Ebeid Walid M, Elkady Ehab F, El-Zaher Asmaa A, El-Bagary Ramzia I, Patonay Gabor
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt. ; Department of Chemistry, Georgia State University, Atlanta, GA, USA.
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Anal Chem Insights. 2014 May 7;9:33-40. doi: 10.4137/ACI.S13768. eCollection 2014.
The recently approved angiotensin II receptor blocker, azilsartan medoxomil (AZL), was determined spectrophotometrically and spectrofluorimetrically in its combination with chlorthalidone (CLT) in their combined dosage form. The UV-spectrophotometric technique depends on simultaneous measurement of the first derivative spectra for AZL and CLT at 286 and 257 nm, respectively, in methanol. The spectrofluorimetric technique depends on measurement of the fourth derivative of the synchronous spectra intensities of AZL in presence of CLT at 298 nm in methanol. The effects of different solvents on spectrophotometric and spectrofluorimetric responses were studied. For, the spectrofluorimetric study, the effect of pH and micelle-assisted fluorescence enhancement were also studied. Linearity, accuracy, and precision were found to be satisfactory over the concentration ranges of 8-50 μg mL(-1) and 2-20 μg mL(-1) for AZL and CLT, respectively, in the spectrophotometric method as well as 0.01-0.08 μg mL(-1) for AZL in the spectrofluorimetric method. The methods were successfully applied for the determination of the studied drugs in their co-formulated tablets. The developed methods are inexpensive and simple for the quality control and routine analysis of the cited drugs in bulk and in pharmaceuticals.
最近获批的血管紧张素II受体阻滞剂阿齐沙坦美洛昔酯(AZL),采用分光光度法和荧光分光光度法对其与氢氯噻嗪(CLT)的复方剂型进行测定。紫外分光光度法是在甲醇中,分别于286 nm和257 nm处同时测量AZL和CLT的一阶导数光谱。荧光分光光度法是在甲醇中,于298 nm处测量CLT存在下AZL同步光谱强度的四阶导数。研究了不同溶剂对分光光度和荧光分光光度响应的影响。对于荧光分光光度研究,还研究了pH值和胶束辅助荧光增强的影响。分光光度法中,AZL和CLT的线性范围分别为8 - 50 μg mL(-1)和2 - 20 μg mL(-1),荧光分光光度法中AZL的线性范围为0.01 - 0.08 μg mL(-1),线性、准确度和精密度均令人满意。这些方法成功应用于复方片剂中所研究药物的测定。所建立的方法对于所提及药物的原料药和制剂的质量控制及常规分析而言,成本低廉且操作简单。