Patel Sejal, Patel N J, Patel S A
S. K. Patel College of Pharmaceutical Education and Research, Department of Pharmaceutical Chemistry, Ganpat University, Kherva, Mehsana-382 711, India.
Indian J Pharm Sci. 2009 Jul;71(4):468-72. doi: 10.4103/0250-474X.57304.
A binary mixture of imipramine HCl and chlordiazepoxide was determined by three different spectrophotometric methods. The first method involved determination of imipramine HCl and chlordiazepoxide using the simultaneous equations and the second method involved absorbance ratio method. Imipramine has absorbance maxima at 251 nm, chlordiazepoxide has absorbance maxima at 264.5 nm and isoabsorptive point is at 220 nm in methanol. Linearity was obtained in the concentration ranges of 1-25 and 1-10 mug/ml for Imipramine HCL and Chlordiazepoxide, respectively. The third method involved determination of these two drugs using the first-derivative spectrophotometric technique at 219 and 231.5 nm over the concentration ranges of 1-20 and 2-24 mug/ml with mean accuracies 99.46+/-0.78 and 101.43+/-1.20%, respectively. These methods were successively applied to pharmaceutical formulations because no interferences from the tablet excipients were found. The suitability of these methods for the quantitative determination of the compounds was proved by validation.
采用三种不同的分光光度法测定盐酸丙咪嗪和氯氮卓的二元混合物。第一种方法是利用联立方程法测定盐酸丙咪嗪和氯氮卓,第二种方法是吸光度比值法。在甲醇中,丙咪嗪在251nm处有最大吸收峰,氯氮卓在264.5nm处有最大吸收峰,等吸收点在220nm处。盐酸丙咪嗪和氯氮卓的线性范围分别为1 - 25μg/ml和1 - 10μg/ml。第三种方法是在219nm和231.5nm处采用一阶导数分光光度技术测定这两种药物,浓度范围分别为1 - 20μg/ml和2 - 24μg/ml,平均准确度分别为99.46±0.78%和101.43±1.20%。由于未发现片剂辅料的干扰,这些方法相继应用于药物制剂。通过验证证明了这些方法对化合物定量测定的适用性。