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机构地区:[1]中国科学技术大学研究生院化学部,北京100039
出 处:《分析化学》2002年第1期9-12,共4页Chinese Journal of Analytical Chemistry
摘 要:基于头孢唑啉在 0.10mol/L NaOH溶液中水浴降解产物中含有巯基(-SH),在 pH 5.0NaAc-HAc介质中,于银亚微盘电极上产生一灵敏的吸附伏安氧化还原峰,其峰电位分别为 Epa=-0.530V和 EPc=-0.400V。动力学研究表明:电极反应的电子转移数为0.91,表观电子传递速率为ks=0.10s-1,峰电流与头孢唑啉浓度在1.0×10-6~50×10-1mol/L范围内呈良好的线性关系。方法可应用于人工合成样品头孢啉的检测。The electrochemical behavior of degradation product of cefazolin (CFL) at silver sub-microdisk electrode has been studied. The degradation progress was carried out in 0.10 mol/L NaOH at 100degreesC for 20 minutes. The method was based on the degradation product of CFL containing thiohydroxy group (-SH), Which can combine with Ag+ to form an insoluble thiolate. In a medium, of 0.1 mol/L HAc-NaAc (pH 5.0), A pair of redox peaks were observed with the peak potential E-p1 = -0.53 V(reduction) and E-p2 = -0.40 V(oxidation). The electron-transfer rate constant (k(s)) and electron-transfer number are 0.10 s(-1) and 0.91 respectively at the scan rate of 100 mV/s. The linear range between the peak currents and the concentration of cefazolin was 5.0 x 10(-4) similar to 1.0 x 10(-6) mol/L. The electrode reaction process was quasi-reversible with adsorptive characteristic. This method has been successfully applied to the determination of CFL in simulate sample.
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