Prussian blue nanocubes peroxidase mimetic-based colorimetric assay for screening acetylcholinesterase activity and its inhibitor

被引:46
|
作者
Ni, Pengjuan [1 ,2 ]
Sun, Yujing [1 ]
Dai, Haichao [1 ,2 ]
Lu, Wangdong [1 ,2 ]
Jiang, Shu [1 ,2 ]
Wang, Yilin [1 ,2 ]
Li, Zhen [1 ,2 ]
Li, Zhuang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electronalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Acetylcholinesterase; Neostigmine bromide; Prussian blue nanocubes; Peroxidase mimetic; GOLD NANOPARTICLES; HYDROGEN-PEROXIDE; VISUAL DETECTION; QUANTUM DOTS; CATALYTIC PERFORMANCE; FLUOROMETRIC ASSAY; PHOTONIC CRYSTAL; GRAPHENE OXIDE; GLUCOSE; NANOSHEETS;
D O I
10.1016/j.snb.2016.09.048
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this paper, a novel, convenient and sensitive colorimetric assay for acetylcholinesterase (AChE) activity and its inhibitor screening is successfully proposed based on the peroxidase-like activity of Prussian blue nanocubes (PB NCs). PB NCs can catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) by H2O2 to develop a blue color and an absorption peak centered at 652 nm. AChE mediates the hydrolysis of acetylthiocholine (ATCh) to yield a reducing agent thiocholine (TCh) that cause the reduction of oxidized TMB and it can also chelate with Fe3+, both of which result in a blue color fading and a decrease of the absorbance. The generation of TCh is inhibited and the absorbance intensity is recovered after the introduction of AChE inhibitor. Consequently, the assay is also utilized in AChE inhibitor screening. The PB NCs-H2O2-TMB based platform is highly sensitive for AChE activity sensing with a low detection limit of 0.04 mU/mL. In addition, this assay has great potential in discriminatively determining AChE over other enzymes. The proposed method is fairly novel, simple and sensitive, which may pave the way for the detection of other hydrolytic enzyme activities with properly selected substrates. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1314 / 1320
页数:7
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