A Validated RP-HPLC-UV Method for Identification of Reference Standards of Degradation Products of Fenofibrate

S. Mulgund, S. Anbazhegan, B. P. Pawaskar, S. Gabhe
{"title":"A Validated RP-HPLC-UV Method for Identification of Reference Standards of Degradation Products of Fenofibrate","authors":"S. Mulgund, S. Anbazhegan, B. P. Pawaskar, S. Gabhe","doi":"10.5530/PHM.2014.2.6","DOIUrl":null,"url":null,"abstract":"Background: During the stress degradation studies of Fenofibrate the structures of two major degradation products, namely 2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl propanoic acid and methyl 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate, were characterized using LC-MS/MS studies under alkaline and acidic hydrolytic conditions, respectively. The present communication deals with synthesis, spectral characterization and further application of those reference standards of degradation products in identification of degradation products in bulk sample of drug through retention time matching studies. Methods: The reference standards of the degradation products were synthesized in the laboratory and their identity were confirmed using spectral studies. These were employed for retention matching studies using HPLC studies. The chromatographic conditions were as follows: stationary phase: Waters X Bridge C 18 column (250x4.6 mm, internal diameter, particle size 5 μm), mobile phase: acetonitrile: water in 75:25 v/v, column oven temperature: ambient, proportion. The chromatograms were monitored at 286 nm with a flowrate of 1 mL/min. The method was validated according to the ICH. guidelines. Results: Retention time values of synthesized reference standards were found to be identical with retention time values of those degradation products in stressed samples. The calibration curves showed good linear regression (r 2 >0.999) within test ranges. The method showed good reproducibility and sensitivity for quantification of both degradation products in samples. Method was precise and %recovery of both reference products was within 98-102%. Conclusion: This communication emphasizes use of non-compendial reference standards for quantification of degradation products by chromatographic methods. Quantitative validation parameters like Limit of detection and Limit of quantitation were established. Key words: Degradation impurities, Fenofibrate, Non-compendial reference standards, RP-HPLC, Retention time matching.","PeriodicalId":19960,"journal":{"name":"Pharmaceutical Methods","volume":"26 1","pages":"79"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/PHM.2014.2.6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Background: During the stress degradation studies of Fenofibrate the structures of two major degradation products, namely 2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl propanoic acid and methyl 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate, were characterized using LC-MS/MS studies under alkaline and acidic hydrolytic conditions, respectively. The present communication deals with synthesis, spectral characterization and further application of those reference standards of degradation products in identification of degradation products in bulk sample of drug through retention time matching studies. Methods: The reference standards of the degradation products were synthesized in the laboratory and their identity were confirmed using spectral studies. These were employed for retention matching studies using HPLC studies. The chromatographic conditions were as follows: stationary phase: Waters X Bridge C 18 column (250x4.6 mm, internal diameter, particle size 5 μm), mobile phase: acetonitrile: water in 75:25 v/v, column oven temperature: ambient, proportion. The chromatograms were monitored at 286 nm with a flowrate of 1 mL/min. The method was validated according to the ICH. guidelines. Results: Retention time values of synthesized reference standards were found to be identical with retention time values of those degradation products in stressed samples. The calibration curves showed good linear regression (r 2 >0.999) within test ranges. The method showed good reproducibility and sensitivity for quantification of both degradation products in samples. Method was precise and %recovery of both reference products was within 98-102%. Conclusion: This communication emphasizes use of non-compendial reference standards for quantification of degradation products by chromatographic methods. Quantitative validation parameters like Limit of detection and Limit of quantitation were established. Key words: Degradation impurities, Fenofibrate, Non-compendial reference standards, RP-HPLC, Retention time matching.
非诺贝特降解产物标准品的RP-HPLC-UV鉴别方法
背景:在非诺贝特的应力降解研究中,分别在碱性和酸性水解条件下,采用LC-MS/MS表征了2-[4-(4-氯苯甲酰)苯氧基]-2-甲基丙酸和2-[4-(4-氯苯甲酰)苯氧基]-2-甲基丙酸两种主要降解产物的结构。本文介绍了降解产物参考标准的合成、光谱表征和进一步应用,并通过保留时间匹配研究对药物散装样品中的降解产物进行鉴定。方法:在实验室合成降解产物的标准品,用波谱法对其进行鉴定。这些被用于HPLC研究的保留匹配研究。色谱条件为:固定相:Waters X Bridge c18色谱柱(250x4.6 mm,内径,粒径5 μm),流动相:乙腈:水75:25 v/v,柱箱温度:常温,比例。以1 mL/min的流速在286 nm处监测色谱。根据ICH对方法进行了验证。指导方针。结果:合成标准品的保留时间与这些降解产物在应力样品中的保留时间相同。校准曲线在测试范围内线性回归良好(r 2 >0.999)。该方法对样品中两种降解产物的定量具有良好的重现性和灵敏度。方法精密度高,两种标准品回收率在98 ~ 102%之间。结论:本通讯强调使用非药典参考标准品通过色谱法定量降解产物。建立了检出限、定量限等定量验证参数。关键词:降解杂质,非诺贝特,非药典标准品,反相高效液相色谱,保留时间匹配
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信