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通过将葡萄糖氧化酶固定在自组装单分子层表面的多层膜中来制备电流型葡萄糖酶电极。

Amperometric glucose enzyme electrode by immobilizing glucose oxidase in multilayers on self-assembled monolayers surface.

作者信息

Hou S F, Yang K S, Fang H Q, Chen H Y

机构信息

Department of Chemistry, the State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, PR China.

出版信息

Talanta. 1998 Nov;47(3):561-7. doi: 10.1016/s0039-9140(98)00081-2.

DOI:10.1016/s0039-9140(98)00081-2
PMID:18967358
Abstract

A novel and robust amperometric enzyme electrode for the determination of glucose was constructed by immobilizing glucose oxidase (GOD) and Os(bpy)(2)Cl-poly(4-vinyl)pyridine (Os-PVP) complex multilayers on thiol self-assembled monolayers surface. The apparent Michaelis-Menton constant K(m)' increased with increasing the number of Os-PVP/GOD multilayers. The concentration range of linear response and detection limit were 0.1-10 and 0.05 mM, the interference of ascorbic acid and uric acid were eliminated by the presence of SAMs and the enzyme electrodes were stable over 3 weeks. The preparation technique may be useful for controlling the performance of multilayer enzyme electrodes by changing the enzyme content.

摘要

通过将葡萄糖氧化酶(GOD)和Os(bpy)(2)Cl-聚(4-乙烯基)吡啶(Os-PVP)复合物多层膜固定在硫醇自组装单分子层表面,构建了一种用于测定葡萄糖的新型且稳健的安培型酶电极。表观米氏常数K(m)' 随着Os-PVP/GOD多层膜层数的增加而增大。线性响应的浓度范围和检测限分别为0.1 - 10 mM和0.05 mM,硫醇自组装单分子层的存在消除了抗坏血酸和尿酸的干扰,并且酶电极在3周内保持稳定。该制备技术可能有助于通过改变酶含量来控制多层酶电极的性能。

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