Abstract

In this study, we have developed an imidazole centered fluorescent probe 3-(2-(2-(5-bromo-2-hydroxyphenyl)-4,5-diphenyl-1H-imidazol-1-yl)thiazol-4-yl)-6-chloro-2H-chromen-2-one (SICT), achieving exceptional selectivity for Cu2+ ion detection. These probes exhibit rapid responsiveness (109 nM detection limit) and strong binding constants (0.214 × 105 M−1). Employing an aqueous ethanol system, we assessed their sensing capabilities through both in vitro and in vivo studies, using zebrafish as our model organism. Notably, the SICT probe displays a high quantum yield of 0.62 and follows a 1:1 binding mechanism with Cu2+ ions, validated by Job's plot and ESI-Mass spectrum analyses. Furthermore, our probe demonstrates minimal cytotoxicity in both in vitro (MDA-MB-231 cells) experiments. These promising results motivate us to apply the SICT probe for intracellular Cu2+ ion tracking in zebrafish embryos, showcasing its potential in diverse fields like biomedicine and environmental monitoring.

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