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Amperometric Determination of Urea Using Enzyme-Modified Carbon Paste Electrode

机译:酶修饰碳糊电极安培法测定尿素

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An amperometric biosensor based on carbon paste electrodes(CPEs)for the determination of urea was constructed by enzyme(urease/GL-DH)-modified method.Urea was hydrolyzed to NH_4~+by catalyzing urease onto the enzyme-modified electrode surface in sample solution.In the presence of alpha-ketoglutarate and reduced nicotinamide adenine dinucleotide(NADH),a liberated NH_4~+ produce to L-glutamate and NAD~+ by L-glutamate dehydrogenase(GL-DH).After the chemical reaction was proceeded,the electrochemical reaction was occurred that an excess of the NADH was oxidized to NAD~+.The oxidation current of NADH was monitored at +1.10 volt vs.Ag/AgCl.An optimum conditions of biosensor were investigated:The optimum pH range for catalyzed hydrolysis reaction of urea was pH 7.0-7.4.The linear response range and detection limit were 2.0 X 10~(-5)approx2.0 X 10~(-4)M and 5.0 x 10~6 M,respectively.Another physiological species did not interfere,except L-ascorbic acid.
机译:通过酶(尿素酶/ GL-DH)修饰的方法构建了一种基于碳糊电极(CPEs)测定尿素的生物电流传感器,将尿素催化到样品中酶修饰的电极表面,将尿素水解为NH_4〜+。在存在α-酮戊二酸和还原烟酰胺腺嘌呤二核苷酸(NADH)的情况下,L-谷氨酸脱氢酶(GL-DH)释放出NH_4〜+生成L-谷氨酸和NAD〜+。进行化学反应后,电化学反应发生,将过量的NADH氧化为NAD〜+。在+1.10伏特对Ag / AgCl的条件下监测NADH的氧化电流。研究了生物传感器的最佳条件:催化水解的最佳p​​H范围尿素反应的pH值为7.0-7.4。线性响应范围和检出限分别为2.0 X 10〜(-5)约2.0 X 10〜(-4)M和5.0 x 10〜6 M.除L-抗坏血酸外,均不干扰。

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