Simple Extractive Spectrophotometric Method for Determination of Favipiravir from Pharmaceutical Formulation

R. V. Rele, Prathamesh P. Tiwatane
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引用次数: 3

Abstract

Simple sensitive and accurate extractive spectrophotometric methods have developed for the estimation of favipiravir in pharmaceutical dosage form. The methods are based on the formation of coloured complexes by the drug with reagents like bromophenol blue, solochrome dark blue and bromocresol green in acidic medium. The ion associated complexes were formed and quantitatively extracted under the experimental condition in chloroform. The absorbance values were measured at 420nm, 495nm and 430nm respectively. The proposed methods were validated statistically. Recoveries of methods were carried out by standard addition methods. The linearity was found to be 1.0-12.0μg/ml, 2-20μg/ml, 1-16μg/ml for methods 1, 2 and 3 respectively. The low values of standard deviation and percentage RSD indicate high precision of methods. Hence these methods are useful for routine estimation of favipiravir in tablets.
简单萃取分光光度法测定制剂中法匹拉韦的含量
建立了一种简单、灵敏、准确的提取分光光度法测定药物剂型中法匹拉韦含量的方法。这些方法是基于药物在酸性介质中与溴酚蓝、茄色素深蓝和溴甲酚绿等试剂形成有色络合物。在实验条件下,在氯仿中形成离子缔合物并定量提取。分别在420nm、495nm和430nm处测定吸光度值。提出的方法经统计学验证。采用标准加样法进行回收率测定。方法1、方法2、方法3的线性范围分别为1.0 ~ 12.0μg/ml、2 ~ 20μg/ml、1 ~ 16μg/ml。标准偏差和RSD百分比值较低,表明该方法精度较高。因此,这些方法可用于法匹拉韦片剂的常规测定。
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