Pathak A, Rajput S J
Quality Assurance Laboratory, Pharmacy Department, Faculty of Technology and Engineering, The Maharaja Sayajirao University of Baroda, Vadodara-390 001, India.
Indian J Pharm Sci. 2008 Jul-Aug;70(4):513-7. doi: 10.4103/0250-474X.44607.
Two UV spectrophotometric methods have been developed, based on first derivative spectrophotometry for simultaneous estimation of doxylamine succinate, pyridoxine hydrochloride, and folic acid in tablet formulations. In method I, the concentrations of these drugs were determined by using linear regression equation. Method II is also based on first derivative spectrophotometry however simultaneous equations (Vierdot's method) were derived on derivative spectra. The first derivative amplitudes at 270.0, 332.8 and 309.2 nm were utilized for simultaneous estimation of these drugs respectively by both methods. In both the methods, linearity was obtained in the concentration range 2.5-50 mug/ml, 1-40 mug/ml and 1-30 mug/ml for doxylamine succinate, pyridoxine hydrochloride, and folic acid respectively. The developed methods show best results in terms of linearity, accuracy, precision, LOD, LOQ and ruggedness for standard laboratory mixtures of pure drugs and marketed formulations. The common excipients and additives did not interfere in their determinations.
已开发出两种紫外分光光度法,基于一阶导数分光光度法同时测定片剂制剂中的琥珀酸多西拉敏、盐酸吡哆醇和叶酸。在方法I中,通过使用线性回归方程测定这些药物的浓度。方法II也基于一阶导数分光光度法,不过是在导数光谱上推导联立方程(维尔多特法)。两种方法分别利用在270.0、332.8和309.2nm处的一阶导数振幅同时测定这些药物。在两种方法中,琥珀酸多西拉敏、盐酸吡哆醇和叶酸的浓度范围分别在2.5 - 50μg/ml、1 - 40μg/ml和1 - 30μg/ml内呈线性。对于纯药物的标准实验室混合物和市售制剂,所开发的方法在线性、准确度、精密度、检测限、定量限和耐用性方面显示出最佳结果。常见的辅料和添加剂在其测定中不产生干扰。