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dc.contributor.authorMiyazaki, Junen_US
dc.contributor.authorTsurui, Hiromichien_US
dc.contributor.authorKawasumi, Koshien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2019-04-03T06:41:30Z-
dc.date.available2019-04-03T06:41:30Z-
dc.date.issued2015-02-09en_US
dc.identifier.issn1094-4087en_US
dc.identifier.urihttp://dx.doi.org/10.1364/OE.23.003647en_US
dc.identifier.urihttp://hdl.handle.net/11536/124331-
dc.description.abstractMulti-wavelength microscopic imaging is essential to visualize a variety of nanoscale cellular components with high specificity and high spatial resolution. However, previous techniques are based on fluorescence, and thus cannot visualize nonfluorescent species, which are much less suffered from photodamage or photobleaching and hence are intrinsically useful in wider range of optical microscopy. Here, we show that simultaneous multi-wavelength imaging of nonfluorescent species can be achieved with the use of a photothermal microscope. Dual-wavelength subdiffraction imaging of biological tissues stained with hematoxylin and eosin is demonstrated. Three-dimensional label-free imaging of mouse melanoma tissue section is also presented to demonstrate the effectiveness of the enhanced spatial resolution. Our technique can be implemented using cost-effective and compact laser diodes and is applicable for various types of both fluorescent and nonfluorescent tissues. (C) 2015 Optical Society of Americaen_US
dc.language.isoen_USen_US
dc.titleSimultaneous dual-wavelength imaging of nonfluorescent tissues with 3D subdiffraction photothermal microscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1364/OE.23.003647en_US
dc.identifier.journalOPTICS EXPRESSen_US
dc.citation.volume23en_US
dc.citation.issue3en_US
dc.citation.spage3647en_US
dc.citation.epage3656en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000349688800174en_US
dc.citation.woscount15en_US
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