{"title":"UV-Spectrophotometric Estimation and Forced Degradation Studies of Tenofovir Alafenamide Fumarate (TAF) in its Bulk and Tablet Dosage Form","authors":"K. Bhavyasri, M. Manisha","doi":"10.5958/0974-360x.2020.00227.9","DOIUrl":null,"url":null,"abstract":"A simple, sensitive and reproducible Spectrophotometric method is developed for estimation of Tenofovir Alafenamide Fumarate (TAF) in bulk and its tablet dosage form. Forced degradation studies are also conducted on standard TAF and % degradation of drug under various stress conditions is reported. Different concentrations of TAF are prepared using distilled water: acetonitrile as diluent. The absorption maximum of TAF is found to be at 261nm. Linearity was established in the range of 6.25-37.5 μg/ml with regression coefficient of 0.999. The drug was subjected to acid and alkali hydrolysis, oxidation degradation, thermal and photo degradation conditions. © 2020 iGlobal Research and Publishing Foundation. All rights reserved. Cite this article as: Bhavyasri, K.; Manisha, M.; Rambabu, D. UV-spectrophotometric estimation and forced degradation studies of tenofovir alafenamide fumarate (TAF) in its bulk and tablet dosage form. Indo Global J. Pharm. Sci., 2020; 10(4): 1-5. DOI: http://doi.org/10.35652/IGJPS.2020.10401 . Indo Global Journal of Pharmaceutical Sciences, 2020; 10(4): 1-5 2 Simultaneous estimation of TAF and Emtricitabine by UV spectroscopic method is found in a literature. The method involving determination of TAF and Emtricitabine at 260nm and 280nm over the concentration ranges of 5-30μg/ml for both drugs has been described [6]. Most of the reported methods are often time consuming, expensive, use multi or expensive reagents, cumbersome and required expertise operational personnel. UV spectrophotometry, because of simplicity, reproducibility and speed and also it requires minimum solvent/reagent system and less analysis time, is widely used for the assay of the therapeutic compounds used as medications. MATERIALS AND METHODS Apparatus The Spectrophotometric measurements were carried out using Elico SL 210 UV/Visible spectrophotometer.","PeriodicalId":13366,"journal":{"name":"Indo Global Journal of Pharmaceutical Sciences","volume":"29 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indo Global Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5958/0974-360x.2020.00227.9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
富马酸替诺福韦阿拉那胺(TAF)原料药和片剂的紫外分光光度测定及强制降解研究
建立了一种简便、灵敏、重复性好的富马酸替诺福韦阿拉那胺(TAF)原料药和片剂含量测定方法。对标准TAF进行了强制降解研究,并报道了不同应力条件下药物的降解率。以蒸馏水乙腈为稀释剂制备不同浓度的TAF。TAF的最大吸收波长为261nm。在6.25 ~ 37.5 μg/ml范围内呈线性关系,回归系数为0.999。药物经过酸、碱水解、氧化降解、热降解和光降解等条件。©2020全球研究与出版基金会。版权所有。引用本文如下:Bhavyasri, K.;Manisha m;紫外分光光度法测定富马酸替诺福韦(TAF)原料药和片剂的强制降解研究。印度国际制药公司。科学。, 2020;10(4): 1 - 5。DOI: http://doi.org/10.35652/IGJPS.2020.10401。印度全球药物科学杂志,2020;10(4): 1-5有文献报道紫外光谱法同时测定TAF和恩曲他滨。已有文献报道了两种药物在260nm和280nm,浓度范围为5-30μg/ml下测定TAF和恩曲他滨的方法[6]。多数报道的方法往往耗时长、价格昂贵,使用多种或昂贵的试剂,操作繁琐且需要专业操作人员。紫外分光光度法具有简便、快速、重现性好、所需溶剂/试剂系统少、分析时间短等优点,被广泛应用于药物治疗性化合物的分析。采用Elico SL 210紫外/可见分光光度计进行分光光度测定。
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