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dc.contributor.authorKim, Ki Hean
dc.contributor.authorSo, Peter T. C.
dc.contributor.authorSun, Tzu-Lin
dc.contributor.authorLiu, Yuan
dc.contributor.authorSung, Ming-Chin
dc.contributor.authorYang, Chun-Hui
dc.contributor.authorHovhannisyan, Vladimir
dc.contributor.authorChen, Wei-Liang
dc.contributor.authorChen, Yang-Fang
dc.contributor.authorChen, Hsiao-Ching
dc.contributor.authorChiou, Ling-Ling
dc.contributor.authorHuang, Guan-Tarn
dc.contributor.authorLin, Wei-Chou
dc.contributor.authorJeng, Yung-Ming
dc.contributor.authorLee, Hsuan-Shu
dc.contributor.authorDong, Chen-Yuan
dc.date.accessioned2011-02-18T16:48:09Z
dc.date.available2011-02-18T16:48:09Z
dc.date.issued2010-06
dc.date.submitted2009-11
dc.identifier.issn1083-3668
dc.identifier.urihttp://hdl.handle.net/1721.1/60985
dc.description.abstractConventionally, liver fibrosis is diagnosed using histopathological techniques. The traditional method is time-consuming in that the specimen preparation procedure requires sample fixation, slicing, and labeling. Our goal is to apply multiphoton microscopy to efficiently image and quantitatively analyze liver fibrosis specimens bypassing steps required in histological preparation. In this work, the combined imaging modality of multiphoton autofluorescence (MAF) and second-harmonic generation (SHG) was used for the qualitative imaging of liver fibrosis of different METAVIR grades under label-free, ex vivo conditions. We found that while MAF is effective in identifying cellular architecture in the liver specimens, it is the spectrally distinct SHG signal that allows the characterization of the extent of fibrosis. We found that qualitative SHG imaging can be used for the effective identification of the associated features of liver fibrosis specimens graded METAVIR 0 to 4. In addition, we attempted to associate quantitative SHG signal to the different METAVIR grades and found that an objective determination of the extent of disease progression can be made. Our approach demonstrates the potential of using multiphoton imaging in rapid classification of ex vivo liver fibrosis in the clinical setting and investigation of liver fibrosis–associated physiopathology in animal models in vivo.en_US
dc.description.sponsorshipNational Science Council (China) (NSC 98-2112-M-002-008-MY3)en_US
dc.language.isoen_US
dc.publisherSPIEen_US
dc.relation.isversionofhttp://dx.doi.org/10.1117/1.3427146en_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.titleEx vivo imaging and quantification of liver fibrosis using second-harmonic generation microscopyen_US
dc.typeArticleen_US
dc.identifier.citationSun, Tzu-Lin et al. “Ex vivo imaging and quantification of liver fibrosis using second-harmonic generation microscopy.” Journal of Biomedical Optics 15.3 (2010): 036002-6. © 2010 Society of Photo-Optical Instrumentation Engineersen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.approverSo, Peter T. C.
dc.contributor.mitauthorKim, Ki Hean
dc.contributor.mitauthorSo, Peter T. C.
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.orderedauthorsSun, Tzu-Lin; Liu, Yuan; Sung, Ming-Chin; Chen, Hsiao-Ching; Yang, Chun-Hui; Hovhannisyan, Vladimir; Lin, Wei-Chou; Jeng, Yung-Ming; Chen, Wei-Liang; Chiou, Ling-Ling; Huang, Guan-Tarn; Kim, Ki-Hean; So, Peter T. C.; Chen, Yang-Fang; Lee, Hsuan-Shu; Dong, Chen-Yuanen
dc.identifier.orcidhttps://orcid.org/0000-0003-4698-6488
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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