Spectrophotometric methods for the simultaneous estimation of losartan potassium and hydrochlorothiazide in tablet dosage forms

K. S. Rao, M. Panda, N. K. Keshar
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引用次数: 10

Abstract

Aim: This work deals with the simultaneous determination of Losartan potassium (LSP) and Hydrochlorothiazide (HZ) in a binary mixture form, without prior separation, by three different techniques. Materials and Methods: The present 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. Standard gift sample of LSP and HZ were obtained from Torrent pharmaceuticals Ltd, Baddi, Himachal Pradesh. Combined LSP and HZ tablets were purchased from local market. Methanol from Merck Ltd. and distilled water are used as solvent. Results: The first method is the application of simultaneous equation. Where the linearity ranges for LSP and HZ were 5-25 μg/ml and 1-20 μg/ml, respectively. The second method is the determination of ratio of absorbance at 272 nm, the maximum absorption of HZ and isosbestic wavelength 266.5nm, the linearity ranges for LSP and HZ were 5-80μg/ml and 1-25μg/ml respectively. The third method is the first order derivative method, where the linearity ranges for LSP 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 99.06±1.210 and 99.30±1.159 using the simultaneous equation method, 99.66±0.573 and 99.95±0.272 using the graphical absorbance ratio method and 99.64±0.301 and 99.91±0.614 using first derivative method, for LSP and HZ respectively. Conclusions: 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.
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分光光度法同时测定片剂中氯沙坦钾和氢氯噻嗪的含量
目的:采用三种不同的方法,在不预先分离的情况下,同时测定氯沙坦钾(LSP)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。LSP和HZ的标准礼品样品来自喜马偕尔邦巴迪Torrent制药有限公司。LSP和HZ联合片从当地市场购买。使用默克公司的甲醇和蒸馏水作为溶剂。结果:第一种方法是应用联立方程。其中,LSP和HZ的线性范围分别为5 ~ 25 μg/ml和1 ~ 20 μg/ml。第二种方法是在272 nm处测定吸光度,HZ和等吸光度的最大吸收波长为266.5nm, LSP和HZ的线性范围分别为5 ~ 80μg/ml和1 ~ 25μg/ml。第三种方法为一阶导数法,LSP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,对LSP和HZ的加标回收率分别为99.06±1.210和99.30±1.159,对图形吸光度法的加标回收率分别为99.66±0.573和99.95±0.272,对一阶导数法的加标回收率分别为99.64±0.301和99.91±0.614。结论:所建立的方法快速、简便,无需前期分离步骤,可用于两种药物在质控实验室的常规分析。
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