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dc.contributor.authorSchmolze, Daniel B.
dc.contributor.authorVardeh, Hilde
dc.contributor.authorFaulkner-Jones, Beverly E.
dc.contributor.authorConnolly, James L.
dc.contributor.authorYoshitake, Tadayuki
dc.contributor.authorGiacomelli, Michael
dc.contributor.authorCahill, Lucas Christopher
dc.contributor.authorFujimoto, James G
dc.date.accessioned2017-06-15T13:40:58Z
dc.date.available2017-06-15T13:40:58Z
dc.date.issued2016-12
dc.date.submitted2016-10
dc.identifier.issn1083-3668
dc.identifier.issn1560-2281
dc.identifier.urihttp://hdl.handle.net/1721.1/109880
dc.description.abstractRapid histopathological examination of surgical specimen margins using fluorescence microscopy during breast conservation therapy has the potential to reduce the rate of positive margins on postoperative histopathology and the need for repeat surgeries. To assess the suitability of imaging modalities, we perform a direct comparison between confocal fluorescence microscopy and multiphoton microscopy for imaging unfixed tissue and compare to paraffin-embedded histology. An imaging protocol including dual channel detection of two contrast agents to implement virtual hematoxylin and eosin images is introduced that provides high quality imaging under both one and two photon excitation. Corresponding images of unfixed human breast tissue show that both confocal and multiphoton microscopy can reproduce the appearance of conventional histology without the need for physical sectioning. We further compare normal breast tissue and invasive cancer specimens imaged at multiple magnifications, and assess the effects of photobleaching for both modalities using the staining protocol. The results demonstrate that confocal fluorescence microscopy is a promising and cost-effective alternative to multiphoton microscopy for rapid histopathological evaluation of ex vivo breast tissue.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-CA178636-02)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-CA075289-18)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant F32-CA183400-03)en_US
dc.description.sponsorshipUnited States. Air Force. Office of Scientific Research (Grant FA9550-12-1-0551)en_US
dc.description.sponsorshipUnited States. Air Force. Office of Scientific Research (Grant FA9550-15-1-0473)en_US
dc.language.isoen_US
dc.publisherSPIEen_US
dc.relation.isversionofhttp://dx.doi.org/10.1117/1.jbo.21.12.126021en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSPIEen_US
dc.titleDirect comparison between confocal and multiphoton microscopy for rapid histopathological evaluation of unfixed human breast tissueen_US
dc.typeArticleen_US
dc.identifier.citationYoshitake, Tadayuki et al. “Direct Comparison between Confocal and Multiphoton Microscopy for Rapid Histopathological Evaluation of Unfixed Human Breast Tissue.” Journal of Biomedical Optics 21.12 (2016): 126021. © 2016 SPIEen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.mitauthorYoshitake, Tadayuki
dc.contributor.mitauthorGiacomelli, Michael
dc.contributor.mitauthorCahill, Lucas Christopher
dc.contributor.mitauthorFujimoto, James G
dc.relation.journalJournal of Biomedical Opticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsYoshitake, Tadayuki; Giacomelli, Michael G.; Cahill, Lucas C.; Schmolze, Daniel B.; Vardeh, Hilde; Faulkner-Jones, Beverly E.; Connolly, James L.; Fujimoto, James G.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4156-6484
dc.identifier.orcidhttps://orcid.org/0000-0002-2570-0770
dc.identifier.orcidhttps://orcid.org/0000-0003-3425-9486
dc.identifier.orcidhttps://orcid.org/0000-0002-0828-4357
mit.licensePUBLISHER_POLICYen_US


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