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dc.contributor.authorSo, Peter T. C.
dc.contributor.authorKim, Daekeun
dc.contributor.authorKim, Ki Hean
dc.contributor.authorDong, Chen-Yuan
dc.contributor.authorLin, Sung-Jan
dc.contributor.authorTsai, Tsung-Hua
dc.contributor.authorTan, Hsin-Yuan
dc.contributor.authorJee, Shiou-Hwa
dc.contributor.authorChen, Yang-Fang
dc.contributor.authorLin, Ming-Gu
dc.contributor.authorChou, Chen-Kuan
dc.contributor.authorChen, Wei-Liang
dc.date.accessioned2010-03-15T16:47:57Z
dc.date.available2010-03-15T16:47:57Z
dc.date.issued2009-10
dc.date.submitted2009-08
dc.identifier.govdoc1560-2281
dc.identifier.issn1083-3668
dc.identifier.urihttp://hdl.handle.net/1721.1/52580
dc.description.abstractBoth reflected confocal and multiphoton microscopy can have clinical diagnostic applications. The successful combination of both modalities in tissue imaging enables unique image contrast to be achieved, especially if a single laser excitation wavelength is used. We apply this approach for skin and corneal imaging using the 780-nm output of a femtosecond, titanium-sapphire laser. We find that the near-IR, reflected confocal (RC) signal is useful in characterizing refractive index varying boundaries in bovine cornea and porcine skin, while the multiphoton autofluorescence (MAF) and second-harmonic generation (SHG) intensities can be used to image cytoplasm and connective tissues (collagen), respectively. In addition, quantitative analysis shows that we are able to detect MAF from greater imaging depths than with the near-IR RC signal. Furthermore, by performing RC imaging at 488, 543, and 633 nm, we find that a longer wavelength leads to better image contrast for deeper imaging of the bovine cornea and porcine skin tissue. Finally, by varying power of the 780-nm source, we find that comparable RC image quality was achieved in the 2.7 to 10.7-mW range.en
dc.description.sponsorshipNational Research Program for Genomic Medicine of the National Science Council of Taiwan (NSC93-3112-B-002-033, NSC93-3112-B-002-034, and NSC-95-3112-B-002-019)en
dc.language.isoen_US
dc.publisherSociety of Photo-Optical Instrumentation Engineersen
dc.relation.isversionofhttp://dx.doi.org/10.1117/1.3247157en
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
dc.sourceSPIEen
dc.titleSingle-wavelength reflected confocal and multiphoton microscopy for tissue imagingen
dc.typeArticleen
dc.identifier.citationChen, Wei-Liang et al. “Single-wavelength reflected confocal and multiphoton microscopy for tissue imaging.” Journal of Biomedical Optics 14.5 (2009): 054026-8. © 2009 Society of Photo-Optical Instrumentation Engineersen
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.approverSo, Peter T. C.
dc.contributor.mitauthorSo, Peter T. C.
dc.contributor.mitauthorKim, Daekeun
dc.contributor.mitauthorKim, Ki Hean
dc.relation.journalJournal of Biomedical Opticsen
dc.eprint.versionFinal published versionen
dc.type.urihttp://purl.org/eprint/type/JournalArticleen
eprint.statushttp://purl.org/eprint/status/PeerRevieweden
dspace.orderedauthorsChen, Wei-Liang; Chou, Chen-Kuan; Lin, Ming-Gu; Chen, Yang-Fang; Jee, Shiou-Hwa; Tan, Hsin-Yuan; Tsai, Tsung-Hua; Kim, Ki-Hean; Kim, Daekeun; So, Peter T. C.; Lin, Sung-Jan; Dong, Chen-Yuanen
dc.identifier.orcidhttps://orcid.org/0000-0003-4698-6488
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen
mit.metadata.statusComplete


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