Hadad Ghada M, El-Gindy Alaa, Mahmoud Waleed M M
Suez Canal University, Faculty of Pharmacy, Pharmaceutical Analytical Chemistry Department, Ismailia 41522, Egypt.
J AOAC Int. 2008 Jan-Feb;91(1):39-51.
Multivariate spectrophotometric calibration and liquid chromatographic (LC) methods were applied to the determination of 2 multicomponent mixtures containing diprophylline, guaiphenesin, methylparaben, and propylparaben (Mixture 1), or clobutinol, orciprenaline, saccharin sodium, and sodium benzoate (Mixture 2). For the multivariate spectrophotometric calibration methods, principal component regression (PCR) and partial least-squares regression (PLS-1), a calibration set of the mixtures consisting of the components of each mixture was prepared in 0.1 M HCl. Analytical figures of merit such as sensitivity, selectivity, limit of quantitation, and limit of detection were determined for both PLS-1 and PCR. The LC separation was achieved on a reversed-phase C18 analytical column by using isocratic elution with 20 mM potassium dihydrogen phosphate, pH 3.3-acetonitrile (55 + 45, v/v) as the mobile phase and UV detection at 260 and 220 nm for Mixture 1 and Mixture 2, respectively. The proposed methods were validated and successfully applied to the analysis of pharmaceutical formulations and laboratory-prepared mixtures containing the 2 multicomponent combinations.
采用多元分光光度校准法和液相色谱(LC)法测定了两种多组分混合物,其中一种含有二羟丙茶碱、愈创甘油醚、对羟基苯甲酸甲酯和对羟基苯甲酸丙酯(混合物1),另一种含有氯丁醇、间羟异丙肾上腺素、糖精钠和苯甲酸钠(混合物2)。对于多元分光光度校准法,即主成分回归(PCR)和偏最小二乘回归(PLS-1),在0.1 M盐酸中制备了由每种混合物的成分组成的混合物校准集。测定了PLS-1和PCR的灵敏度、选择性、定量限和检测限等分析性能指标。在反相C18分析柱上进行LC分离,流动相采用20 mM磷酸二氢钾(pH 3.3)-乙腈(55 + 45,v/v)等度洗脱,混合物1和混合物2分别在260和220 nm处进行紫外检测。所提出的方法经过验证,并成功应用于含有这两种多组分组合的药物制剂和实验室制备混合物的分析。