\nvolume = {25},<br \/>\r\nnumber = {18},<br \/>\r\npages = {22164-22177},<br \/>\r\nabstract = {We present a new paradigm for performing two-dimensional scanning called dual-beam manually-actuated distortion-corrected imaging (DMDI). DMDI operates by imaging the same object with two spatially-separated beams that are being mechanically scanned rapidly in one dimension with slower manual actuation along a second dimension. Registration of common features between the two imaging channels allows remapping of the images to correct for distortions due to manual actuation. We demonstrate DMDI using a 4.7 mm OD rotationally scanning dual-beam micromotor catheter (DBMC). The DBMC requires a simple, one-time calibration of the beam paths by imaging a patterned phantom. DMDI allows for distortion correction of non-uniform axial speed and rotational motion of the DBMC. We show the utility of this technique by demonstrating en face OCT image distortion correction of a manually-scanned checkerboard phantom and fingerprint scan.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('151','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_151\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a new paradigm for performing two-dimensional scanning called dual-beam manually-actuated distortion-corrected imaging (DMDI). DMDI operates by imaging the same object with two spatially-separated beams that are being mechanically scanned rapidly in one dimension with slower manual actuation along a second dimension. Registration of common features between the two imaging channels allows remapping of the images to correct for distortions due to manual actuation. We demonstrate DMDI using a 4.7 mm OD rotationally scanning dual-beam micromotor catheter (DBMC). The DBMC requires a simple, one-time calibration of the beam paths by imaging a patterned phantom. DMDI allows for distortion correction of non-uniform axial speed and rotational motion of the DBMC. We show the utility of this technique by demonstrating en face OCT image distortion correction of a manually-scanned checkerboard phantom and fingerprint scan.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('151','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_151\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2017.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.25.022164\" title=\"Follow DOI:10.1364\/OE.25.022164\" target=\"_blank\">doi:10.1364\/OE.25.022164<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('151','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Dual-mode endomicroscopy for detection of epithelial dysplasia in the mouth: a descriptive pilot study\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Bodenschatz-2017.jpg\" width=\"128\" alt=\"Dual-mode endomicroscopy for detection of epithelial dysplasia in the mouth: a descriptive pilot study\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Bodenschatz, Nico;  Poh, Catherine F.;  Lam, Sylvia;  Lane, Pierre M.;  Guillaud, Martial;  MacAulay, Calum E.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.22.8.086005\" title=\"Dual-mode endomicroscopy for detection of epithelial dysplasia in the mouth: a descriptive pilot study\" target=\"blank\">Dual-mode endomicroscopy for detection of epithelial dysplasia in the mouth: a descriptive pilot study<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 22, <\/span><span class=\"tp_pub_additional_number\">no. 8, <\/span><span class=\"tp_pub_additional_pages\">pp. 086005, <\/span><span class=\"tp_pub_additional_year\">2017<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_150\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('150','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_150\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('150','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_150\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('150','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_150\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Bodenschatz2017,<br \/>\r\ntitle = {Dual-mode endomicroscopy for detection of epithelial dysplasia in the mouth: a descriptive pilot study},<br \/>\r\nauthor = {Nico Bodenschatz and Catherine F. Poh and Sylvia Lam and Pierre M. Lane and Martial Guillaud and Calum E. MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Bodenschatz-2017.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1117\/1.JBO.22.8.086005},<br \/>\r\nyear  = {2017},<br \/>\r\ndate = {2017-08-19},<br \/>\r\njournal = {Journal of Biomedical Optics},<br \/>\r\nvolume = {22},<br \/>\r\nnumber = {8},<br \/>\r\npages = {086005},<br \/>\r\nabstract = {Dual-mode endomicroscopy is a diagnostic tool for early cancer detection. It combines the high-resolution nuclear tissue contrast of fluorescence endomicroscopy with quantified depth-dependent epithelial backscattering as obtained by diffuse optical microscopy. In an in vivo pilot imaging study of 27 oral lesions from 21 patients, we demonstrate the complementary diagnostic value of both modalities and show correlations between grade of epithelial dysplasia and relative depth-dependent shifts in light backscattering. When combined, the two modalities provide diagnostic sensitivity to both moderate and severe epithelial dysplasia in vivo.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('150','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_150\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Dual-mode endomicroscopy is a diagnostic tool for early cancer detection. It combines the high-resolution nuclear tissue contrast of fluorescence endomicroscopy with quantified depth-dependent epithelial backscattering as obtained by diffuse optical microscopy. In an in vivo pilot imaging study of 27 oral lesions from 21 patients, we demonstrate the complementary diagnostic value of both modalities and show correlations between grade of epithelial dysplasia and relative depth-dependent shifts in light backscattering. When combined, the two modalities provide diagnostic sensitivity to both moderate and severe epithelial dysplasia in vivo.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('150','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_150\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Bodenschatz-2017.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.22.8.086005\" title=\"Follow DOI:10.1117\/1.JBO.22.8.086005\" target=\"_blank\">doi:10.1117\/1.JBO.22.8.086005<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('150','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2016\">2016<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fluorescence confocal endomicroscopy of the cervix: pilot study on the potential and limitations for clinical implementation\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Schlosser-2016.jpg\" width=\"128\" alt=\"Fluorescence confocal endomicroscopy of the cervix: pilot study on the potential and limitations for clinical implementation\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Schlosser, Colin;  Bodenschatz, Nico;  Lam, Sylvia;  Lee, Marette;  McAlpine, Jessica N.;  Miller, Dianne M.;  Niekerk, Dirk J. T. Van;  Follen, Michele;  Guillaud, Martial;  MacAulay, Calum E.;  Lane, Pierre M.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1. JBO.21.12.126011\" title=\"Fluorescence confocal endomicroscopy of the cervix: pilot study on the potential and limitations for clinical implementation\" target=\"blank\">Fluorescence confocal endomicroscopy of the cervix: pilot study on the potential and limitations for clinical implementation<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of Biomedical Optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 21, <\/span><span class=\"tp_pub_additional_number\">no. 12, <\/span><span class=\"tp_pub_additional_pages\">pp. 126011, <\/span><span class=\"tp_pub_additional_year\">2016<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_149\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('149','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_149\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('149','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_149\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('149','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_149\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Schlosser2016,<br \/>\r\ntitle = {Fluorescence confocal endomicroscopy of the cervix: pilot study on the potential and limitations for clinical implementation},<br \/>\r\nauthor = {Colin Schlosser and Nico Bodenschatz and Sylvia Lam and Marette Lee and Jessica N. McAlpine and Dianne M. Miller and Dirk J. T. Van Niekerk and Michele Follen and Martial Guillaud and Calum E. MacAulay and Pierre M. Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Schlosser-2016.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1117\/1. JBO.21.12.126011},<br \/>\r\nyear  = {2016},<br \/>\r\ndate = {2016-12-01},<br \/>\r\njournal = {Journal of Biomedical Optics},<br \/>\r\nvolume = {21},<br \/>\r\nnumber = {12},<br \/>\r\npages = {126011},<br \/>\r\nabstract = {Current diagnostic capabilities and limitations of fluorescence endomicroscopy in the cervix are assessed by qualitative and quantitative image analysis. Four cervical tissue types are investigated: normal columnar epithelium, normal and precancerous squamous epithelium, and stromal tissue. This study focuses on the perceived variability within and the subtle differences between the four tissue groups in the context of endomicroscopic in vivo pathology. Conclusions are drawn on the general ability to distinguish and diagnose tissue types, on the need for imaging depth control to enhance differentiation, and on the possible risks for diagnostic misinterpretations.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('149','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_149\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Current diagnostic capabilities and limitations of fluorescence endomicroscopy in the cervix are assessed by qualitative and quantitative image analysis. Four cervical tissue types are investigated: normal columnar epithelium, normal and precancerous squamous epithelium, and stromal tissue. This study focuses on the perceived variability within and the subtle differences between the four tissue groups in the context of endomicroscopic in vivo pathology. Conclusions are drawn on the general ability to distinguish and diagnose tissue types, on the need for imaging depth control to enhance differentiation, and on the possible risks for diagnostic misinterpretations.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('149','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_149\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Schlosser-2016.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1. JBO.21.12.126011\" title=\"Follow DOI:10.1117\/1. JBO.21.12.126011\" target=\"_blank\">doi:10.1117\/1. JBO.21.12.126011<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('149','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Endoscopic high-resolution autofluorescence imaging and OCT of pulmonary vascular networks\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2016.jpg\" width=\"128\" alt=\"Endoscopic high-resolution autofluorescence imaging and OCT of pulmonary vascular networks\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony MD;  Hohert, Geoffrey;  Lam, Stephen;  Shaipanich, Tawimas;  Beaudoin, Eve-Lea;  MacAulay, Calum;  Boudoux, Caroline;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/OL.41.003209\" title=\"Endoscopic high-resolution autofluorescence imaging and OCT of pulmonary vascular networks\" target=\"blank\">Endoscopic high-resolution autofluorescence imaging and OCT of pulmonary vascular networks<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Letters, <\/span><span class=\"tp_pub_additional_volume\">vol. 41, <\/span><span class=\"tp_pub_additional_number\">no. 14, <\/span><span class=\"tp_pub_additional_pages\">pp. 3209-32-12, <\/span><span class=\"tp_pub_additional_year\">2016<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_148\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('148','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_148\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('148','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_148\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('148','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_148\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Pahlevaninezhad2016,<br \/>\r\ntitle = {Endoscopic high-resolution autofluorescence imaging and OCT of pulmonary vascular networks},<br \/>\r\nauthor = {Hamid Pahlevaninezhad and Anthony MD Lee and Geoffrey Hohert and Stephen Lam and Tawimas Shaipanich and Eve-Lea Beaudoin and Calum MacAulay and Caroline Boudoux and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2016.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1364\/OL.41.003209},<br \/>\r\nyear  = {2016},<br \/>\r\ndate = {2016-07-15},<br \/>\r\njournal = {Optics Letters},<br \/>\r\nvolume = {41},<br \/>\r\nnumber = {14},<br \/>\r\npages = {3209-32-12},<br \/>\r\nabstract = {High-resolution imaging from within airways may allow new methods for studying lung disease. In this work, we report an endoscopic imaging system capable of high-resolution autofluorescence imaging (AFI) and optical coherence tomography (OCT) in peripheral airways using a 0.9 mm diameter double-clad fiber (DCF) catheter. In this system, AFI excitation light is coupled into the core of the DCF, enabling tightly focused excitation light while maintaining efficient collection of autofluorescence emission through the large diameter inner cladding of the DCF. We demonstrate the ability of this imaging system to visualize pulmonary vasculature as small as 12 \u03bcm in vivo.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('148','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_148\" style=\"display:none;\"><div class=\"tp_abstract_entry\">High-resolution imaging from within airways may allow new methods for studying lung disease. In this work, we report an endoscopic imaging system capable of high-resolution autofluorescence imaging (AFI) and optical coherence tomography (OCT) in peripheral airways using a 0.9 mm diameter double-clad fiber (DCF) catheter. In this system, AFI excitation light is coupled into the core of the DCF, enabling tightly focused excitation light while maintaining efficient collection of autofluorescence emission through the large diameter inner cladding of the DCF. We demonstrate the ability of this imaging system to visualize pulmonary vasculature as small as 12 \u03bcm in vivo.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('148','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_148\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2016.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/OL.41.003209\" title=\"Follow DOI:10.1364\/OL.41.003209\" target=\"_blank\">doi:10.1364\/OL.41.003209<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('148','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_inbook\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Measurement of pulmonary structure and function\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2016.jpg\" width=\"128\" alt=\"Measurement of pulmonary structure and function\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kirby, Miranda;  Lane, Pierre;  Coxson, Harvey<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1183\/2312508X.10003415\" title=\"Measurement of pulmonary structure and function\" target=\"blank\">Measurement of pulmonary structure and function<\/a> <span class=\"tp_pub_type tp_  inbook\">Book Chapter<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span> Barr, R. Graham;  Parr, David G.;  Vogel-Claussen, Jens (Ed.): <span class=\"tp_pub_additional_booktitle\">Imaging, <\/span><span class=\"tp_pub_additional_number\">no. 70, <\/span><span class=\"tp_pub_additional_chapter\"> Chapter 14, <\/span><span class=\"tp_pub_additional_pages\">pp. 216-232, <\/span><span class=\"tp_pub_additional_publisher\">European Respiratory Society, <\/span><span class=\"tp_pub_additional_year\">2016<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_147\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('147','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_147\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('147','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_147\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('147','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_147\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@inbook{Kirby2016,<br \/>\r\ntitle = {Measurement of pulmonary structure and function},<br \/>\r\nauthor = {Miranda Kirby and Pierre Lane and Harvey Coxson},<br \/>\r\neditor = {R. Graham Barr and David G. Parr and Jens Vogel-Claussen},<br \/>\r\ndoi = {10.1183\/2312508X.10003415},<br \/>\r\nyear  = {2016},<br \/>\r\ndate = {2016-03-01},<br \/>\r\nbooktitle = {Imaging},<br \/>\r\nnumber = {70},<br \/>\r\npages = {216-232},<br \/>\r\npublisher = {European Respiratory Society},<br \/>\r\nchapter = {14},<br \/>\r\nabstract = {Much of our understanding of both healthy and diseased lung is based on quantitative morphological assessment using pathology.  However, the development of new therapies for lung disease requires measurements and tools that can non-invasively measure lung structure and function both on a global and a regional scale.  Medical imaging technologies allows us to \u201csee\u201d the complex internal structures of the lung in three-dimensions so that detailed anatomic measurements can be performed, while other imaging modalities can also measure how the lung functions.  Here we have highlighted three techniques that have impacted pulmonary imaging research with emphasis on quantitative measurements:  computed tomography (CT), hyperpolarized noble gas magnetic resonance imaging (MRI) and optical coherence tomography (OCT).  For each of these imaging modalities, we discuss the quantitative measurements that can be derived as well as discuss the pulmonary diseases where each technique has demonstrated utility, discuss some drawbacks that are unique to each technique, and, finally, discuss some important directions for future research.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {inbook}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('147','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_147\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Much of our understanding of both healthy and diseased lung is based on quantitative morphological assessment using pathology.  However, the development of new therapies for lung disease requires measurements and tools that can non-invasively measure lung structure and function both on a global and a regional scale.  Medical imaging technologies allows us to \u201csee\u201d the complex internal structures of the lung in three-dimensions so that detailed anatomic measurements can be performed, while other imaging modalities can also measure how the lung functions.  Here we have highlighted three techniques that have impacted pulmonary imaging research with emphasis on quantitative measurements:  computed tomography (CT), hyperpolarized noble gas magnetic resonance imaging (MRI) and optical coherence tomography (OCT).  For each of these imaging modalities, we discuss the quantitative measurements that can be derived as well as discuss the pulmonary diseases where each technique has demonstrated utility, discuss some drawbacks that are unique to each technique, and, finally, discuss some important directions for future research.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('147','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_147\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1183\/2312508X.10003415\" title=\"Follow DOI:10.1183\/2312508X.10003415\" target=\"_blank\">doi:10.1183\/2312508X.10003415<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('147','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2015\">2015<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Reproducibility of optical coherence tomography airway imaging\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015a.jpg\" width=\"128\" alt=\"Reproducibility of optical coherence tomography airway imaging\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kirby, Miranda;  Ohtani, Keishi;  Nickens, Taylor;  Lisbona, Rosa Maria Lopez;  Lee, Anthony M. D.;  Shaipanich, Tawimas;  Lane, Pierre;  MacAulay, Calum;  Lam, Stephen;  Coxson, Harvey O.<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.004365\" title=\"Reproducibility of optical coherence tomography airway imaging\" target=\"blank\">Reproducibility of optical coherence tomography airway imaging<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomed. Opt. Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 6, <\/span><span class=\"tp_pub_additional_number\">no. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 4365\u20134377, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_145\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('145','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_145\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('145','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_145\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('145','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_145\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Kirby:15,<br \/>\r\ntitle = {Reproducibility of optical coherence tomography airway imaging},<br \/>\r\nauthor = {Miranda Kirby and Keishi Ohtani and Taylor Nickens and Rosa Maria Lopez Lisbona and Anthony M. D. Lee and Tawimas Shaipanich and Pierre Lane and Calum MacAulay and Stephen Lam and Harvey O. Coxson},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015a.pdf, Full Text (PDF)<br \/>\r\n},<br \/>\r\ndoi = {10.1364\/BOE.6.004365},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-11-01},<br \/>\r\njournal = {Biomed. Opt. Express},<br \/>\r\nvolume = {6},<br \/>\r\nnumber = {11},<br \/>\r\npages = {4365--4377},<br \/>\r\npublisher = {OSA},<br \/>\r\nabstract = {Optical coherence tomography (OCT) is a promising imaging technique to evaluate small airway remodeling. However, the short-term insertion-reinsertion reproducibility of OCT for evaluating the same bronchial pathway has yet to be established. We evaluated 74 OCT data sets from 38 current or former smokers twice within a single imaging session. Although the overall insertion-reinsertion airway wall thickness (WT) measurement coefficient of variation (CV) was moderate at 12%, much of the variability between repeat imaging was attributed to the observer; CV for repeated measurements of the same airway (intra-observer CV) was 9%. Therefore, reproducibility may be improved by introduction of automated analysis approaches suggesting that OCT has potential to be an in-vivo method for evaluating airway remodeling in future longitudinal and intervention studies.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('145','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_145\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Optical coherence tomography (OCT) is a promising imaging technique to evaluate small airway remodeling. However, the short-term insertion-reinsertion reproducibility of OCT for evaluating the same bronchial pathway has yet to be established. We evaluated 74 OCT data sets from 38 current or former smokers twice within a single imaging session. Although the overall insertion-reinsertion airway wall thickness (WT) measurement coefficient of variation (CV) was moderate at 12%, much of the variability between repeat imaging was attributed to the observer; CV for repeated measurements of the same airway (intra-observer CV) was 9%. Therefore, reproducibility may be improved by introduction of automated analysis approaches suggesting that OCT has potential to be an in-vivo method for evaluating airway remodeling in future longitudinal and intervention studies.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('145','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_145\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015a.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.004365\" title=\"Follow DOI:10.1364\/BOE.6.004365\" target=\"_blank\">doi:10.1364\/BOE.6.004365<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('145','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Quantification of\u00a0confocal fluorescence microscopy for\u00a0the detection of\u00a0cervical intraepithelial neoplasia\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Sheikhzadeh-2015.jpg\" width=\"128\" alt=\"Quantification of\u00a0confocal fluorescence microscopy for\u00a0the detection of\u00a0cervical intraepithelial neoplasia\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Sheikhzadeh, Fahime;  Ward, Rabab K.;  Carraro, Anita;  Chen, Zhao Yang; van Niekerk, Dirk;  Miller, Dianne;  Ehlen, Tom;  MacAulay, Calum E.;  Follen, Michele;  Lane, Pierre M.;  Guillaud, Martial<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1186\/s12938-015-0093-6\" title=\"Quantification of\u00a0confocal fluorescence microscopy for\u00a0the detection of\u00a0cervical intraepithelial neoplasia\" target=\"blank\">Quantification of\u00a0confocal fluorescence microscopy for\u00a0the detection of\u00a0cervical intraepithelial neoplasia<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomedical Engineering Online, <\/span><span class=\"tp_pub_additional_volume\">vol. 14, <\/span><span class=\"tp_pub_additional_number\">no. 96, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_146\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('146','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_146\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('146','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_146\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('146','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_146\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Sheikhzadeh2015,<br \/>\r\ntitle = {Quantification of\u00a0confocal fluorescence microscopy for\u00a0the detection of\u00a0cervical intraepithelial neoplasia},<br \/>\r\nauthor = {Fahime Sheikhzadeh and Rabab K. Ward and Anita Carraro and Zhao Yang Chen and Dirk van Niekerk and Dianne Miller and Tom Ehlen and Calum E. MacAulay and Michele Follen and Pierre M. Lane and Martial Guillaud },<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Sheikhzadeh-2015.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1186\/s12938-015-0093-6},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-10-24},<br \/>\r\njournal = {Biomedical Engineering Online},<br \/>\r\nvolume = {14},<br \/>\r\nnumber = {96},<br \/>\r\nabstract = {Background<br \/>\r\nCervical cancer remains a major health problem, especially in developing countries. Colposcopic examination is used to detect high-grade lesions in patients with a history of abnormal pap smears. New technologies are needed to improve the sensitivity and specificity of this technique. We propose to test the potential of fluorescence confocal microscopy to identify high-grade lesions.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\nWe examined the quantification of ex vivo confocal fluorescence microscopy to differentiate among normal cervical tissue, low-grade Cervical Intraepithelial Neoplasia (CIN), and high-grade CIN. We sought to (1) quantify nuclear morphology and tissue architecture features by analyzing images of cervical biopsies; and (2) determine the accuracy of high-grade CIN detection via confocal microscopy relative to the accuracy of detection by colposcopic impression. Forty-six biopsies obtained from colposcopically normal and abnormal cervical sites were evaluated. Confocal images were acquired at different depths from the epithelial surface and histological images were analyzed using in-house software.<br \/>\r\n<br \/>\r\nResults<br \/>\r\nThe features calculated from the confocal images compared well with those features obtained from the histological images and histopathological reviews of the specimens (obtained by a gynecologic pathologist). The correlations between two of these features (the nuclear-cytoplasmic ratio and the average of three nearest Delaunay-neighbors distance) and the grade of dysplasia were higher than that of colposcopic impression. The sensitivity of detecting high-grade dysplasia by analysing images collected at the surface of the epithelium, and at 15 and 30 \u03bcm below the epithelial surface were respectively 100, 100, and 92 %.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\nQuantitative analysis of confocal fluorescence images showed its capacity for discriminating high-grade CIN lesions vs. low-grade CIN lesions and normal tissues, at different depth of imaging. This approach could be used to help clinicians identify high-grade CIN in clinical settings.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('146','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_146\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Background<br \/>\r\nCervical cancer remains a major health problem, especially in developing countries. Colposcopic examination is used to detect high-grade lesions in patients with a history of abnormal pap smears. New technologies are needed to improve the sensitivity and specificity of this technique. We propose to test the potential of fluorescence confocal microscopy to identify high-grade lesions.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\nWe examined the quantification of ex vivo confocal fluorescence microscopy to differentiate among normal cervical tissue, low-grade Cervical Intraepithelial Neoplasia (CIN), and high-grade CIN. We sought to (1) quantify nuclear morphology and tissue architecture features by analyzing images of cervical biopsies; and (2) determine the accuracy of high-grade CIN detection via confocal microscopy relative to the accuracy of detection by colposcopic impression. Forty-six biopsies obtained from colposcopically normal and abnormal cervical sites were evaluated. Confocal images were acquired at different depths from the epithelial surface and histological images were analyzed using in-house software.<br \/>\r\n<br \/>\r\nResults<br \/>\r\nThe features calculated from the confocal images compared well with those features obtained from the histological images and histopathological reviews of the specimens (obtained by a gynecologic pathologist). The correlations between two of these features (the nuclear-cytoplasmic ratio and the average of three nearest Delaunay-neighbors distance) and the grade of dysplasia were higher than that of colposcopic impression. The sensitivity of detecting high-grade dysplasia by analysing images collected at the surface of the epithelium, and at 15 and 30 \u03bcm below the epithelial surface were respectively 100, 100, and 92 %.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\nQuantitative analysis of confocal fluorescence images showed its capacity for discriminating high-grade CIN lesions vs. low-grade CIN lesions and normal tissues, at different depth of imaging. This approach could be used to help clinicians identify high-grade CIN in clinical settings.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('146','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_146\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Sheikhzadeh-2015.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1186\/s12938-015-0093-6\" title=\"Follow DOI:10.1186\/s12938-015-0093-6\" target=\"_blank\">doi:10.1186\/s12938-015-0093-6<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('146','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Endoscopic Doppler optical coherence tomography and autofluorescence imaging of peripheral pulmonary nodules and vasculature\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2015.jpg\" width=\"128\" alt=\"Endoscopic Doppler optical coherence tomography and autofluorescence imaging of peripheral pulmonary nodules and vasculature\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony M. D.;  Ritchie, Alexander;  Shaipanich, Tawimas;  Zhang, Wei;  Ionescu, Diana N.;  Hohert, Geoffrey;  MacAulay, Calum;  Lam, Stephen;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.004191\" title=\"Endoscopic Doppler optical coherence tomography and autofluorescence imaging of peripheral pulmonary nodules and vasculature\" target=\"blank\">Endoscopic Doppler optical coherence tomography and autofluorescence imaging of peripheral pulmonary nodules and vasculature<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomedical Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 6, <\/span><span class=\"tp_pub_additional_number\">no. 10, <\/span><span class=\"tp_pub_additional_pages\">pp. 4191-4199, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_144\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('144','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_144\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('144','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_144\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('144','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_144\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{Pahlevaninezhad:15,<br \/>\r\ntitle = {Endoscopic Doppler optical coherence tomography and autofluorescence imaging of peripheral pulmonary nodules and vasculature},<br \/>\r\nauthor = {Hamid Pahlevaninezhad and Anthony M. D. Lee and Alexander Ritchie and Tawimas Shaipanich and Wei Zhang and Diana N. Ionescu and Geoffrey Hohert and Calum MacAulay and Stephen Lam and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2015.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1364\/BOE.6.004191},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-10-01},<br \/>\r\njournal = {Biomedical Optics Express},<br \/>\r\nvolume = {6},<br \/>\r\nnumber = {10},<br \/>\r\npages = {4191-4199},<br \/>\r\npublisher = {OSA},<br \/>\r\nabstract = {We present the first endoscopic Doppler optical coherence tomography and co-registered autofluorescence imaging (DOCT-AFI) of peripheral pulmonary nodules and vascular networks in vivo using a small 0.9 mm diameter catheter. Using exemplary images from volumetric data sets collected from 31 patients during flexible bronchoscopy, we demonstrate how DOCT and AFI offer complementary information that may increase the ability to locate and characterize pulmonary nodules. AFI offers a sensitive visual presentation for the rapid identification of suspicious airway sites, while co-registered OCT provides detailed structural information to assess the airway morphology. We demonstrate the ability of AFI to visualize vascular networks in vivo and validate this finding using Doppler and structural OCT. Given the advantages of higher resolution, smaller probe size, and ability to visualize vasculature, DOCT-AFI has the potential to increase diagnostic accuracy and minimize bleeding to guide biopsy of pulmonary nodules compared to radial endobronchial ultrasound, the current standard of care.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('144','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_144\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present the first endoscopic Doppler optical coherence tomography and co-registered autofluorescence imaging (DOCT-AFI) of peripheral pulmonary nodules and vascular networks in vivo using a small 0.9 mm diameter catheter. Using exemplary images from volumetric data sets collected from 31 patients during flexible bronchoscopy, we demonstrate how DOCT and AFI offer complementary information that may increase the ability to locate and characterize pulmonary nodules. AFI offers a sensitive visual presentation for the rapid identification of suspicious airway sites, while co-registered OCT provides detailed structural information to assess the airway morphology. We demonstrate the ability of AFI to visualize vascular networks in vivo and validate this finding using Doppler and structural OCT. Given the advantages of higher resolution, smaller probe size, and ability to visualize vasculature, DOCT-AFI has the potential to increase diagnostic accuracy and minimize bleeding to guide biopsy of pulmonary nodules compared to radial endobronchial ultrasound, the current standard of care.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('144','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_144\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2015.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.004191\" title=\"Follow DOI:10.1364\/BOE.6.004191\" target=\"_blank\">doi:10.1364\/BOE.6.004191<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('144','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015.jpg\" width=\"128\" alt=\"Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kirby, Miranda;  Ohtani, Keishi;  Lisbona, Rosa Maria Lopez;  Lee, Anthony MD;  Zhang, Wei;  Lane, Pierre;  Varfolomeva, Nina;  Hui, Linda;  Ionescu, Diana;  Coxson, Harvey O;  MacAulay, Calum;  FitzGerald, J. Mark;  Lam, Stephen<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1183\/09031936.00016815\" title=\"Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography\" target=\"blank\">Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">European Respiratory Journal, <\/span><span class=\"tp_pub_additional_volume\">vol. 46, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 859-862, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_121\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('121','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_121\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('121','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_121\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('121','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_121\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{kirby2015bronchial,<br \/>\r\ntitle = {Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography},<br \/>\r\nauthor = { Miranda Kirby and Keishi Ohtani and Rosa Maria Lopez Lisbona and Anthony MD Lee and Wei Zhang and Pierre Lane and Nina Varfolomeva and Linda Hui and Diana Ionescu and Harvey O Coxson and Calum MacAulay and J. Mark FitzGerald and Stephen Lam},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.1183\/09031936.00016815},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-01-01},<br \/>\r\njournal = {European Respiratory Journal},<br \/>\r\nvolume = {46},<br \/>\r\nnumber = {3},<br \/>\r\npages = {859-862},<br \/>\r\npublisher = {Eur Respiratory Soc},<br \/>\r\nabstract = {We evaluated two severe asthmatics immediately prior to and longitudinally following BT, and demonstrated a reduction in airway wall thickness that persisted 2 years following treatment in the BT responder, as well as differences in airway wall features between the responder and nonresponder prior to treatment. These observations generate hypotheses for a larger study to determine if airway changes defined by OCT imaging can identify asthma patients who will benefit from BT and to determine the long-term effects of the treatment.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('121','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_121\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We evaluated two severe asthmatics immediately prior to and longitudinally following BT, and demonstrated a reduction in airway wall thickness that persisted 2 years following treatment in the BT responder, as well as differences in airway wall features between the responder and nonresponder prior to treatment. These observations generate hypotheses for a larger study to determine if airway changes defined by OCT imaging can identify asthma patients who will benefit from BT and to determine the long-term effects of the treatment.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('121','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_121\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Kirby-2015.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1183\/09031936.00016815\" title=\"Follow DOI:10.1183\/09031936.00016815\" target=\"_blank\">doi:10.1183\/09031936.00016815<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('121','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Wide-field in vivo oral OCT imaging\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2015.jpg\" width=\"128\" alt=\"Wide-field in vivo oral OCT imaging\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony MD;  Cahill, Lucas;  Liu, Kelly;  MacAulay, Calum;  Poh, Catherine;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.002664\" title=\"Wide-field in vivo oral OCT imaging\" target=\"blank\">Wide-field in vivo oral OCT imaging<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomedical Optics Express, <\/span><span class=\"tp_pub_additional_volume\">vol. 6, <\/span><span class=\"tp_pub_additional_number\">no. 7, <\/span><span class=\"tp_pub_additional_pages\">pp. 2664-2674, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_141\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('141','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_141\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('141','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_141\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('141','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_141\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lee2015wide,<br \/>\r\ntitle = {Wide-field in vivo oral OCT imaging},<br \/>\r\nauthor = { Anthony MD Lee and Lucas Cahill and Kelly Liu and Calum MacAulay and Catherine Poh and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2015.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26203389, PubMed},<br \/>\r\ndoi = {10.1364\/BOE.6.002664},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-01-01},<br \/>\r\njournal = {Biomedical Optics Express},<br \/>\r\nvolume = {6},<br \/>\r\nnumber = {7},<br \/>\r\npages = {2664-2674},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We have built a polarization-sensitive swept source Optical Coherence Tomography (OCT) instrument capable of wide-field in vivo imaging in the oral cavity. This instrument uses a hand-held side-looking fiber-optic rotary pullback catheter that can cover two dimensional tissue imaging fields approximately 2.5 mm wide by up to 90 mm length in a single image acquisition. The catheter spins at 100 Hz with pullback speeds up to 15 mm\/s allowing imaging of areas up to 225 mm2 field-of-view in seconds. A catheter sheath and two optional catheter sheath holders have been designed to allow imaging at all locations within the oral cavity. Image quality of 2-dimensional image slices through the data can be greatly enhanced by averaging over the orthogonal dimension to reduce speckle. Initial in vivo imaging results reveal a wide-field view of features such as epithelial thickness and continuity of the basement membrane that may be useful in clinic for chair-side management of oral lesions.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('141','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_141\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We have built a polarization-sensitive swept source Optical Coherence Tomography (OCT) instrument capable of wide-field in vivo imaging in the oral cavity. This instrument uses a hand-held side-looking fiber-optic rotary pullback catheter that can cover two dimensional tissue imaging fields approximately 2.5 mm wide by up to 90 mm length in a single image acquisition. The catheter spins at 100 Hz with pullback speeds up to 15 mm\/s allowing imaging of areas up to 225 mm2 field-of-view in seconds. A catheter sheath and two optional catheter sheath holders have been designed to allow imaging at all locations within the oral cavity. Image quality of 2-dimensional image slices through the data can be greatly enhanced by averaging over the orthogonal dimension to reduce speckle. Initial in vivo imaging results reveal a wide-field view of features such as epithelial thickness and continuity of the basement membrane that may be useful in clinic for chair-side management of oral lesions.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('141','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_141\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2015.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26203389\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.6.002664\" title=\"Follow DOI:10.1364\/BOE.6.002664\" target=\"_blank\">doi:10.1364\/BOE.6.002664<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('141','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2014\">2014<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fiber-optic polarization diversity detection for rotary probe optical coherence tomography\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014.jpg\" width=\"128\" alt=\"Fiber-optic polarization diversity detection for rotary probe optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony;  Pahlevaninezhad, Hamid;  Yang, Victor XD;  Lam, Stephen;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/OL.39.003638\" title=\"Fiber-optic polarization diversity detection for rotary probe optical coherence tomography\" target=\"blank\">Fiber-optic polarization diversity detection for rotary probe optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics Letters, <\/span><span class=\"tp_pub_additional_volume\">vol. 39, <\/span><span class=\"tp_pub_additional_number\">no. 12, <\/span><span class=\"tp_pub_additional_pages\">pp. 3638\u20133641, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_79\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('79','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_79\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lee2014fiber,<br \/>\r\ntitle = {Fiber-optic polarization diversity detection for rotary probe optical coherence tomography},<br \/>\r\nauthor = { Anthony Lee and Hamid Pahlevaninezhad and Victor XD Yang and Stephen Lam and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24978556, Pubmed},<br \/>\r\ndoi = {10.1364\/OL.39.003638},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Optics Letters},<br \/>\r\nvolume = {39},<br \/>\r\nnumber = {12},<br \/>\r\npages = {3638--3641},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We report a polarization diversity detection scheme for optical coherence tomography with a new, custom, miniaturized fiber coupler with single mode (SM) fiber inputs and polarization maintaining (PM) fiber outputs. The SM fiber inputs obviate matching the optical lengths of the X and Y OCT polarization channels prior to interference and the PM fiber outputs ensure defined X and Y axes after interference. Advantages for this scheme include easier alignment, lower cost, and easier miniaturization compared to designs with free-space bulk optical components. We demonstrate the utility of the detection system to mitigate the effects of rapidly changing polarization states when imaging with rotating fiber optic probes in Intralipid suspension and during in vivo imaging of human airways.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_79\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We report a polarization diversity detection scheme for optical coherence tomography with a new, custom, miniaturized fiber coupler with single mode (SM) fiber inputs and polarization maintaining (PM) fiber outputs. The SM fiber inputs obviate matching the optical lengths of the X and Y OCT polarization channels prior to interference and the PM fiber outputs ensure defined X and Y axes after interference. Advantages for this scheme include easier alignment, lower cost, and easier miniaturization compared to designs with free-space bulk optical components. We demonstrate the utility of the detection system to mitigate the effects of rapidly changing polarization states when imaging with rotating fiber optic probes in Intralipid suspension and during in vivo imaging of human airways.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_79\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24978556\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/OL.39.003638\" title=\"Follow DOI:10.1364\/OL.39.003638\" target=\"_blank\">doi:10.1364\/OL.39.003638<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('79','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"A high-efficiency fiber-based imaging system for co-registered autofluorescence and optical coherence tomography\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014.jpg\" width=\"128\" alt=\"A high-efficiency fiber-based imaging system for co-registered autofluorescence and optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony;  Shaipanich, Tawimas;  Raizada, Rashika;  Cahill, Lucas;  Hohert, Geoffrey;  Yang, Victor XD;  Lam, Stephen;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.5.002978\" title=\"A high-efficiency fiber-based imaging system for co-registered autofluorescence and optical coherence tomography\" target=\"blank\">A high-efficiency fiber-based imaging system for co-registered autofluorescence and optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Biomedical optics express, <\/span><span class=\"tp_pub_additional_volume\">vol. 5, <\/span><span class=\"tp_pub_additional_number\">no. 9, <\/span><span class=\"tp_pub_additional_pages\">pp. 2978\u20132987, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_81\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('81','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_81\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{pahlevaninezhad2014high,<br \/>\r\ntitle = {A high-efficiency fiber-based imaging system for co-registered autofluorescence and optical coherence tomography},<br \/>\r\nauthor = { Hamid Pahlevaninezhad and Anthony Lee and Tawimas Shaipanich and Rashika Raizada and Lucas Cahill and Geoffrey Hohert and Victor XD Yang and Stephen Lam and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25401011, PubMed},<br \/>\r\ndoi = {10.1364\/BOE.5.002978},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Biomedical optics express},<br \/>\r\nvolume = {5},<br \/>\r\nnumber = {9},<br \/>\r\npages = {2978--2987},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We present a power-efficient fiber-based imaging system capable of co-registered autofluorescence imaging and optical coherence tomography (AF\/OCT). The system employs a custom fiber optic rotary joint (FORJ) with an embedded dichroic mirror to efficiently combine the OCT and AF pathways. This three-port wavelength multiplexing FORJ setup has a throughput of more than 83% for collected AF emission, significantly more efficient compared to previously reported fiber-based methods. A custom 900 \u00b5m diameter catheter \u2012 consisting of a rotating lens assembly, double-clad fiber (DCF), and torque cable in a stationary plastic tube \u2012 was fabricated to allow AF\/OCT imaging of small airways in vivo. We demonstrate the performance of this system ex vivo in resected porcine airway specimens and in vivo in human on fingers, in the oral cavity, and in peripheral airways.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_81\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a power-efficient fiber-based imaging system capable of co-registered autofluorescence imaging and optical coherence tomography (AF\/OCT). The system employs a custom fiber optic rotary joint (FORJ) with an embedded dichroic mirror to efficiently combine the OCT and AF pathways. This three-port wavelength multiplexing FORJ setup has a throughput of more than 83% for collected AF emission, significantly more efficient compared to previously reported fiber-based methods. A custom 900 \u00b5m diameter catheter \u2012 consisting of a rotating lens assembly, double-clad fiber (DCF), and torque cable in a stationary plastic tube \u2012 was fabricated to allow AF\/OCT imaging of small airways in vivo. We demonstrate the performance of this system ex vivo in resected porcine airway specimens and in vivo in human on fingers, in the oral cavity, and in peripheral airways.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_81\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25401011\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/BOE.5.002978\" title=\"Follow DOI:10.1364\/BOE.5.002978\" target=\"_blank\">doi:10.1364\/BOE.5.002978<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('81','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"High speed, wide velocity dynamic range Doppler optical coherence tomography (Part IV): split spectrum processing in rotary catheter probes\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Vuong-2014.jpg\" width=\"128\" alt=\"High speed, wide velocity dynamic range Doppler optical coherence tomography (Part IV): split spectrum processing in rotary catheter probes\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Vuong, Barry;  Lee, Anthony;  Luk, Timothy WH;  Sun, Cuiru;  Lam, Stephen;  Lane, Pierre;  Yang, Victor XD<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.22.007399\" title=\"High speed, wide velocity dynamic range Doppler optical coherence tomography (Part IV): split spectrum processing in rotary catheter probes\" target=\"blank\">High speed, wide velocity dynamic range Doppler optical coherence tomography (Part IV): split spectrum processing in rotary catheter probes<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics express, <\/span><span class=\"tp_pub_additional_volume\">vol. 22, <\/span><span class=\"tp_pub_additional_number\">no. 7, <\/span><span class=\"tp_pub_additional_pages\">pp. 7399\u20137415, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_84\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('84','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_84\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{vuong2014high,<br \/>\r\ntitle = {High speed, wide velocity dynamic range Doppler optical coherence tomography (Part IV): split spectrum processing in rotary catheter probes},<br \/>\r\nauthor = { Barry Vuong and Anthony Lee and Timothy WH Luk and Cuiru Sun and Stephen Lam and Pierre Lane and Victor XD Yang},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Vuong-2014.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24718115, Pubmed},<br \/>\r\ndoi = {10.1364\/OE.22.007399},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Optics express},<br \/>\r\nvolume = {22},<br \/>\r\nnumber = {7},<br \/>\r\npages = {7399--7415},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We report a technique for blood flow detection using split spectrum Doppler optical coherence tomography (ssDOCT) that shows improved sensitivity over existing Doppler OCT methods. In ssDOCT, the Doppler signal is averaged over multiple sub-bands of the interferogram, increasing the SNR of the Doppler signal. We explore the parameterization of this technique in terms of number of sub-band windows, width and overlap of the windows, and their effect on the Doppler signal to noise in a flow phantom. Compared to conventional DOCT, ssDOCT processing has increased flow sensitivity. We demonstrate the effectiveness of ssDOCT in-vivo for intravascular flow detection within a porcine carotid artery and for microvascular vessel detection in human pulmonary imaging, using rotary catheter probes. To our knowledge, this is the first report of visualizing in-vivo Doppler flow patterns adjacent to stent struts in the carotid artery.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_84\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We report a technique for blood flow detection using split spectrum Doppler optical coherence tomography (ssDOCT) that shows improved sensitivity over existing Doppler OCT methods. In ssDOCT, the Doppler signal is averaged over multiple sub-bands of the interferogram, increasing the SNR of the Doppler signal. We explore the parameterization of this technique in terms of number of sub-band windows, width and overlap of the windows, and their effect on the Doppler signal to noise in a flow phantom. Compared to conventional DOCT, ssDOCT processing has increased flow sensitivity. We demonstrate the effectiveness of ssDOCT in-vivo for intravascular flow detection within a porcine carotid artery and for microvascular vessel detection in human pulmonary imaging, using rotary catheter probes. To our knowledge, this is the first report of visualizing in-vivo Doppler flow patterns adjacent to stent struts in the carotid artery.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_84\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Vuong-2014.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24718115\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/OE.22.007399\" title=\"Follow DOI:10.1364\/OE.22.007399\" target=\"_blank\">doi:10.1364\/OE.22.007399<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('84','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Coregistered autofluorescence-optical coherence tomography imaging of human lung sections\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014a.jpg\" width=\"128\" alt=\"Coregistered autofluorescence-optical coherence tomography imaging of human lung sections\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony MD;  Lam, Stephen;  MacAulay, Calum;  Lane, Pierre M<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.19.3.036022\" title=\"Coregistered autofluorescence-optical coherence tomography imaging of human lung sections\" target=\"blank\">Coregistered autofluorescence-optical coherence tomography imaging of human lung sections<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 19, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 036022\u2013036022, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_85\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('85','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_85\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('85','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_85\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('85','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_85\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{pahlevaninezhad2014coregistered,<br \/>\r\ntitle = {Coregistered autofluorescence-optical coherence tomography imaging of human lung sections},<br \/>\r\nauthor = { Hamid Pahlevaninezhad and Anthony MD Lee and Stephen Lam and Calum MacAulay and Pierre M Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014a.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24687614, PubMed},<br \/>\r\ndoi = {10.1117\/1.JBO.19.3.036022},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {19},<br \/>\r\nnumber = {3},<br \/>\r\npages = {036022--036022},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {Autofluorescence (AF) imaging can provide valuable information about the structural and metabolic state of tissue that can be useful for elucidating physiological and pathological processes. Optical coherence tomography (OCT) provides high resolution detailed information about tissue morphology. We present coregistered AF-OCT imaging of human lung sections. Adjacent hematoxylin and eosin stained histological sections are used to identify tissue structures observed in the OCT images. Segmentation of these structures in the OCT images allowed determination of relative AF intensities of human lung components. Since the AF imaging was performed on tissue sections perpendicular to the airway axis, the results show the AF signal originating from the airway wall components free from the effects of scattering and absorption by overlying layers as is the case during endoscopic imaging. Cartilage and dense connective tissue (DCT) are found to be the dominant fluorescing components with the average cartilage AF intensity about four times greater than that of DCT. The epithelium, lamina propria, and loose connective tissue near basement membrane generate an order of magnitude smaller AF signal than the cartilage fluorescence.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('85','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_85\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Autofluorescence (AF) imaging can provide valuable information about the structural and metabolic state of tissue that can be useful for elucidating physiological and pathological processes. Optical coherence tomography (OCT) provides high resolution detailed information about tissue morphology. We present coregistered AF-OCT imaging of human lung sections. Adjacent hematoxylin and eosin stained histological sections are used to identify tissue structures observed in the OCT images. Segmentation of these structures in the OCT images allowed determination of relative AF intensities of human lung components. Since the AF imaging was performed on tissue sections perpendicular to the airway axis, the results show the AF signal originating from the airway wall components free from the effects of scattering and absorption by overlying layers as is the case during endoscopic imaging. Cartilage and dense connective tissue (DCT) are found to be the dominant fluorescing components with the average cartilage AF intensity about four times greater than that of DCT. The epithelium, lamina propria, and loose connective tissue near basement membrane generate an order of magnitude smaller AF signal than the cartilage fluorescence.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('85','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_85\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014a.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24687614\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.19.3.036022\" title=\"Follow DOI:10.1117\/1.JBO.19.3.036022\" target=\"_blank\">doi:10.1117\/1.JBO.19.3.036022<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('85','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Validation of airway wall measurements by optical coherence tomography in porcine airways\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014a.jpg\" width=\"128\" alt=\"Validation of airway wall measurements by optical coherence tomography in porcine airways\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony MD;  Kirby, Miranda;  Ohtani, Keishi;  Candido, Tara;  Shalansky, Rebecca;  MacAulay, Calum;  English, John;  Finley, Richard;  Lam, Stephen;  Coxson, Harvey O;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1371\/journal.pone.0100145\" title=\"Validation of airway wall measurements by optical coherence tomography in porcine airways\" target=\"blank\">Validation of airway wall measurements by optical coherence tomography in porcine airways<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">PloS one, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. e100145, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_99\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('99','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_99\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('99','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_99\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('99','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_99\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lee2014validation,<br \/>\r\ntitle = {Validation of airway wall measurements by optical coherence tomography in porcine airways},<br \/>\r\nauthor = { Anthony MD Lee and Miranda Kirby and Keishi Ohtani and Tara Candido and Rebecca Shalansky and Calum MacAulay and John English and Richard Finley and Stephen Lam and Harvey O Coxson and Pierre Lane },<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014a.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24949633, Pubmed},<br \/>\r\ndoi = {10.1371\/journal.pone.0100145},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {PloS one},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {6},<br \/>\r\npages = {e100145},<br \/>\r\nabstract = {Examining and quantifying changes in airway morphology is critical for studying longitudinal pathogenesis and interventions in diseases such as chronic obstructive pulmonary disease and asthma. Here we present fiber-optic optical coherence tomography (OCT) as a nondestructive technique to precisely and accurately measure the 2-dimensional cross-sectional areas of airway wall substructure divided into the mucosa (WAmuc), submucosa (WAsub), cartilage (WAcart), and the airway total wall area (WAt). Porcine lung airway specimens were dissected from freshly resected lung lobes (N\u200a=\u200a10). Three-dimensional OCT imaging using a fiber-optic rotary-pullback probe was performed immediately on airways greater than 0.9 mm in diameter on the fresh airway specimens and subsequently on the same specimens post-formalin-fixation. The fixed specimens were serially sectioned and stained with H&E. OCT images carefully matched to selected sections stained with Movat's pentachrome demonstrated that OCT effectively identifies airway epithelium, lamina propria, and cartilage. Selected H&E sections were digitally scanned and airway total wall areas were measured. Traced measurements of WAmuc, WAsub, WAcart, and WAt from OCT images of fresh specimens by two independent observers found there were no significant differences (p&gt;0.05) between the observer's measurements. The same wall area measurements from OCT images of formalin-fixed specimens found no significant differences for WAsub, WAcart and WAt, and a small but significant difference for WAmuc. Bland-Altman analysis indicated there were negligible biases between the observers for OCT wall area measurements in both fresh and formalin-fixed specimens. Bland-Altman analysis also indicated there was negligible bias between histology and OCT wall area measurements for both fresh and formalin-fixed specimens. We believe this study sets the groundwork for quantitatively monitoring pathogenesis and interventions in the airways using OCT.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('99','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_99\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Examining and quantifying changes in airway morphology is critical for studying longitudinal pathogenesis and interventions in diseases such as chronic obstructive pulmonary disease and asthma. Here we present fiber-optic optical coherence tomography (OCT) as a nondestructive technique to precisely and accurately measure the 2-dimensional cross-sectional areas of airway wall substructure divided into the mucosa (WAmuc), submucosa (WAsub), cartilage (WAcart), and the airway total wall area (WAt). Porcine lung airway specimens were dissected from freshly resected lung lobes (N\u200a=\u200a10). Three-dimensional OCT imaging using a fiber-optic rotary-pullback probe was performed immediately on airways greater than 0.9 mm in diameter on the fresh airway specimens and subsequently on the same specimens post-formalin-fixation. The fixed specimens were serially sectioned and stained with H&amp;E. OCT images carefully matched to selected sections stained with Movat's pentachrome demonstrated that OCT effectively identifies airway epithelium, lamina propria, and cartilage. Selected H&amp;E sections were digitally scanned and airway total wall areas were measured. Traced measurements of WAmuc, WAsub, WAcart, and WAt from OCT images of fresh specimens by two independent observers found there were no significant differences (p&gt;0.05) between the observer's measurements. The same wall area measurements from OCT images of formalin-fixed specimens found no significant differences for WAsub, WAcart and WAt, and a small but significant difference for WAmuc. Bland-Altman analysis indicated there were negligible biases between the observers for OCT wall area measurements in both fresh and formalin-fixed specimens. Bland-Altman analysis also indicated there was negligible bias between histology and OCT wall area measurements for both fresh and formalin-fixed specimens. We believe this study sets the groundwork for quantitatively monitoring pathogenesis and interventions in the airways using OCT.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('99','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_99\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2014a.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24949633\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1371\/journal.pone.0100145\" title=\"Follow DOI:10.1371\/journal.pone.0100145\" target=\"_blank\">doi:10.1371\/journal.pone.0100145<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('99','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fiber-Based Polarization Diversity Detection for Polarization-Sensitive Optical Coherence Tomography\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014b.jpg\" width=\"128\" alt=\"Fiber-Based Polarization Diversity Detection for Polarization-Sensitive Optical Coherence Tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony;  Cahill, Lucas;  Lam, Stephen;  MacAulay, Calum;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.3390\/photonics1040283\" title=\"Fiber-Based Polarization Diversity Detection for Polarization-Sensitive Optical Coherence Tomography\" target=\"blank\">Fiber-Based Polarization Diversity Detection for Polarization-Sensitive Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Photonics, <\/span><span class=\"tp_pub_additional_volume\">vol. 1, <\/span><span class=\"tp_pub_additional_number\">no. 4, <\/span><span class=\"tp_pub_additional_pages\">pp. 283\u2013295, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_102\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('102','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_102\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('102','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_102\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('102','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_102\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{pahlevaninezhad2014fiber,<br \/>\r\ntitle = {Fiber-Based Polarization Diversity Detection for Polarization-Sensitive Optical Coherence Tomography},<br \/>\r\nauthor = { Hamid Pahlevaninezhad and Anthony Lee and Lucas Cahill and Stephen Lam and Calum MacAulay and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014b.pdf, Full Text (PDF)},<br \/>\r\ndoi = {10.3390\/photonics1040283},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Photonics},<br \/>\r\nvolume = {1},<br \/>\r\nnumber = {4},<br \/>\r\npages = {283--295},<br \/>\r\npublisher = {Multidisciplinary Digital Publishing Institute},<br \/>\r\nabstract = {We present a new fiber-based polarization diversity detection (PDD) scheme for polarization sensitive optical coherence tomography (PSOCT). This implementation uses a new custom miniaturized polarization-maintaining fiber coupler with single mode (SM) fiber inputs and polarization maintaining (PM) fiber outputs. The SM fiber inputs obviate matching the optical lengths of the two orthogonal OCT polarization channels prior to interference while the PM fiber outputs ensure defined orthogonal axes after interference. Advantages of this detection scheme over those with bulk optics PDD include lower cost, easier miniaturization, and more relaxed alignment and handling issues. We incorporate this PDD scheme into a galvanometer-scanned OCT system to demonstrate system calibration and PSOCT imaging of an achromatic quarter-wave plate, fingernail in vivo, and chicken breast, salmon, cow leg, and basa fish muscle samples ex vivo.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('102','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_102\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a new fiber-based polarization diversity detection (PDD) scheme for polarization sensitive optical coherence tomography (PSOCT). This implementation uses a new custom miniaturized polarization-maintaining fiber coupler with single mode (SM) fiber inputs and polarization maintaining (PM) fiber outputs. The SM fiber inputs obviate matching the optical lengths of the two orthogonal OCT polarization channels prior to interference while the PM fiber outputs ensure defined orthogonal axes after interference. Advantages of this detection scheme over those with bulk optics PDD include lower cost, easier miniaturization, and more relaxed alignment and handling issues. We incorporate this PDD scheme into a galvanometer-scanned OCT system to demonstrate system calibration and PSOCT imaging of an achromatic quarter-wave plate, fingernail in vivo, and chicken breast, salmon, cow leg, and basa fish muscle samples ex vivo.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('102','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_102\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014b.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.3390\/photonics1040283\" title=\"Follow DOI:10.3390\/photonics1040283\" target=\"_blank\">doi:10.3390\/photonics1040283<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('102','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"A statistical model for removing inter-device differences in spectroscopy\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Wang-2014.jpg\" width=\"128\" alt=\"A statistical model for removing inter-device differences in spectroscopy\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Wang, Lu;  Lee, Jong Soo;  Lane, Pierre;  Atkinson, E Neely;  Zuluaga, Andres;  Follen, Michele;  MacAulay, Calum;  Cox, Dennis D<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/ 10.1364\/OE.22.007617\" title=\"A statistical model for removing inter-device differences in spectroscopy\" target=\"blank\">A statistical model for removing inter-device differences in spectroscopy<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics express, <\/span><span class=\"tp_pub_additional_volume\">vol. 22, <\/span><span class=\"tp_pub_additional_number\">no. 7, <\/span><span class=\"tp_pub_additional_pages\">pp. 7617\u20137624, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_128\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('128','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_128\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('128','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_128\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('128','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_128\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{wang2014statistical,<br \/>\r\ntitle = {A statistical model for removing inter-device differences in spectroscopy},<br \/>\r\nauthor = { Lu Wang and Jong Soo Lee and Pierre Lane and E Neely Atkinson and Andres Zuluaga and Michele Follen and Calum MacAulay and Dennis D Cox},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Wang-2014.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24718136, Pubmed},<br \/>\r\ndoi = { 10.1364\/OE.22.007617},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {Optics express},<br \/>\r\nvolume = {22},<br \/>\r\nnumber = {7},<br \/>\r\npages = {7617--7624},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We are investigating spectroscopic devices designed to make in vivo cervical tissue measurements to detect pre-cancerous and cancerous lesions. All devices have the same design and ideally should record identical measurements. However, we observed consistent differences among them. An experiment was designed to study the sources of variation in the measurements recorded. Here we present a log additive statistical model that incorporates the sources of variability we identified. Based on this model, we estimated correction factors from the experimental data needed to eliminate the inter-device variability and other sources of variation. These correction factors are intended to improve the accuracy and repeatability of such devices when making future measurements on patient tissue.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('128','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_128\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We are investigating spectroscopic devices designed to make in vivo cervical tissue measurements to detect pre-cancerous and cancerous lesions. All devices have the same design and ideally should record identical measurements. However, we observed consistent differences among them. An experiment was designed to study the sources of variation in the measurements recorded. Here we present a log additive statistical model that incorporates the sources of variability we identified. Based on this model, we estimated correction factors from the experimental data needed to eliminate the inter-device variability and other sources of variation. These correction factors are intended to improve the accuracy and repeatability of such devices when making future measurements on patient tissue.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('128','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_128\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Wang-2014.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24718136\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/ 10.1364\/OE.22.007617\" title=\"Follow DOI: 10.1364\/OE.22.007617\" target=\"_blank\">doi: 10.1364\/OE.22.007617<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('128','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Optical Coherence Tomography and Autofluorescence Imaging of Human Tonsil\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014c.jpg\" width=\"128\" alt=\"Optical Coherence Tomography and Autofluorescence Imaging of Human Tonsil\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Lee, Anthony MD;  Rosin, Miriam;  Sun, Ivan;  Zhang, Lewei;  Hakimi, Mehrnoush;  MacAulay, Calum;  Lane, Pierre M<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1371\/journal.pone.0115889\" title=\"Optical Coherence Tomography and Autofluorescence Imaging of Human Tonsil\" target=\"blank\">Optical Coherence Tomography and Autofluorescence Imaging of Human Tonsil<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">PloS one, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 12, <\/span><span class=\"tp_pub_additional_pages\">pp. e115889, <\/span><span class=\"tp_pub_additional_year\">2014<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_136\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('136','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_136\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('136','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_136\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('136','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_136\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{pahlevaninezhad2014optical,<br \/>\r\ntitle = {Optical Coherence Tomography and Autofluorescence Imaging of Human Tonsil},<br \/>\r\nauthor = { Hamid Pahlevaninezhad and Anthony MD Lee and Miriam Rosin and Ivan Sun and Lewei Zhang and Mehrnoush Hakimi and Calum MacAulay and Pierre M Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014c.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25542010, Pubmed},<br \/>\r\ndoi = {10.1371\/journal.pone.0115889},<br \/>\r\nyear  = {2014},<br \/>\r\ndate = {2014-01-01},<br \/>\r\njournal = {PloS one},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {12},<br \/>\r\npages = {e115889},<br \/>\r\npublisher = {Public Library of Science},<br \/>\r\nabstract = {For the first time, we present co-registered autofluorescence imaging and optical coherence tomography (AF\/OCT) of excised human palatine tonsils to evaluate the capabilities of OCT to visualize tonsil tissue components. Despite limited penetration depth, OCT can provide detailed structural information about tonsil tissue with much higher resolution than that of computed tomography, magnetic resonance imaging, and Ultrasound. Different tonsil tissue components such as epithelium, dense connective tissue, lymphoid nodules, and crypts can be visualized by OCT. The co-registered AF imaging can provide matching biochemical information. AF\/OCT scans may provide a non-invasive tool for detecting tonsillar cancers and for studying the natural history of their development.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('136','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_136\" style=\"display:none;\"><div class=\"tp_abstract_entry\">For the first time, we present co-registered autofluorescence imaging and optical coherence tomography (AF\/OCT) of excised human palatine tonsils to evaluate the capabilities of OCT to visualize tonsil tissue components. Despite limited penetration depth, OCT can provide detailed structural information about tonsil tissue with much higher resolution than that of computed tomography, magnetic resonance imaging, and Ultrasound. Different tonsil tissue components such as epithelium, dense connective tissue, lymphoid nodules, and crypts can be visualized by OCT. The co-registered AF imaging can provide matching biochemical information. AF\/OCT scans may provide a non-invasive tool for detecting tonsillar cancers and for studying the natural history of their development.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('136','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_136\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2014c.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25542010\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1371\/journal.pone.0115889\" title=\"Follow DOI:10.1371\/journal.pone.0115889\" target=\"_blank\">doi:10.1371\/journal.pone.0115889<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('136','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2013\">2013<\/h3><div class=\"tp_publication tp_publication_inbook\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Endoscopic Confocal Microscopy\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/9780367379070.jpeg\" width=\"128\" alt=\"Endoscopic Confocal Microscopy\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre;  MacAulay, Calum;  Follen, Michele<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/book\/9781420099584\" title=\"https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/book\/9781420099584\" target=\"blank\">Endoscopic Confocal Microscopy<\/a> <span class=\"tp_pub_type tp_  inbook\">Book Chapter<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span> Zeng, Haishan (Ed.): <span class=\"tp_pub_additional_chapter\"> Chapter 8, <\/span><span class=\"tp_pub_additional_pages\">pp. 103, <\/span><span class=\"tp_pub_additional_publisher\">Taylor &amp; Francis, <\/span><span class=\"tp_pub_additional_year\">2013<\/span>, <span class=\"tp_pub_additional_isbn\">ISBN: 9781420083460<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_120\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('120','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_120\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('120','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_120\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@inbook{lane20138,<br \/>\r\ntitle = {Endoscopic Confocal Microscopy},<br \/>\r\nauthor = { Pierre Lane and Calum MacAulay and Michele Follen},<br \/>\r\neditor = {Haishan Zeng},<br \/>\r\nurl = {https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/book\/9781420099584},<br \/>\r\nisbn = {9781420083460},<br \/>\r\nyear  = {2013},<br \/>\r\ndate = {2013-12-09},<br \/>\r\nurldate = {2013-12-09},<br \/>\r\njournal = {Diagnostic Endoscopy},<br \/>\r\npages = {103},<br \/>\r\npublisher = {Taylor & Francis},<br \/>\r\nchapter = {8},<br \/>\r\nseries = {Series in Medical Physics and Biomedical Engineering},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {inbook}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('120','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_120\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/book\/9781420099584\" title=\"https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/bo[...]\" target=\"_blank\">https:\/\/www.routledge.com\/Medical-Equipment-Management\/Willson-Ison-Tabakov\/p\/bo[...]<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('120','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"In vivo lung microvasculature visualized in three dimensions using fiber-optic color Doppler optical coherence tomography\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2013.jpg\" width=\"128\" alt=\"In vivo lung microvasculature visualized in three dimensions using fiber-optic color Doppler optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lee, Anthony MD;  Ohtani, Keishi;  MacAulay, Calum;  McWilliams, Annette;  Shaipanich, Tawimas;  Yang, Victor XD;  Lam, Stephen;  Lane, Pierre<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.18.5.050501\" title=\"In vivo lung microvasculature visualized in three dimensions using fiber-optic color Doppler optical coherence tomography\" target=\"blank\">In vivo lung microvasculature visualized in three dimensions using fiber-optic color Doppler optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 18, <\/span><span class=\"tp_pub_additional_number\">no. 5, <\/span><span class=\"tp_pub_additional_pages\">pp. 050501\u2013050501, <\/span><span class=\"tp_pub_additional_year\">2013<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_75\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('75','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_75\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('75','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_75\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('75','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_75\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lee2013vivo,<br \/>\r\ntitle = {In vivo lung microvasculature visualized in three dimensions using fiber-optic color Doppler optical coherence tomography},<br \/>\r\nauthor = { Anthony MD Lee and Keishi Ohtani and Calum MacAulay and Annette McWilliams and Tawimas Shaipanich and Victor XD Yang and Stephen Lam and Pierre Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2013.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/ 23625308, PubMed},<br \/>\r\ndoi = {10.1117\/1.JBO.18.5.050501},<br \/>\r\nyear  = {2013},<br \/>\r\ndate = {2013-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {18},<br \/>\r\nnumber = {5},<br \/>\r\npages = {050501--050501},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {For the first time, the use of fiber-optic color Doppler optical coherence tomography (CDOCT) to map in vivo the three-dimensional (3-D) vascular network of airway segments in human lungs is demonstrated. Visualizing the 3-D vascular network in the lungs may provide new opportunities for detecting and monitoring lung diseases such as asthma, chronic obstructive pulmonary disease, and lung cancer. Our CDOCT instrument employs a rotary fiber-optic probe that provides simultaneous two-dimensional (2-D) real-time structural optical coherence tomography (OCT) and CDOCT imaging at frame rates up to 12.5 frames per second. Controlled pullback of the probe allows 3-D vascular mapping in airway segments up to 50 mm in length in a single acquisition. We demonstrate the ability of CDOCT to map both small and large vessels. In one example, CDOCT imaging allows assignment of a feature in the structural OCT image as a large (\u223c1\u2009 mm diameter) blood vessel. In a second example, a smaller vessel (\u223c80\u2009 \u03bcm diameter) that is indistinguishable in the structural OCT image is fully visualized in 3-D using CDOCT.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('75','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_75\" style=\"display:none;\"><div class=\"tp_abstract_entry\">For the first time, the use of fiber-optic color Doppler optical coherence tomography (CDOCT) to map in vivo the three-dimensional (3-D) vascular network of airway segments in human lungs is demonstrated. Visualizing the 3-D vascular network in the lungs may provide new opportunities for detecting and monitoring lung diseases such as asthma, chronic obstructive pulmonary disease, and lung cancer. Our CDOCT instrument employs a rotary fiber-optic probe that provides simultaneous two-dimensional (2-D) real-time structural optical coherence tomography (OCT) and CDOCT imaging at frame rates up to 12.5 frames per second. Controlled pullback of the probe allows 3-D vascular mapping in airway segments up to 50 mm in length in a single acquisition. We demonstrate the ability of CDOCT to map both small and large vessels. In one example, CDOCT imaging allows assignment of a feature in the structural OCT image as a large (\u223c1\u2009 mm diameter) blood vessel. In a second example, a smaller vessel (\u223c80\u2009 \u03bcm diameter) that is indistinguishable in the structural OCT image is fully visualized in 3-D using CDOCT.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('75','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_75\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lee-2013.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/ 23625308\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.18.5.050501\" title=\"Follow DOI:10.1117\/1.JBO.18.5.050501\" target=\"_blank\">doi:10.1117\/1.JBO.18.5.050501<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('75','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Ex vivo confocal imaging with contrast agents for the detection of oral potentially malignant lesions\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Hallani-2013.jpg\" width=\"128\" alt=\"Ex vivo confocal imaging with contrast agents for the detection of oral potentially malignant lesions\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Hallani, S El;  Poh, CF;  Macaulay, CE;  Follen, M;  Guillaud, M;  Lane, P<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.oraloncology.2013.01.009\" title=\"Ex vivo confocal imaging with contrast agents for the detection of oral potentially malignant lesions\" target=\"blank\">Ex vivo confocal imaging with contrast agents for the detection of oral potentially malignant lesions<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Oral oncology, <\/span><span class=\"tp_pub_additional_volume\">vol. 49, <\/span><span class=\"tp_pub_additional_number\">no. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. 582\u2013590, <\/span><span class=\"tp_pub_additional_year\">2013<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_77\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('77','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_77\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{el2013ex,<br \/>\r\ntitle = {Ex vivo confocal imaging with contrast agents for the detection of oral potentially malignant lesions},<br \/>\r\nauthor = { S El Hallani and CF Poh and CE Macaulay and M Follen and M Guillaud and P Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Hallani-2013.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/23415144, PubMed},<br \/>\r\ndoi = {10.1016\/j.oraloncology.2013.01.009},<br \/>\r\nyear  = {2013},<br \/>\r\ndate = {2013-01-01},<br \/>\r\njournal = {Oral oncology},<br \/>\r\nvolume = {49},<br \/>\r\nnumber = {6},<br \/>\r\npages = {582--590},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {Objectives<br \/>\r\n<br \/>\r\nWe investigated the potential use of real-time confocal microscpy in the non-invasive detection of occult oral potentially malignant lesions. Our objectives were to select the best fluorescence contrast agent for cellular morphology enhancement, to build an atlas of confocal microscopic images of normal human oral mucosa, and to determine the accuracy of confocal microscopy to recognise oral high-grade dysplasia lesions on live human tissue.<br \/>\r\n<br \/>\r\nMaterials and Methods<br \/>\r\n<br \/>\r\nFive clinically used fluorescent contrast agents were tested in vitro on cultured human cells and validated ex vivo on human oral mucosa. Images acquired ex vivo from normal and diseased human oral biopsies with bench-top fluorescent confocal microscope were compared to conventional histology. Image analyzer software was used as an adjunct tool to objectively compare high-grade dysplasia versus low-grade dysplasia and normal epithelium.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nAcriflavine Hydrochloride provided the best cellular contrast by preferentially staining the nuclei of the epithelium. Using topical application of Acriflavine Hydrochloride followed by confocal microscopy, we could define morphological characteristics of each cellular layer of the normal human oral mucosa, building an atlas of histology-like images. Applying this technique to diseased oral tissue specimen, we were also able to accurately diagnose the presence of high-grade dysplasia through the increased cellularity and changes in nuclear morphological features. Objective measurement of cellular density by quantitative image analysis was a strong discriminant to differentiate between high-grade dysplasia and low-grade dysplasia lesions.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nPending clinical investigation, real-time confocal microscopy may become a useful adjunct to detect precancerous lesions that are at high risk of cancer progression, direct biopsy and delineate excision margins.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_77\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Objectives<br \/>\r\n<br \/>\r\nWe investigated the potential use of real-time confocal microscpy in the non-invasive detection of occult oral potentially malignant lesions. Our objectives were to select the best fluorescence contrast agent for cellular morphology enhancement, to build an atlas of confocal microscopic images of normal human oral mucosa, and to determine the accuracy of confocal microscopy to recognise oral high-grade dysplasia lesions on live human tissue.<br \/>\r\n<br \/>\r\nMaterials and Methods<br \/>\r\n<br \/>\r\nFive clinically used fluorescent contrast agents were tested in vitro on cultured human cells and validated ex vivo on human oral mucosa. Images acquired ex vivo from normal and diseased human oral biopsies with bench-top fluorescent confocal microscope were compared to conventional histology. Image analyzer software was used as an adjunct tool to objectively compare high-grade dysplasia versus low-grade dysplasia and normal epithelium.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nAcriflavine Hydrochloride provided the best cellular contrast by preferentially staining the nuclei of the epithelium. Using topical application of Acriflavine Hydrochloride followed by confocal microscopy, we could define morphological characteristics of each cellular layer of the normal human oral mucosa, building an atlas of histology-like images. Applying this technique to diseased oral tissue specimen, we were also able to accurately diagnose the presence of high-grade dysplasia through the increased cellularity and changes in nuclear morphological features. Objective measurement of cellular density by quantitative image analysis was a strong discriminant to differentiate between high-grade dysplasia and low-grade dysplasia lesions.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nPending clinical investigation, real-time confocal microscopy may become a useful adjunct to detect precancerous lesions that are at high risk of cancer progression, direct biopsy and delineate excision margins.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_77\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Hallani-2013.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/23415144\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.oraloncology.2013.01.009\" title=\"Follow DOI:10.1016\/j.oraloncology.2013.01.009\" target=\"_blank\">doi:10.1016\/j.oraloncology.2013.01.009<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('77','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Oral mucosa optical biopsy by a novel handheld fluorescent confocal microscope specifically developed: technologic improvements and future prospects\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Contaldo-2013.jpg\" width=\"128\" alt=\"Oral mucosa optical biopsy by a novel handheld fluorescent confocal microscope specifically developed: technologic improvements and future prospects\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Contaldo, Maria;  Poh, Catherine F;  Guillaud, Martial;  Lucchese, Alberta;  Rullo, Rosario;  Lam, Sylvia;  Serpico, Rosario;  MacAulay, Calum E;  Lane, Pierre M<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.oooo.2013.09.006\" title=\"Oral mucosa optical biopsy by a novel handheld fluorescent confocal microscope specifically developed: technologic improvements and future prospects\" target=\"blank\">Oral mucosa optical biopsy by a novel handheld fluorescent confocal microscope specifically developed: technologic improvements and future prospects<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Oral surgery, oral medicine, oral pathology and oral radiology, <\/span><span class=\"tp_pub_additional_volume\">vol. 116, <\/span><span class=\"tp_pub_additional_number\">no. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. 752\u2013758, <\/span><span class=\"tp_pub_additional_year\">2013<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_82\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('82','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_82\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{contaldo2013oral,<br \/>\r\ntitle = {Oral mucosa optical biopsy by a novel handheld fluorescent confocal microscope specifically developed: technologic improvements and future prospects},<br \/>\r\nauthor = { Maria Contaldo and Catherine F Poh and Martial Guillaud and Alberta Lucchese and Rosario Rullo and Sylvia Lam and Rosario Serpico and Calum E MacAulay and Pierre M Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Contaldo-2013.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24237726, Pubmed},<br \/>\r\ndoi = {10.1016\/j.oooo.2013.09.006},<br \/>\r\nyear  = {2013},<br \/>\r\ndate = {2013-01-01},<br \/>\r\njournal = {Oral surgery, oral medicine, oral pathology and oral radiology},<br \/>\r\nvolume = {116},<br \/>\r\nnumber = {6},<br \/>\r\npages = {752--758},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {Objective<br \/>\r\n<br \/>\r\nThis pilot study evaluated the baseline effectiveness of a novel handheld fluorescent confocal microscope (FCM) specifically developed for oral mucosa imaging and compared the results with the literature.<br \/>\r\n<br \/>\r\nStudy Design<br \/>\r\n<br \/>\r\nFour different oral sites (covering the mucosa of the lip and of the ventral tongue, the masticatory mucosa of the gingiva, and the specialized mucosa of the dorsal tongue) in 6 healthy nonsmokers were imaged by an FCM made up of a confocal fiberoptic probe ergonomically designed for in vivo oral examination, using light at the wavelength of 457 nm able to excite the fluorophore acriflavine hydrochloride, topically administered. In total, 24 mucosal areas were examined.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nThe FCM was able to distinctly define epithelial cells, bacterial plaque, and inflammatory cells and to image submucosal structures by detecting their intrinsic fluorescence.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nWhen compared with other devices, this FCM allowed the user to image each oral site at higher magnification, thus resulting in a clearer view.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_82\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Objective<br \/>\r\n<br \/>\r\nThis pilot study evaluated the baseline effectiveness of a novel handheld fluorescent confocal microscope (FCM) specifically developed for oral mucosa imaging and compared the results with the literature.<br \/>\r\n<br \/>\r\nStudy Design<br \/>\r\n<br \/>\r\nFour different oral sites (covering the mucosa of the lip and of the ventral tongue, the masticatory mucosa of the gingiva, and the specialized mucosa of the dorsal tongue) in 6 healthy nonsmokers were imaged by an FCM made up of a confocal fiberoptic probe ergonomically designed for in vivo oral examination, using light at the wavelength of 457 nm able to excite the fluorophore acriflavine hydrochloride, topically administered. In total, 24 mucosal areas were examined.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nThe FCM was able to distinctly define epithelial cells, bacterial plaque, and inflammatory cells and to image submucosal structures by detecting their intrinsic fluorescence.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nWhen compared with other devices, this FCM allowed the user to image each oral site at higher magnification, thus resulting in a clearer view.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_82\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Contaldo-2013.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24237726\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.oooo.2013.09.006\" title=\"Follow DOI:10.1016\/j.oooo.2013.09.006\" target=\"_blank\">doi:10.1016\/j.oooo.2013.09.006<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('82','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Multimodal tissue imaging: using coregistered optical tomography data to estimate tissue autofluorescence intensity change due to scattering and absorption by neoplastic epithelial cells\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2013.jpg\" width=\"128\" alt=\"Multimodal tissue imaging: using coregistered optical tomography data to estimate tissue autofluorescence intensity change due to scattering and absorption by neoplastic epithelial cells\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Pahlevaninezhad, Hamid;  Cecic, Ivana;  Lee, Anthony MD;  Kyle, Alastair H;  Lam, Stephen;  MacAulay, Calum;  Lane, Pierre M<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.18.10.106007\" title=\"Multimodal tissue imaging: using coregistered optical tomography data to estimate tissue autofluorescence intensity change due to scattering and absorption by neoplastic epithelial cells\" target=\"blank\">Multimodal tissue imaging: using coregistered optical tomography data to estimate tissue autofluorescence intensity change due to scattering and absorption by neoplastic epithelial cells<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 18, <\/span><span class=\"tp_pub_additional_number\">no. 10, <\/span><span class=\"tp_pub_additional_pages\">pp. 106007\u2013106007, <\/span><span class=\"tp_pub_additional_year\">2013<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_101\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('101','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_101\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{pahlevaninezhad2013multimodal,<br \/>\r\ntitle = {Multimodal tissue imaging: using coregistered optical tomography data to estimate tissue autofluorescence intensity change due to scattering and absorption by neoplastic epithelial cells},<br \/>\r\nauthor = { Hamid Pahlevaninezhad and Ivana Cecic and Anthony MD Lee and Alastair H Kyle and Stephen Lam and Calum MacAulay and Pierre M Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2013.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24108573, Pubmed},<br \/>\r\ndoi = {10.1117\/1.JBO.18.10.106007},<br \/>\r\nyear  = {2013},<br \/>\r\ndate = {2013-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {18},<br \/>\r\nnumber = {10},<br \/>\r\npages = {106007--106007},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {Autofluorescence (AF) imaging provides valuable information about the structural and chemical states of tissue that can be used for early cancer detection. Optical scattering and absorption of excitation and emission light by the epithelium can significantly affect observed tissue AF intensity. Determining the effect of epithelial attenuation on the AF intensity could lead to a more accurate interpretation of AF intensity. We propose to use optical coherence tomography coregistered with AF imaging to characterize the AF attenuation due to the epithelium. We present imaging results from three vital tissue models, each consisting of a three-dimensional tissue culture grown from one of three epithelial cell lines (HCT116, OVCAR8, and MCF7) and immobilized on a fluorescence substrate. The AF loss profiles in the tissue layer show two different regimes, each approximately linearly decreasing with thickness. For thin cell cultures (&lt;300 \u03bcm), the AF signal changes as AF(t)\/AF(0)=1-1.3t (t is the thickness in millimeter). For thick cell cultures (&gt;400 \u03bcm), the AF loss profiles have different intercepts but similar slopes. The data presented here can be used to estimate AF loss due to a change in the epithelial layer thickness and potentially to reduce AF bronchoscopy false positives due to inflammation and non-neoplastic epithelial thickening.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_101\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Autofluorescence (AF) imaging provides valuable information about the structural and chemical states of tissue that can be used for early cancer detection. Optical scattering and absorption of excitation and emission light by the epithelium can significantly affect observed tissue AF intensity. Determining the effect of epithelial attenuation on the AF intensity could lead to a more accurate interpretation of AF intensity. We propose to use optical coherence tomography coregistered with AF imaging to characterize the AF attenuation due to the epithelium. We present imaging results from three vital tissue models, each consisting of a three-dimensional tissue culture grown from one of three epithelial cell lines (HCT116, OVCAR8, and MCF7) and immobilized on a fluorescence substrate. The AF loss profiles in the tissue layer show two different regimes, each approximately linearly decreasing with thickness. For thin cell cultures (&lt;300 \u03bcm), the AF signal changes as AF(t)\/AF(0)=1-1.3t (t is the thickness in millimeter). For thick cell cultures (&gt;400 \u03bcm), the AF loss profiles have different intercepts but similar slopes. The data presented here can be used to estimate AF loss due to a change in the epithelial layer thickness and potentially to reduce AF bronchoscopy false positives due to inflammation and non-neoplastic epithelial thickening.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_101\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Pahlevaninezhad-2013.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24108573\" title=\"Pubmed\" target=\"_blank\">Pubmed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.JBO.18.10.106007\" title=\"Follow DOI:10.1117\/1.JBO.18.10.106007\" target=\"_blank\">doi:10.1117\/1.JBO.18.10.106007<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('101','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2012\">2012<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Has fluorescence spectroscopy come of age? A case series of oral precancers and cancers using white light, fluorescent light at 405 nm, and reflected light at 545 nm using the Trimira Identafi 3000\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012.jpg\" width=\"128\" alt=\"Has fluorescence spectroscopy come of age? A case series of oral precancers and cancers using white light, fluorescent light at 405 nm, and reflected light at 545 nm using the Trimira Identafi 3000\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre;  Follen, Michele;  MacAulay, Calum<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.09.031\" title=\"Has fluorescence spectroscopy come of age? A case series of oral precancers and cancers using white light, fluorescent light at 405 nm, and reflected light at 545 nm using the Trimira Identafi 3000\" target=\"blank\">Has fluorescence spectroscopy come of age? A case series of oral precancers and cancers using white light, fluorescent light at 405 nm, and reflected light at 545 nm using the Trimira Identafi 3000<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Gender medicine, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. S25\u2013S35, <\/span><span class=\"tp_pub_additional_year\">2012<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_72\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('72','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_72\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('72','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_72\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('72','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_72\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2012has,<br \/>\r\ntitle = {Has fluorescence spectroscopy come of age? A case series of oral precancers and cancers using white light, fluorescent light at 405 nm, and reflected light at 545 nm using the Trimira Identafi 3000},<br \/>\r\nauthor = { Pierre Lane and Michele Follen and Calum MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/22340638, PubMed},<br \/>\r\ndoi = {10.1016\/j.genm.2011.09.031},<br \/>\r\nyear  = {2012},<br \/>\r\ndate = {2012-01-01},<br \/>\r\njournal = {Gender medicine},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {1},<br \/>\r\npages = {S25--S35},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {Objectives<br \/>\r\n<br \/>\r\nThe objective of this study was to present a case series of oral precancers and cancers that have been photographed during larger ongoing clinical trials.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nOver 300 patients were measured at 2 clinical sites that are comprehensive cancer centers and a faculty practice associated with a major dental school. Each site is conducting independent research on the sensitivity and specificity of several optical technologies for the diagnosis of oral neoplasia. The cases presented in this case series were taken from the larger database of images from the clinical trials using the aforementioned device. Optical spectroscopy was performed and biopsies obtained from all sites measured, representing abnormal and normal areas on comprehensive white light examination and after use of the fluorescence and reflectance spectroscopy device. The gold standard of test accuracy was the histologic report of biopsies read by the study histopathologists at each of the 3 study sites.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nComprehensive white light examination showed some lesions; however, the addition of a fluorescence image and a selected reflectance wavelength was helpful in identifying other characteristics of the lesions. The addition of the violet light-induced fluorescence excited at 405 nm provided an additional view of both the stromal neovasculature of the lesions and the stromal changes associated with lesion growth that were biologically indicative of stromal breakdown. The addition of 545 nm green\u2013amber light reflectance increased the view of the keratinized image and allowed the abnormal surface vasculature to be more prominent.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nOptical spectroscopy is a promising technology for the diagnosis of oral neoplasia. The conclusion of several ongoing clinical trials and an eventual randomized Phase III clinical trial will provide definitive findings that sensitivity is or is not increased over comprehensive white light examination.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('72','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_72\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Objectives<br \/>\r\n<br \/>\r\nThe objective of this study was to present a case series of oral precancers and cancers that have been photographed during larger ongoing clinical trials.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nOver 300 patients were measured at 2 clinical sites that are comprehensive cancer centers and a faculty practice associated with a major dental school. Each site is conducting independent research on the sensitivity and specificity of several optical technologies for the diagnosis of oral neoplasia. The cases presented in this case series were taken from the larger database of images from the clinical trials using the aforementioned device. Optical spectroscopy was performed and biopsies obtained from all sites measured, representing abnormal and normal areas on comprehensive white light examination and after use of the fluorescence and reflectance spectroscopy device. The gold standard of test accuracy was the histologic report of biopsies read by the study histopathologists at each of the 3 study sites.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nComprehensive white light examination showed some lesions; however, the addition of a fluorescence image and a selected reflectance wavelength was helpful in identifying other characteristics of the lesions. The addition of the violet light-induced fluorescence excited at 405 nm provided an additional view of both the stromal neovasculature of the lesions and the stromal changes associated with lesion growth that were biologically indicative of stromal breakdown. The addition of 545 nm green\u2013amber light reflectance increased the view of the keratinized image and allowed the abnormal surface vasculature to be more prominent.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nOptical spectroscopy is a promising technology for the diagnosis of oral neoplasia. The conclusion of several ongoing clinical trials and an eventual randomized Phase III clinical trial will provide definitive findings that sensitivity is or is not increased over comprehensive white light examination.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('72','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_72\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/22340638\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.09.031\" title=\"Follow DOI:10.1016\/j.genm.2011.09.031\" target=\"_blank\">doi:10.1016\/j.genm.2011.09.031<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('72','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Oral fluorescence imaging using 405-nm excitation, aiding the discrimination of cancers and precancers by identifying changes in collagen and elastic breakdown and neovascularization in the underlying stroma\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012a.jpg\" width=\"128\" alt=\"Oral fluorescence imaging using 405-nm excitation, aiding the discrimination of cancers and precancers by identifying changes in collagen and elastic breakdown and neovascularization in the underlying stroma\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre;  Lam, Sylvia;  Follen, Michele;  MacAulay, Calum<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.11.006\" title=\"Oral fluorescence imaging using 405-nm excitation, aiding the discrimination of cancers and precancers by identifying changes in collagen and elastic breakdown and neovascularization in the underlying stroma\" target=\"blank\">Oral fluorescence imaging using 405-nm excitation, aiding the discrimination of cancers and precancers by identifying changes in collagen and elastic breakdown and neovascularization in the underlying stroma<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Gender medicine, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. S78\u2013S82, <\/span><span class=\"tp_pub_additional_year\">2012<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_86\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('86','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_86\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('86','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_86\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('86','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_86\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2012oral,<br \/>\r\ntitle = {Oral fluorescence imaging using 405-nm excitation, aiding the discrimination of cancers and precancers by identifying changes in collagen and elastic breakdown and neovascularization in the underlying stroma},<br \/>\r\nauthor = { Pierre Lane and Sylvia Lam and Michele Follen and Calum MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012a.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/22340643, PubMed},<br \/>\r\ndoi = {10.1016\/j.genm.2011.11.006},<br \/>\r\nyear  = {2012},<br \/>\r\ndate = {2012-01-01},<br \/>\r\njournal = {Gender medicine},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {1},<br \/>\r\npages = {S78--S82},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {Background<br \/>\r\n<br \/>\r\nOptical spectroscopy and imaging devices are being developed and tested for the screening and diagnosis of cancer and precancer in multiple organ sites.<br \/>\r\n<br \/>\r\nObjective<br \/>\r\n<br \/>\r\nThe aim of the study reported here is to optimize the capability of an optical imaging device to discriminate precancerous tissue from other lesions by identifying ideal excitation wavelengths.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nThe studies reported here used a prototype of a direct fluorescence imaging device that uses 405-nm illumination to excite tissue.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nThere is ample evidence in the literature that 405 nm can distinguish oral cancers from normal tissue. Higher wavelengths may be necessary to differentiate potential confounding lesions, such as abrasions, burns, viral infections, inflammation, and gingivitis.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nImaging at 405 nm could help doctors detect precancerous and cancerous oral lesions. Such imaging could be used by dentists, family practitioners, otorhinolaryngologists, general surgeons, obstetrician gynecologists, and internists, and could greatly increase the number of patients who have lesions detected in the precancerous phase.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('86','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_86\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Background<br \/>\r\n<br \/>\r\nOptical spectroscopy and imaging devices are being developed and tested for the screening and diagnosis of cancer and precancer in multiple organ sites.<br \/>\r\n<br \/>\r\nObjective<br \/>\r\n<br \/>\r\nThe aim of the study reported here is to optimize the capability of an optical imaging device to discriminate precancerous tissue from other lesions by identifying ideal excitation wavelengths.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nThe studies reported here used a prototype of a direct fluorescence imaging device that uses 405-nm illumination to excite tissue.<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nThere is ample evidence in the literature that 405 nm can distinguish oral cancers from normal tissue. Higher wavelengths may be necessary to differentiate potential confounding lesions, such as abrasions, burns, viral infections, inflammation, and gingivitis.<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nImaging at 405 nm could help doctors detect precancerous and cancerous oral lesions. Such imaging could be used by dentists, family practitioners, otorhinolaryngologists, general surgeons, obstetrician gynecologists, and internists, and could greatly increase the number of patients who have lesions detected in the precancerous phase.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('86','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_86\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2012a.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/22340643\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.11.006\" title=\"Follow DOI:10.1016\/j.genm.2011.11.006\" target=\"_blank\">doi:10.1016\/j.genm.2011.11.006<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('86','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Optical technologies and molecular imaging for cervical neoplasia: a program project update\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Buys-2012.jpg\" width=\"128\" alt=\"Optical technologies and molecular imaging for cervical neoplasia: a program project update\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Buys, Timon PH;  Cantor, Scott B;  Guillaud, Martial;  Adler-Storthz, Karen;  Cox, Dennis D;  Okolo, Clement;  Arulogon, Oyedunni;  Oladepo, Oladimeji;  Basen-Engquist, Karen;  Shinn, Eileen;  Yamal, Jos\u00e9-Miguel;  Beck, J. Robert;  Scheurer, Michael E.; van Niekerk, Dirk;  Malpica, Anais;  Matisic, Jasenka;  Staerkel, Gregg;  Atkinson, Edward Neely;  Bidaut, Luc;  Lane, Pierre;  Benedet, J. Lou;  Miller, Dianne;  Ehlen, Tom;  Price, Roderick;  Adewole, Isaac F.;  MacAulay, Calum;  Follen, Michele<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.08.002\" title=\"Optical technologies and molecular imaging for cervical neoplasia: a program project update\" target=\"blank\">Optical technologies and molecular imaging for cervical neoplasia: a program project update<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Gender medicine, <\/span><span class=\"tp_pub_additional_volume\">vol. 9, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. S7\u2013S24, <\/span><span class=\"tp_pub_additional_year\">2012<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_88\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('88','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_88\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{buys2012optical,<br \/>\r\ntitle = {Optical technologies and molecular imaging for cervical neoplasia: a program project update},<br \/>\r\nauthor = { Timon PH Buys and Scott B Cantor and Martial Guillaud and Karen Adler-Storthz and Dennis D Cox and Clement Okolo and Oyedunni Arulogon and Oladimeji Oladepo and Karen Basen-Engquist and Eileen Shinn and Jos\u00e9-Miguel Yamal and J. Robert Beck and Michael E. Scheurer and Dirk van Niekerk and Anais Malpica and Jasenka Matisic and Gregg Staerkel and Edward Neely Atkinson and Luc Bidaut and Pierre Lane and J. Lou Benedet and Dianne Miller and Tom Ehlen and Roderick Price and Isaac F. Adewole and Calum MacAulay and Michele Follen },<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Buys-2012.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/21944317, PubMed},<br \/>\r\ndoi = {10.1016\/j.genm.2011.08.002},<br \/>\r\nyear  = {2012},<br \/>\r\ndate = {2012-01-01},<br \/>\r\njournal = {Gender medicine},<br \/>\r\nvolume = {9},<br \/>\r\nnumber = {1},<br \/>\r\npages = {S7--S24},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {There is an urgent global need for effective and affordable approaches to cervical cancer screening and diagnosis. In developing nations, cervical malignancies remain the leading cause of cancer-related deaths in women. This reality may be difficult to accept given that these deaths are largely preventable; where cervical screening programs have been implemented, cervical cancer-related deaths have decreased dramatically. In developed countries, the challenges of cervical disease stem from high costs and overtreatment. The National Cancer Institute-funded Program Project is evaluating the applicability of optical technologies in cervical cancer. The mandate of the project is to create tools for disease detection and diagnosis that are inexpensive, require minimal expertise, are more accurate than existing modalities, and can be feasibly implemented in a variety of clinical settings. This article presents the status and long-term goals of the project.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_88\" style=\"display:none;\"><div class=\"tp_abstract_entry\">There is an urgent global need for effective and affordable approaches to cervical cancer screening and diagnosis. In developing nations, cervical malignancies remain the leading cause of cancer-related deaths in women. This reality may be difficult to accept given that these deaths are largely preventable; where cervical screening programs have been implemented, cervical cancer-related deaths have decreased dramatically. In developed countries, the challenges of cervical disease stem from high costs and overtreatment. The National Cancer Institute-funded Program Project is evaluating the applicability of optical technologies in cervical cancer. The mandate of the project is to create tools for disease detection and diagnosis that are inexpensive, require minimal expertise, are more accurate than existing modalities, and can be feasibly implemented in a variety of clinical settings. This article presents the status and long-term goals of the project.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_88\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Buys-2012.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/21944317\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.genm.2011.08.002\" title=\"Follow DOI:10.1016\/j.genm.2011.08.002\" target=\"_blank\">doi:10.1016\/j.genm.2011.08.002<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('88','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2011\">2011<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Autofluorescence imaging can identify preinvasive or clinically occult lesions in fallopian tube epithelium: a promising step towards screening and early detection\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/McAlpine-2011.jpg\" width=\"128\" alt=\"Autofluorescence imaging can identify preinvasive or clinically occult lesions in fallopian tube epithelium: a promising step towards screening and early detection\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> McAlpine, JN;  Hallani, S El;  Lam, SF;  Kalloger, SE;  Luk, M;  Huntsman, DG;  MacAulay, C;  Gilks, CB;  Miller, DM;  Lane, PM<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1016\/j.ygyno.2010.12.333\" title=\"Autofluorescence imaging can identify preinvasive or clinically occult lesions in fallopian tube epithelium: a promising step towards screening and early detection\" target=\"blank\">Autofluorescence imaging can identify preinvasive or clinically occult lesions in fallopian tube epithelium: a promising step towards screening and early detection<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Gynecologic oncology, <\/span><span class=\"tp_pub_additional_volume\">vol. 120, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 385\u2013392, <\/span><span class=\"tp_pub_additional_year\">2011<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_68\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('68','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_68\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('68','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_68\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('68','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_68\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{mcalpine2011autofluorescence,<br \/>\r\ntitle = {Autofluorescence imaging can identify preinvasive or clinically occult lesions in fallopian tube epithelium: a promising step towards screening and early detection},<br \/>\r\nauthor = { JN McAlpine and S El Hallani and SF Lam and SE Kalloger and M Luk and DG Huntsman and C MacAulay and CB Gilks and DM Miller and PM Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/McAlpine-2011.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/ 21237503, PubMed},<br \/>\r\ndoi = {10.1016\/j.ygyno.2010.12.333},<br \/>\r\nyear  = {2011},<br \/>\r\ndate = {2011-01-01},<br \/>\r\njournal = {Gynecologic oncology},<br \/>\r\nvolume = {120},<br \/>\r\nnumber = {3},<br \/>\r\npages = {385--392},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nabstract = {Background<br \/>\r\n<br \/>\r\nOptical imaging systems are robust, portable, relatively inexpensive, and have proven utility in detecting precancerous lesions in the lung, esophagus, colon, oral cavity and cervix. We describe the use of light-induced endogenous fluorescence (autofluorescence) in identifying preinvasive and occult carcinomas in ex vivo samples of human fallopian tube (FT) epithelium.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nWomen undergoing surgery for an i) ovarian mass, ii) a history suggestive of hereditary breast-ovarian cancer, or iii) known serous ovarian cancer following neoadjuvant chemotherapy (NAC) were approached for informed consent. Immediately following surgery, FT's were photographed in reflectance and fluorescence at high resolution. Images included: (1) white-light reflectance of luminal\/epithelial surface; (2) narrow-band green reflectance (570 nm) (3) green autofluorescence (405\/436 nm excitation); and (4) blue autofluorescence (405 nm excitation). Areas revealing a loss of natural tissue fluorescence or marked increase in tissue microvasculature were recorded and compared to final histopathologic diagnosis (SEE-FIM protocol).<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nFifty-six cases involving one or both fallopian tubes underwent reflectance and fluorescence visualization. Nine cases were excluded, either secondary to non-ovarian primary pathology (7) or excessive trauma (2) rendering tissue interpretation impossible. Of the 47 cases remaining, there were 11 high grade serous (HGS) and 9 non-serous ovarian carcinomas undergoing primary debulking surgery, 5 serous carcinomas having received NAC, 8 benign ovarian tumors, and 14 women undergoing risk-reducing bilateral salpingo-oophorectomy (RRBSO). Methodology was feasible, efficient, and reproducible. TIC or carcinoma was identified in 7\/11 HGS, 3\/5 NAC, and 1\/14 RRBSO. Optical images were reviewed to determine test positive or negative based on standardized criteria. Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated for the entire cohort (73%; 83%; 57%; 91%) and in a subgroup that excluded non-serous histology (87.5%; 92%; 78%; 96%).<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nAbnormal FT lesions can be identified using ex vivo optical imaging technologies. With this platform, we will move towards genomic interrogation of identified lesions, and developing in vivo screening modalities via falloposcopy.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('68','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_68\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Background<br \/>\r\n<br \/>\r\nOptical imaging systems are robust, portable, relatively inexpensive, and have proven utility in detecting precancerous lesions in the lung, esophagus, colon, oral cavity and cervix. We describe the use of light-induced endogenous fluorescence (autofluorescence) in identifying preinvasive and occult carcinomas in ex vivo samples of human fallopian tube (FT) epithelium.<br \/>\r\n<br \/>\r\nMethods<br \/>\r\n<br \/>\r\nWomen undergoing surgery for an i) ovarian mass, ii) a history suggestive of hereditary breast-ovarian cancer, or iii) known serous ovarian cancer following neoadjuvant chemotherapy (NAC) were approached for informed consent. Immediately following surgery, FT's were photographed in reflectance and fluorescence at high resolution. Images included: (1) white-light reflectance of luminal\/epithelial surface; (2) narrow-band green reflectance (570 nm) (3) green autofluorescence (405\/436 nm excitation); and (4) blue autofluorescence (405 nm excitation). Areas revealing a loss of natural tissue fluorescence or marked increase in tissue microvasculature were recorded and compared to final histopathologic diagnosis (SEE-FIM protocol).<br \/>\r\n<br \/>\r\nResults<br \/>\r\n<br \/>\r\nFifty-six cases involving one or both fallopian tubes underwent reflectance and fluorescence visualization. Nine cases were excluded, either secondary to non-ovarian primary pathology (7) or excessive trauma (2) rendering tissue interpretation impossible. Of the 47 cases remaining, there were 11 high grade serous (HGS) and 9 non-serous ovarian carcinomas undergoing primary debulking surgery, 5 serous carcinomas having received NAC, 8 benign ovarian tumors, and 14 women undergoing risk-reducing bilateral salpingo-oophorectomy (RRBSO). Methodology was feasible, efficient, and reproducible. TIC or carcinoma was identified in 7\/11 HGS, 3\/5 NAC, and 1\/14 RRBSO. Optical images were reviewed to determine test positive or negative based on standardized criteria. Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated for the entire cohort (73%; 83%; 57%; 91%) and in a subgroup that excluded non-serous histology (87.5%; 92%; 78%; 96%).<br \/>\r\n<br \/>\r\nConclusions<br \/>\r\n<br \/>\r\nAbnormal FT lesions can be identified using ex vivo optical imaging technologies. With this platform, we will move towards genomic interrogation of identified lesions, and developing in vivo screening modalities via falloposcopy.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('68','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_68\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/McAlpine-2011.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/ 21237503\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1016\/j.ygyno.2010.12.333\" title=\"Follow DOI:10.1016\/j.ygyno.2010.12.333\" target=\"_blank\">doi:10.1016\/j.ygyno.2010.12.333<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('68','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2009\">2009<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Confocal fluorescence microendoscopy of bronchial epithelium\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009.jpg\" width=\"128\" alt=\"Confocal fluorescence microendoscopy of bronchial epithelium\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre M;  Lam, Stephen;  McWilliams, Annette;  LeRiche, Jean C.;  Anderson, Marshall W;  MacAulay, Calum E<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.3103583\" title=\"Confocal fluorescence microendoscopy of bronchial epithelium\" target=\"blank\">Confocal fluorescence microendoscopy of bronchial epithelium<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 14, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 024008\u2013024008, <\/span><span class=\"tp_pub_additional_year\">2009<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_64\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('64','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_64\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('64','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_64\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('64','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_64\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2009confocal,<br \/>\r\ntitle = {Confocal fluorescence microendoscopy of bronchial epithelium},<br \/>\r\nauthor = { Pierre M Lane and Stephen Lam and Annette McWilliams and Jean C. LeRiche and Marshall W Anderson and Calum E MacAulay },<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/19405738, PubMed},<br \/>\r\ndoi = {10.1117\/1.3103583},<br \/>\r\nyear  = {2009},<br \/>\r\ndate = {2009-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {14},<br \/>\r\nnumber = {2},<br \/>\r\npages = {024008--024008},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {Confocal microendoscopy permits the acquisition of high-resolution real-time confocal images of bronchial mucosa via the instrument channel of an endoscope. We report here on the construction and validation of a confocal fluorescence microendoscope and its use to acquire images of bronchial epithelium in vivo. Our objective is to develop an imaging method that can distinguish preneoplastic lesions from normal epithelium to enable us to study the natural history of these lesions and the efficacy of chemopreventive agents without biopsy removal of the lesion that can introduce a spontaneous regression bias. The instrument employs a laser-scanning engine and bronchoscope-compatible confocal probe consisting of a fiber-optic image guide and a graded-index objective lens. We assessed the potential of topical application of physiological pH cresyl violet (CV) as a fluorescence contrast-enhancing agent for the visualization of tissue morphology. Images acquired ex vivo with the confocal microendoscope were first compared with a bench-top confocal fluorescence microscope and conventional histology. Confocal images from five sites topically stained with CV were then acquired in vivo from high-risk smokers and compared to hematoxylin and eosin stained sections of biopsies taken from the same site. Sufficient contrast in the confocal imagery was obtained to identify cells in the bronchial epithelium. However, further improvements in the miniature objective lens are required to provide sufficient axial resolution for accurate classification of preneoplastic lesions.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('64','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_64\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Confocal microendoscopy permits the acquisition of high-resolution real-time confocal images of bronchial mucosa via the instrument channel of an endoscope. We report here on the construction and validation of a confocal fluorescence microendoscope and its use to acquire images of bronchial epithelium in vivo. Our objective is to develop an imaging method that can distinguish preneoplastic lesions from normal epithelium to enable us to study the natural history of these lesions and the efficacy of chemopreventive agents without biopsy removal of the lesion that can introduce a spontaneous regression bias. The instrument employs a laser-scanning engine and bronchoscope-compatible confocal probe consisting of a fiber-optic image guide and a graded-index objective lens. We assessed the potential of topical application of physiological pH cresyl violet (CV) as a fluorescence contrast-enhancing agent for the visualization of tissue morphology. Images acquired ex vivo with the confocal microendoscope were first compared with a bench-top confocal fluorescence microscope and conventional histology. Confocal images from five sites topically stained with CV were then acquired in vivo from high-risk smokers and compared to hematoxylin and eosin stained sections of biopsies taken from the same site. Sufficient contrast in the confocal imagery was obtained to identify cells in the bronchial epithelium. However, further improvements in the miniature objective lens are required to provide sufficient axial resolution for accurate classification of preneoplastic lesions.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('64','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_64\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/19405738\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.3103583\" title=\"Follow DOI:10.1117\/1.3103583\" target=\"_blank\">doi:10.1117\/1.3103583<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('64','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Terminal reflections in fiber-optic image guides\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009b.jpg\" width=\"128\" alt=\"Terminal reflections in fiber-optic image guides\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre M<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1364\/AO.48.005802\" title=\"Terminal reflections in fiber-optic image guides\" target=\"blank\">Terminal reflections in fiber-optic image guides<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Applied optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 48, <\/span><span class=\"tp_pub_additional_number\">no. 30, <\/span><span class=\"tp_pub_additional_pages\">pp. 5802\u20135810, <\/span><span class=\"tp_pub_additional_year\">2009<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_83\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('83','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_83\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2009terminal,<br \/>\r\ntitle = {Terminal reflections in fiber-optic image guides},<br \/>\r\nauthor = { Pierre M Lane},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009b.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/19844318, PubMed},<br \/>\r\ndoi = {10.1364\/AO.48.005802},<br \/>\r\nyear  = {2009},<br \/>\r\ndate = {2009-01-01},<br \/>\r\njournal = {Applied optics},<br \/>\r\nvolume = {48},<br \/>\r\nnumber = {30},<br \/>\r\npages = {5802--5810},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {Fibered image guides for confocal reflectance endomicroscopy suffer from Fresnel reflections at the fiber terminals, which can limit signal-to-noise ratio in these systems. A model that describes these terminal reflections is presented to better understand how they can be managed most effectively. An expression for the refractive index of termination that minimizes the reflection as a function of the fiber's normalized frequency is derived for step-index fibers, while a graphical solution is presented for graded-index fibers. The model predicts that terminal reflections from graded-index fibers are more sensitive to variations in fiber size and changes in wavelength than step-index fibers. A method is also presented to measure the refractive index that allows one to minimize the terminal reflections in an image guide. The technique uses the inherent mode coupling of the fibers in the image guide, allowing the isolation and measurement of reflections from only one end of the fiber. An achievable minimum backreflection of -36 dB was measured at 635 nm in a commercial image guide with 30,000 fibers.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_83\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Fibered image guides for confocal reflectance endomicroscopy suffer from Fresnel reflections at the fiber terminals, which can limit signal-to-noise ratio in these systems. A model that describes these terminal reflections is presented to better understand how they can be managed most effectively. An expression for the refractive index of termination that minimizes the reflection as a function of the fiber's normalized frequency is derived for step-index fibers, while a graphical solution is presented for graded-index fibers. The model predicts that terminal reflections from graded-index fibers are more sensitive to variations in fiber size and changes in wavelength than step-index fibers. A method is also presented to measure the refractive index that allows one to minimize the terminal reflections in an image guide. The technique uses the inherent mode coupling of the fibers in the image guide, allowing the isolation and measurement of reflections from only one end of the fiber. An achievable minimum backreflection of -36 dB was measured at 635 nm in a commercial image guide with 30,000 fibers.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_83\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009b.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/19844318\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1364\/AO.48.005802\" title=\"Follow DOI:10.1364\/AO.48.005802\" target=\"_blank\">doi:10.1364\/AO.48.005802<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('83','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Reflection-contrast limit of fiber-optic image guides\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009a.jpg\" width=\"128\" alt=\"Reflection-contrast limit of fiber-optic image guides\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre M;  MacAulay, Calum E<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.3269679\" title=\"Reflection-contrast limit of fiber-optic image guides\" target=\"blank\">Reflection-contrast limit of fiber-optic image guides<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 14, <\/span><span class=\"tp_pub_additional_number\">no. 6, <\/span><span class=\"tp_pub_additional_pages\">pp. 064028\u2013064028, <\/span><span class=\"tp_pub_additional_year\">2009<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_96\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('96','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_96\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('96','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_96\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('96','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_96\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2009reflection,<br \/>\r\ntitle = {Reflection-contrast limit of fiber-optic image guides},<br \/>\r\nauthor = { Pierre M Lane and Calum E MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009a.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/20059266, PubMed},<br \/>\r\ndoi = {10.1117\/1.3269679},<br \/>\r\nyear  = {2009},<br \/>\r\ndate = {2009-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {14},<br \/>\r\nnumber = {6},<br \/>\r\npages = {064028--064028},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {Fiber-optic image guides in confocal reflectance endomicroscopes introduce background backscatter that limits the achievable contrast in these devices. We show the dominant source of backscatter from the image guide is due to Rayleigh scattering at short wavelengths and terminal reflections of the fibers at long wavelengths. The effective Rayleigh scattering coefficient and the wavelength-independent reflectivity due terminal reflections are measured experimentally in a commercial image guide. The Rayleigh scattering component of backscatter can be accurately predicted using the fractional refractive-index difference and length of the fibers in the image guide. We also presented a simple model that can be used to predict signal-to-background ratio in a fiber-optic confocal reflectance endomicroscope for biologically relevant tissues and contrast agents that cover a wide range of reflectivity.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('96','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_96\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Fiber-optic image guides in confocal reflectance endomicroscopes introduce background backscatter that limits the achievable contrast in these devices. We show the dominant source of backscatter from the image guide is due to Rayleigh scattering at short wavelengths and terminal reflections of the fibers at long wavelengths. The effective Rayleigh scattering coefficient and the wavelength-independent reflectivity due terminal reflections are measured experimentally in a commercial image guide. The Rayleigh scattering component of backscatter can be accurately predicted using the fractional refractive-index difference and length of the fibers in the image guide. We also presented a simple model that can be used to predict signal-to-background ratio in a fiber-optic confocal reflectance endomicroscope for biologically relevant tissues and contrast agents that cover a wide range of reflectivity.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('96','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_96\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2009a.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/20059266\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.3269679\" title=\"Follow DOI:10.1117\/1.3269679\" target=\"_blank\">doi:10.1117\/1.3269679<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('96','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2007\">2007<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Direct fluorescence visualization of clinically occult high-risk oral premalignant disease using a simple hand-held device\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Poh-2007.jpg\" width=\"128\" alt=\"Direct fluorescence visualization of clinically occult high-risk oral premalignant disease using a simple hand-held device\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Poh, Catherine F;  Ng, Samson P;  Williams, P Michele;  Zhang, Lewei;  Laronde, Denise M;  Lane, Pierre;  MacAulay, Calum;  Rosin, Miriam P<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1002\/hed.20468\" title=\"Direct fluorescence visualization of clinically occult high-risk oral premalignant disease using a simple hand-held device\" target=\"blank\">Direct fluorescence visualization of clinically occult high-risk oral premalignant disease using a simple hand-held device<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Head &amp; neck, <\/span><span class=\"tp_pub_additional_volume\">vol. 29, <\/span><span class=\"tp_pub_additional_number\">no. 1, <\/span><span class=\"tp_pub_additional_pages\">pp. 71\u201376, <\/span><span class=\"tp_pub_additional_year\">2007<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_59\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('59','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_59\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('59','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_59\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('59','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_59\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{poh2007direct,<br \/>\r\ntitle = {Direct fluorescence visualization of clinically occult high-risk oral premalignant disease using a simple hand-held device},<br \/>\r\nauthor = { Catherine F Poh and Samson P Ng and P Michele Williams and Lewei Zhang and Denise M Laronde and Pierre Lane and Calum MacAulay and Miriam P Rosin},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Poh-2007.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16983693, PubMed},<br \/>\r\ndoi = {10.1002\/hed.20468},<br \/>\r\nyear  = {2007},<br \/>\r\ndate = {2007-01-01},<br \/>\r\njournal = {Head & neck},<br \/>\r\nvolume = {29},<br \/>\r\nnumber = {1},<br \/>\r\npages = {71--76},<br \/>\r\npublisher = {Wiley Online Library},<br \/>\r\nabstract = {A considerable proportion of oral cancer and precancer is not clinically apparent and could contribute significantly to the late diagnosis and high mortality of oral cancer. A simple method to identify such occult change is needed.<br \/>\r\n<br \/>\r\nMETHODS:<br \/>\r\nPatients in the Oral Dysplasia Clinics at British Columbia are currently being examined with a simple hand-held device that permits the direct visualization of alterations to autofluorescence in the oral cavity. Tissue showing loss of autofluorescence is biopsied.<br \/>\r\n<br \/>\r\nRESULTS:<br \/>\r\nWe present 3 representative cases in which occult lesions were identified with fluorescence visualization during longitudinal follow-up, resulting in the diagnosis of a primary dysplasia in case 1, a second primary cancer in case 2, and cancer recurrence in case 3.<br \/>\r\n<br \/>\r\nCONCLUSIONS:<br \/>\r\nThis is the first report of the diagnosis of occult oral disease using a simple noninvasive device. These early examples indicate the potential value of this technology to guide the management of patients with oral lesions, facilitating the detection of high-risk changes not apparent with white-light visualization.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('59','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_59\" style=\"display:none;\"><div class=\"tp_abstract_entry\">A considerable proportion of oral cancer and precancer is not clinically apparent and could contribute significantly to the late diagnosis and high mortality of oral cancer. A simple method to identify such occult change is needed.<br \/>\r\n<br \/>\r\nMETHODS:<br \/>\r\nPatients in the Oral Dysplasia Clinics at British Columbia are currently being examined with a simple hand-held device that permits the direct visualization of alterations to autofluorescence in the oral cavity. Tissue showing loss of autofluorescence is biopsied.<br \/>\r\n<br \/>\r\nRESULTS:<br \/>\r\nWe present 3 representative cases in which occult lesions were identified with fluorescence visualization during longitudinal follow-up, resulting in the diagnosis of a primary dysplasia in case 1, a second primary cancer in case 2, and cancer recurrence in case 3.<br \/>\r\n<br \/>\r\nCONCLUSIONS:<br \/>\r\nThis is the first report of the diagnosis of occult oral disease using a simple noninvasive device. These early examples indicate the potential value of this technology to guide the management of patients with oral lesions, facilitating the detection of high-risk changes not apparent with white-light visualization.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('59','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_59\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Poh-2007.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16983693\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1002\/hed.20468\" title=\"Follow DOI:10.1002\/hed.20468\" target=\"_blank\">doi:10.1002\/hed.20468<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('59','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2006\">2006<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Simple device for the direct visualization of oral-cavity tissue fluorescence\" src=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2006.jpg\" width=\"128\" alt=\"Simple device for the direct visualization of oral-cavity tissue fluorescence\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre M;  Gilhuly, Terence;  Whitehead, Peter;  Zeng, Haishan;  Poh, Catherine F;  Ng, Samson;  Williams, P Michele;  Zhang, Lewei;  Rosin, Miriam P;  MacAulay, Calum E<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.1117\/1.2193157\" title=\"Simple device for the direct visualization of oral-cavity tissue fluorescence\" target=\"blank\">Simple device for the direct visualization of oral-cavity tissue fluorescence<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Journal of biomedical optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 11, <\/span><span class=\"tp_pub_additional_number\">no. 2, <\/span><span class=\"tp_pub_additional_pages\">pp. 024006\u2013024006, <\/span><span class=\"tp_pub_additional_year\">2006<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_58\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('58','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_58\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('58','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_58\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('58','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_58\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2006simple,<br \/>\r\ntitle = {Simple device for the direct visualization of oral-cavity tissue fluorescence},<br \/>\r\nauthor = { Pierre M Lane and Terence Gilhuly and Peter Whitehead and Haishan Zeng and Catherine F Poh and Samson Ng and P Michele Williams and Lewei Zhang and Miriam P Rosin and Calum E MacAulay},<br \/>\r\nurl = {http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2006.pdf, Full Text (PDF)<br \/>\r\nhttp:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16674196, PubMed},<br \/>\r\ndoi = {10.1117\/1.2193157},<br \/>\r\nyear  = {2006},<br \/>\r\ndate = {2006-01-01},<br \/>\r\njournal = {Journal of biomedical optics},<br \/>\r\nvolume = {11},<br \/>\r\nnumber = {2},<br \/>\r\npages = {024006--024006},<br \/>\r\npublisher = {International Society for Optics and Photonics},<br \/>\r\nabstract = {Early identification of high-risk disease could greatly reduce both mortality and morbidity due to oral cancer. We describe a simple handheld device that facilitates the direct visualization of oral-cavity fluorescence for the detection of high-risk precancerous and early cancerous lesions. Blue excitation light (400 to 460 nm) is employed to excite green-red fluorescence from fluorophores in the oral tissues. Tissue fluorescence is viewed directly along an optical axis collinear with the axis of excitation to reduce inter- and intraoperator variability. This robust, field-of-view device enables the direct visualization of fluorescence in the context of surrounding normal tissue. Results from a pilot study of 44 patients are presented. Using histology as the gold standard, the device achieves a sensitivity of 98% and specificity of 100% when discriminating normal mucosa from severe dysplasia\/carcinoma in situ (CIS) or invasive carcinoma. We envisage this device as a suitable adjunct for oral cancer screening, biopsy guidance, and margin delineation.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('58','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_58\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Early identification of high-risk disease could greatly reduce both mortality and morbidity due to oral cancer. We describe a simple handheld device that facilitates the direct visualization of oral-cavity fluorescence for the detection of high-risk precancerous and early cancerous lesions. Blue excitation light (400 to 460 nm) is employed to excite green-red fluorescence from fluorophores in the oral tissues. Tissue fluorescence is viewed directly along an optical axis collinear with the axis of excitation to reduce inter- and intraoperator variability. This robust, field-of-view device enables the direct visualization of fluorescence in the context of surrounding normal tissue. Results from a pilot study of 44 patients are presented. Using histology as the gold standard, the device achieves a sensitivity of 98% and specificity of 100% when discriminating normal mucosa from severe dysplasia\/carcinoma in situ (CIS) or invasive carcinoma. We envisage this device as a suitable adjunct for oral cancer screening, biopsy guidance, and margin delineation.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('58','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_58\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/biophotonics.bccrc.ca\/pubs\/Lane-2006.pdf\" title=\"Full Text (PDF)\" target=\"_blank\">Full Text (PDF)<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16674196\" title=\"PubMed\" target=\"_blank\">PubMed<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.1117\/1.2193157\" title=\"Follow DOI:10.1117\/1.2193157\" target=\"_blank\">doi:10.1117\/1.2193157<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('58','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2005\">2005<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Spectrally programmable light engine for in vitro or in vivo molecular imaging and spectroscopy\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Screenshot-2025-09-30-141516-e1759266980532.png\" width=\"128\" alt=\"Spectrally programmable light engine for in vitro or in vivo molecular imaging and spectroscopy\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> MacKinnon, Nicholas;  Stange, Ulrich;  Lane, Pierre;  MacAulay, Calum;  Quatrevalet, Mathieu<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf\" target=\"blank\">Spectrally programmable light engine for in vitro or in vivo molecular imaging and spectroscopy<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Applied optics, <\/span><span class=\"tp_pub_additional_volume\">vol. 44, <\/span><span class=\"tp_pub_additional_number\">no. 11, <\/span><span class=\"tp_pub_additional_pages\">pp. 2033\u20132040, <\/span><span class=\"tp_pub_additional_year\">2005<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_62\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('62','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_62\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('62','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_62\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{mackinnon2005spectrally,<br \/>\r\ntitle = {Spectrally programmable light engine for in vitro or in vivo molecular imaging and spectroscopy},<br \/>\r\nauthor = { Nicholas MacKinnon and Ulrich Stange and Pierre Lane and Calum MacAulay and Mathieu Quatrevalet},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf},<br \/>\r\nyear  = {2005},<br \/>\r\ndate = {2005-01-01},<br \/>\r\nurldate = {2005-01-01},<br \/>\r\njournal = {Applied optics},<br \/>\r\nvolume = {44},<br \/>\r\nnumber = {11},<br \/>\r\npages = {2033--2040},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('62','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_62\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacKinnon-2005.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('62','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2004\">2004<\/h3><div class=\"tp_publication tp_publication_inbook\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"In vivo pathology: microendoscopy as a new endoscopic imaging modality\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Screenshot-2025-09-30-142240.png\" width=\"128\" alt=\"In vivo pathology: microendoscopy as a new endoscopic imaging modality\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> MacAulay, Calum;  Lane, Pierre;  Richards-Kortum, Rebecca<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf\" target=\"blank\">In vivo pathology: microendoscopy as a new endoscopic imaging modality<\/a> <span class=\"tp_pub_type tp_  inbook\">Book Chapter<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_volume\">vol. 14, <\/span><span class=\"tp_pub_additional_number\">no. 3, <\/span><span class=\"tp_pub_additional_pages\">pp. 595\u2013620, <\/span><span class=\"tp_pub_additional_publisher\">Elsevier, <\/span><span class=\"tp_pub_additional_year\">2004<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_61\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('61','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_61\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('61','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_61\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@inbook{macaulay2004vivo,<br \/>\r\ntitle = {In vivo pathology: microendoscopy as a new endoscopic imaging modality},<br \/>\r\nauthor = { Calum MacAulay and Pierre Lane and Rebecca Richards-Kortum},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf<br \/>\r\nhttps:\/\/doi.org\/10.1016\/j.giec.2004.03.014},<br \/>\r\nyear  = {2004},<br \/>\r\ndate = {2004-01-01},<br \/>\r\nurldate = {2004-01-01},<br \/>\r\njournal = {Gastrointestinal endoscopy clinics of North America},<br \/>\r\nvolume = {14},<br \/>\r\nnumber = {3},<br \/>\r\npages = {595--620},<br \/>\r\npublisher = {Elsevier},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {inbook}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('61','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_61\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/MacAulay-2004.pdf<\/a><\/li><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/doi.org\/10.1016\/j.giec.2004.03.014\" title=\"https:\/\/doi.org\/10.1016\/j.giec.2004.03.014\" target=\"_blank\">https:\/\/doi.org\/10.1016\/j.giec.2004.03.014<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('61','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Optical computed-tomographic microscope for three-dimensional quantitative histology\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Screenshot-2025-09-30-143205.png\" width=\"128\" alt=\"Optical computed-tomographic microscope for three-dimensional quantitative histology\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Chamgoulov, Ravil;  Lane, Pierre;  MacAulay, Calum<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf\" target=\"blank\">Optical computed-tomographic microscope for three-dimensional quantitative histology<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Analytical Cellular Pathology, <\/span><span class=\"tp_pub_additional_volume\">vol. 26, <\/span><span class=\"tp_pub_additional_number\">no. 5-6, <\/span><span class=\"tp_pub_additional_pages\">pp. 319\u2013327, <\/span><span class=\"tp_pub_additional_year\">2004<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_resource_link\"><a id=\"tp_links_sh_70\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('70','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_70\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('70','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_70\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{chamgoulov2004optical,<br \/>\r\ntitle = {Optical computed-tomographic microscope for three-dimensional quantitative histology},<br \/>\r\nauthor = { Ravil Chamgoulov and Pierre Lane and Calum MacAulay},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf},<br \/>\r\nyear  = {2004},<br \/>\r\ndate = {2004-01-01},<br \/>\r\nurldate = {2004-01-01},<br \/>\r\njournal = {Analytical Cellular Pathology},<br \/>\r\nvolume = {26},<br \/>\r\nnumber = {5-6},<br \/>\r\npages = {319--327},<br \/>\r\npublisher = {Hindawi Publishing Corporation},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('70','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_70\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Chamgoulov-2004.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('70','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2000\">2000<\/h3><div class=\"tp_publication tp_publication_article\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Fiber-optic confocal microscopy using a spatial light modulator\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Screenshot-2025-09-30-144219.png\" width=\"128\" alt=\"Fiber-optic confocal microscopy using a spatial light modulator\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Lane, Pierre M;  Dlugan, Andrew LP;  Richards-Kortum, Rebecca;  MacAulay, Calum E<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf\" target=\"blank\">Fiber-optic confocal microscopy using a spatial light modulator<\/a> <span class=\"tp_pub_type tp_  article\">Journal Article<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_in\">In: <\/span><span class=\"tp_pub_additional_journal\">Optics letters, <\/span><span class=\"tp_pub_additional_volume\">vol. 25, <\/span><span class=\"tp_pub_additional_number\">no. 24, <\/span><span class=\"tp_pub_additional_pages\">pp. 1780\u20131782, <\/span><span class=\"tp_pub_additional_year\">2000<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_60\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('60','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_60\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('60','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_60\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('60','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_60\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@article{lane2000fiber,<br \/>\r\ntitle = {Fiber-optic confocal microscopy using a spatial light modulator},<br \/>\r\nauthor = { Pierre M Lane and Andrew LP Dlugan and Rebecca Richards-Kortum and Calum E MacAulay},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf},<br \/>\r\nyear  = {2000},<br \/>\r\ndate = {2000-01-01},<br \/>\r\nurldate = {2000-01-01},<br \/>\r\njournal = {Optics letters},<br \/>\r\nvolume = {25},<br \/>\r\nnumber = {24},<br \/>\r\npages = {1780--1782},<br \/>\r\npublisher = {Optical Society of America},<br \/>\r\nabstract = {We present a novel fiber-optic confocal microscope in which the scanning operation is achieved by use of a spatial light modulator (SLM) to sequentially illuminate individual fibers or patterns of multiple fibers. Experimental images are presented, and the optical-sectioning capability of the device is demonstrated. The novel SLM-based system is more optically efficient, achieves higher contrast, and has improved optical-sectioning capabilities compared with those of other proposed instruments for confocal microendoscopy.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {article}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('60','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_60\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We present a novel fiber-optic confocal microscope in which the scanning operation is achieved by use of a spatial light modulator (SLM) to sequentially illuminate individual fibers or patterns of multiple fibers. Experimental images are presented, and the optical-sectioning capability of the device is demonstrated. The novel SLM-based system is more optically efficient, achieves higher contrast, and has improved optical-sectioning capabilities compared with those of other proposed instruments for confocal microendoscopy.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('60','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_60\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Lane-2000.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('60','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><\/div><\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"theses\">Theses<\/h2>\n\n\n<div class=\"teachpress_pub_list\"><form name=\"tppublistform\" method=\"get\"><a name=\"tppubs\" id=\"tppubs\"><\/a><\/form><div class=\"teachpress_publication_list\"><h3 class=\"tp_h3\" id=\"tp_h3_2025\">2025<\/h3><div class=\"tp_publication tp_publication_phdthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Towards endoscopic optical imaging of the fallopian tubes for tubo-ovarian cancer detection\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/01\/thumbnail_image1-e1759257145539-150x150.jpg\" width=\"128\" alt=\"Towards endoscopic optical imaging of the fallopian tubes for tubo-ovarian cancer detection\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Malone, Jeanie<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0447698\" title=\"Towards endoscopic optical imaging of the fallopian tubes for tubo-ovarian cancer detection\" target=\"blank\">Towards endoscopic optical imaging of the fallopian tubes for tubo-ovarian cancer detection<\/a> <span class=\"tp_pub_type tp_  phdthesis\">PhD Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Biomedical Engineering, University of British Columbia, <\/span><span class=\"tp_pub_additional_year\">2025<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_176\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('176','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_176\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('176','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_176\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('176','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_176\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@phdthesis{Malone2025,<br \/>\r\ntitle = {Towards endoscopic optical imaging of the fallopian tubes for tubo-ovarian cancer detection},<br \/>\r\nauthor = {Jeanie Malone},<br \/>\r\nurl = {http:\/\/hdl.handle.net\/2429\/90069},<br \/>\r\ndoi = {10.14288\/1.0447698},<br \/>\r\nyear  = {2025},<br \/>\r\ndate = {2025-07-01},<br \/>\r\nurldate = {2025-07-01},<br \/>\r\norganization = {University of British Columbia},<br \/>\r\nschool = {School of Biomedical Engineering, University of British Columbia},<br \/>\r\nabstract = {Tubo-ovarian cancers are the most lethal gynecologic cancer. Early diagnosis is associated with better patient outcomes, but there are currently no effective screening measures. This thesis is a series of translational studies which explore whether novel optical imaging catheters can detect early or occult (otherwise undetectable) tubo-ovarian cancers where they originate in the fallopian tubes. Endoscopic optical coherence tomography (OCT) is uniquely positioned to provide detailed examination of subsurface tissue structures in small luminal organs deep within the body. It can be paired with autofluorescence imaging (AFI), to provide complimentary functional information, and achieved in a single fiber optic (sub-millimeter diameter) catheter. This thesis aims to develop methods for imaging the fallopian tubes, discover image features related to tubo-ovarian cancers, and assess the clinical feasibility of in vivo optical falloposcopy. These aims are explored first through a pre-clinical study of resected fallopian tubes, and later through work towards an in vivo human trial. High grade serous ovarian carcinoma is visualized and quantified via imaging biomarkers, motivating future study and providing direction for the future design of optical falloposcopy devices. In parallel with these primary aims, two adjacent studies are presented to provide context for the opportunities and challenges associated with optical imaging for tubo-ovarian cancer detection. First, an in vivo oral cancer imaging study using similar devices in a different clinical application. Second, an exploration of multipath artifacts inherent to multimodal endoscopic OCT including a novel strategy to leverage these artifacts. This work demonstrates promise in an optical imaging technique which is near in vivo translation. Tools that allow for high-resolution, detailed qualitative and quantitative assessment of fallopian tubes may support new care strategies for tubo-ovarian cancer patients, with the ultimate aim of reducing mortality and improving quality of life.<br \/>\r\n},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {phdthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('176','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_176\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Tubo-ovarian cancers are the most lethal gynecologic cancer. Early diagnosis is associated with better patient outcomes, but there are currently no effective screening measures. This thesis is a series of translational studies which explore whether novel optical imaging catheters can detect early or occult (otherwise undetectable) tubo-ovarian cancers where they originate in the fallopian tubes. Endoscopic optical coherence tomography (OCT) is uniquely positioned to provide detailed examination of subsurface tissue structures in small luminal organs deep within the body. It can be paired with autofluorescence imaging (AFI), to provide complimentary functional information, and achieved in a single fiber optic (sub-millimeter diameter) catheter. This thesis aims to develop methods for imaging the fallopian tubes, discover image features related to tubo-ovarian cancers, and assess the clinical feasibility of in vivo optical falloposcopy. These aims are explored first through a pre-clinical study of resected fallopian tubes, and later through work towards an in vivo human trial. High grade serous ovarian carcinoma is visualized and quantified via imaging biomarkers, motivating future study and providing direction for the future design of optical falloposcopy devices. In parallel with these primary aims, two adjacent studies are presented to provide context for the opportunities and challenges associated with optical imaging for tubo-ovarian cancer detection. First, an in vivo oral cancer imaging study using similar devices in a different clinical application. Second, an exploration of multipath artifacts inherent to multimodal endoscopic OCT including a novel strategy to leverage these artifacts. This work demonstrates promise in an optical imaging technique which is near in vivo translation. Tools that allow for high-resolution, detailed qualitative and quantitative assessment of fallopian tubes may support new care strategies for tubo-ovarian cancer patients, with the ultimate aim of reducing mortality and improving quality of life.<br \/>\r\n<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('176','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_176\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/hdl.handle.net\/2429\/90069\" title=\"http:\/\/hdl.handle.net\/2429\/90069\" target=\"_blank\">http:\/\/hdl.handle.net\/2429\/90069<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0447698\" title=\"Follow DOI:10.14288\/1.0447698\" target=\"_blank\">doi:10.14288\/1.0447698<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('176','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2024\">2024<\/h3><div class=\"tp_publication tp_publication_phdthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Leveraging multipath effects in multimodal optical coherence tomography for cancer detection\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Adrian-2-scaled-e1759257984514.jpg\" width=\"128\" alt=\"Leveraging multipath effects in multimodal optical coherence tomography for cancer detection\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Tanskanen, Adrian<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0445584\" title=\"Leveraging multipath effects in multimodal optical coherence tomography for cancer detection\" target=\"blank\">Leveraging multipath effects in multimodal optical coherence tomography for cancer detection<\/a> <span class=\"tp_pub_type tp_  phdthesis\">PhD Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Biomedical Engineering, University of British Columbia, <\/span><span class=\"tp_pub_additional_year\">2024<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_177\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('177','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_177\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('177','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_177\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('177','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_177\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@phdthesis{nokey,<br \/>\r\ntitle = {Leveraging multipath effects in multimodal optical coherence tomography for cancer detection},<br \/>\r\nauthor = {Adrian Tanskanen},<br \/>\r\nurl = {http:\/\/hdl.handle.net\/2429\/89428},<br \/>\r\ndoi = {10.14288\/1.0445584},<br \/>\r\nyear  = {2024},<br \/>\r\ndate = {2024-10-17},<br \/>\r\nurldate = {2024-10-17},<br \/>\r\nschool = {School of Biomedical Engineering, University of British Columbia},<br \/>\r\nabstract = {This thesis explores multipath artifacts in multimodal endoscopic optical coherence tomography (OCT). In non-multimodal systems, endoscopic OCT is generated using single-mode fibers (SMF) to ensure that the backscattered light is collected by the fundamental mode. To add a secondary type of imaging without increasing endoscope size, multimodal OCT systems use double-clad fiber (DCF). DCF has a single-mode core for OCT, and a high numerical aperture inner-cladding for the secondary modality. Unfortunately, multimodal systems come at the cost of multipath artifacts. Multipath artifacts are blurred ghost images inherent to the use of DCF which degrade OCT image quality. The initial goal of this thesis was to develop a method to mitigate multipath artifacts and improve the image quality of multimodal OCT systems to the same as SMF-based OCT. First, using experimental methods such as spatially and spectrally resolved imaging, I discovered that multipath artifacts are generated by LP11-like inner-cladding modes. Leveraging this research, I demonstrated that catheters fabricated with a triple-clad W-Type fiber in place of DCF can be used to remove multipath artifacts without degrading the quality of the secondary modality (autofluorescence imaging). However, in the process of studying multipath artifacts, I discovered that they could be projected from blurred images in 3D, to high-quality en face images. These images contain different features than an equivalent projection of the OCT image carried by the DCFs fundamental mode. Using modelling and experimentation, I revealed that the higher-order modes of the multipath artifact couple off-axis backscattering. This discovery essentially changed a bug into a feature, providing the basis for multipath contract imaging (MCI). MCI is a ratiometric measure of the total power coupled into the fundamental mode divided by the higher-order modes: providing a visualization of tissues angular diversity. As multipath artifacts are inherent to multimodal OCT devices, MCI can be generated from old datasets meaning that a wealth of clinical data could be retrospectively analyzed.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {phdthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('177','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_177\" style=\"display:none;\"><div class=\"tp_abstract_entry\">This thesis explores multipath artifacts in multimodal endoscopic optical coherence tomography (OCT). In non-multimodal systems, endoscopic OCT is generated using single-mode fibers (SMF) to ensure that the backscattered light is collected by the fundamental mode. To add a secondary type of imaging without increasing endoscope size, multimodal OCT systems use double-clad fiber (DCF). DCF has a single-mode core for OCT, and a high numerical aperture inner-cladding for the secondary modality. Unfortunately, multimodal systems come at the cost of multipath artifacts. Multipath artifacts are blurred ghost images inherent to the use of DCF which degrade OCT image quality. The initial goal of this thesis was to develop a method to mitigate multipath artifacts and improve the image quality of multimodal OCT systems to the same as SMF-based OCT. First, using experimental methods such as spatially and spectrally resolved imaging, I discovered that multipath artifacts are generated by LP11-like inner-cladding modes. Leveraging this research, I demonstrated that catheters fabricated with a triple-clad W-Type fiber in place of DCF can be used to remove multipath artifacts without degrading the quality of the secondary modality (autofluorescence imaging). However, in the process of studying multipath artifacts, I discovered that they could be projected from blurred images in 3D, to high-quality en face images. These images contain different features than an equivalent projection of the OCT image carried by the DCFs fundamental mode. Using modelling and experimentation, I revealed that the higher-order modes of the multipath artifact couple off-axis backscattering. This discovery essentially changed a bug into a feature, providing the basis for multipath contract imaging (MCI). MCI is a ratiometric measure of the total power coupled into the fundamental mode divided by the higher-order modes: providing a visualization of tissues angular diversity. As multipath artifacts are inherent to multimodal OCT devices, MCI can be generated from old datasets meaning that a wealth of clinical data could be retrospectively analyzed.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('177','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_177\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/hdl.handle.net\/2429\/89428\" title=\"http:\/\/hdl.handle.net\/2429\/89428\" target=\"_blank\">http:\/\/hdl.handle.net\/2429\/89428<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0445584\" title=\"Follow DOI:10.14288\/1.0445584\" target=\"_blank\">doi:10.14288\/1.0445584<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('177','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2023\">2023<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Rehill, Mehar<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/summit.sfu.ca\/item\/37772\" title=\"https:\/\/summit.sfu.ca\/item\/37772\" target=\"blank\">Methods for the Estimation of Depth-resolved Attenuation in OCT<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_185\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('185','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_185\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('185','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_185\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('185','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_185\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{Rehill2023,<br \/>\r\ntitle = {Methods for the Estimation of Depth-resolved Attenuation in OCT},<br \/>\r\nauthor = {Mehar Rehill},<br \/>\r\nurl = {https:\/\/summit.sfu.ca\/item\/37772},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-12-11},<br \/>\r\nurldate = {2023-12-11},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Cancer is one of the major causes of mortality, accounting for one in six deaths worldwide in 2020. The majority of cancers can be prevented , cured , or reversed if early detected. Early diagnosis and screening are vital components, with screening focusing on detecting cancer before the symptoms manifest, and diagnosis involving the identification of cancer in its early stages through methods like biopsies and imaging techniques.<br \/>\r\nOptical coherence tomography (OCT) has shown potential for early cancer diagnosis, due to its non-invasive nature and potential to guide biopsies site selection, reducing the invasiveness of certain procedures by enabling the clinicians to obtain fewer biopsies and minimizing errors associated with surgical biopsies. Researchers have proposed several models linking the attenuation coefficient (\u03bc), which describes the exponential decay of the OCT signal, with tissue optical structural properties. Presently , two methods, layer-wise extraction through curve fitting and depth-resolved methods, are employed for attenuation coefficient calculation. However, challenges persist in achieving accurate and precise estimations.<br \/>\r\nThis thesis entails a comparison of four methods to calculate the attenuation coefficient from OCT intensity data-: slope-fitting, Vermeer, Jain Lui and Kaiyan Li. Validation of theses methods on various types of milk serves as a preliminary evaluation, with further comparisons of estimated attenuation coefficients from OCT images against measurements from a power meter using various intralipid concentrations. The identified optimal algorithm is subsequently applied to OCT images for both cancerous and normal oral tissues.<br \/>\r\nThe study extends its evaluation to explore critical factors influencing the performance of the four methods. Pre-processing, including frames averaging, is found to enhance data quality and signal-to-noise ratio (SNR). The noise floor, particularly prominent at greater imaging depth, poses challenges common to all methods. Overlooked confocal effects, especially in samples with lower attenuation coefficients, contribute to underestimation in the Jain Lui and Kaiyan Li methods. While the validation experiments establish a linear relationship between intralipid concentration and attenuation coefficient, multiple scattering at higher intralipid concentrations challenges the assumption of constant backscattering fraction. Each method exhibits strengths and shortcomings, emphasizing the need for further research to explicitly incorporate confocal effects and multiple scattering to enhance depth-resolved algorithms for improved biomedical applications.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('185','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_185\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Cancer is one of the major causes of mortality, accounting for one in six deaths worldwide in 2020. The majority of cancers can be prevented , cured , or reversed if early detected. Early diagnosis and screening are vital components, with screening focusing on detecting cancer before the symptoms manifest, and diagnosis involving the identification of cancer in its early stages through methods like biopsies and imaging techniques.<br \/>\r\nOptical coherence tomography (OCT) has shown potential for early cancer diagnosis, due to its non-invasive nature and potential to guide biopsies site selection, reducing the invasiveness of certain procedures by enabling the clinicians to obtain fewer biopsies and minimizing errors associated with surgical biopsies. Researchers have proposed several models linking the attenuation coefficient (\u03bc), which describes the exponential decay of the OCT signal, with tissue optical structural properties. Presently , two methods, layer-wise extraction through curve fitting and depth-resolved methods, are employed for attenuation coefficient calculation. However, challenges persist in achieving accurate and precise estimations.<br \/>\r\nThis thesis entails a comparison of four methods to calculate the attenuation coefficient from OCT intensity data-: slope-fitting, Vermeer, Jain Lui and Kaiyan Li. Validation of theses methods on various types of milk serves as a preliminary evaluation, with further comparisons of estimated attenuation coefficients from OCT images against measurements from a power meter using various intralipid concentrations. The identified optimal algorithm is subsequently applied to OCT images for both cancerous and normal oral tissues.<br \/>\r\nThe study extends its evaluation to explore critical factors influencing the performance of the four methods. Pre-processing, including frames averaging, is found to enhance data quality and signal-to-noise ratio (SNR). The noise floor, particularly prominent at greater imaging depth, poses challenges common to all methods. Overlooked confocal effects, especially in samples with lower attenuation coefficients, contribute to underestimation in the Jain Lui and Kaiyan Li methods. While the validation experiments establish a linear relationship between intralipid concentration and attenuation coefficient, multiple scattering at higher intralipid concentrations challenges the assumption of constant backscattering fraction. Each method exhibits strengths and shortcomings, emphasizing the need for further research to explicitly incorporate confocal effects and multiple scattering to enhance depth-resolved algorithms for improved biomedical applications.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('185','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_185\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/summit.sfu.ca\/item\/37772\" title=\"https:\/\/summit.sfu.ca\/item\/37772\" target=\"_blank\">https:\/\/summit.sfu.ca\/item\/37772<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('185','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Lumen Segmentation in Endobronchial Optical Coherence Tomography with Deep Learning\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Allan-e1759366172750.jpg\" width=\"128\" alt=\"Lumen Segmentation in Endobronchial Optical Coherence Tomography with Deep Learning\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Zuckermann, Allan<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/summit.sfu.ca\/item\/37774\" title=\"https:\/\/summit.sfu.ca\/item\/37774\" target=\"blank\">Lumen Segmentation in Endobronchial Optical Coherence Tomography with Deep Learning<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_184\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('184','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_184\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('184','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_184\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('184','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_184\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Lumen Segmentation in Endobronchial Optical Coherence Tomography with Deep Learning},<br \/>\r\nauthor = {Allan Zuckermann},<br \/>\r\nurl = {https:\/\/summit.sfu.ca\/item\/37774},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-12-01},<br \/>\r\nurldate = {2023-12-01},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Chronic lung allograft dysfunction (CLAD) is a condition that kills approximately 50% of lung transplant (LTx) patients who survive their first year post-surgery. A correlation between CLAD status and dilation of the small airways has been shown, and assessment of these airways by endobronchial optical coherence tomography (EB-OCT) could prove beneficial in identifying CLAD in its early stages.<br \/>\r\nTo perform this task, a deep learning approach is presented to segment cross-sections of EB-OCT, identifying the luminal boundary. With this information, assessment of dilation is likely possible, and further correlations between airway morphology and CLAD could be investigated.<br \/>\r\nThe proposed method utilizes a U-Net architecture implemented in PyTorch, designed for the segmentation of medical images. The model is trained from scratch on 532 cross-sections acquired in vivo from 44 patients (9 CLAD), utilizing cross-validation as a model-building technique and an external validation set to report metrics. Key metrics are the average Hausdorff distance (AVD), precision, and recall.<br \/>\r\nResults on external data show an AVD of 1.25 pixels, or approximately 12.5 \u03bcm. Precision and recall were 0.631 and 0.847, respectively. These values are satisfactory and reflect the challenging nature of the task.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('184','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_184\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Chronic lung allograft dysfunction (CLAD) is a condition that kills approximately 50% of lung transplant (LTx) patients who survive their first year post-surgery. A correlation between CLAD status and dilation of the small airways has been shown, and assessment of these airways by endobronchial optical coherence tomography (EB-OCT) could prove beneficial in identifying CLAD in its early stages.<br \/>\r\nTo perform this task, a deep learning approach is presented to segment cross-sections of EB-OCT, identifying the luminal boundary. With this information, assessment of dilation is likely possible, and further correlations between airway morphology and CLAD could be investigated.<br \/>\r\nThe proposed method utilizes a U-Net architecture implemented in PyTorch, designed for the segmentation of medical images. The model is trained from scratch on 532 cross-sections acquired in vivo from 44 patients (9 CLAD), utilizing cross-validation as a model-building technique and an external validation set to report metrics. Key metrics are the average Hausdorff distance (AVD), precision, and recall.<br \/>\r\nResults on external data show an AVD of 1.25 pixels, or approximately 12.5 \u03bcm. Precision and recall were 0.631 and 0.847, respectively. These values are satisfactory and reflect the challenging nature of the task.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('184','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_184\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/summit.sfu.ca\/item\/37774\" title=\"https:\/\/summit.sfu.ca\/item\/37774\" target=\"_blank\">https:\/\/summit.sfu.ca\/item\/37774<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('184','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_mastersthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Segmentation of oral optical coherence tomography with deep learning\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Chloe-1.png\" width=\"128\" alt=\"Segmentation of oral optical coherence tomography with deep learning\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Hill, Chloe<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/summit.sfu.ca\/item\/36497\" title=\"https:\/\/summit.sfu.ca\/item\/36497\" target=\"blank\">Segmentation of oral optical coherence tomography with deep learning<\/a> <span class=\"tp_pub_type tp_  mastersthesis\">Masters Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2023<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_178\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('178','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_178\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('178','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_178\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('178','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_178\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@mastersthesis{nokey,<br \/>\r\ntitle = {Segmentation of oral optical coherence tomography with deep learning},<br \/>\r\nauthor = {Chloe Hill},<br \/>\r\nurl = {https:\/\/summit.sfu.ca\/item\/36497},<br \/>\r\nyear  = {2023},<br \/>\r\ndate = {2023-08-16},<br \/>\r\nurldate = {2023-08-16},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Diagnosis of oral cancer involves collecting multiple biopsies to increase the likelihood of sampling the most pathologic site within a lesion. Optical coherence tomography (OCT) allows for examination of subsurface morphology, and has shown potential in biopsy guidance. OCT captures changes in tissue stratification related to depth, topology, and presence of the stromal-epithelial boundary which are structural biomarkers for pre-invasive and invasive oral cancer. This thesis presents a four-part neural network pipeline to simplify OCT interpretation by providing en face maps of epithelial depth and stratification. U-nets models are employed to segment the stromal-epithelial boundary, and supporting convolutional neural networks are used for identification of the imaging field and artifacts. Training was conducted on a variety of non-cancerous and cancerous pathologies across the oral cavity to promote generalizability. Predictions demonstrate as-good-as or better agreement than inter-rater agreement, suggesting strong predictive power.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {mastersthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('178','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_178\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Diagnosis of oral cancer involves collecting multiple biopsies to increase the likelihood of sampling the most pathologic site within a lesion. Optical coherence tomography (OCT) allows for examination of subsurface morphology, and has shown potential in biopsy guidance. OCT captures changes in tissue stratification related to depth, topology, and presence of the stromal-epithelial boundary which are structural biomarkers for pre-invasive and invasive oral cancer. This thesis presents a four-part neural network pipeline to simplify OCT interpretation by providing en face maps of epithelial depth and stratification. U-nets models are employed to segment the stromal-epithelial boundary, and supporting convolutional neural networks are used for identification of the imaging field and artifacts. Training was conducted on a variety of non-cancerous and cancerous pathologies across the oral cavity to promote generalizability. Predictions demonstrate as-good-as or better agreement than inter-rater agreement, suggesting strong predictive power.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('178','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_178\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/summit.sfu.ca\/item\/36497\" title=\"https:\/\/summit.sfu.ca\/item\/36497\" target=\"_blank\">https:\/\/summit.sfu.ca\/item\/36497<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('178','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2022\">2022<\/h3><div class=\"tp_publication tp_publication_phdthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Kaur, Mandeep<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/summit.sfu.ca\/item\/36510\" title=\"https:\/\/summit.sfu.ca\/item\/36510\" target=\"blank\">Design of scanning fiber micro-cantilever based catheter for ultra-small endoscopes<\/a> <span class=\"tp_pub_type tp_  phdthesis\">PhD Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2022<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_183\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('183','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_183\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('183','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_183\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('183','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_183\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@phdthesis{nokey,<br \/>\r\ntitle = {Design of scanning fiber micro-cantilever based catheter for ultra-small endoscopes},<br \/>\r\nauthor = {Mandeep Kaur},<br \/>\r\nurl = {https:\/\/summit.sfu.ca\/item\/36510},<br \/>\r\nyear  = {2022},<br \/>\r\ndate = {2022-05-20},<br \/>\r\nurldate = {2022-05-20},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {During the past few decades, optical devices are frequently being used in medical applications to image lesions and malignancies, and to assist with surgical procedures. An endoscopic procedure requires the distal end of the scope to be placed close to the imageable target area through an opening such as nose, mouth, etc. Thus, the size of an endoscopic device dictates the area of the body that can be imaged using that device. The continuous evolution of micro-electro-mechanical systems (MEMSs) along with the development in optics enable the fabrication of flexible endoscopes having diameters just over a millimeter. As a result, medical users are able to image smaller areas of the body that were inaccessible in the past. Thus, lesions and tumors can be detected at preliminary cancerous stages permitting more accurate diagnoses and supporting an increased life expectancy of the patients. The overarching goal of this work has been to develop a sub-millimeter sized optical scanner that sets the bases for a miniaturized endoscope able to image previously inaccessible luminal organs in real time, at high resolution, in a minimally invasive manner without compromising the comfort of the subject, nor introduce additional risk. Thus, an initial diagnosis can be made, or a small precancerous lesion may be detected, in a small-diameter luminal organ that would not have otherwise been possible. This work sets out to present an optical-fiber scanner for a scanning fiber endoscope design that has an insertion tube diameter in the sub-millimeter range; small enough to potentially be inserted into the smallest airways of the lung and other small diameter tubes, which may include narrow sections of the pancreatic duct, and the narrowest section at the openings of the fallopian tubes. To attain this goal, a novel approach based on exciting a single mode optical fiber at resonance with the help of an electro-thermal actuator is proposed where an asymmetric conducting element expands due to the Joule effect in presence of an electric current. The actuator provides base excitation motion to a cantilevered based optical fiber whose free end follows a closed line pattern. It has been seen experimentally that the area inside the circle can be scanned by offsetting the excitation frequency from the resonant value to achieve the bi-dimensional scanning. The backscattered reflected light from the target sample is set to be captured using multiple multimode fibers placed at the periphery of the device in a ring shape.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {phdthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('183','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_183\" style=\"display:none;\"><div class=\"tp_abstract_entry\">During the past few decades, optical devices are frequently being used in medical applications to image lesions and malignancies, and to assist with surgical procedures. An endoscopic procedure requires the distal end of the scope to be placed close to the imageable target area through an opening such as nose, mouth, etc. Thus, the size of an endoscopic device dictates the area of the body that can be imaged using that device. The continuous evolution of micro-electro-mechanical systems (MEMSs) along with the development in optics enable the fabrication of flexible endoscopes having diameters just over a millimeter. As a result, medical users are able to image smaller areas of the body that were inaccessible in the past. Thus, lesions and tumors can be detected at preliminary cancerous stages permitting more accurate diagnoses and supporting an increased life expectancy of the patients. The overarching goal of this work has been to develop a sub-millimeter sized optical scanner that sets the bases for a miniaturized endoscope able to image previously inaccessible luminal organs in real time, at high resolution, in a minimally invasive manner without compromising the comfort of the subject, nor introduce additional risk. Thus, an initial diagnosis can be made, or a small precancerous lesion may be detected, in a small-diameter luminal organ that would not have otherwise been possible. This work sets out to present an optical-fiber scanner for a scanning fiber endoscope design that has an insertion tube diameter in the sub-millimeter range; small enough to potentially be inserted into the smallest airways of the lung and other small diameter tubes, which may include narrow sections of the pancreatic duct, and the narrowest section at the openings of the fallopian tubes. To attain this goal, a novel approach based on exciting a single mode optical fiber at resonance with the help of an electro-thermal actuator is proposed where an asymmetric conducting element expands due to the Joule effect in presence of an electric current. The actuator provides base excitation motion to a cantilevered based optical fiber whose free end follows a closed line pattern. It has been seen experimentally that the area inside the circle can be scanned by offsetting the excitation frequency from the resonant value to achieve the bi-dimensional scanning. The backscattered reflected light from the target sample is set to be captured using multiple multimode fibers placed at the periphery of the device in a ring shape.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('183','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_183\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/summit.sfu.ca\/item\/36510\" title=\"https:\/\/summit.sfu.ca\/item\/36510\" target=\"_blank\">https:\/\/summit.sfu.ca\/item\/36510<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('183','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2021\">2021<\/h3><div class=\"tp_publication tp_publication_phdthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Optimization of multimodal OCT for early cancer detection and diagnosis\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/0-e1759266142909.jpg\" width=\"128\" alt=\"Optimization of multimodal OCT for early cancer detection and diagnosis\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Abouei, Elham<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0401900\" title=\"Optimization of multimodal OCT for early cancer detection and diagnosis\" target=\"blank\">Optimization of multimodal OCT for early cancer detection and diagnosis<\/a> <span class=\"tp_pub_type tp_  phdthesis\">PhD Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Biomedical Engineering, University of British Columbia, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_179\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('179','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_179\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('179','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_179\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('179','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_179\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@phdthesis{nokey,<br \/>\r\ntitle = {Optimization of multimodal OCT for early cancer detection and diagnosis},<br \/>\r\nauthor = {Elham Abouei},<br \/>\r\nurl = {http:\/\/hdl.handle.net\/2429\/79596},<br \/>\r\ndoi = {10.14288\/1.0401900},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-09-02},<br \/>\r\nurldate = {2021-09-02},<br \/>\r\nschool = {School of Biomedical Engineering, University of British Columbia},<br \/>\r\nabstract = {In this thesis, I present improved optical imaging modalities for early cancer detection, diagnosis and prognosis of lung and cervical cancers in a minimally invasive fashion. Optical coherence tomography (OCT), which is based on low coherence interferometry of backscattered light, offers high resolution three-dimensional visualization of structures below the tissue surface. In contrast, autofluorescence imaging (AFI) detects spectral differences in fluorescence and absorption characteristics of endogenous fluorophores. A combined OCT\u2013AFI system uses both complementary modalities to examine structural and molecular information, which may enable increased detection and characterization of features associated with disease. The motivation of this thesis is to improve the capabilities of OCT and OCT-AFI for the in vivo detection and localization of early cancers. Rotary-pullback catheter-based OCT or OCT-AFI systems suffer from motion-induced artifacts. In this thesis, I developed a method for the correction of these motion artifacts present in both 2D and 3D images collected with an endoscopic OCT-AFI system. I optimized and demonstrated the suitability of this method using real and simulated NURD (non-uniform rotation distortion) phantoms and in vivo endoscopic pulmonary OCT-AFI. Presented is a qualitative evaluation of this method showing an enhancement of the image quality and a proposed metric to quantitatively evaluate the correction method. Next, I evaluated a high resolution OCT system for early cervical cancer screening and diagnosis. My work characterized diagnostic OCT features of normal cervix as well as low-grade squamous intraepithelial lesions (LSIL), and high-grade squamous intraepithelial lesions (HSIL). We determined the sensitivity (100%), specificity (83%) and accuracy (85%) of this diagnostic technique in differentiating low-risk and high-risk cervical lesions. Lastly, I present a design for a forward-viewing fiber scanning high resolution OCT probe for in vivo cervical imaging in the clinic. To enable high resolution imaging but allow for sufficient depth penetration into tissue, OCT systems use near-infrared light ~1000 nm in wavelength. As well, I have investigated the suitability of a new supercontinuum light source for this application.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {phdthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('179','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_179\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In this thesis, I present improved optical imaging modalities for early cancer detection, diagnosis and prognosis of lung and cervical cancers in a minimally invasive fashion. Optical coherence tomography (OCT), which is based on low coherence interferometry of backscattered light, offers high resolution three-dimensional visualization of structures below the tissue surface. In contrast, autofluorescence imaging (AFI) detects spectral differences in fluorescence and absorption characteristics of endogenous fluorophores. A combined OCT\u2013AFI system uses both complementary modalities to examine structural and molecular information, which may enable increased detection and characterization of features associated with disease. The motivation of this thesis is to improve the capabilities of OCT and OCT-AFI for the in vivo detection and localization of early cancers. Rotary-pullback catheter-based OCT or OCT-AFI systems suffer from motion-induced artifacts. In this thesis, I developed a method for the correction of these motion artifacts present in both 2D and 3D images collected with an endoscopic OCT-AFI system. I optimized and demonstrated the suitability of this method using real and simulated NURD (non-uniform rotation distortion) phantoms and in vivo endoscopic pulmonary OCT-AFI. Presented is a qualitative evaluation of this method showing an enhancement of the image quality and a proposed metric to quantitatively evaluate the correction method. Next, I evaluated a high resolution OCT system for early cervical cancer screening and diagnosis. My work characterized diagnostic OCT features of normal cervix as well as low-grade squamous intraepithelial lesions (LSIL), and high-grade squamous intraepithelial lesions (HSIL). We determined the sensitivity (100%), specificity (83%) and accuracy (85%) of this diagnostic technique in differentiating low-risk and high-risk cervical lesions. Lastly, I present a design for a forward-viewing fiber scanning high resolution OCT probe for in vivo cervical imaging in the clinic. To enable high resolution imaging but allow for sufficient depth penetration into tissue, OCT systems use near-infrared light ~1000 nm in wavelength. As well, I have investigated the suitability of a new supercontinuum light source for this application.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('179','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_179\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/hdl.handle.net\/2429\/79596\" title=\"http:\/\/hdl.handle.net\/2429\/79596\" target=\"_blank\">http:\/\/hdl.handle.net\/2429\/79596<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0401900\" title=\"Follow DOI:10.14288\/1.0401900\" target=\"_blank\">doi:10.14288\/1.0401900<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('179','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Development of a Modular Microcontroller-Based Scanner for Optical Coherence Tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/malcolm-e1759266255322.jpg\" width=\"128\" alt=\"Development of a Modular Microcontroller-Based Scanner for Optical Coherence Tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Brown, Malcolm<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf\" target=\"blank\">Development of a Modular Microcontroller-Based Scanner for Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_186\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('186','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_186\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('186','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_186\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('186','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_186\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Development of a Modular Microcontroller-Based Scanner for Optical Coherence Tomography},<br \/>\r\nauthor = {Malcolm Brown},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-06-01},<br \/>\r\nurldate = {2021-06-01},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {The purpose of this thesis was to develop a scanner for an existing optical coherence tomography (OCT)<br \/>\r\nsystem at the BC Cancer Research Center. Work included adding features, reducing response times,<br \/>\r\nincreasing reliability, and modularizing the current imaging system\u2019s design. The system is normally used<br \/>\r\nin fiber optic imaging using a Rotary Pullback Device (RPD) and other scanning geometries can be<br \/>\r\nimplemented with these improvements.<br \/>\r\nScanning methods including the RPD generally involve two motors, which allow for scanning in two axes.<br \/>\r\nThis project\u2019s goal was to design and validate microcontroller (MCU) firmware for the scanner\u2019s motor<br \/>\r\ncontrol and peripheral systems. The MCU receives commands from the imaging system\u2019s main software<br \/>\r\nand translates them to control the motors and command the rest of the system.<br \/>\r\nIn the previous design, the scanner\u2019s RPD motors were controlled through software and a data<br \/>\r\nacquisition board (DAQ), which generated signals to control the RPD motors and acquire sample data.<br \/>\r\nHowever, this implementation was not ideal. This project replaces the DAQ\u2019s control of the scanner<br \/>\r\nmotors, leaving it to only acquire sample data.<br \/>\r\nModularity was the main motivation for design changes, but there are other benefits. The RPD hardware<br \/>\r\nrequires prompt, reliable responses from software. Previously, if the imaging system Windows software<br \/>\r\ncrashed, it could damage hardware if the scanning motors continued to move unintentionally. Using a<br \/>\r\ndedicated MCU allows for faster response times and if software fails, the MCU still functions as<br \/>\r\nintended.<br \/>\r\nAn MCU and peripherals were selected for this task, with the MCU firmware being the main<br \/>\r\ndevelopment step. The firmware was developed to facilitate multiple lines of communication and<br \/>\r\nreplaces the existing interface while adding to existing functionality and robustness. Testing and<br \/>\r\nvalidation of the design followed in order to ensure the device operates safely and reliably. These steps<br \/>\r\nare intended to allow for implementation of a custom printed circuit board (PCB) in the project\u2019s future.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('186','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_186\" style=\"display:none;\"><div class=\"tp_abstract_entry\">The purpose of this thesis was to develop a scanner for an existing optical coherence tomography (OCT)<br \/>\r\nsystem at the BC Cancer Research Center. Work included adding features, reducing response times,<br \/>\r\nincreasing reliability, and modularizing the current imaging system\u2019s design. The system is normally used<br \/>\r\nin fiber optic imaging using a Rotary Pullback Device (RPD) and other scanning geometries can be<br \/>\r\nimplemented with these improvements.<br \/>\r\nScanning methods including the RPD generally involve two motors, which allow for scanning in two axes.<br \/>\r\nThis project\u2019s goal was to design and validate microcontroller (MCU) firmware for the scanner\u2019s motor<br \/>\r\ncontrol and peripheral systems. The MCU receives commands from the imaging system\u2019s main software<br \/>\r\nand translates them to control the motors and command the rest of the system.<br \/>\r\nIn the previous design, the scanner\u2019s RPD motors were controlled through software and a data<br \/>\r\nacquisition board (DAQ), which generated signals to control the RPD motors and acquire sample data.<br \/>\r\nHowever, this implementation was not ideal. This project replaces the DAQ\u2019s control of the scanner<br \/>\r\nmotors, leaving it to only acquire sample data.<br \/>\r\nModularity was the main motivation for design changes, but there are other benefits. The RPD hardware<br \/>\r\nrequires prompt, reliable responses from software. Previously, if the imaging system Windows software<br \/>\r\ncrashed, it could damage hardware if the scanning motors continued to move unintentionally. Using a<br \/>\r\ndedicated MCU allows for faster response times and if software fails, the MCU still functions as<br \/>\r\nintended.<br \/>\r\nAn MCU and peripherals were selected for this task, with the MCU firmware being the main<br \/>\r\ndevelopment step. The firmware was developed to facilitate multiple lines of communication and<br \/>\r\nreplaces the existing interface while adding to existing functionality and robustness. Testing and<br \/>\r\nvalidation of the design followed in order to ensure the device operates safely and reliably. These steps<br \/>\r\nare intended to allow for implementation of a custom printed circuit board (PCB) in the project\u2019s future.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('186','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_186\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Brown-2021.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('186','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Bernard, Scott<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf\" target=\"blank\">Design of a Three-Phase Micromotor Driver for use in Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2021<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_191\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('191','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_191\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('191','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_191\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('191','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_191\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Design of a Three-Phase Micromotor Driver for use in Optical Coherence Tomography},<br \/>\r\nauthor = {Scott Bernard},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf},<br \/>\r\nyear  = {2021},<br \/>\r\ndate = {2021-05-06},<br \/>\r\nurldate = {2021-05-06},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Optical coherence tomography (OCT) is a photonics-based medical imaging technique under active research within the BC Cancer Research Centre&#039;s (BCCRC) Optical Cancer Imaging Lab (OCIL). A current focus within the OCIL is the development and applications of micromotor-driven catheter probes for OCT imaging. The current micromotor driver used in the OCIL&#039;s research is independent from the imaging system and suffers from frequency mismatches between imaging and motor rotation speeds, resulting in instability of the output images. Image instability limits clinical applications of the micromotor probes that require analysis and comparison between consecutively acquired images.<br \/>\r\nTo eliminate rotational instabilities from the micromotor catheter probes we design and construct a micromotor driver that is frequency-matched with the OCT imaging system. The new micromotor driver generates three-phase motor drive waveforms through updating a digital-to-analog converter (DAC) synchronously with the OCT imaging sample rate. DAC outputs are fed through analog filtering and current amplification circuitry to allow for smooth rotation of the micromotor. The new micromotor driver was designed for control through software developed within the OCIL.<br \/>\r\nTo validate the new micromotor driver we use a printed paper phantom with regularly-spaced azimuthal fiducial markings to compare the imaging performance of the current micromotor driver to the performance of the new micromotor driver. We find that the new micromotor driver solves the frequency-mismatch issue in the current micromotor imaging system and allows for stable imaging with micromotor probes.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('191','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_191\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Optical coherence tomography (OCT) is a photonics-based medical imaging technique under active research within the BC Cancer Research Centre&#039;s (BCCRC) Optical Cancer Imaging Lab (OCIL). A current focus within the OCIL is the development and applications of micromotor-driven catheter probes for OCT imaging. The current micromotor driver used in the OCIL&#039;s research is independent from the imaging system and suffers from frequency mismatches between imaging and motor rotation speeds, resulting in instability of the output images. Image instability limits clinical applications of the micromotor probes that require analysis and comparison between consecutively acquired images.<br \/>\r\nTo eliminate rotational instabilities from the micromotor catheter probes we design and construct a micromotor driver that is frequency-matched with the OCT imaging system. The new micromotor driver generates three-phase motor drive waveforms through updating a digital-to-analog converter (DAC) synchronously with the OCT imaging sample rate. DAC outputs are fed through analog filtering and current amplification circuitry to allow for smooth rotation of the micromotor. The new micromotor driver was designed for control through software developed within the OCIL.<br \/>\r\nTo validate the new micromotor driver we use a printed paper phantom with regularly-spaced azimuthal fiducial markings to compare the imaging performance of the current micromotor driver to the performance of the new micromotor driver. We find that the new micromotor driver solves the frequency-mismatch issue in the current micromotor imaging system and allows for stable imaging with micromotor probes.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('191','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_191\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Bernard-2021.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('191','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2020\">2020<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Design and Construction of A Forward Viewing, Wide-Field Gastroscope Endcap Imager\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Andrea-e1759266411102.jpg\" width=\"128\" alt=\"Design and Construction of A Forward Viewing, Wide-Field Gastroscope Endcap Imager\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Manjarres, Andrea<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf\" target=\"blank\">Design and Construction of A Forward Viewing, Wide-Field Gastroscope Endcap Imager<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2020<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_187\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('187','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_187\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('187','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_187\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('187','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_187\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Design and Construction of A Forward Viewing, Wide-Field Gastroscope Endcap Imager},<br \/>\r\nauthor = {Andrea Manjarres},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf},<br \/>\r\nyear  = {2020},<br \/>\r\ndate = {2020-07-15},<br \/>\r\nurldate = {2020-07-15},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Gastric cancer is the third most common cause of cancer-related deaths worldwide [1]. It has a 25% 5-year survival rate, which is most likely due to the fact that 45% of cases are diagnosed in stage IV, when the cancer has already metastasized [2]. It is diagnosed through pathological examination of histological biopsies obtained during gastroscopies. A gastroscopy is a procedure in which a doctor examines the stomach using different imaging modalities, such as white light imaging (WLI) and narrowband imaging (NBI) [3].<br \/>\r\nIn order to increase the diagnostic ability of gastroscopies, an assistive device called a gastroscope endcap imager (GEI) is being proposed. The GEI presents a large \feld of view (FOV) using the imaging paradigm dual-beam manually actuated distortion corrected<br \/>\r\nimaging (DMDI) [4, 5]. The proposed GEI will be a multi-modal imaging device that is designed to be attachable to the distal end of a gastroscope, and will provide two imaging modalities, namely optical coherence tomography (OCT) and NBI. The work covered in this thesis project is the mechanical and optical mechanisms that will be used to develop a GEI prototype. More speci\fcally, a detailed discussion of<br \/>\r\nthe simulations, manufacturing processes, experiments, and iterative design processes is presented. It was found that it is feasible to manufacture collimators that can achieve a resolution of \u0014 50 mm, and to mechanically actuate \ffibers to create stable scans with a<br \/>\r\nFOV of 9 mm.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('187','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_187\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Gastric cancer is the third most common cause of cancer-related deaths worldwide [1]. It has a 25% 5-year survival rate, which is most likely due to the fact that 45% of cases are diagnosed in stage IV, when the cancer has already metastasized [2]. It is diagnosed through pathological examination of histological biopsies obtained during gastroscopies. A gastroscopy is a procedure in which a doctor examines the stomach using different imaging modalities, such as white light imaging (WLI) and narrowband imaging (NBI) [3].<br \/>\r\nIn order to increase the diagnostic ability of gastroscopies, an assistive device called a gastroscope endcap imager (GEI) is being proposed. The GEI presents a large \feld of view (FOV) using the imaging paradigm dual-beam manually actuated distortion corrected<br \/>\r\nimaging (DMDI) [4, 5]. The proposed GEI will be a multi-modal imaging device that is designed to be attachable to the distal end of a gastroscope, and will provide two imaging modalities, namely optical coherence tomography (OCT) and NBI. The work covered in this thesis project is the mechanical and optical mechanisms that will be used to develop a GEI prototype. More speci\fcally, a detailed discussion of<br \/>\r\nthe simulations, manufacturing processes, experiments, and iterative design processes is presented. It was found that it is feasible to manufacture collimators that can achieve a resolution of \u0014 50 mm, and to mechanically actuate \ffibers to create stable scans with a<br \/>\r\nFOV of 9 mm.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('187','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_187\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Manjarres-2020.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('187','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2019\">2019<\/h3><div class=\"tp_publication tp_publication_phdthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Zarei, Nilgoon<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0387343\" title=\"Machine learning for cancer detection, grading, and prognosis: automated segmentation, patterning recognition, and AL-based analysis\" target=\"blank\">Machine learning for cancer detection, grading, and prognosis: automated segmentation, patterning recognition, and AL-based analysis<\/a> <span class=\"tp_pub_type tp_  phdthesis\">PhD Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">Interdisciplinary Oncology, University of British Columbia, <\/span><span class=\"tp_pub_additional_year\">2019<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_180\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('180','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_180\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('180','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_180\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('180','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_180\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@phdthesis{nokey,<br \/>\r\ntitle = {Machine learning for cancer detection, grading, and prognosis: automated segmentation, patterning recognition, and AL-based analysis},<br \/>\r\nauthor = {Nilgoon Zarei},<br \/>\r\nurl = {http:\/\/hdl.handle.net\/2429\/72960},<br \/>\r\ndoi = {10.14288\/1.0387343},<br \/>\r\nyear  = {2019},<br \/>\r\ndate = {2019-12-24},<br \/>\r\nurldate = {2019-12-24},<br \/>\r\nschool = {Interdisciplinary Oncology, University of British Columbia},<br \/>\r\nabstract = {In this thesis, we presented the design steps for developing new, reliable, and cost-effective diagnostic and prognostic tools for cancer using advanced Machine Learning (ML) techniques. We proposed tools to improve the diagnostic, prognostic and detection accuracy of quantitative digital pathology by incorporating advanced image analysis, image processing, and classification methods. In this thesis we presented our ML image-based analytic approaches for three cancer types (prostate, cervix, and kidney) with different scale ranges from the sub-micron to multiple centimeters. In this thesis, we demonstrated the full workflow to design an automated prognostic and grading system specially designed for prostate cancer. We started with demonstrating techniques for prostate glandular structures detection. Next, we introduced an automated cell segmentation method along with an interactive segmentation correction method requiring minimum user-interaction and finally, we introduced our ML classification algorithms. We trained our ML method on the features extracted from cells\/nuclei that were segmented via our proposed techniques. Next, we studied renal carcinoma. We presented the workflow of renal carcinoma classification from image processing to feature selection and development of machine learning classification techniques. We extracted the features from renal vessel structures and demonstrated the design steps of machine learning classifiers to discriminate between different renal carcinoma subtypes using these features. The last cancer site studied was the cervix. We applied our techniques for cervical pre-cancer abnormality detection. We showed the whole pipeline of designing an automated classification method starting from tissue imaging to the development of ML classifiers using both classical and deep-learning methods. Although we conducted these studies on specific cancer types, a modified version of our algorithm could be applied to other cancers and disease sites. These techniques have great potential to improve the healthcare environment by providing extra information\/second opinion to the medical experts or to be used as a part of the first line of a screening program.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {phdthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('180','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_180\" style=\"display:none;\"><div class=\"tp_abstract_entry\">In this thesis, we presented the design steps for developing new, reliable, and cost-effective diagnostic and prognostic tools for cancer using advanced Machine Learning (ML) techniques. We proposed tools to improve the diagnostic, prognostic and detection accuracy of quantitative digital pathology by incorporating advanced image analysis, image processing, and classification methods. In this thesis we presented our ML image-based analytic approaches for three cancer types (prostate, cervix, and kidney) with different scale ranges from the sub-micron to multiple centimeters. In this thesis, we demonstrated the full workflow to design an automated prognostic and grading system specially designed for prostate cancer. We started with demonstrating techniques for prostate glandular structures detection. Next, we introduced an automated cell segmentation method along with an interactive segmentation correction method requiring minimum user-interaction and finally, we introduced our ML classification algorithms. We trained our ML method on the features extracted from cells\/nuclei that were segmented via our proposed techniques. Next, we studied renal carcinoma. We presented the workflow of renal carcinoma classification from image processing to feature selection and development of machine learning classification techniques. We extracted the features from renal vessel structures and demonstrated the design steps of machine learning classifiers to discriminate between different renal carcinoma subtypes using these features. The last cancer site studied was the cervix. We applied our techniques for cervical pre-cancer abnormality detection. We showed the whole pipeline of designing an automated classification method starting from tissue imaging to the development of ML classifiers using both classical and deep-learning methods. Although we conducted these studies on specific cancer types, a modified version of our algorithm could be applied to other cancers and disease sites. These techniques have great potential to improve the healthcare environment by providing extra information\/second opinion to the medical experts or to be used as a part of the first line of a screening program.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('180','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_180\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/hdl.handle.net\/2429\/72960\" title=\"http:\/\/hdl.handle.net\/2429\/72960\" target=\"_blank\">http:\/\/hdl.handle.net\/2429\/72960<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0387343\" title=\"Follow DOI:10.14288\/1.0387343\" target=\"_blank\">doi:10.14288\/1.0387343<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('180','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><div class=\"tp_publication tp_publication_mastersthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Identification of qualitative and quantitative features in wide-field in vivo oral optical coherence tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Rashika-Raizada-2018-web-e1759266519778.jpg\" width=\"128\" alt=\"Identification of qualitative and quantitative features in wide-field in vivo oral optical coherence tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Raizada, Rashika<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0375828\" title=\"Identification of qualitative and quantitative features in wide-field in vivo oral optical coherence tomography\" target=\"blank\">Identification of qualitative and quantitative features in wide-field in vivo oral optical coherence tomography<\/a> <span class=\"tp_pub_type tp_  mastersthesis\">Masters Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Biomedical Engineering, University of British Columbia, <\/span><span class=\"tp_pub_additional_year\">2019<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_182\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('182','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_182\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('182','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_182\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('182','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_182\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@mastersthesis{Raizada2019,<br \/>\r\ntitle = {Identification of qualitative and quantitative features in wide-field in vivo oral optical coherence tomography},<br \/>\r\nauthor = {Rashika Raizada},<br \/>\r\nurl = {http:\/\/hdl.handle.net\/2429\/68141},<br \/>\r\ndoi = {10.14288\/1.0375828},<br \/>\r\nyear  = {2019},<br \/>\r\ndate = {2019-01-02},<br \/>\r\nurldate = {2019-01-02},<br \/>\r\nschool = {School of Biomedical Engineering, University of British Columbia},<br \/>\r\nabstract = {Optical coherence tomography (OCT), the optical analogue of ultrasound with resolution approaching that of histology, has shown great potential in the detection of pre-cancerous and cancerous lesions in the oral cavity. The objective of this thesis is to identify qualitative and quantitative features from OCT that are associated with normal, benign, pre-cancerous and cancerous lesions. In this work, OCT images were acquired from patients in vivo during their visits to the oral pathology clinic. The data were then analyzed both qualitatively and quantitatively. In the qualitative analysis, structural changes in tissue, associated with abnormalities, were compared and matched between their appearance in OCT and the corresponding histology images. In the quantitative analysis, MATLAB was used to automate extraction of numerical values associated with the structural changes, present in the OCT images. As a result of the qualitative analysis, it was found that a set of five features \u2014 epithelium thickness, epithelium stratification, rete-ridges visibility, basement membrane presence, and connective tissue appearance relative to the epithelium \u2014 can together qualitatively help to identify normal as well as various benign, pre-cancerous and cancerous conditions. To the best of my knowledge, this is the first time that epithelium stratification and high-resolution rete-ridges visibility have been presented as OCT features relevant for cancer detection. Furthermore, quantitative analysis revealed that the numerical values of two of the features \u2014 epithelium thickness and stratification \u2014 significantly vary going from normal tissue to benign and finally to pre-cancers and cancer. As a result, this work lays the ground work for showing the potential of OCT as a biopsy guidance tool, that can be used in vivo, to find regions of severe abnormalities and thus minimize multiple and unnecessary biopsies.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {mastersthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('182','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_182\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Optical coherence tomography (OCT), the optical analogue of ultrasound with resolution approaching that of histology, has shown great potential in the detection of pre-cancerous and cancerous lesions in the oral cavity. The objective of this thesis is to identify qualitative and quantitative features from OCT that are associated with normal, benign, pre-cancerous and cancerous lesions. In this work, OCT images were acquired from patients in vivo during their visits to the oral pathology clinic. The data were then analyzed both qualitatively and quantitatively. In the qualitative analysis, structural changes in tissue, associated with abnormalities, were compared and matched between their appearance in OCT and the corresponding histology images. In the quantitative analysis, MATLAB was used to automate extraction of numerical values associated with the structural changes, present in the OCT images. As a result of the qualitative analysis, it was found that a set of five features \u2014 epithelium thickness, epithelium stratification, rete-ridges visibility, basement membrane presence, and connective tissue appearance relative to the epithelium \u2014 can together qualitatively help to identify normal as well as various benign, pre-cancerous and cancerous conditions. To the best of my knowledge, this is the first time that epithelium stratification and high-resolution rete-ridges visibility have been presented as OCT features relevant for cancer detection. Furthermore, quantitative analysis revealed that the numerical values of two of the features \u2014 epithelium thickness and stratification \u2014 significantly vary going from normal tissue to benign and finally to pre-cancers and cancer. As a result, this work lays the ground work for showing the potential of OCT as a biopsy guidance tool, that can be used in vivo, to find regions of severe abnormalities and thus minimize multiple and unnecessary biopsies.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('182','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_182\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-globe\"><\/i><a class=\"tp_pub_list\" href=\"http:\/\/hdl.handle.net\/2429\/68141\" title=\"http:\/\/hdl.handle.net\/2429\/68141\" target=\"_blank\">http:\/\/hdl.handle.net\/2429\/68141<\/a><\/li><li><i class=\"ai ai-doi\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/dx.doi.org\/10.14288\/1.0375828\" title=\"Follow DOI:10.14288\/1.0375828\" target=\"_blank\">doi:10.14288\/1.0375828<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('182','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2018\">2018<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Harlow, Madeline<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf\" target=\"blank\">Dual-beam manually-actuated distortion-corrected imaging (DMDI): 2D scanning using single-axis galvanometer with automated distortion correction<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">Swiss Federal Institute of Technology in Z\u00fcrich (ETH Z\u00fcrich), <\/span><span class=\"tp_pub_additional_year\">2018<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_181\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('181','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_181\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('181','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_181\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('181','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_181\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Dual-beam manually-actuated distortion-corrected imaging (DMDI): 2D scanning using single-axis galvanometer with automated distortion correction},<br \/>\r\nauthor = {Madeline Harlow},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf},<br \/>\r\nyear  = {2018},<br \/>\r\ndate = {2018-03-20},<br \/>\r\nurldate = {2018-03-20},<br \/>\r\nschool = {Swiss Federal Institute of Technology in Z\u00fcrich (ETH Z\u00fcrich)},<br \/>\r\nabstract = {High resolution optical imaging modalities, such as optical coherence tomography, confocal, and multiphoton microscopy, continue to show promise for diagnostic imaging. These modalities are commonly employed using 2D scanners, however such scanners can often have limited field-of-view and are susceptible to clinician or patient motion artefacts. A number of techniques have been investigated to overcome these shortcomings, including allowing for manual actuation of handheld probes. Recently our research group at BC Cancer Research Centre demonstrated a new imaging paradigm, called dual-beam manually-actuated distortion-corrected imaging (DMDI), which exploits the predictable path and spatial separation of two beams to calculate and correct the scanning distortion caused by manual actuation of the imaging apparatus and\/or the sample. DMDI was first implemented using a rotating dual-beam micromotor catheter which demonstrated the feasibility of DMDI, however the complex scan pattern as a result of the catheter design resulted in tedious and manual distortion correction. Further, alternative implementations of DMDI should be explored to demonstrate the versatility and applicability of this modality.<br \/>\r\nIn this thesis, I demonstrate a galvanometer implementation of DMDI with automated distortion correction. The single-axis galvanometer allows for tracing of two roughly parallel lines onto a sample which can be manually actuated. Distortion caused by the scanning pattern and manual actuation can be corrected by estimating the effective beam path of both beams onto the sample. The effective beam path is determined by characterizing the scanning pattern, achieved by a one-time calibration, and estimating the effective sample displacement, achieved by estimating the velocity profile through identifying common and unique features in the images of the two beams. With a scanning pattern of two roughly parallel lines, identifying common and unique features can be done in an automated fashion. Specifically I developed automated frame correlation to allow for detecting common features with potential displacement in two dimensions, thus sensitive to 2D actuation. Only the information from two distorted images and the calibrated scan pattern are used to produce two corrected images.<br \/>\r\nUsing en face OCT as the imaging modality, I demonstrate DMDI with automated distortion correction in imaging of a printed paper phantom, beef tongue, kiwi, dragon fruit, and fingerprint. Distortion correction is possible for manually-actuated motion both perpendicular and parallel to the galvanonmeter-scanned lines. Through biological validations, the correction method estimated constant velocities with an average error of 0.99% and produced favorable results in the correction of 2D manual actuation. Additionally, I developed a simulation of the imaging system and actuation to allow for fast investigation of scanning parameters and arbitrary velocity profiles. For example it was observed that beam separation influences the range of velocity sensitivity. With this work as a foundation, DMDI with automated distortion correction becomes a more attractive and accessible imaging modality with a promising future in clinical applications.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('181','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_181\" style=\"display:none;\"><div class=\"tp_abstract_entry\">High resolution optical imaging modalities, such as optical coherence tomography, confocal, and multiphoton microscopy, continue to show promise for diagnostic imaging. These modalities are commonly employed using 2D scanners, however such scanners can often have limited field-of-view and are susceptible to clinician or patient motion artefacts. A number of techniques have been investigated to overcome these shortcomings, including allowing for manual actuation of handheld probes. Recently our research group at BC Cancer Research Centre demonstrated a new imaging paradigm, called dual-beam manually-actuated distortion-corrected imaging (DMDI), which exploits the predictable path and spatial separation of two beams to calculate and correct the scanning distortion caused by manual actuation of the imaging apparatus and\/or the sample. DMDI was first implemented using a rotating dual-beam micromotor catheter which demonstrated the feasibility of DMDI, however the complex scan pattern as a result of the catheter design resulted in tedious and manual distortion correction. Further, alternative implementations of DMDI should be explored to demonstrate the versatility and applicability of this modality.<br \/>\r\nIn this thesis, I demonstrate a galvanometer implementation of DMDI with automated distortion correction. The single-axis galvanometer allows for tracing of two roughly parallel lines onto a sample which can be manually actuated. Distortion caused by the scanning pattern and manual actuation can be corrected by estimating the effective beam path of both beams onto the sample. The effective beam path is determined by characterizing the scanning pattern, achieved by a one-time calibration, and estimating the effective sample displacement, achieved by estimating the velocity profile through identifying common and unique features in the images of the two beams. With a scanning pattern of two roughly parallel lines, identifying common and unique features can be done in an automated fashion. Specifically I developed automated frame correlation to allow for detecting common features with potential displacement in two dimensions, thus sensitive to 2D actuation. Only the information from two distorted images and the calibrated scan pattern are used to produce two corrected images.<br \/>\r\nUsing en face OCT as the imaging modality, I demonstrate DMDI with automated distortion correction in imaging of a printed paper phantom, beef tongue, kiwi, dragon fruit, and fingerprint. Distortion correction is possible for manually-actuated motion both perpendicular and parallel to the galvanonmeter-scanned lines. Through biological validations, the correction method estimated constant velocities with an average error of 0.99% and produced favorable results in the correction of 2D manual actuation. Additionally, I developed a simulation of the imaging system and actuation to allow for fast investigation of scanning parameters and arbitrary velocity profiles. For example it was observed that beam separation influences the range of velocity sensitivity. With this work as a foundation, DMDI with automated distortion correction becomes a more attractive and accessible imaging modality with a promising future in clinical applications.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('181','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_181\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/09\/Harlow_MasterThesis.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('181','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2017\">2017<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Custom Optimized Galvanometer Scanning for Micro Optical Coherence Tomography\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2022\/02\/Adrian-2-scaled-e1759257984514.jpg\" width=\"128\" alt=\"Custom Optimized Galvanometer Scanning for Micro Optical Coherence Tomography\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Tanskanen, Adrian<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis-FINAL.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis-FINAL.pdf\" target=\"blank\">Custom Optimized Galvanometer Scanning for Micro Optical Coherence Tomography<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2017<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_189\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('189','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_189\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('189','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_189\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('189','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_189\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Custom Optimized Galvanometer Scanning for Micro Optical Coherence Tomography},<br \/>\r\nauthor = {Adrian Tanskanen},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis-FINAL.pdf},<br \/>\r\nyear  = {2017},<br \/>\r\ndate = {2017-04-30},<br \/>\r\nurldate = {2017-04-30},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {We document the fabrication of a Galvanometer scanner to be integrated into a novel Micro Optical Coherence Tomography system. Using an of-the-shelf Thorlabs Small Beam Diameter Scanning Galvo Mirror System and an OCT scan lens, a prototype model is assembled and controlled using custom software developed for the application. The custom software is programmed to allow for seamless control of the scanner hardware. The hardware and the software are tested together along with an added photo-detector, beam splitter and Helium Neon laser in order to generate images from the resections of an ultra resolution target. A theoretical maximum resolution value of R = 14.2 \u00b5m is calculated given the wavelength of the laser \u03bb = 632.8 nm, the focal length of the lens fe = 18 mm and the beam waist of the laser entering the lens D = 0.59 mm. This resolution value is validated by generating a Modulation Transfer Function from the images taken from the target. Lastly a number of potential designs for specialized optics capable of being used in a Micro Optical Coherence Tomography system are discussed.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('189','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_189\" style=\"display:none;\"><div class=\"tp_abstract_entry\">We document the fabrication of a Galvanometer scanner to be integrated into a novel Micro Optical Coherence Tomography system. Using an of-the-shelf Thorlabs Small Beam Diameter Scanning Galvo Mirror System and an OCT scan lens, a prototype model is assembled and controlled using custom software developed for the application. The custom software is programmed to allow for seamless control of the scanner hardware. The hardware and the software are tested together along with an added photo-detector, beam splitter and Helium Neon laser in order to generate images from the resections of an ultra resolution target. A theoretical maximum resolution value of R = 14.2 \u00b5m is calculated given the wavelength of the laser \u03bb = 632.8 nm, the focal length of the lens fe = 18 mm and the beam waist of the laser entering the lens D = 0.59 mm. This resolution value is validated by generating a Modulation Transfer Function from the images taken from the target. Lastly a number of potential designs for specialized optics capable of being used in a Micro Optical Coherence Tomography system are discussed.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('189','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_189\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis-FINAL.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis[...]\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Adrian-Tanskanen-Thesis[...]<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('189','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2016\">2016<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Goldan, Ryan<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf\" target=\"blank\">Real-Time Automated Segmentation of Oral Mucosa from OCT Images<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2016<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_188\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('188','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_188\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('188','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_188\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('188','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_188\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Real-Time Automated Segmentation of Oral Mucosa from OCT Images},<br \/>\r\nauthor = {Ryan Goldan},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf},<br \/>\r\nyear  = {2016},<br \/>\r\ndate = {2016-08-01},<br \/>\r\nurldate = {2016-08-01},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {Diagnosing and treating oral cancers can be challenging for clinicians using current practices which rely on histopathology to make decisions. There is currently little technology readily available to assist clinicians in assessing the morphology of abnormal tissue beneath the surface in order to determine the best biopsy site or to delineate sufficient margins during surgery. Biopsies can be traumatic for patients, and therefore determining whether it is necessary using a non-invasive method is of great interest. Additionally, determining the best place to take a biopsy with greater confidence would reduce the likelihood of requiring multiple biopsies.<br \/>\r\nOptical Coherence Tomography (OCT) can discriminate morphological tissue features important for oral cancer detection such as the presence or absence of basement membrane and epithelial thickness. We previously developed a proof of concept algorithm and MATLAB implementation capable of automatically segmenting the epithelial surface and basement membrane surfaces in 3D OCT images of oral mucosa from a wide-field OCT system developed at the BC Cancer Research Centre (BCCRC). Using these segmentations, maps of epithelial thickness and basement membrane continuity over the tissue surface can be generated to give clinicians visualizations of tissue morphology in abnormal tissue. Using these maps they can localize the most severely affected areas where they can take biopsies. The maps can also be used to determine the margins of tumors, by looking at where the abnormal tissue begins to end and normal tissue begins. <br \/>\r\nThe MATLAB implementation was validated using a test set of images to ensure that it had been trained to perform well on a wide variety of sites and diagnoses. Once it was validated, the next step was to implement a compiled software implementation in order to provide these visualizations quickly in clinical settings in order to make quick bedside decisions regarding biopsy site guidance and tumor margin selection. <br \/>\r\nThe compiled software implementation was written in C++, making use of Intel Integrated Performance Primitives to implement equivalent functions and libraries to those found in the Matlab image processing toolbox. Parallelization of tasks using multithreaded programming increased the speed of the software in order to meet the sufficiently fast processing requirements of the software necessary to provide visualizations quickly in the clinic.<br \/>\r\nFinally, the real-time software was validated against the proof of concept implementation to ensure that the performance of the software was consistent after the transition to C++.<br \/>\r\n},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('188','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_188\" style=\"display:none;\"><div class=\"tp_abstract_entry\">Diagnosing and treating oral cancers can be challenging for clinicians using current practices which rely on histopathology to make decisions. There is currently little technology readily available to assist clinicians in assessing the morphology of abnormal tissue beneath the surface in order to determine the best biopsy site or to delineate sufficient margins during surgery. Biopsies can be traumatic for patients, and therefore determining whether it is necessary using a non-invasive method is of great interest. Additionally, determining the best place to take a biopsy with greater confidence would reduce the likelihood of requiring multiple biopsies.<br \/>\r\nOptical Coherence Tomography (OCT) can discriminate morphological tissue features important for oral cancer detection such as the presence or absence of basement membrane and epithelial thickness. We previously developed a proof of concept algorithm and MATLAB implementation capable of automatically segmenting the epithelial surface and basement membrane surfaces in 3D OCT images of oral mucosa from a wide-field OCT system developed at the BC Cancer Research Centre (BCCRC). Using these segmentations, maps of epithelial thickness and basement membrane continuity over the tissue surface can be generated to give clinicians visualizations of tissue morphology in abnormal tissue. Using these maps they can localize the most severely affected areas where they can take biopsies. The maps can also be used to determine the margins of tumors, by looking at where the abnormal tissue begins to end and normal tissue begins. <br \/>\r\nThe MATLAB implementation was validated using a test set of images to ensure that it had been trained to perform well on a wide variety of sites and diagnoses. Once it was validated, the next step was to implement a compiled software implementation in order to provide these visualizations quickly in clinical settings in order to make quick bedside decisions regarding biopsy site guidance and tumor margin selection. <br \/>\r\nThe compiled software implementation was written in C++, making use of Intel Integrated Performance Primitives to implement equivalent functions and libraries to those found in the Matlab image processing toolbox. Parallelization of tasks using multithreaded programming increased the speed of the software in order to meet the sufficiently fast processing requirements of the software necessary to provide visualizations quickly in the clinic.<br \/>\r\nFinally, the real-time software was validated against the proof of concept implementation to ensure that the performance of the software was consistent after the transition to C++.<br \/>\r\n<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('188','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_188\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Goldan-2016.pdf<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('188','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><h3 class=\"tp_h3\" id=\"tp_h3_2015\">2015<\/h3><div class=\"tp_publication tp_publication_bachelorthesis\"><div class=\"tp_pub_image_left\"><img decoding=\"async\" name=\"Automatic Segmentation of Airway Wall Components in Optical Coherence Tomography Images\" src=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2018\/10\/Rashika-Raizada-2018-web-e1759266519778.jpg\" width=\"128\" alt=\"Automatic Segmentation of Airway Wall Components in Optical Coherence Tomography Images\" \/><\/div><div class=\"tp_pub_info\"><p class=\"tp_pub_author\"> Raizada, Rashika<\/p><p class=\"tp_pub_title\"><a class=\"tp_title_link\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-Segmentation-of-Airway-Wall-Components-in-OCT-Images-FINAL.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-Segmentation-of-Airway-Wall-Components-in-OCT-Images-FINAL.pdf\" target=\"blank\">Automatic Segmentation of Airway Wall Components in Optical Coherence Tomography Images<\/a> <span class=\"tp_pub_type tp_  bachelorthesis\">Bachelor Thesis<\/span> <\/p><p class=\"tp_pub_additional\"><span class=\"tp_pub_additional_school\">School of Engineering Science, Simon Fraser University, <\/span><span class=\"tp_pub_additional_year\">2015<\/span>.<\/p><p class=\"tp_pub_menu\"><span class=\"tp_abstract_link\"><a id=\"tp_abstract_sh_190\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('190','tp_abstract')\" title=\"Show abstract\" style=\"cursor:pointer;\">Abstract<\/a><\/span> | <span class=\"tp_resource_link\"><a id=\"tp_links_sh_190\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('190','tp_links')\" title=\"Show links and resources\" style=\"cursor:pointer;\">Links<\/a><\/span> | <span class=\"tp_bibtex_link\"><a id=\"tp_bibtex_sh_190\" class=\"tp_show\" onclick=\"teachpress_pub_showhide('190','tp_bibtex')\" title=\"Show BibTeX entry\" style=\"cursor:pointer;\">BibTeX<\/a><\/span><\/p><div class=\"tp_bibtex\" id=\"tp_bibtex_190\" style=\"display:none;\"><div class=\"tp_bibtex_entry\"><pre>@bachelorthesis{nokey,<br \/>\r\ntitle = {Automatic Segmentation of Airway Wall Components in Optical Coherence Tomography Images},<br \/>\r\nauthor = {Rashika Raizada},<br \/>\r\nurl = {https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-Segmentation-of-Airway-Wall-Components-in-OCT-Images-FINAL.pdf},<br \/>\r\nyear  = {2015},<br \/>\r\ndate = {2015-01-17},<br \/>\r\nurldate = {2015-01-17},<br \/>\r\nschool = {School of Engineering Science, Simon Fraser University},<br \/>\r\nabstract = {This thesis presents the investigation and experimental results on various image processing techniques as well as segmentation and analysis of volumetric Porcine Airway data. The Porcine airway data was acquired using Optical Coherence Tomography (OCT) using a fiber based probe. The data set used in this project comprised of ten Porcine Airway volumes. Six frames were manually segmented by two expert observers per porcine airway volume. Three hundred frames were automatically segmented in this thesis project per porcine airway volume and were compared against the manually segmented frames. Root mean square errors and Jaccard similarity were used to compare the segmentation contours and Bland-Altman plots were used to compare measurements with the manually segmented frames. Results and analysis of all three hundred frames automatically segmented form the final results of the thesis project.},<br \/>\r\nkeywords = {},<br \/>\r\npubstate = {published},<br \/>\r\ntppubtype = {bachelorthesis}<br \/>\r\n}<br \/>\r\n<\/pre><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('190','tp_bibtex')\">Close<\/a><\/p><\/div><div class=\"tp_abstract\" id=\"tp_abstract_190\" style=\"display:none;\"><div class=\"tp_abstract_entry\">This thesis presents the investigation and experimental results on various image processing techniques as well as segmentation and analysis of volumetric Porcine Airway data. The Porcine airway data was acquired using Optical Coherence Tomography (OCT) using a fiber based probe. The data set used in this project comprised of ten Porcine Airway volumes. Six frames were manually segmented by two expert observers per porcine airway volume. Three hundred frames were automatically segmented in this thesis project per porcine airway volume and were compared against the manually segmented frames. Root mean square errors and Jaccard similarity were used to compare the segmentation contours and Bland-Altman plots were used to compare measurements with the manually segmented frames. Results and analysis of all three hundred frames automatically segmented form the final results of the thesis project.<\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('190','tp_abstract')\">Close<\/a><\/p><\/div><div class=\"tp_links\" id=\"tp_links_190\" style=\"display:none;\"><div class=\"tp_links_entry\"><ul class=\"tp_pub_list\"><li><i class=\"fas fa-file-pdf\"><\/i><a class=\"tp_pub_list\" href=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-Segmentation-of-Airway-Wall-Components-in-OCT-Images-FINAL.pdf\" title=\"https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-[...]\" target=\"_blank\">https:\/\/biophotonics.bccrc.ca\/wp-content\/uploads\/2025\/10\/Raizada-2015-Automatic-[...]<\/a><\/li><\/ul><\/div><p class=\"tp_close_menu\"><a class=\"tp_close\" onclick=\"teachpress_pub_showhide('190','tp_links')\">Close<\/a><\/p><\/div><\/div><\/div><\/div><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Journal Articles Theses<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":3,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-19","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.0 - 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