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Label-free multimodal microscopy using a single light source and detector for biological imaging

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dc.contributor.authorKang, Juehyung-
dc.contributor.authorKang, Ungyo-
dc.contributor.authorNam, Hyeong Soo-
dc.contributor.authorKim, Wooseop-
dc.contributor.authorKim, Hyun Jung-
dc.contributor.authorKim, Ryeong Hyeon-
dc.contributor.authorKim, Jin Won-
dc.contributor.authorYoo, Hongki-
dc.date.accessioned2021-08-30T02:59:48Z-
dc.date.available2021-08-30T02:59:48Z-
dc.date.created2021-06-18-
dc.date.issued2021-02-15-
dc.identifier.issn0146-9592-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/49581-
dc.description.abstractMultimodal nonlinear microscopy has been widely applied in biology and medicine due to its relatively deep penetration into tissue and its label-free manner. However, current multimodal systems require the use of multiple sources and detectors, leading to bulky, complex, and expensive systems. In this Letter, we present a novel method of using a single light source and detector for nonlinear multimodal imaging of biological samples. Using a photonic crystal fiber, a pulse picker, and multimode fibers, our developed system successfully acquired multimodal images of swine coronary arteries, including two-photon excitation fluorescence, second-harmonic generation, coherent anti-Stokes Raman scattering, and backreflection. The developed system could be a valuable tool for various biomedical applications. (C) 2021 Optical Society of America-
dc.languageEnglish-
dc.language.isoen-
dc.publisherOPTICAL SOC AMER-
dc.subjectIN-VIVO-
dc.subject2-PHOTON-
dc.subjectFLUORESCENCE-
dc.subjectHISTOLOGY-
dc.titleLabel-free multimodal microscopy using a single light source and detector for biological imaging-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jin Won-
dc.identifier.doi10.1364/OL.415938-
dc.identifier.scopusid2-s2.0-85101470855-
dc.identifier.wosid000618473600049-
dc.identifier.bibliographicCitationOPTICS LETTERS, v.46, no.4, pp.892 - 895-
dc.relation.isPartOfOPTICS LETTERS-
dc.citation.titleOPTICS LETTERS-
dc.citation.volume46-
dc.citation.number4-
dc.citation.startPage892-
dc.citation.endPage895-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOptics-
dc.relation.journalWebOfScienceCategoryOptics-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlus2-PHOTON-
dc.subject.keywordPlusFLUORESCENCE-
dc.subject.keywordPlusHISTOLOGY-
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