Target-triggered inhibiting oxidase-mimicking activity of platinum nanoparticles for ultrasensitive colorimetric detection of silver ion

被引:37
作者
Deng, Haohua [1 ]
He, Shaobin [1 ]
Lin, Xiuling [1 ]
Yang, Lu [1 ]
Lin, Zhen [1 ]
Chen, Ruiting [1 ]
Peng, Huaping [1 ]
Chen, Wei [1 ]
机构
[1] Fujian Med Univ, Dept Pharmaceut Anal, Higher Educ Key Lab Nano Biomed Technol Fujian Pr, Fuzhou 350004, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorimetric detection; Oxidase-like activity; Platinum nanoparticle; Tetramethylbenzidine; Silver ion; PEROXIDASE MIMETICS; HEAVY-METALS; GOLD; FLUORESCENCE; CARBON; H2O2; AG; NANOSENSOR; PALLADIUM; PROBE;
D O I
10.1016/j.cclet.2019.05.032
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of efficient methods for the detection of hazardous and toxic elements is extremely important for environmental security and public health. In this work, we developed a facile colorimetric assaying system for Ag+ detection in aqueous solution. Chitosan-stabilized platinum nanoparticles (Ch-PtNPs) were synthesized and severed as an artificial oxidase to catalyze the oxidation of the substrate 3,3',5,5'-tetramethylbenzidine (TMB) and generate color signal. In the presence of Ag+, due to the strong metallophilic interactions between Ag+ and Pt2+ on the surface of Ch-PtNPs, Ag+ can weaken the affinity to the substrates and inactivate the catalytic activity of Ch-PtNPs, leading to decreased absorbance signal to varying degrees depending on Ag+ amount. Combing the specific binding between Ch-PtNPs and Ag+ with signal amplification procedure based on the Ch-PtNPs-catalyzed TMB oxidation, a sensitive, selective, simple, cost-effective, and rapid detection method for Ag+ can be realized. Ag+ ions in tap and lake waters have been successfully detected. We ensured that the proposed method can be a potential alternative for Ag+ determination in environmental samples. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1659 / 1662
页数:4
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