A near-infrared fluorescence probe for the detection of bisulfite in vivo and food samples

化学 荧光 滴定法 电负性 光化学 部分 有机化学 量子力学 物理
作者
Zhuye Shang,Jianhua Liu,Zhizhi Hu,Qingtao Meng,Yue Wang,Run Zhang,Zhiqiang Zhang
出处
期刊:Dyes and Pigments [Elsevier BV]
卷期号:200: 110119-110119 被引量:14
标识
DOI:10.1016/j.dyepig.2022.110119
摘要

The evaluation of the HSO3− levels in the biological systems and food samples is of great significance in the understanding its physiological/pathological roles and realizing food security supervision. In this work, a near-infrared (NIR) emitted fluorescence probe (QNP) has been successfully developed to detect HSO3− in live animals and food samples. QNP was designed with a large π-conjugation structure by conjugating of quinolinium with 3H-naphtho[2,1-b]pyran moiety through a reactive C=C double bond. Spectroscopic titration, high resolution mass spectrometry (HR MS), 1H NMR titration and theoretical computation indicates that HSO3− attacks to the C=C double bond through an established 1,4-nucleophilic addition reaction leads to the interruption of the π-conjugation system of QNP, resulting in dramatic decline of the UV–vis absorption and fluorescence spectra. QNP was featured with near infrared emission (centered at 690 nm), high water-solubility (98% water), large Stokes shift (218 nm), perfect selectivity, fast response time (within 50 s) to HSO3−, reliability in broad pH range (6.5–11.5) and low cytotoxicity. The application of QNP in biological systems has been demonstrated by the monitoring of exogenous HSO3− in live adult zebrafish and nude mouse. Furthermore, the evaluation of HSO3− level in several food samples including sugar, white wine, canned fruits and jasmine tea drinks were also determined by fluorescence colorimetric method using QNP.
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