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dc.contributor.authorChou, Cho-Yenen_US
dc.contributor.authorLiu, Shi-Rongen_US
dc.contributor.authorWu, Shu-Paoen_US
dc.date.accessioned2014-12-08T15:30:44Z-
dc.date.available2014-12-08T15:30:44Z-
dc.date.issued2013en_US
dc.identifier.issn0003-2654en_US
dc.identifier.urihttp://hdl.handle.net/11536/21960-
dc.identifier.urihttp://dx.doi.org/10.1039/c3an00286aen_US
dc.description.abstractIn this study, a boron-dipyrromethene (BODIPY)-based fluorescent chemosensor CBS was developed for metal ion sensing. It was found that CBS containing an NSe2 moiety exhibited high selectivity for Cu2+ detection while CBS in the presence of Cu2+ displayed significant fluorescence enhancement. However, the metal ions Ag+, Ca2+, Co2+, Cr3+, Fe2+, Fe3+, Hg2+, K+, Mg2+, Mn2+, Ni2+, Pb2+, and Zn2+ produced only minor changes in the fluorescence values of the system. The binding constant (K-a) of Cu2+ binding to CBS was found to be 7.28 x 10(3) M-1. The binding ratio of CBS-Cu2+ complexes was determined from the Job plot to be 1 : 1. The maximum fluorescence enhancement caused by Cu2+ binding to CBS was observed over the pH range 5.0-9.0. Additionally, the methyl thiazolyl tetrazolium (MTT) assay demonstrated the CBS to have low cytotoxicity. Confocal fluorescence microscopy imaging using RAW264.7 cells showed that CBS could be used as an effective fluorescent probe for detecting Cu2+ in living cells.en_US
dc.language.isoen_USen_US
dc.titleA highly selective turn-on fluorescent sensor for Cu(II) based on an NSe2 chelating moiety and its application in living cell imagingen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3an00286aen_US
dc.identifier.journalANALYSTen_US
dc.citation.volume138en_US
dc.citation.issue11en_US
dc.citation.spage3264en_US
dc.citation.epage3270en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000318513500027-
dc.citation.woscount17-
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