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一种新型基于 4-氨基-7-硝基-2,1,3-苯并恶二唑(ANBD)的荧光探针,用于 Hg 的检测。

A new 4-Amino-7-Nitro-2,1,3-Benzoxadiazole (ANBD)-Based Fluorescent Probe for the Detection of Hg.

机构信息

Shijiazhuang Center for Disease Control and Prevention, Shijiazhuang, 050011, China.

College of Chemistry and Material Science, Hebei Normal University, Shijiazhuang, 050024, China.

出版信息

J Fluoresc. 2017 Sep;27(5):1739-1745. doi: 10.1007/s10895-017-2112-4. Epub 2017 May 13.

DOI:10.1007/s10895-017-2112-4
PMID:28501902
Abstract

Based on the photoinduced electron transfer (PET) principle, 4-amino-7-nitro-2,1,3-benzoxadiazole (ANBD) has been used as a fluorophore to develop a new fluorescent probe, 4-(2-N,N-dimethylthioacetamide)amino-7-nitro-2,1,3-benzoxadiazole (2), for the detection of Hg. Upon the addition of Hg, a 46-fold fluorescence enhancement occurs. Moreover the probe 2 exhibits a high selectivity and sensitivity to Hg, even in the presence of other common metal ions. Under optimal reaction conditions, a good linearity can be obtained in the range of 0.5-2.5 μM, and the detection limit is 0.05 μM. In addition, the desulfurization reaction mechanism is proposed based on electrospray ionization mass spectrum. The present study is not only a supplement to the detection method of Hg, but also a merit to the development of ANBD-based fluorescent probes.

摘要

基于光诱导电子转移(PET)原理,4-氨基-7-硝基-2,1,3-苯并恶二唑(ANBD)被用作荧光团,开发了一种新的荧光探针 4-(2-N,N-二甲基硫代乙酰胺)氨基-7-硝基-2,1,3-苯并恶二唑(2),用于检测 Hg。加入 Hg 后,荧光增强了 46 倍。此外,探针 2 对 Hg 具有高选择性和灵敏度,即使存在其他常见金属离子也是如此。在最佳反应条件下,在 0.5-2.5 μM 范围内可以得到良好的线性关系,检测限为 0.05 μM。此外,还基于电喷雾电离质谱提出了脱硫反应机理。本研究不仅是 Hg 检测方法的补充,也是基于 ANBD 的荧光探针发展的一个优点。

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本文引用的文献

1
Organic Material Based Fluorescent Sensor for Hg: a Brief Review on Recent Development.基于有机材料的汞荧光传感器:最新进展简述。
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Visible light excitable Zn2+ fluorescent sensor derived from an intramolecular charge transfer fluorophore and its in vitro and in vivo application.基于分子内电荷转移荧光团的可见光可激发锌离子荧光传感器及其体外和体内应用
J Am Chem Soc. 2009 Feb 4;131(4):1460-8. doi: 10.1021/ja806489y.
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10
Inhibition of the human thioredoxin system. A molecular mechanism of mercury toxicity.人类硫氧还蛋白系统的抑制:汞毒性的一种分子机制
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