Suppr超能文献

含痕量甲醛的高效液相色谱级甲醇中药物的降解。

Degradation of a pharmaceutical in HPLC grade methanol containing trace level formaldehyde.

机构信息

Department of Small Molecule Pharmaceutical Sciences, Genentech, Inc. 1 DNA Way, South San Francisco, CA, USA.

出版信息

Pharm Dev Technol. 2013 Jul-Aug;18(4):877-82. doi: 10.3109/10837450.2012.696265. Epub 2012 Jun 12.

Abstract

An anomalous peak was observed in the HPLC/UV analysis of a developmental drug product. High resolution LC/MS revealed that the mass of this degradant was 12 Da greater than the drug substance, corresponding to a net gain of a single carbon atom. The degradant was reproduced by incubating the drug substance with formaldehyde, followed by isolation using normal phase chromatography and structure elucidation by NMR. It was determined to be an analytical artifact caused by the nucleophilic reaction of the drug substance with trace levels of formaldehyde in the methanol diluent. Typical formaldehyde levels in various grades of methanol were determined, leading to the adoption of spectrophotometric purity solvent to mitigate the recurrence of this artifact. This work demonstrates that even ppm levels of impurities in solvents can cause significant degradation of drug product and the HPLC grade solvents are not always suitable for HPLC analysis in drug product development.

摘要

在对一种开发中的药物产品进行 HPLC/UV 分析时,观察到一个异常峰。高分辨率 LC/MS 显示,该降解产物的质量比药物母体大 12 Da,对应于单个碳原子的净增加。通过使药物母体与甲醛孵育,然后使用正相色谱法分离,并通过 NMR 进行结构阐明,可重现该降解产物。确定它是由药物母体与甲醇稀释剂中痕量甲醛的亲核反应引起的分析性假象。测定了各种级别的甲醇中的典型甲醛水平,导致采用分光光度纯度溶剂来减轻该假象的重现。这项工作表明,即使溶剂中的杂质 ppm 水平也会导致药物产品的显著降解,并且 HPLC 级溶剂并不总是适合药物产品开发中的 HPLC 分析。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验