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首页> 外文期刊>Analytica chimica acta >Hydrogen peroxide sensor based on horseradish peroxidase-labeled Au colloids immobilized on gold electrode surface by cysteamine monolayer
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Hydrogen peroxide sensor based on horseradish peroxidase-labeled Au colloids immobilized on gold electrode surface by cysteamine monolayer

机译:基于辣根过氧化物酶标记的金胶体通过半胱胺单层固定在金电极表面的过氧化氢传感器

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摘要

A novel strategy to construct a sensitive amperometric sensor of H2O2 was described. Horseradish peroxidase (HRP) was successfully immobilized on nanometer-sized Au colloids, which were supported by thiol-tailed groups of cysteamine monolayer. The thiol-tailed groups were formed through the covalent binding of glutaraldehyde on a cysteamine-modified gold electrode. With the aid of the catechol mediator in the solution, HRP-labeled Au colloids displayed excellent electrocatalytical response to the reduction of H2O2, which increased with decreasing size of Au colloids. The sensors responded to H2O2 in the concentration range of 0.39 mu M-0.33 mM, and reached 95% of the steady-state current in less than 5 s with the detection limit of 0.15 mu M. The response showed a Michaelis-Menten behavior at larger H2O2 concentrations. The K-M(app) values for the sensors based on different sized HRP-labeled Au colloids (colloid A-D) were found to be 0.11, 0.094, 0.054 and 0.064 mM, respectively. The low K-M(app) values demonstrated that HRP immobilized on An colloids exhibited a high affinity to H2O2 with no loss of enzymatic activity. (C) 1999 Elsevier Science B.V. All rights reserved. [References: 42]
机译:描述了一种构造H2O2灵敏安培传感器的新策略。辣根过氧化物酶(HRP)已成功固定在纳米级Au胶体上,该胶体由巯基尾巴的半胱胺单分子层支撑。通过戊二醛在半胱胺修饰的金电极上的共价结合形成硫醇尾基。在溶液中邻苯二酚介体的帮助下,HRP标记的Au胶体对H2O2的还原表现出出色的电催化响应,并随着Au胶体尺寸的减小而增加。传感器在0.39μM-0.33mM的浓度范围内对H2O2作出响应,并在不到5 s的时间内达到稳态电流的95%,检测极限为0.15μM。该响应显示出Michaelis-Menten行为在较高的H2O2浓度。发现基于不同大小的HRP标记的Au胶体(胶体A-D)的传感器的K-M(app)值分别为0.11、0.094、0.054和0.064 mM。低的K-M(app)值表明固定在An胶体上的HRP对H2O2表现出高亲和力,而没有酶活性的损失。 (C)1999 Elsevier Science B.V.保留所有权利。 [参考:42]

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