Nanomolar Detection of H2S in an Aqueous Medium: Application in Endogenous and Exogenous Imaging of HeLa Cells and Zebrafish
Author(s) -
Sanay Naha,
Natesan Thirumalaivasan,
Somenath Garai,
ShuPao Wu,
Sivan Velmathi
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c02963
Subject(s) - chemistry , hydrogen sulfide , quenching (fluorescence) , photochemistry , electrospray ionization , mass spectrometry , fluorescence , sulfur , organic chemistry , chromatography , physics , quantum mechanics
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.
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