葡萄糖氧化酶
化学
生物传感器
单糖
催化作用
分子印迹聚合物
组合化学
固定化酶
纳米技术
有机化学
生物化学
材料科学
选择性
作者
Yujun Cheng,Tao Chen,Donglei Fu,Maosheng Liu,Zhongfa Cheng,Yanfei Hua,Jingquan Liu
出处
期刊:Talanta
[Elsevier]
日期:2022-05-01
卷期号:242: 123279-123279
被引量:8
标识
DOI:10.1016/j.talanta.2022.123279
摘要
It is generally accepted that glucose oxidase (GOx) shows unique specificity in β-d-glucose catalysis. However, it has been found that GOx can catalyze diverse monosaccharides. Therefore, the sensing accuracy for glucose biosensors using GOx as probes will be largely compromised by the presence of other monosaccharides. Herein, multifunctional bi-nanospheres (Fe3O4@Au NCs), which show both peroxidase-like and catalase-like catalytic activities in different working conditions, are successfully constructed and served as desirable platform with huge surface area for the immobilization of large amount of GOx probes. In acidic environment, hydroxyl radicals could be generated via the cascaded catalysis of β-d-glucose by Fe3O4@Au-GOx, and then employed to initiate the polymerization of boric acid derivative to prepare molecularly imprinted polymers (MIPs) on the surface of GOx using β-d-glucose as template. Then, the molecularly imprinted GOx are immobilized on the surface of highly oriented pyrolytic graphite (HOPG) electrode and an electrochemical biosensor (Fe3O4@Au-GOx-HOPG) for glucose sensing is successfully obtained. Interestingly, the as-prepared biosensors could selectively detect glucose in the range of 10.0 μM - 5.0 mM with a LOD = 5.0 μM with the help of MIPs, which is comparable or better than other glucose sensors reported recently.
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