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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A miniaturized urea sensor based on the integration of both ammonium based urea enzyme field effect transistor and a reference field effect transistor in a single chip
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A miniaturized urea sensor based on the integration of both ammonium based urea enzyme field effect transistor and a reference field effect transistor in a single chip

机译:基于铵基尿素酶场效应晶体管和参考场效应晶体管集成在单个芯片中的小型尿素传感器

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摘要

A urea biosensor prepared by covalent binding of urease directly to the surface of an ammonium-sensitive field effect transistor (FET) is described. Nonactin incorporated in carboxylated polyvinyl chloride was used to obtain the sensitive membrane of the ammonium-sensitive FET. The grafting of urease on the polyvinylchloride-COOH membrane surface was performed through carbodiimide coupling. The activity of the immobilized enzyme was spectrometrically controlled through the time-dependent disappearance of the absorbance of NADH at 340 nm. An apparent activity of 50% was found, compared with free enzyme. The sensitivity of the urea enzyme FET is 50 mV/pUrea working in a differential mode of 2 #mu#M to 1 mM, this sensitivity being constant during 15 days. Finally, in order to test the potentialities of the urea biosensor for the environmental applications, the detection of heavy metal ions such as Cu(II) and Hg(II) is solution was performed by measuring the remaining activity of the inhibited enzyme.
机译:描述了通过将尿素酶直接共价结合到铵敏感的场效应晶体管(FET)的表面而制备的尿素生物传感器。使用掺入羧化聚氯乙烯中的非肌动蛋白来获得铵敏感型FET的敏感膜。通过碳二亚胺偶联进行脲酶在聚氯乙烯-COOH膜表面上的接枝。通过340 nm处NADH的吸光度随时间的消失,通过光谱法控制固定化酶的活性。与游离酶相比,发现表观活性为50%。尿素酶FET的灵敏度为50 mV / pUrea,工作在2#mu#M至1 mM的差分模式下,该灵敏度在15天内保持不变。最后,为了测试尿素生物传感器在环境中的潜力,通过测量被抑制酶的剩余活性来对重金属离子(例如Cu(II)和Hg(II))进行溶液检测。

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