A chromogenic and fluorogenic rhodol-based chemosensor for hydrazine detection and its application in live cell bioimaging.

Spectrochim Acta A Mol Biomol Spectrosc

Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand; Center for Excellence in Protein and Enzyme Technology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand. Electronic address:

Published: April 2018

AI Article Synopsis

  • A new fluorescent probe called rhodol levulinate (RL) has been created for detecting hydrazine, showing high selectivity and sensitivity compared to other substances.
  • The color of the RL solution changes from colorless to pink when hydrazine is present, and it emits strong fluorescence under specific light.
  • The probe can detect hydrazine at very low levels (26 nM), which is below the safety limit set by the EPA, and it can also be used to visualize hydrazine in live cells using advanced imaging techniques.

Article Abstract

A rhodol-based fluorescent probe has been developed as a selective hydrazine chemosensor using levulinate as a recognition site. The rhodol levulinate probe (RL) demonstrated high selectivity and sensitivity toward hydrazine among other molecules. The chromogenic response of RL solution to hydrazine from colorless to pink could be readily observed by the naked eye, while strong fluorescence emission could be monitored upon excitation at 525 nm. The detection process occurred via a ring-opening process of the spirolactone initiated by hydrazinolysis, triggering the fluorescence emission with a 53-fold enhancement. The probe rapidly reacted with hydrazine in aqueous medium with the detection limit of 26 nM (0.83 ppb), lower than the threshold limit value (TLV) of 10 ppb suggested by the U.S. Environmental Protection Agency. Furthermore, RL-impregnated paper strips could detect hydrazine vapor. For biological applicability of RL, its membrane-permeable property led to bioimaging of hydrazine in live HepG2 cells by confocal fluorescence microscopy.

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Source
http://dx.doi.org/10.1016/j.saa.2018.01.033DOI Listing

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