过氧化氢
生物传感器
化学
基质(水族馆)
过氧化物酶
显色的
催化作用
核化学
组合化学
检出限
谷胱甘肽
三元运算
三元络合物
磁性纳米粒子
色谱法
抗氧化剂
荧光
纳米复合材料
磁选
纳米颗粒
无机化学
滴定法
信号(编程语言)
谷胱甘肽过氧化物酶
过氧化物
作者
Wei Yang,Chenyuan Weng,Xiaoyun Li,Hongliang He,Jianwen Fei,Wei Xu,Xiaoqiang Yan,Wanying Zhu,Hongsong Zhang,Xuemin Zhou
标识
DOI:10.1016/j.snb.2021.129844
摘要
Abstract At present, artificial mimic enzyme has become a powerful substitute for natural enzyme. In particular, the biosensors based on nano-enzymes have been the focus of current research. Herein, a novel magnetic ternary nanocomposite hemin-Fe3O4@polypyrrole (h-Fe3O4@ppy) was synthesized by chemical oxidation polymerization. The results showed that the h-Fe3O4@ppy had stronger peroxidase activity than Fe3O4 nanoparticles (Fe3O4 NPs) and h-ppy NPs, and was indicated by Michaelis-Menten constant (Km) and maximum initial velocity (Vmax). Therefore, we used h-Fe3O4@ppy catalyzing H2O2 to oxidize the chromogenic substrate TMB, and built Hydrogen peroxide (H2O2) and Glutathione (GSH) colorimetric biosensors with the help of signal intrinsic exponential amplification and easy operation. The controllable catalysis was realized by h-Fe3O4@ppy which was prone to separation. The method of removing h-Fe3O4@ppy by magnetic separation effectively eliminated the effect of residual catalysis when terminating the reaction. The sensor was then applied to the determination of GSH in biological samples from acute coronary syndrome patients. The linear ranges of H2O2 and GSH were 0.2–100 μM and 0.5–80 μM, respectively. The detection limits of H2O2 and GSH are 0.18 μM and 0.15 μM, respectively. This research not only proposes a new type of nanoenzyme, but also shows the multiple advantages of magnetic nano-enzymes for the construction of biosensors.
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