Bakry R S, Abdel Razak O, el Walily A F, Belal S F
Pharmaceutical Analytical Chemistry Department, College of Pharmacy, University of Alexandria, Egypt.
Acta Pharm Hung. 1996 Mar;66(2):83-8.
Simple and selective spectrophotometric procedures for the determination of mequitazine in its pharmaceutical tablets are described. The method was based on the formation of complex between mequitazine and palladium in presence of methyl cellulose in buffered or unbuffered media. The two procedures provide a mean of following the oxidative decomposition of the investigated drug. The apparent molar absorptivities at 460 and 500 nm were 2810 and 2840 and with Sandell's sensitivity of 0.116 and 0.103 for the buffered and unbuffered solutions, respectively. At the same time, Beer's law was obeyed in a concentration range of 2.4-7.2 mg% and the regression line equations were derived with correlation coefficients of 0.9997 and 0.9999 for buffered and unbuffered reactions, respectively. The validity of the method was further confirmed using the standard addition method. The proposed procedures demonstrate high percentage of recovery with good accuracy and precision.
本文描述了用于测定其药物片剂中美喹他嗪的简单且选择性的分光光度法。该方法基于在缓冲或非缓冲介质中,美喹他嗪与钯在甲基纤维素存在下形成络合物。这两种方法提供了一种追踪所研究药物氧化分解的手段。在460和500nm处的表观摩尔吸光系数分别为2810和2840,缓冲溶液和非缓冲溶液的桑德尔灵敏度分别为0.116和0.103。同时,在2.4 - 7.2mg%的浓度范围内符合比尔定律,缓冲和非缓冲反应的回归线方程分别具有0.9997和0.9999的相关系数。使用标准加入法进一步证实了该方法的有效性。所提出的方法显示出高回收率,具有良好的准确度和精密度。