Iodide/metal-organic frameworks (MOF) -mediated signal amplification strategy for the colorimetric detection of H2O2, Cr2O72- and H2S

被引:19
|
作者
Chi, Kuan-Neng [1 ]
Guan, Yan [1 ]
Zhang, Xi [1 ]
Yang, Tong [1 ]
Meng, Shuang [1 ]
Hu, Rong [1 ]
Yang, Yun-Hui [1 ]
机构
[1] Yunnan Normal Univ, Coll Chem & Chem Engn, Kunming 650092, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorimetric assay; Iodide-catalyzed reaction; Signal amplification; Cu-MOFs; GOLD NANOPARTICLES; GLUCOSE; NANOSTRUCTURES; NANOMATERIALS; PERFORMANCE; TRICLOSAN; PLATFORM; SORPTION; PROBE; DNA;
D O I
10.1016/j.aca.2021.338378
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The analytical methods based on colorimetric detection of various analytes have attracted intensive interest. However, most of them display relatively low sensitivity. Herein, a novel colorimetric strategy based on iodide/metal-organic frameworks (MOF)-mediated amplification was developed for low-cost, naked-eye detection and quantification of H2O2,Cr2O72-, and H2S. Cu-MOFs could catalyze the oxidation of the colorless peroxidase substrate TMB to produce a blue product. The published researches mainly focused on the immobilization or integration of a macromolecule, such as natural enzymes, to enhance MOFs catalytic abilities. The use of small molecules to improve the catalytic performance of MOFs has rarely reported. Due to the negligible steric hindrance, iodide could easily be adsorbed in the framework pore of MOFs to conduct the synergic catalytic effect, and shows a high catalytic effect. As a result, the catalytic activity of Cu-MOFs was dramatically enhanced, and thus, the nanocatalyst could act as an amplifier system for target detection. The detection limits obtained by the amplified method are 25, 30, and 0.2 nM, respectively, which are about 200-fold lower than that of the unamplified colorimetric assays. The colorimetric strategy developed herein provides a novel system for the detection of low concentrations of analytes in complex biological samples. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:9
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