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A reagentless hydrogen peroxide biosensor based on the coimmobilization of thionine and horseradish peroxidase by their cross-linking with glutaraldehyde on glassy carbon electrode

机译:基于乙二胺和辣根过氧化物酶与戊二醛在玻璃碳电极上的交联共固定化的无试剂过氧化氢生物传感器

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摘要

A novel reagentless H2O2 sensor, based on the coimmobilization of horseradish peroxidase (HRP) and the redox dye thionine by their cross-linking with glutaraldehyde on the surface of a glassy carbon electrode, was fabricated. This resulting modified electrode exhibited good electrochemical activity in aqueous solution, and the electron transfer rate constant between the derivative thionine and glassy carbon electrode was about 0.097 s(-1) (calculated from Laviron method). The apparent surface coverage of thionine was about 8.54 x 10(-12) mol cm(-2). It was found that thionine could mediate the electron transfer of HRP with the electrode substrate. Performance and characteristics of the biosensor were evaluated with respect to response time, detection limit, applied potential, pH, and temperature. The results indicate that this biosensor is of high sensitivity to hydrogen peroxide with a low detection limit down to 1.0 x 10(-7) molL(-1). Moreover, dopamine, ascorbic acid, and uric acid did not interfere with the determination of H2O2. Meanwhile, this enzyme electrode also showed good stability and reproducibility for long-term use. [References: 33]
机译:基于辣根过氧化物酶(HRP)和氧化还原染料硫氨酸通过与戊二醛在玻璃碳电极表面的交联而共固定化的新型无试剂H2O2传感器。该所得修饰电极在水溶液中显示出良好的电化学活性,并且在衍生的硫氨酸和玻璃碳电极之间的电子转移速率常数为约0.097 s(-1)(根据拉维尔方法计算)。硫氨酸的表观表面覆盖率约为8.54 x 10(-12)mol cm(-2)。已经发现,硫氨酸可以介导HRP与电极基底的电子转移。关于响应时间,检测极限,施加的电势,pH和温度,评估了生物传感器的性能和特性。结果表明,该生物传感器对过氧化氢具有高灵敏度,检测限低至1.0 x 10(-7)molL(-1)。此外,多巴胺,抗坏血酸和尿酸不会干扰H2O2的测定。同时,该酶电极对于长期使用也显示出良好的稳定性和再现性。 [参考:33]

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