酮洛芬大醇400酯测定方法的证实

E. Bezuglaya, I. Zinchenko, N. Lyapunov, Hanna S. Vlasenko, V. Musatov
{"title":"酮洛芬大醇400酯测定方法的证实","authors":"E. Bezuglaya, I. Zinchenko, N. Lyapunov, Hanna S. Vlasenko, V. Musatov","doi":"10.15587/2519-4852.2021.235980","DOIUrl":null,"url":null,"abstract":"The aim: The work is concerned with the substantiation of the approach to the identification and quantitative determination of ketoprofen macrogol 400 esters. Materials and methods: Ketoprofen, macrogol 400, ketoprofen macrogol 400 ester (KM400E), as well as model cream-gels were studied by the following methods: absorption spectrophotometry ultraviolet (UV) and visible, high-performance liquid chromatography (HPLC), gas chromatography (GC), GC / mass spectrometry, nuclear magnetic resonance (NMR) spectrometry and thermogravimetry. Results: It was found by GC and GC / mass spectrometry that the average molecular mass (Mr) of the test macrogol 400 is 383.50 and it contains oligomers with molecular masses from 150.17 to 546.65. KM400E, which is a mixture of esters of ketoprofen with macrogol oligomers, was synthesized. The formed esters were characterized by 1H NMR spectra. It was shown that the ratio of the average molecular mass of KM400E, calculated for monoesters, and the molecular mass of ketoprofen corresponds to the ratio of specific absorbances of solutions of ketoprofen and solutions of KM400E, this fact indicated the formation of monoesters. Taking into account the risk of variability of the fractional composition of macrogol 400 in different batches, it is advisable to quantify KM400E using ketoprofen reference standard (RS) and not KM400E RS. Using HPLC with diode array detection the peak of KM400E should be identified by the UV absorption spectrum with λmax≈255 nm, which is characteristic for ketoprofen, and the relative retention time (RRt) of the peak; KM400E should be quantified by the content of ketoprofen in this impurity. During storage of model cream-gels the content of KM400E impurity is significantly lower than the content of ketoprofen propylene glycol ester (mixture of isomers). Conclusions: The approach to the identification and quantitative determination of KM400E is substantiated. The analytical procedure for determination of KM400E impurity by HPLC with a diode array detection using ketoprofen RS was developed. Correctness of the procedure was proved by the results of the validation studies.","PeriodicalId":9858,"journal":{"name":"Chemical Engineering (Engineering) eJournal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Substantiation of an Approach to Determination of Ketoprofen Macrogol 400 Esters\",\"authors\":\"E. Bezuglaya, I. Zinchenko, N. Lyapunov, Hanna S. Vlasenko, V. Musatov\",\"doi\":\"10.15587/2519-4852.2021.235980\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The aim: The work is concerned with the substantiation of the approach to the identification and quantitative determination of ketoprofen macrogol 400 esters. Materials and methods: Ketoprofen, macrogol 400, ketoprofen macrogol 400 ester (KM400E), as well as model cream-gels were studied by the following methods: absorption spectrophotometry ultraviolet (UV) and visible, high-performance liquid chromatography (HPLC), gas chromatography (GC), GC / mass spectrometry, nuclear magnetic resonance (NMR) spectrometry and thermogravimetry. Results: It was found by GC and GC / mass spectrometry that the average molecular mass (Mr) of the test macrogol 400 is 383.50 and it contains oligomers with molecular masses from 150.17 to 546.65. KM400E, which is a mixture of esters of ketoprofen with macrogol oligomers, was synthesized. The formed esters were characterized by 1H NMR spectra. It was shown that the ratio of the average molecular mass of KM400E, calculated for monoesters, and the molecular mass of ketoprofen corresponds to the ratio of specific absorbances of solutions of ketoprofen and solutions of KM400E, this fact indicated the formation of monoesters. Taking into account the risk of variability of the fractional composition of macrogol 400 in different batches, it is advisable to quantify KM400E using ketoprofen reference standard (RS) and not KM400E RS. Using HPLC with diode array detection the peak of KM400E should be identified by the UV absorption spectrum with λmax≈255 nm, which is characteristic for ketoprofen, and the relative retention time (RRt) of the peak; KM400E should be quantified by the content of ketoprofen in this impurity. During storage of model cream-gels the content of KM400E impurity is significantly lower than the content of ketoprofen propylene glycol ester (mixture of isomers). Conclusions: The approach to the identification and quantitative determination of KM400E is substantiated. The analytical procedure for determination of KM400E impurity by HPLC with a diode array detection using ketoprofen RS was developed. Correctness of the procedure was proved by the results of the validation studies.\",\"PeriodicalId\":9858,\"journal\":{\"name\":\"Chemical Engineering (Engineering) eJournal\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering (Engineering) eJournal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15587/2519-4852.2021.235980\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering (Engineering) eJournal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15587/2519-4852.2021.235980","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

目的:建立酮洛芬大醇400酯的鉴别和定量测定方法。材料与方法:采用吸收分光光度法、紫外分光光度法、可见分光光度法、高效液相色谱法、气相色谱法、气相质谱法、核磁共振谱法和热重法对酮洛芬、大醇400、酮洛芬大醇400酯(KM400E)以及模型乳凝胶进行了研究。结果:通过GC和GC /质谱分析发现,所测巨醇400的平均分子质量(Mr)为383.50,含有分子量为150.17 ~ 546.65的低聚物。合成了酮洛芬酯与大醇低聚物的混合物KM400E。形成的酯用1H NMR谱进行了表征。结果表明,以单酯计算的KM400E的平均分子质量与酮洛芬的分子质量之比对应于酮洛芬溶液与KM400E溶液的比吸光度之比,这一事实表明了单酯的形成。考虑到不同批次大醇400的组分存在差异的风险,建议采用酮洛芬标准品(RS)而非KM400E标准品(RS)对KM400E进行定量。采用二极管阵列高效液相色谱法检测时,KM400E的峰应采用酮洛芬特有的紫外吸收光谱(λmax≈255 nm)和峰的相对保留时间(RRt)进行鉴别;KM400E应通过该杂质中酮洛芬的含量进行定量。在模型乳凝胶的储存过程中,KM400E杂质的含量明显低于酮洛芬丙二醇酯(异构体混合物)的含量。结论:建立了KM400E的鉴别及定量测定方法。建立了酮洛芬光谱二极管阵列高效液相色谱法测定KM400E杂质的分析方法。验证研究的结果证明了该方法的正确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Substantiation of an Approach to Determination of Ketoprofen Macrogol 400 Esters
The aim: The work is concerned with the substantiation of the approach to the identification and quantitative determination of ketoprofen macrogol 400 esters. Materials and methods: Ketoprofen, macrogol 400, ketoprofen macrogol 400 ester (KM400E), as well as model cream-gels were studied by the following methods: absorption spectrophotometry ultraviolet (UV) and visible, high-performance liquid chromatography (HPLC), gas chromatography (GC), GC / mass spectrometry, nuclear magnetic resonance (NMR) spectrometry and thermogravimetry. Results: It was found by GC and GC / mass spectrometry that the average molecular mass (Mr) of the test macrogol 400 is 383.50 and it contains oligomers with molecular masses from 150.17 to 546.65. KM400E, which is a mixture of esters of ketoprofen with macrogol oligomers, was synthesized. The formed esters were characterized by 1H NMR spectra. It was shown that the ratio of the average molecular mass of KM400E, calculated for monoesters, and the molecular mass of ketoprofen corresponds to the ratio of specific absorbances of solutions of ketoprofen and solutions of KM400E, this fact indicated the formation of monoesters. Taking into account the risk of variability of the fractional composition of macrogol 400 in different batches, it is advisable to quantify KM400E using ketoprofen reference standard (RS) and not KM400E RS. Using HPLC with diode array detection the peak of KM400E should be identified by the UV absorption spectrum with λmax≈255 nm, which is characteristic for ketoprofen, and the relative retention time (RRt) of the peak; KM400E should be quantified by the content of ketoprofen in this impurity. During storage of model cream-gels the content of KM400E impurity is significantly lower than the content of ketoprofen propylene glycol ester (mixture of isomers). Conclusions: The approach to the identification and quantitative determination of KM400E is substantiated. The analytical procedure for determination of KM400E impurity by HPLC with a diode array detection using ketoprofen RS was developed. Correctness of the procedure was proved by the results of the validation studies.
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
期刊最新文献
Deep Eutectic Solvent Assisted Facile and Efficient Synthesis of Nitrogen-Doped Magnetic Biochar for Hexavalent Chromium Elimination: Mechanism and Performance Insights Computational Simulation of Ionization Processes in Single-Bubble and Multi-Bubble Sonoluminescence Microbubbles for Effective Cleaning of Metal Surfaces Without Chemical Agents Unprecedented Age-Hardening and its Structural Requirement in a Severely Deformed Al-Cu-Mg Alloy Elucidating the Interaction of Enantiomeric Cu(Ii) Complexes with DNA, Rna and Hsa: A Comparative Study
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1