Real-time cancer detection with an integrated lensless fluorescence contact imager
Microscopic tumor cell foci left in a patient after surgery significantly increase the chance of cancer recurrence. However, fluorescence microscopes used for intraoperative navigation lack the necessary sensitivity for imaging microscopic disease and are too bulky to maneuver within the resection c...
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Veröffentlicht in: | Biomedical optics express 2018-08, Vol.9 (8), p.3607-3623 |
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creator | Papageorgiou, Efthymios P Zhang, Hui Giverts, Simeon Park, Catherine Boser, Bernhard E Anwar, Mekhail |
description | Microscopic tumor cell foci left in a patient after surgery significantly increase the chance of cancer recurrence. However, fluorescence microscopes used for intraoperative navigation lack the necessary sensitivity for imaging microscopic disease and are too bulky to maneuver within the resection cavity. We have developed a scalable chip-scale fluorescence contact imager for detecting microscopic cancer
and in real-time. The imager has been characterized under simulated
conditions using
samples, providing strong evidence that our device can be used
. Angle-selective gratings enhance the resolution of the imager without impacting its physical size. We demonstrate detection of cancer cell clusters containing as few as 25 HCC1569 breast cancer cells and 400 LNCaP prostate cancer cells with integration times of only 50 ms and 70 ms, respectively. A cell cluster recognition algorithm is used to achieve both a sensitivity and specificity of 92 % for HCC1569 cell samples, indicating the reliability of the imager. The signal-to-noise ratio (SNR) degradation with increased separation is only 1.5 dB at 250 μm. Blood scattering and absorption reduce the SNR by less than 2 dB for typical concentrations. Moreover, HER2+ breast cancer tissue taken from a patient is distinguished from normal breast tissue with an integration time of only 75 ms. |
doi_str_mv | 10.1364/BOE.9.003607 |
format | Article |
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and in real-time. The imager has been characterized under simulated
conditions using
samples, providing strong evidence that our device can be used
. Angle-selective gratings enhance the resolution of the imager without impacting its physical size. We demonstrate detection of cancer cell clusters containing as few as 25 HCC1569 breast cancer cells and 400 LNCaP prostate cancer cells with integration times of only 50 ms and 70 ms, respectively. A cell cluster recognition algorithm is used to achieve both a sensitivity and specificity of 92 % for HCC1569 cell samples, indicating the reliability of the imager. The signal-to-noise ratio (SNR) degradation with increased separation is only 1.5 dB at 250 μm. Blood scattering and absorption reduce the SNR by less than 2 dB for typical concentrations. Moreover, HER2+ breast cancer tissue taken from a patient is distinguished from normal breast tissue with an integration time of only 75 ms.</description><identifier>ISSN: 2156-7085</identifier><identifier>EISSN: 2156-7085</identifier><identifier>DOI: 10.1364/BOE.9.003607</identifier><identifier>PMID: 30338143</identifier><language>eng</language><publisher>United States: Optical Society of America</publisher><ispartof>Biomedical optics express, 2018-08, Vol.9 (8), p.3607-3623</ispartof><rights>2018 Optical Society of America under the terms of the 2018 Optical Society of America</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-684bc5c0759e8c2d423af065297d308a80009a6149478eb8a836992b3288f5e33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191610/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191610/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30338143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Papageorgiou, Efthymios P</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Giverts, Simeon</creatorcontrib><creatorcontrib>Park, Catherine</creatorcontrib><creatorcontrib>Boser, Bernhard E</creatorcontrib><creatorcontrib>Anwar, Mekhail</creatorcontrib><title>Real-time cancer detection with an integrated lensless fluorescence contact imager</title><title>Biomedical optics express</title><addtitle>Biomed Opt Express</addtitle><description>Microscopic tumor cell foci left in a patient after surgery significantly increase the chance of cancer recurrence. However, fluorescence microscopes used for intraoperative navigation lack the necessary sensitivity for imaging microscopic disease and are too bulky to maneuver within the resection cavity. We have developed a scalable chip-scale fluorescence contact imager for detecting microscopic cancer
and in real-time. The imager has been characterized under simulated
conditions using
samples, providing strong evidence that our device can be used
. Angle-selective gratings enhance the resolution of the imager without impacting its physical size. We demonstrate detection of cancer cell clusters containing as few as 25 HCC1569 breast cancer cells and 400 LNCaP prostate cancer cells with integration times of only 50 ms and 70 ms, respectively. A cell cluster recognition algorithm is used to achieve both a sensitivity and specificity of 92 % for HCC1569 cell samples, indicating the reliability of the imager. The signal-to-noise ratio (SNR) degradation with increased separation is only 1.5 dB at 250 μm. Blood scattering and absorption reduce the SNR by less than 2 dB for typical concentrations. Moreover, HER2+ breast cancer tissue taken from a patient is distinguished from normal breast tissue with an integration time of only 75 ms.</description><issn>2156-7085</issn><issn>2156-7085</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpVUU1LxDAQDaLoot48S44e7Jqv5uMi6OIXCAuLnkOaTtdKt9UkVfz3RnZdNJcJM2_evJmH0AklU8qluLie30zNlBAuidpBE0ZLWSiiy90__wN0HOMryU8IRbjeRweccK6p4BO0WIDritSuAHvXewi4hgQ-tUOPP9v0gl2P2z7BMrgENe6gjx3EiJtuHAJED7kH-6FPzifcrtwSwhHaa1wX4XgTD9Hz7c3T7L54nN89zK4eCy-YSoXUovKlJ6o0oD2rBeOuIbJkRtWcaKezYOMkFUYoDVVOcGkMqzjTuimB80N0ueZ9G6sV1FlKCq6zbyHLCF92cK39X-nbF7scPqykhkpKMsHZhiAM7yPEZFdt3qjrXA_DGC2jjCuqSEkz9HwN9WGIMUCzHUOJ_XHCZiessWsnMvz0r7Qt-Pfu_BtcjoPL</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Papageorgiou, Efthymios P</creator><creator>Zhang, Hui</creator><creator>Giverts, Simeon</creator><creator>Park, Catherine</creator><creator>Boser, Bernhard E</creator><creator>Anwar, Mekhail</creator><general>Optical Society of America</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180801</creationdate><title>Real-time cancer detection with an integrated lensless fluorescence contact imager</title><author>Papageorgiou, Efthymios P ; Zhang, Hui ; Giverts, Simeon ; Park, Catherine ; Boser, Bernhard E ; Anwar, Mekhail</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-684bc5c0759e8c2d423af065297d308a80009a6149478eb8a836992b3288f5e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Papageorgiou, Efthymios P</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Giverts, Simeon</creatorcontrib><creatorcontrib>Park, Catherine</creatorcontrib><creatorcontrib>Boser, Bernhard E</creatorcontrib><creatorcontrib>Anwar, Mekhail</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biomedical optics express</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Papageorgiou, Efthymios P</au><au>Zhang, Hui</au><au>Giverts, Simeon</au><au>Park, Catherine</au><au>Boser, Bernhard E</au><au>Anwar, Mekhail</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-time cancer detection with an integrated lensless fluorescence contact imager</atitle><jtitle>Biomedical optics express</jtitle><addtitle>Biomed Opt Express</addtitle><date>2018-08-01</date><risdate>2018</risdate><volume>9</volume><issue>8</issue><spage>3607</spage><epage>3623</epage><pages>3607-3623</pages><issn>2156-7085</issn><eissn>2156-7085</eissn><abstract>Microscopic tumor cell foci left in a patient after surgery significantly increase the chance of cancer recurrence. However, fluorescence microscopes used for intraoperative navigation lack the necessary sensitivity for imaging microscopic disease and are too bulky to maneuver within the resection cavity. We have developed a scalable chip-scale fluorescence contact imager for detecting microscopic cancer
and in real-time. The imager has been characterized under simulated
conditions using
samples, providing strong evidence that our device can be used
. Angle-selective gratings enhance the resolution of the imager without impacting its physical size. We demonstrate detection of cancer cell clusters containing as few as 25 HCC1569 breast cancer cells and 400 LNCaP prostate cancer cells with integration times of only 50 ms and 70 ms, respectively. A cell cluster recognition algorithm is used to achieve both a sensitivity and specificity of 92 % for HCC1569 cell samples, indicating the reliability of the imager. The signal-to-noise ratio (SNR) degradation with increased separation is only 1.5 dB at 250 μm. Blood scattering and absorption reduce the SNR by less than 2 dB for typical concentrations. Moreover, HER2+ breast cancer tissue taken from a patient is distinguished from normal breast tissue with an integration time of only 75 ms.</abstract><cop>United States</cop><pub>Optical Society of America</pub><pmid>30338143</pmid><doi>10.1364/BOE.9.003607</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
title | Real-time cancer detection with an integrated lensless fluorescence contact imager |
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