紫外可见分光光度计定量分析原料药和药剂型的法匹拉韦

K. Ramadoss
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引用次数: 0

摘要

本研究的主要目的是建立一种快速、廉价的紫外分光光度法测定片剂中Favipiravir (400mg)的含量,并根据国际协调会议(ICH)的指导方针进行验证。本方法采用乙醇:水(30:70)溶剂测定Favipiravir, λmax为231nm。该方法在2 ~ 10 μg/ml范围内呈线性关系。采用标准加法法计算精度,通过计算相对标准偏差确定精密度。建立了一种廉价、快速的紫外分光光度法测定法匹拉韦的含量,可用于常规药物分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative analysis of favipiravir in bulk and pharmaceutical dosage forms using UV visible spectrophotometer
The main aim of this study is to develop a rapid and cheap Ultraviolet (UV) spectrophotometric method for the estimation of Favipiravir (400mg) in tablets and validate as per International Conference on Harmonization (ICH) guidelines. The developed method uses the solvent Ethanol: Water (30:70) for the assay of Favipiravir whose λmax was found to be 231nm. In this method, Favipiravirshows linearity in the range 2-10 μg/ml. The accuracy was carried out by using standard addition method and the precision is ascertained by calculating the relative standard deviation. A cheap and rapid UV spectrophotometric method was developed and validated for the estimation of Favipiravir and hence it can be used for the routine pharmaceutical analysis.
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