Senthil Kumar Pichandi Mohanraj, R. Tulasi, Venkatesan Chidambaram Subramanian, B. Dandu, Vinodh Guvvala, Srinivas Kota
{"title":"用LC/ESI/QTOF/MS/MS和NMR表征糖madex钠潜在杂质的结构","authors":"Senthil Kumar Pichandi Mohanraj, R. Tulasi, Venkatesan Chidambaram Subramanian, B. Dandu, Vinodh Guvvala, Srinivas Kota","doi":"10.2139/ssrn.3856020","DOIUrl":null,"url":null,"abstract":"The first selective relaxant binding agent (SRBA), Sugammadex sodium (SGS) is used to reverse anesthesia. A study of the process related and degradation products will help to optimize process parameters and also to develop the analytical methods and set the quality standard for a quality control strategy in pharmaceutical industry. During the manufacture of SGS, all the process related impurities are controlled in every stage and process related and degradation products are controlled in the active pharmaceutical ingredient (API) as per ICH guidelines. A total of nine process related and degradation impurities of SGS (Impurity-A to Impurity-I) were isolated and characterized by using LC/ESI/QTOF/MS/MS and NMR studies.","PeriodicalId":19957,"journal":{"name":"PharmSciRN: Analytical Chemistry Techniques & Methods (Topic)","volume":"149 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"A Study on Structural Characterization of Potential Impurities of Sugammadex Sodium Using LC/ESI/QTOF/MS/MS and NMR\",\"authors\":\"Senthil Kumar Pichandi Mohanraj, R. Tulasi, Venkatesan Chidambaram Subramanian, B. Dandu, Vinodh Guvvala, Srinivas Kota\",\"doi\":\"10.2139/ssrn.3856020\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The first selective relaxant binding agent (SRBA), Sugammadex sodium (SGS) is used to reverse anesthesia. A study of the process related and degradation products will help to optimize process parameters and also to develop the analytical methods and set the quality standard for a quality control strategy in pharmaceutical industry. During the manufacture of SGS, all the process related impurities are controlled in every stage and process related and degradation products are controlled in the active pharmaceutical ingredient (API) as per ICH guidelines. A total of nine process related and degradation impurities of SGS (Impurity-A to Impurity-I) were isolated and characterized by using LC/ESI/QTOF/MS/MS and NMR studies.\",\"PeriodicalId\":19957,\"journal\":{\"name\":\"PharmSciRN: Analytical Chemistry Techniques & Methods (Topic)\",\"volume\":\"149 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"PharmSciRN: Analytical Chemistry Techniques & Methods (Topic)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2139/ssrn.3856020\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"PharmSciRN: Analytical Chemistry Techniques & Methods (Topic)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2139/ssrn.3856020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Study on Structural Characterization of Potential Impurities of Sugammadex Sodium Using LC/ESI/QTOF/MS/MS and NMR
The first selective relaxant binding agent (SRBA), Sugammadex sodium (SGS) is used to reverse anesthesia. A study of the process related and degradation products will help to optimize process parameters and also to develop the analytical methods and set the quality standard for a quality control strategy in pharmaceutical industry. During the manufacture of SGS, all the process related impurities are controlled in every stage and process related and degradation products are controlled in the active pharmaceutical ingredient (API) as per ICH guidelines. A total of nine process related and degradation impurities of SGS (Impurity-A to Impurity-I) were isolated and characterized by using LC/ESI/QTOF/MS/MS and NMR studies.