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Nanomolar Detection of H(2)S in an Aqueous Medium: Application in Endogenous and Exogenous Imaging of HeLa Cells and Zebrafish

[Image: see text] The homeostasis of short-lived reactive species such as hydrogen sulfide/hypochlorous acid (H(2)S/HOCl) in biological systems is essential for maintaining intercellular balance. An unchecked increase in biological H(2)S concentrations impedes homeostasis. In this report, we present...

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Detalles Bibliográficos
Autores principales: Naha, Sanay, Thirumalaivasan, Natesan, Garai, Somenath, Wu, Shu-Pao, Velmathi, Sivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424736/
https://www.ncbi.nlm.nih.gov/pubmed/32803086
http://dx.doi.org/10.1021/acsomega.0c02963
Descripción
Sumario:[Image: see text] The homeostasis of short-lived reactive species such as hydrogen sulfide/hypochlorous acid (H(2)S/HOCl) in biological systems is essential for maintaining intercellular balance. An unchecked increase in biological H(2)S concentrations impedes homeostasis. In this report, we present a molecular probe pyrene-based sulfonyl hydrazone derived from pyrene for the selective detection of H(2)S endogenously as well as exogenously through a “turn-off” response in water. The structure of the receptor is confirmed by Fourier-transform infrared spectroscopy, (1)H and (13)C nuclear magnetic resonance spectroscopy, electrospray ionization mass spectrometry, and single-crystal X-ray diffraction studies. The receptor shows excellent green emission in both the aqueous phase and solid state. Quenching of green emission of the receptor is observed only when H(2)S is present in water with a detection limit of 18 nM. Other competing anions and cations do not have any influence on the receptor’s optical properties. The efficiency of H(2)S detection is not negatively impacted by other reactive sulfur species too. The sensing mechanism of H(2)S follows a chemodosimetric reductive elimination of sulfur dioxide, which is supported by product isolation. The receptor is found to be biocompatible, as evident by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and its utility is extended to endogenous and exogenous fluorescence imaging of HeLa cells and zebrafish.