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在钴-水杨醛缩邻苯二胺修饰的碳糊电极上对头孢菌素进行电催化检测。

The electrocatalytic examination of cephalosporins at carbon paste electrode modified with CoSalophen.

作者信息

Jamasbi E S, Rouhollahi A, Shahrokhian S, Haghgoo S, Aghajani S

机构信息

Chemistry Department, Faculty of Science, K.N. Toosi University of Technology, Tehran 15418, Iran.

出版信息

Talanta. 2007 Mar 15;71(4):1669-74. doi: 10.1016/j.talanta.2006.07.058. Epub 2006 Sep 25.

Abstract

The electrocatalytic oxidation of cephalexin and cefazolin has been studied at a carbon paste electrode modified with cobalt salophen (CoSal) by cyclic voltammetry. The selectivity of the carbon paste modified with CoSal in detecting cephalexin and cefazolin was examined. To suggest the electrocatalytic mechanism for electro-oxidation of cefazolin, the electrochemical behavior of ceftriaxone was investigated which has a thiol group out of the beta lactam ring. The electrocatalytic oxidation of these antibiotics is shown to be irreversible at the CoSal modified electrode. Scan rate dependence of cefazolin, which is a sulfur-containing compound, has been examined. The results indicated that the electrocatalytic oxidation of the compounds is diffusion controlled. The responses of the modified electrode were compared with those of unmodified electrode and it has shown that the modified electrode has better sensitivity than unmodified electrode to the detection of cefazolin. The overall number of electrons contributed to the oxidation of cefazolin is obtained 1 by chronoamperometry; the number of electron involved in the rate-determining step was 1. The results of differential pulse voltammetry (DPV) using the modified electrode with high sensitivity were applied for the determination of cefazolin in human synthetic serum samples. The linear range was obtained from 1x10(-5) to 1x10(-3)M for DPV determination of cefazolin in buffered solutions (pH 3.0).

摘要

通过循环伏安法研究了在钴酞菁修饰的碳糊电极上头孢氨苄和头孢唑啉的电催化氧化。考察了钴酞菁修饰碳糊在检测头孢氨苄和头孢唑啉时的选择性。为了揭示头孢唑啉电氧化的电催化机理,研究了头孢曲松的电化学行为,其β-内酰胺环外有一个巯基。这些抗生素在钴酞菁修饰电极上的电催化氧化显示为不可逆。考察了含硫化合物头孢唑啉的扫描速率依赖性。结果表明,化合物的电催化氧化受扩散控制。将修饰电极与未修饰电极的响应进行比较,结果表明修饰电极对头孢唑啉的检测比未修饰电极具有更好的灵敏度。通过计时电流法得到头孢唑啉氧化的总电子数为1;速率决定步骤中涉及的电子数为1。使用具有高灵敏度的修饰电极的差分脉冲伏安法(DPV)结果用于测定人合成血清样品中的头孢唑啉。在缓冲溶液(pH 3.0)中,DPV测定头孢唑啉的线性范围为1×10⁻⁵至1×10⁻³M。

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