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dc.contributor.authorYan, Jie
dc.contributor.authorKang, Yuzhan
dc.contributor.authorXu, Shuoyu
dc.contributor.authorOng, Lee Ling
dc.contributor.authorZhuo, Shuangmu
dc.contributor.authorBunte, Ralph M.
dc.contributor.authorChen, Nanguang
dc.contributor.authorWanless, Ian R.
dc.contributor.authorYu, Hanry
dc.contributor.authorAsada, Harry
dc.contributor.authorSo, Peter T. C.
dc.date.accessioned2015-01-12T17:12:03Z
dc.date.available2015-01-12T17:12:03Z
dc.date.issued2014-11
dc.date.submitted2014-07
dc.identifier.issn1083-3668
dc.identifier.issn1560-2281
dc.identifier.urihttp://hdl.handle.net/1721.1/92790
dc.description.abstractMicrocirculation lesion is a common symptom of chronic liver diseases in the form of vasculature deformation and circulation alteration. In acute to chronic liver diseases such as biliary atresia, microcirculation lesion can have an early onset. Detection of microcirculation lesion is meaningful for studying the progression of liver disease. We have combined wide-field fluorescence microscopy and a laser speckle contrast technique to characterize hepatic microcirculation in vivo without labeling in a bile-duct ligation rat fibrosis model of biliary atresia. Through quantitative image analysis of four microcirculation parameters, we observed significant microcirculation lesion in the early to middle stages of fibrosis. This bimodal imaging method is useful to assess hepatic microcirculation lesion for the study of liver diseases.en_US
dc.description.sponsorshipSingapore-MIT Alliance for Research and Technologyen_US
dc.description.sponsorshipSingapore-MIT Alliance Computational and Systems Biology Flagship Project (C-382-641-001-091)en_US
dc.description.sponsorshipInstitute of Bioengineering and Nanotechnology (Singapore)en_US
dc.description.sponsorshipSingapore. Biomedical Research Councilen_US
dc.description.sponsorshipSingapore. Agency for Science, Technology and Researchen_US
dc.description.sponsorshipJanssen Pharmaceutical Ltd. (Grant R-185-000-182-592)en_US
dc.description.sponsorshipJanssen Pharmaceutical Ltd. (Grant R-185-000-228-592)en_US
dc.description.sponsorshipMechanobiology Institute, Singapore (Grant R-714-001-003-271)en_US
dc.language.isoen_US
dc.publisherSPIEen_US
dc.relation.isversionofhttp://dx.doi.org/10.1117/1.jbo.19.11.116006en_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.titleIn Vivo Label-Free Quantification of Liver Microcirculation Using Dual-Modality Microscopyen_US
dc.typeArticleen_US
dc.identifier.citationYan, Jie, Yuzhan Kang, Shuoyu Xu, Lee-Ling S. Ong, Shuangmu Zhuo, Ralph M Bunte, Nanguang Chen, et al. “ In Vivo Label-Free Quantification of Liver Microcirculation Using Dual-Modality Microscopy .” Journal of Biomedical Optics 19, no. 11 (November 1, 2014): 116006. © 2014 Society of Photo-Optical Instrumentation Engineersen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorAsada, Harryen_US
dc.contributor.mitauthorSo, Peter T. C.en_US
dc.contributor.mitauthorYu, Hanryen_US
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.orderedauthorsYan, Jie; Kang, Yuzhan; Xu, Shuoyu; Ong, Lee-Ling S.; Zhuo, Shuangmu; Bunte, Ralph M; Chen, Nanguang; Asada, H. Harry; So, Peter T. C.; Wanless, Ian R.; Yu, Hanryen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0339-3685
dc.identifier.orcidhttps://orcid.org/0000-0003-3155-6223
dc.identifier.orcidhttps://orcid.org/0000-0003-4698-6488
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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