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Tunable Triazole-Dansyl Fluorescent Probes for Glutathione Detection: Modulating Probe-Biomarker Interactions for Enhanced Sensitivity and Selectivity in Biological, Environmental, and Cellular Systems.

Created on 17 Aug 2026

Authors

Geethanjali Anand, Karthika Kannan, Jaseela Keedakkadan, Sushabhan Sadhukhan, Mintu Porel

Published in

ACS applied bio materials. Volume 9. Issue 16. Pages 7419-7427. Aug 17, 2026.

Abstract

A structurally tunable library of six triazole-dansyl fluorophores was investigated for substitution-dependent recognition of glutathione (GSH). All probes showed fluorescence quenching upon GSH addition, with the aliphatic-aliphatic derivative P4 exhibiting the highest sensitivity (LOD: 123 nM). High selectivity toward GSH was observed over competing amino acids, metal ions, and biomolecules, with minimal interference under competitive conditions. Mechanistic studies (UV-Vis, ESI-MS, 1H NMR, FTIR, PXRD, molecular docking, and DFT) revealed multivalent noncovalent interactions with a 2:1 binding stoichiometry, inducing perturbation of the intramolecular charge transfer (ICT) state. Time-resolved fluorescence confirmed a dynamic quenching pathway, while quantum yield measurements showed up to 49% quenching. pH- and temperature-dependent studies established optimal performance under physiological conditions. Practical applicability was demonstrated in human serum, cow urine, and goat blood with recoveries of 95-115% and negligible matrix effects. P4 did not exhibit any significant cytotoxicity in HeLa cells even at 100 μM. Fluorescence-based detection of GSH in HeLa cells and A549 cells confirmed the probe's sensing capability in mammalian cells, while cellular imaging established its suitability for bioimaging applications.

PMID:
42606046
Bibliographic data and abstract were imported from PubMed on 17 Aug 2026.

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