多奈哌齐测定的应力降解研究及稳定性指示方法的建立

H. AhmedReema, Bhusari K.P, Tajne Mr
{"title":"多奈哌齐测定的应力降解研究及稳定性指示方法的建立","authors":"H. AhmedReema, Bhusari K.P, Tajne Mr","doi":"10.1234/JGPT.V3I11.458","DOIUrl":null,"url":null,"abstract":"This study describes the development and validation of stability indicating RP-HPLC method for Mirtazapine, an antidepressant drug. In order to investigate the stability of drug, a stress testing of drug sample by exposing it to variety of forced degradation conditions has been recommended. Mirtazapine was subjected to stress degradation 1 under different conditions recommended by International conference on Harmonization (ICH). The ICH guideline gives parameters to be considered when validating methods, the objective of validation of an analytical procedure is to demonstrate that it is suitable for its intended purpose. Stress testing methods are screening methods to be used to understand the degradation chemistry of a drug and therefore do not need to be validate to the extent of final control methods. The sample so generated was used to develop a stability indicating High Performance liquid Chromatographic method for Mirtazapine. The chromatographic separation of Mirtazapine and its degradation products was done on C18 column. The mobile phase containing mixture of Water and Acetonitrile in ratio 80:20 was found to be most satisfactory at a flow rate of 1mllmin. Detection was carried out using single wavelength detector at 225nm. The retention time under optimized chromatographic condition was found to be 8.43 minutes, with asymmetry of 1.50. A good linear response was observed in the range of 5-25ug/ml. The method showed good recoveries (average 101.37).","PeriodicalId":15889,"journal":{"name":"Journal of Global Pharma Technology","volume":"37 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2012-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"STRESS DEGRADATION STUDIES AND DEVELOPMENT OF VALIDATED STABILITY INDICATING METHOD FOR ASSAY OF DONEPEZIL\",\"authors\":\"H. AhmedReema, Bhusari K.P, Tajne Mr\",\"doi\":\"10.1234/JGPT.V3I11.458\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study describes the development and validation of stability indicating RP-HPLC method for Mirtazapine, an antidepressant drug. In order to investigate the stability of drug, a stress testing of drug sample by exposing it to variety of forced degradation conditions has been recommended. Mirtazapine was subjected to stress degradation 1 under different conditions recommended by International conference on Harmonization (ICH). The ICH guideline gives parameters to be considered when validating methods, the objective of validation of an analytical procedure is to demonstrate that it is suitable for its intended purpose. Stress testing methods are screening methods to be used to understand the degradation chemistry of a drug and therefore do not need to be validate to the extent of final control methods. The sample so generated was used to develop a stability indicating High Performance liquid Chromatographic method for Mirtazapine. The chromatographic separation of Mirtazapine and its degradation products was done on C18 column. The mobile phase containing mixture of Water and Acetonitrile in ratio 80:20 was found to be most satisfactory at a flow rate of 1mllmin. Detection was carried out using single wavelength detector at 225nm. The retention time under optimized chromatographic condition was found to be 8.43 minutes, with asymmetry of 1.50. A good linear response was observed in the range of 5-25ug/ml. The method showed good recoveries (average 101.37).\",\"PeriodicalId\":15889,\"journal\":{\"name\":\"Journal of Global Pharma Technology\",\"volume\":\"37 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-02-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Global Pharma Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1234/JGPT.V3I11.458\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Global Pharma Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1234/JGPT.V3I11.458","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

本研究描述了抗抑郁药米氮平稳定性指示反相高效液相色谱法的建立和验证。为了研究药物的稳定性,建议对药物样品进行压力测试,使其暴露于各种强制降解条件下。米氮平在国际统一会议(ICH)推荐的不同条件下进行应激降解1。ICH指南给出了验证方法时要考虑的参数,分析方法验证的目的是证明其适合其预期用途。压力测试方法是用于了解药物降解化学的筛选方法,因此不需要验证到最终控制方法的程度。所生成的样品用于建立稳定性指示的高效液相色谱法测定米氮平。采用C18色谱柱对米氮平及其降解产物进行色谱分离。流动相中水与乙腈的比例为80:20,流速为1mmol / min时效果最佳。采用单波长检测器,检测波长为225nm。优化色谱条件下的保留时间为8.43 min,不对称性为1.50。在5 ~ 25ug/ml范围内具有良好的线性响应。该法回收率高,平均为101.37。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
STRESS DEGRADATION STUDIES AND DEVELOPMENT OF VALIDATED STABILITY INDICATING METHOD FOR ASSAY OF DONEPEZIL
This study describes the development and validation of stability indicating RP-HPLC method for Mirtazapine, an antidepressant drug. In order to investigate the stability of drug, a stress testing of drug sample by exposing it to variety of forced degradation conditions has been recommended. Mirtazapine was subjected to stress degradation 1 under different conditions recommended by International conference on Harmonization (ICH). The ICH guideline gives parameters to be considered when validating methods, the objective of validation of an analytical procedure is to demonstrate that it is suitable for its intended purpose. Stress testing methods are screening methods to be used to understand the degradation chemistry of a drug and therefore do not need to be validate to the extent of final control methods. The sample so generated was used to develop a stability indicating High Performance liquid Chromatographic method for Mirtazapine. The chromatographic separation of Mirtazapine and its degradation products was done on C18 column. The mobile phase containing mixture of Water and Acetonitrile in ratio 80:20 was found to be most satisfactory at a flow rate of 1mllmin. Detection was carried out using single wavelength detector at 225nm. The retention time under optimized chromatographic condition was found to be 8.43 minutes, with asymmetry of 1.50. A good linear response was observed in the range of 5-25ug/ml. The method showed good recoveries (average 101.37).
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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:604180095
Book学术官方微信