El-Bardicy Mohammad G, Lotfy Hayam M, El-Sayed Mohammad A, El-Tarras Mohammad F
Cairo University, Faculty of Pharmacy, Department of Analytical Chemistry, Kaser E1-Aini St, ET 11562, Cairo, Egypt.
J AOAC Int. 2008 Mar-Apr;91(2):299-310.
Ratio subtraction and isosbestic point methods are 2 innovating spectrophotometric methods used to determine vincamine in the presence of its acid degradation product and a mixture of cinnarizine (CN) and nicergoline (NIC). Linear correlations were obtained in the concentration range from 8-40 microg/mL for vincamine (I), 6-22 microg/mL for CN (II), and 6-36 microg/mL for NIC (III), with mean accuracies 99.72 +/- 0.917% for I, 99.91 +/- 0.703% for II, and 99.58 +/- 0.847 and 99.83 +/- 1.039% for III. The ratio subtraction method was utilized for the analysis of laboratory-prepared mixtures containing different ratios of vincamine and its degradation product, and it was valid in the presence of up to 80% degradation product. CN and NIC in synthetic mixtures were analyzed by the 2 proposed methods with the total content of the mixture determined at their respective isosbestic points of 270.2 and 235.8 nm, and the content of CN was determined by the ratio subtraction method. The proposed method was validated and found to be suitable as a stability-indicating assay method for vincamine in pharmaceutical formulations. The standard addition technique was applied to validate the results and to ensure the specificity of the proposed methods.
比值减法和等吸收点法是两种创新的分光光度法,用于在长春胺存在其酸降解产物以及桂利嗪(CN)和尼麦角林(NIC)混合物的情况下测定长春胺。对于长春胺(I),在8 - 40μg/mL浓度范围内获得线性相关性;对于CN(II),在6 - 22μg/mL浓度范围内;对于NIC(III),在6 - 36μg/mL浓度范围内,I的平均准确度为99.72±0.917%,II为99.91±0.703%,III为99.58±0.847%和99.83±1.039%。比值减法用于分析含有不同比例长春胺及其降解产物的实验室制备混合物,在存在高达80%降解产物的情况下有效。合成混合物中的CN和NIC通过两种提议的方法进行分析,混合物的总含量在其各自270.2和235.8nm的等吸收点处测定,CN的含量通过比值减法测定。所提议的方法经过验证,被发现适用于作为药物制剂中长春胺的稳定性指示测定方法。采用标准加入技术验证结果并确保所提议方法的特异性。