Simultaneous estimation of captopril and hydrochlorothiazide in combined dosage forms

K. S. Rao, M. Panda, N. K. Keshar, S. Yadav
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引用次数: 4

Abstract

Aim: This work deals with the simultaneous determination of captopril (CAP) and hydrochlorothiazide (HZ) in two-component solid dosage form, without prior separation, by three different techniques (simultaneous equation, absorbance ratio method, and first-order derivative method). Materials and Methods: This work was carried out on Shimadzu electron UV1800 double-beam UV-Visible spectrophotometer. The absorption spectra of reference and test solutions were carried out in 1 cm matched quartz cell over the range of 200-400 nm. Methanol and distilled water are used as solvent. Results: The first method is the application of simultaneous equation. Where the linearity ranges for both the drugs were 5-35 μg/ml. The second method is the determination of ratio of absorbance at 271 nm, the maximum absorption of HZ and isobestic wavelength 209 nm, the linearity ranges for both the drugs were 10-120 μg/ml The third method is the first-order derivative method, where the CAP shows wavelength at 222 nm and HZ shows at 340 nm, and the linearity ranges for CAP and HZ were 1-30 μg/ml and 1-40 μg/ml, respectively. The proposed procedures were successfully applied for the simultaneous determination of both the drugs in commercial tablet preparation. The validity of the proposed methods was assessed by applying the standard addition technique where the percentage recovery of the added standard was found to be 99.52±0.214 and 99.00±0.165 using the simultaneous equation method, 99.76±0.684 and 99.58±0.279 using the graphical absorbance ratio method, and 99.45±0295 and 99.21±0.678 using first derivative method, for CAP and HZ, respectively. Conclusion: The proposed procedures are rapid, simple, require no preliminary separation steps, and can be used for routine analysis of both drugs in quality control laboratories.
卡托普利与氢氯噻嗪联合剂型的同时评价
目的:采用联立方程法、吸光度法和一阶导数法同时测定两组分固体剂型卡托普利(CAP)和氢氯噻嗪(HZ)的含量。材料与方法:本工作在岛津电子UV1800双光束紫外可见分光光度计上进行。在1 cm匹配的石英池中,在200-400 nm范围内对参比溶液和被试溶液进行吸收光谱分析。甲醇和蒸馏水作为溶剂。结果:第一种方法是应用联立方程。两种药物的线性范围为5 ~ 35 μg/ml。第二种方法是在271 nm处测定吸光度,HZ和等适吸收波长均为209 nm,两种药物的线性范围为10 ~ 120 μg/ml;第三种方法是一阶导数法,其中CAP在222 nm处,HZ在340 nm处,CAP和HZ的线性范围分别为1 ~ 30 μg/ml和1 ~ 40 μg/ml。该方法成功地应用于两种药物在市售片剂制剂中的同时测定。采用标准添加法对方法的有效性进行了评价,加标后的标准品回收率分别为:联立方程法99.52±0.214和99.00±0.165,图形吸光度法99.76±0.684和99.58±0.279,一阶导数法99.45±0295和99.21±0.678。结论:所建立的方法快速、简便,不需要初步分离步骤,可用于两种药物在质控实验室的常规分析。
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