Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99645
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dc.contributorDepartment of Electronic and Information Engineering-
dc.creatorLuo, Yen_US
dc.creatorTseng, MLen_US
dc.creatorVyas, Sen_US
dc.creatorHsieh, TYen_US
dc.creatorWu, JCen_US
dc.creatorChen, SYen_US
dc.creatorPeng, HFen_US
dc.creatorSu, VCen_US
dc.creatorHuang, TTen_US
dc.creatorKuo, HYen_US
dc.creatorChu, CHen_US
dc.creatorChen, MKen_US
dc.creatorChen, JWen_US
dc.creatorChen, YCen_US
dc.creatorHuang, KYen_US
dc.creatorKuan, CHen_US
dc.creatorShi, Xen_US
dc.creatorMisawa, Hen_US
dc.creatorTsai, DPen_US
dc.date.accessioned2023-07-18T03:12:30Z-
dc.date.available2023-07-18T03:12:30Z-
dc.identifier.urihttp://hdl.handle.net/10397/99645-
dc.language.isoenen_US
dc.publisherDe Gruyter Open Ltden_US
dc.rights© 2022 Yuan Luo et al., published by De Gruyter.en_US
dc.rightsThis work is licensed under the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Luo, Yuan, Tseng, Ming Lun, Vyas, Sunil, Hsieh, Ting-Yu, Wu, Jui-Ching, Chen, Shang-Yang, Peng, Hsiao-Fang, Su, Vin-Cent, Huang, Tzu-Ting, Kuo, Hsin Yu, Chu, Cheng Hung, Chen, Mu Ku, Chen, Jia-Wern, Chen, Yu-Chun, Huang, Kuang-Yuh, Kuan, Chieh-Hsiung, Shi, Xu, Misawa, Hiroaki and Tsai, Din Ping. "Meta-lens light-sheet fluorescence microscopy for in vivo imaging" Nanophotonics, vol. 11, no. 9, 2022, pp. 1949-1959 is available at https://doi.org/10.1515/nanoph-2021-0748.en_US
dc.subjectFluorescence microscopyen_US
dc.subjectLight sheet microscopyen_US
dc.subjectMetasurfaceen_US
dc.titleMeta-lens light-sheet fluorescence microscopy for in vivo imagingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1949en_US
dc.identifier.epage1959en_US
dc.identifier.volume11en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1515/nanoph-2021-0748en_US
dcterms.abstractLight-sheet fluorescent microscopy has become the leading technique for in vivo imaging in the fields of disease, medicine, and cell biology research. However, designing proper illumination for high image resolution and optical sectioning is challenging. Another issue is geometric constraints arising from the multiple bulky components for illumination and detection. Here, we demonstrate that those issues can be well addressed by integrating nanophotonic meta-lens as the illumination component for LSFM. The meta-lens is composed of 800-nm-thick GaN nanostructures and is designed for a light-sheet well-adapted to biological specimens such as the nematode Caenorhabditis elegans (C. elegans). With the meta-lens, the complexity of the LSFM system is significantly reduced, and it is capable of performing multicolor fluorescent imaging of live C. elegans with cellular resolution. Considering the miniature size and plane geometry of the meta-lens, our system enables a new design for LSFM to acquire in vivo images of biological specimens with high resolution.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNanophotonics, Apr. 2022, v. 11, no. 9, p. 1949-1959en_US
dcterms.isPartOfNanophotonicsen_US
dcterms.issued2022-04-
dc.identifier.scopus2-s2.0-85126028360-
dc.identifier.eissn2192-8614en_US
dc.description.validate202307 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextDepartment of Electrical Engineering, City University of Hong Kong; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology; Ministry of Science and Technology, Taiwan; National Taiwan University; Guangdong Science and Technology Department; Science, Technology and Innovation Commission of Shenzhen Municipalityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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