Moussa Bahia Abbas, El-Zaher Asmaa Ahmed, Mahrouse Marianne Alphonse, Ahmed Maha Said
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt.
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc. 2016 Aug 5;165:127-137. doi: 10.1016/j.saa.2016.04.003. Epub 2016 Apr 7.
Four new spectrophotometric methods were developed, applied to resolve the overlapped spectra of a ternary mixture of [aliskiren hemifumarate (ALS)-amlodipine besylate (AM)-hydrochlorothiazide (HCT)] and to determine the three drugs in pure form and in combined dosage form. Method A depends on simultaneous determination of ALS, AM and HCT using principal component regression and partial least squares chemometric methods. In Method B, a modified isosbestic spectrophotometric method was applied for the determination of the total concentration of ALS and HCT by measuring the absorbance at 274.5nm (isosbestic point, Aiso). On the other hand, the concentration of HCT in ternary mixture with ALS and AM could be calculated without interference using first derivative spectrophotometric method by measuring the amplitude at 279nm (zero crossing of ALS and zero value of AM). Thus, the content of ALS was calculated by subtraction. Method C, double divisor first derivative ratio spectrophotometry (double divisor (1)DD method), was based on that for the determination of one drug, the ratio spectra were obtained by dividing the absorption spectra of its different concentrations by the sum of the absorption spectra of the other two drugs as a double divisor. The first derivative of the obtained ratio spectra were then recorded using the appropriate smoothing factor. The amplitudes at 291nm, 380nm and 274.5nm were selected for the determination of ALS, AM and HCT in their ternary mixture, respectively. Method D was based on mean centering of ratio spectra. The mean centered values at 287, 295.5 and 269nm were recorded and used for the determination of ALS, AM and HCT, respectively. The developed methods were validated according to ICH guidelines and proved to be accurate, precise and selective. Satisfactory results were obtained by applying the proposed methods to the analysis of pharmaceutical dosage form.
开发了四种新的分光光度法,用于解析阿利吉仑半富马酸盐(ALS)-苯磺酸氨氯地平(AM)-氢氯噻嗪(HCT)三元混合物的重叠光谱,并测定纯品及复方制剂中的这三种药物。方法A依赖于使用主成分回归和偏最小二乘化学计量学方法同时测定ALS、AM和HCT。在方法B中,采用改进的等吸收点分光光度法,通过在274.5nm(等吸收点,Aiso)处测量吸光度来测定ALS和HCT的总浓度。另一方面,在与ALS和AM的三元混合物中,HCT的浓度可通过一阶导数分光光度法,在279nm处测量吸光度(ALS的零交叉点和AM的零值)来计算,不受干扰。因此,通过减法计算出ALS的含量。方法C,双除数一阶导数比光谱法(双除数(1)DD法),其原理是在测定一种药物时,将其不同浓度的吸收光谱除以其他两种药物吸收光谱之和作为双除数,得到比光谱。然后使用适当的平滑因子记录所得比光谱的一阶导数。选择在291nm、380nm和274.5nm处的吸光度分别测定其三元混合物中的ALS、AM和HCT。方法D基于比光谱的均值中心化。记录在287、295.5和269nm处的均值中心化值,分别用于测定ALS、AM和HCT。所开发的方法按照国际人用药品注册技术协调会(ICH)指南进行了验证,结果表明这些方法准确、精密且具有选择性。将所提出的方法应用于药物制剂分析,获得了满意的结果。