Radi Abd-Elgawad, Abd-Elghany Nadia, Wahdan Tarek
Department of Chemistry, Faculty of Science (Dumyat), Mansoura University, Dumyat, Egypt.
Chem Pharm Bull (Tokyo). 2007 Sep;55(9):1379-82. doi: 10.1248/cpb.55.1379.
The electrochemical oxidation of the antineoplastic agent etoposide was studied at carbon paste electrode in Britton-Robinson buffer solutions over the pH range 2.0-10.0 using cyclic, linear sweep and differential pulse voltammetry. Oxidation of the drug was effected in a single reversible, diffusion-controlled step within the pH range 2.0-4.0, a second oxidation process was produced above pH 4.0. Using differential pulse voltammetry (DPV), the drug yielded a well-defined voltammetric response in Britton-Robinson buffer, pH 3.0 at 0.500 V (vs. Ag/AgCl) on carbon paste electrode. This process could be used to determine etoposide concentrations in the range 2.5 x 10(-7) to 2.5 x 10(-5) M with a detection limit of 1.0 x 10(-7) M. The method was successfully applied to the determination of the drug in spiked human serum.
采用循环伏安法、线性扫描伏安法和差分脉冲伏安法,在pH值为2.0 - 10.0的Britton-Robinson缓冲溶液中,于碳糊电极上研究了抗肿瘤药物依托泊苷的电化学氧化。在pH值为2.0 - 4.0范围内,药物的氧化通过一个单一的可逆、扩散控制步骤进行,在pH值高于4.0时产生第二个氧化过程。使用差分脉冲伏安法(DPV),该药物在碳糊电极上于pH 3.0的Britton-Robinson缓冲溶液中,在0.500 V(相对于Ag/AgCl)处产生明确的伏安响应。此方法可用于测定浓度范围为2.5×10⁻⁷至2.5×10⁻⁵ M的依托泊苷,检测限为1.0×10⁻⁷ M。该方法已成功应用于加标人血清中药物的测定。