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dc.contributor.authorOkuno, Masanarien_US
dc.contributor.authorHamaguchi, Hiro-oen_US
dc.date.accessioned2014-12-08T15:38:17Z-
dc.date.available2014-12-08T15:38:17Z-
dc.date.issued2010-12-15en_US
dc.identifier.issn0146-9592en_US
dc.identifier.urihttp://dx.doi.org/10.1364/OL.35.004096en_US
dc.identifier.urihttp://hdl.handle.net/11536/26225-
dc.description.abstractWe have developed a multifocus confocal Raman microspectroscopic system for the fast multimode vibrational imaging of living cells. It consists of an inverted microscope equipped with a microlens array, a pinhole array, a fiber bundle, and a multichannel Raman spectrometer. Forty-eight Raman spectra from 48 foci under the microscope are simultaneously obtained by using multifocus excitation and image-compression techniques. The multifocus confocal configuration suppresses the background generated from the cover glass and the cell culturing medium so that high-contrast images are obtainable with a short accumulation time. The system enables us to obtain multimode (10 different vibrational modes) vibrational images of living cells in tens of seconds with only 1 mW laser power at one focal point. This image acquisition time is more than 10 times faster than that in conventional single-focus Raman microspectroscopy. (C) 2010 Optical Society of Americaen_US
dc.language.isoen_USen_US
dc.titleMultifocus confocal Raman microspectroscopy for fast multimode vibrational imaging of living cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1364/OL.35.004096en_US
dc.identifier.journalOPTICS LETTERSen_US
dc.citation.volume35en_US
dc.citation.issue24en_US
dc.citation.spage4096en_US
dc.citation.epage4098en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000285387300004-
dc.citation.woscount17-
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