阿齐沙坦、美多索米和氯噻酮的分光光度法和荧光光度法研究。

Analytical Chemistry Insights Pub Date : 2014-05-07 eCollection Date: 2014-01-01 DOI:10.4137/ACI.S13768
Walid M Ebeid, Ehab F Elkady, Asmaa A El-Zaher, Ramzia I El-Bagary, Gabor Patonay
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引用次数: 25

摘要

最近批准的血管紧张素II受体阻滞剂阿齐沙坦美多索米(AZL)与氯噻酮(CLT)联合使用的分光光度法和荧光光谱法进行了测定。紫外分光光度技术依赖于同时测量AZL和CLT在甲醇中分别在286和257 nm处的一阶导数光谱。荧光光谱技术依赖于测量在甲醇中存在CLT时AZL在298 nm处的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光度反应的影响。在荧光光谱研究中,还研究了pH和胶束辅助荧光增强的影响。分光光度法测定AZL和CLT的浓度范围分别为8 ~ 50 μ mL(-1)和2 ~ 20 μ mL(-1),荧光光谱法测定AZL的浓度范围为0.01 ~ 0.08 μ mL(-1),线性、准确度和精密度均较好。所建立的方法可用于所研究药物的含量测定。所建立的方法价格低廉、操作简便,适用于上述原料药和制剂的质量控制和常规分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spectrophotometric and spectrofluorimetric studies on azilsartan medoxomil and chlorthalidone to be utilized in their determination in pharmaceuticals.

Spectrophotometric and spectrofluorimetric studies on azilsartan medoxomil and chlorthalidone to be utilized in their determination in pharmaceuticals.

Spectrophotometric and spectrofluorimetric studies on azilsartan medoxomil and chlorthalidone to be utilized in their determination in pharmaceuticals.

Spectrophotometric and spectrofluorimetric studies on azilsartan medoxomil and chlorthalidone to be utilized in their determination in pharmaceuticals.

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.

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