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dc.contributor.authorVelusamy, Nithyaen_US
dc.contributor.authorThirumalaivasan, Natesanen_US
dc.contributor.authorBobba, Kondapa Naiduen_US
dc.contributor.authorWu, Shu-Paoen_US
dc.contributor.authorBhuniya, Sankarprasaden_US
dc.date.accessioned2018-08-21T05:53:15Z-
dc.date.available2018-08-21T05:53:15Z-
dc.date.issued2018-02-07en_US
dc.identifier.issn1144-0546en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7nj04119een_US
dc.identifier.urihttp://hdl.handle.net/11536/144448-
dc.description.abstractWe developed a naphthalimide-based, lysosome-targeting, and self-immolative fluorescent probe for H2S detection. Probe LS-1 comprises a 2-formylbenzoate derivative of the 1,8-naphthalimide fluorophore. H2S forms a thiohemiacetal intermediate by reacting with the formyl group of the 2-formylbenzoate derivative, which subsequently undergoes intramolecular cyclization with the ester moiety to generate a free naphthalimide fluorophore (FL-1). The UV-vis absorbance (lambda(abs)) value of probe LS-1 at 450 nm increased in the presence of H2S. Similarly, with increasing H2S concentrations, the emission band (lambda(em)) centered at 560 nm increased gradually. The probe was found to be highly sensitive and chemoselective towards H2S compared with other biological analytes. Probe LS-1 was nontoxic and very stable across the physiological pH range. The probe LS-1 enables the detection of intracellular endogenous H2S formation in HT29 cells in lysosomes.en_US
dc.language.isoen_USen_US
dc.titleA hydrogen sulfide triggered self-immolative fluorescent probe for lysosome labeling in live cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7nj04119een_US
dc.identifier.journalNEW JOURNAL OF CHEMISTRYen_US
dc.citation.volume42en_US
dc.citation.spage1590en_US
dc.citation.epage1594en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000423702900005en_US
Appears in Collections:Articles