Farghaly O A, Taher M A, Naggar A H, El-Sayed A Y
Chemistry Department, Faculty of Science, Al-Azhar University, Assiut Branch, 71524 Assiut, Egypt.
J Pharm Biomed Anal. 2005 Jun 1;38(1):14-20. doi: 10.1016/j.jpba.2004.11.059. Epub 2005 Jan 15.
A simple, reliable and selective square wave anodic stripping (SWAS) voltammetric method at carbon paste electrode (CPE) of metoclopramide hydrochloride (MCP) in pharmaceutical dosage forms (tablet) and in biological fluids (spiked and real urine samples) has been developed and evaluated. Different parameters such as medium, supporting electrolyte, pH, accumulation potential, scan rate, accumulation time and ionic strength, were tested to optimize the conditions for the determination of MCP. The adsorbed form is oxidized irreversibly under optimal conditions, viz., 0.4M HCl-sodium acetate buffer (pH approximately 6.2), 0.2M KCl, a linear concentration ranges from 0.067 to 0.336, 0.067 to 0.269 and 0.067 to 0.269 ng/mL of MCP, at accumulation times 60, 120 and 180 s, respectively, can be determined successfully. The interferences of some common excipients and some metal ions were studied. The standard addition method was used to determine the MCP in pure solutions, tablets and in biological fluids with satisfactory results. The data obtained are compared with the standard official method.
已开发并评估了一种在碳糊电极(CPE)上用于测定药物剂型(片剂)和生物流体(加标及实际尿液样本)中盐酸甲氧氯普胺(MCP)的简单、可靠且具选择性的方波阳极溶出伏安法(SWAS)。测试了诸如介质、支持电解质、pH值、富集电位、扫描速率、富集时间和离子强度等不同参数,以优化测定MCP的条件。在最佳条件下,即0.4M盐酸 - 醋酸钠缓冲液(pH约为6.2)、0.2M氯化钾,MCP的线性浓度范围分别为0.067至0.336、0.067至0.269和0.067至0.269 ng/mL,富集时间分别为60、120和180 s时,吸附形式会发生不可逆氧化,从而能够成功测定。研究了一些常见辅料和一些金属离子的干扰情况。采用标准加入法测定纯溶液、片剂和生物流体中的MCP,结果令人满意。将所得数据与标准官方方法进行了比较。