首页> 外文期刊>Der Pharmacia Lettre >A Novel Quantification Method for the Simultaneous Estimation of LosartanPotassium and Hydrochlorothiazide in Bulk and Tablet Dosage Form UsingSimultaneous Equation Method
【24h】

A Novel Quantification Method for the Simultaneous Estimation of LosartanPotassium and Hydrochlorothiazide in Bulk and Tablet Dosage Form UsingSimultaneous Equation Method

机译:联立方程法同时估算散剂和片剂中氯沙坦钾和氢氯噻嗪的定量方法

获取原文
           

摘要

In this present paper, a novel, sensitive, UV- Spectrophotometric simultaneous equation method was proposed for the estimation of Losartan Potassium (LOS.P) and Hydrochlorothiazide (HTZ) in bulk and tablet dosage form. Water: Methanol in the ratio of 95:5 v/v was used as a solvent which exhibits maximum absorption at 215nm for LOS.P and 272nm for HTZ. Beers law was obeyed over the linear range for LOS.P is 1-20μg/ml and HTZ. The correlation coefficient (R2) was found 0.980 for LOS.P and 0.992 for HTZ respectively. The method was successfully applied for the assay of the both drugs in tablet with 99.2 % and 98.67 % purity for LOSP and HTZ respectively. The developed method was fully validated as per ICH guidelines. The percentage relative standard deviation (RSD) for accuracy was less than 2. The percentages RSD of the intra-day and inter-day variations were found also less than 2%. The limit of detection and quantification were 0.32μg/ml and 0.97 μg/ml for LOS.P and 0.09 μg/ml and 0.248 μg/ml for HTZ which indicates the sensitivity of the developed method. The present method also demonstrated robust on changing λmax and solvent volume ratio up to ± 2%. Empirical evidence from developed method concludes that it was simple, sensitive, reliable, and useful for the routine quality control analysis of LOS.P and HTZ in bulk and tablet dosage form.
机译:本文提出了一种新颖,灵敏的紫外分光光度联立方程方法,用于估计散装和片剂剂型中的氯沙坦钾(LOS.P)和氢氯噻嗪(HTZ)。水:甲醇以95:5 v / v的比例用作溶剂,对LOS.P和HTZ在215nm处显示最大吸收。 LOS.P在1-20μg/ ml和HTZ的线性范围内遵循比尔斯定律。 LOS.P和HTZ的相关系数(R2)分别为0.980和0.992。该方法已成功用于片剂中两种药物的测定,其LOSP和HTZ的纯度分别为99.2%和98.67%。所开发的方法已按照ICH指南进行了充分验证。准确性的相对标准偏差(RSD)百分比小于2。日内和日间变化的RSD百分比也小于2%。 LOS.P的检出限和定量限分别为0.32μg/ ml和0.97μg/ ml,而HTZ的检出限为0.09μg/ ml和0.248μg/ ml,表明该方法的灵敏度。本方法还证明了在改变λmax和溶剂体积比高达±2%时的鲁棒性。发达方法的经验证据表明,该方法简单,灵敏,可靠,可用于散装和片剂剂型LOS.P和HTZ的常规质量控制分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号