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Electrochemical sensor using glassy carbon electrode modified with acylpyrazolone-multiwalled carbon nanotube composite film for determination of xanthine

机译:酰基吡唑啉酮-多壁碳纳米管复合膜修饰玻碳电极测定黄嘌呤的电化学传感器

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摘要

In this work, an electrochemical sensor 1-phenyl-3-methyl-4-(2-furoyl)-5-pyrazolone/multiwalled carbon nanotubes/glassy carbon electrode (GCE) was prepared for the determination of xanthine (XN) in the presence of an excess of uric acid. Cyclic voltammetry and differential pulse voltammetry were used to characterize the electrode. The oxidation of XN occurred in a well-defined peak having E p 0.73 V in phosphate buffer solution of pH 6.0. Compared with the bare GCE, the electrochemical sensor greatly enhanced the oxidation signal of XN with negative shift in peak potential about 110 mV. Based on this, a sensitive, rapid, and convenient electrochemical method for the determination of XN has been proposed. Under the optimized conditions, the oxidation peak current of XN was found to be proportional to its concentration in the range of 0.3~50 μM with a detection limit of 0.08 μM. The analytical utility of the proposed method was demonstrated by the direct assay of XN in urine samples and was found to be promising at our preliminary experiments.
机译:在这项工作中,制备了一种电化学传感器1-苯基-3-甲基-4-(2-呋喃基)-5-吡唑啉酮/多壁碳纳米管/玻璃碳电极(GCE),用于在存在下测定黄嘌呤(XN)过量的尿酸。循环伏安法和差分脉冲伏安法用于表征电极。 XN的氧化发生在pH为6.0的磷酸盐缓冲溶液中具有E > p 0.73 V的明确定义的峰中。与裸露的GCE相比,该电化学传感器极大地增强了XN的氧化信号,使峰值电势的负位移约为110 mV。基于此,提出了一种灵敏,快速,方便的电化学方法测定XN。在最佳条件下,发现XN的氧化峰电流与其浓度成正比,范围为0.3〜50μM,检出限为0.08μM。尿液样品中XN的直接测定证明了该方法的分析实用性,并在我们的初步实验中被证明是很有前途的。

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