A novel biosensor based on multienzyme microcapsules constructed from covalent-organic framework

生物传感器 葡萄糖氧化酶 化学 电极 固定化酶 辣根过氧化物酶 共价键 电化学 纳米技术 化学工程 组合化学 材料科学 有机化学 工程类 物理化学
作者
Huihui Liang,Linyu Wang,Yuxi Yang,Yonghai Song,Li Wang
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:193: 113553-113553 被引量:54
标识
DOI:10.1016/j.bios.2021.113553
摘要

Electrochemical biosensors based on enzymes modified electrode are attracting special attention due to their broad applications. However, the immobilization of enzymes on electrode is always an important challenge because it's not conducive to conformational expansion of enzymes and affects the bioactivity of enzymes accordingly. Although the imobilization of enzymes in micropores of crystalline covalent-organic framework (COF) and metal-organic framework (MOF) to construct electrochemical biosensors based on pore embedding can achive good reuslts, their micropores can still not guarantee that the enzyme's conformation is well extended. Herein, a multienzyme microcapsules ([email protected]) containing glucose oxidase, horseradish peroxidase and acetylcholinesterase with a 600 nm-sized cavity and a shell of COF was used to construct electrochemical biosensors. The 600 nm-sized cavity ensures free conformation expansion of encapsulated enzymes and the shell of COF with good chemical stablity protects encapsulated enzymes against external harsh environments. And the specific catalytic substrates of the enzymes can infiltrated into the microcapsule through the pores of COF shell. So, the biosensor based on [email protected] microcapsules demonstrated preeminent performances as compared with those of enzymes assembled on electrode. The detection limits were 0.85 μM, 2.81 nM, 3.0×10−13 g/L, and the detection range were 2.83 μM–8.0 mM, 9.53 nM-7.0 μM, 10−12 g/L-10−8 g/L for glucose, H2O2 and malathion detection. This work shows that it is feasible to fabricate electrochemical sensors using [email protected] microcapsules.
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