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Photoelectrochemical glucose biosensor in flow injection analysis system based on glucose dehydrogenase immobilized on poly-hematoxylin modified glassy carbon electrode

机译:固定在聚苏木修饰玻碳电极上的葡萄糖脱氢酶流动注射分析系统中的光电化学葡萄糖生物传感器

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摘要

In this study, a photoelectrochemical glucose biosensor is presented, comprising electropolymerized hematoxylin film on poly-amidoamine (PAMAM) dendrimers adsorbed on glassy carbon electrode (polyHT/PAMAM/GCE). After immobilization of glucose dehydrogenase (GDH) onto the poly-HT/PAMAM/GCE, photoelectrochemical biosensing of glucose was investigated using cyclic voltammetry and amperometry in a flow injection analysis (FIA) system dependent on the NAD+/NADH redox coupledehydrogenase enzyme. The linear range was from 1 x 10(-5) M to 1 x 10(-3) M with a sensitivity of 0.76 mu A mM(-1) and detection limit of 3.0 mM without irradiation in the FIA system. After irradiation, the linear range was from 5 x 10(-6) M to 1 x 10(-3) M with a sensitivity of 1.90 mu A mM(-1) and a detection limit of 1.5 mM. Comparing the results obtained from irradiation of the electrode surface with those from the reaction without irradiation, the sensitivity and the detection limit increased around 2.5- and 2.0-fold, respectively. The photoelectrochemical biosensor showed good performance with high upper detection limit, acceptable repeatability, and selectivity, providing a rapid alternative method for monitoring biomolecules and extending photoelectrochemical determination in the FIA system. The proposed electrochemical and photoelectrochemical biosensor was successfully applied to determination of glucose in real samples. The results obtained from this study provide a basis for future studies in these directions.
机译:在这项研究中,提出了一种光电化学葡萄糖生物传感器,该传感器包括吸附在玻碳电极上的聚酰胺基胺(PAMAM)树状聚合物上的电聚合苏木素膜(polyHT / PAMAM / GCE)。在将葡萄糖脱氢酶(GDH)固定在聚HT / PAMAM / GCE上之后,在依赖于NAD + / NADH氧化还原偶联脱氢酶的流动注射分析(FIA)系统中,使用循环伏安法和安培法研究了葡萄糖的光电化学生物传感。线性范围为1 x 10(-5)M到1 x 10(-3)M,灵敏度为0.76μAmM(-1),检测限为3.0 mM,未在FIA系统中进行辐照。辐照后,线性范围为5 x 10(-6)M到1 x 10(-3)M,灵敏度为1.90μAmM(-1),检测极限为1.5 mM。将通过辐照电极表面获得的结果与未经辐照的反应获得的结果进行比较,灵敏度和检测极限分别提高了约2.5倍和2.0倍。光电化学生物传感器表现出良好的性能,具有较高的检测上限,可接受的重复性和选择性,为监测生物分子和扩展FIA系统中的光电化学测定提供了一种快速的替代方法。提出的电化学和光电化学生物传感器已成功应用于实际样品中葡萄糖的测定。这项研究获得的结果为今后在这些方向上的研究提供了基础。

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