An aggregation-induced emission (AIE)-active fluorescent chemodosimeter for selective sensing of hypochlorite in water and solid state: Endogenous detection of hypochlorite in live cells

次氯酸盐 荧光 四苯乙烯 化学 检出限 光化学 选择性 聚集诱导发射 分子 分析物 次氯酸 内生 活性氧 无机化学 有机化学 色谱法 生物化学 物理 催化作用 量子力学
作者
Sandip Kumar Samanta,Kalipada Maiti,Saikat Kumar Manna,Syed Samim Ali,Uday Narayan Guria,Aritri Ghosh,Pallab Datta,Ajit Kumar Mahapatra
出处
期刊:Dyes and Pigments [Elsevier]
卷期号:196: 109758-109758 被引量:18
标识
DOI:10.1016/j.dyepig.2021.109758
摘要

Hypochlorite (ClO−) being an important reactive oxygen species plays a crucial role in the oxidative damage to tissue and other various diseases. Highly selective, sensitive, and quick detection of aberrant ClO− is vital for the protection of living organisms and the environment. Accordingly, fluorescent molecules are most effective sensor system for ClO−. Herein, we have synthesized and characterized a water soluble AIE-active tetraphenylethylene (TPE)-based fluorescent molecule TPE−Py+ (TPP) for rapid (10 s) and selective detection of ClO− based on ClO− induced oxidation of N-alkylpyridinium to N-methyl-2-pyridone. ClO− mediated aggregation-induced emission (AIE) enhancement corresponds to turn-on response. Scanning electron microscopic (SEM) study supports AIE behavior of the probe upon treatment with ClO−. The detection limit of TPP for ClO− was found to be 8.89 nM and exhibited high selectivity among other possibly interfering analytes (ROS, RNS, other ions). TPP-based handy test kits were developed for the solid-state detection of ClO− in environmental samples. Furthermore, our probe was effective in detecting ClO− in real water samples, fetal bovine serum and able to detect endogenous ClO− in live cell.
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