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Activation-Based Catalase Enzyme Electrode and its Usage for Glucose Determination

机译:基于激活的过氧化氢酶电极及其在葡萄糖测定中的用途

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In this study,a novel type amperometric biosensor,which is based on the activation of catalase enzyme by glucose,was developed and used for the sensitive determination of glucose.For the preparation of the biosensor catalase enzyme was immobilized in gelatin by using cross-Unking agent glutaraldehyde and fixed on a pre-treated teflon membrane of a dissolved oxygen probe.Glucose was used as an activator for the catalase enzyme and determination of glucose is based on the assay of the differences on the catalase activity of the biosensor on the oxygenmeter in the absence and the presence of glucose in the reaction medium.The responses of the activation based catalase biosensor have a linear relation to glucose concentrations and good measurement correlation between 0.5 and 5.0 pM with 2 min response time.In the optimization studies of the biosensor the most suitable catalase amount were found as 1324 U cm~(-2) and also phosphate buffer (pH:7.0;50 mM) and 35°C were obtained as the optimum working conditions.For the characterization studies of the biosensor some parameters such as activator and interference effects of some substances on the biosensor response,reproducibility and operational stability were performed.
机译:本研究开发了一种基于葡萄糖激活过氧化氢酶的新型安培生物传感器,并用于葡萄糖的灵敏测定。为制备生物传感器过氧化氢酶,采用交叉Unking法将其固定在明胶中。试剂戊二醛固定在溶解氧探针的预处理聚四氟乙烯膜上。葡萄糖用作过氧化氢酶的活化剂,葡萄糖的测定是基于测定生物传感器在氧气计上过氧化氢酶活性的差异进行的。基于活化的过氧化氢酶生物传感器的响应与葡萄糖浓度呈线性关系,并且在2分钟响应时间内在0.5和5.0 pM之间具有良好的测量相关性。在生物传感器的优化研究中,发现最合适的过氧化氢酶的量为1324 U cm〜(-2),并且获得了磷酸盐缓冲液(pH:7.0; 50 mM)和35°C为最佳为了进行生物传感器的表征研究,进行了一些参数,例如活化剂和某些物质对生物传感器响应,重现性和操作稳定性的干扰作用。

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