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dc.contributor.authorLiu, Shi-Rongen_US
dc.contributor.authorVedamalai, Manien_US
dc.contributor.authorWu, Shu-Paoen_US
dc.date.accessioned2014-12-08T15:32:56Z-
dc.date.available2014-12-08T15:32:56Z-
dc.date.issued2013-10-24en_US
dc.identifier.issn0003-2670en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.aca.2013.09.018en_US
dc.identifier.urihttp://hdl.handle.net/11536/22969-
dc.description.abstractA boron dipyrromethene (BODIPY)-based fluorometric probe, HCS, has been successfully developed for the highly sensitive and selective detection of hypochlorous acid (HOCl). The probe is based on the specific HOCl-promoted oxidation of methyl phenyl sulfide. The reaction is accompanied by a 160-fold increase in the fluorescent quantum yield (from 0.003 to 0.480). The fluorescent turn-on mechanism is accomplished by suppression of photoinduced electron transfer (PET) from the methyl phenyl sulfide group to BODIPY. The fluorescence intensity of the reaction between HOCl and HCS shows a good linearity in the HOCl concentration range 1-10 mu M. The detection limit is 23.7 nM (S/N = 3). In addition, confocal fluorescence microscopy imaging using RAW264.7 macrophages demonstrates that the HCS probe could be an efficient fluorescent detector for HOCl in living cells. (C) 2013 Published by Elsevier B.V.en_US
dc.language.isoen_USen_US
dc.subjectHypochlorous aciden_US
dc.subjectFluorescent probeen_US
dc.subjectBoron dipyrrometheneen_US
dc.subjectBioimagingen_US
dc.titleHypochlorous acid turn-on boron dipyrromethene probe based on oxidation of methyl phenyl sulfideen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.aca.2013.09.018en_US
dc.identifier.journalANALYTICA CHIMICA ACTAen_US
dc.citation.volume800en_US
dc.citation.issueen_US
dc.citation.spage71en_US
dc.citation.epage76en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000325646100010-
dc.citation.woscount7-
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