Excipient Taxonomy for the 21st Century.

Journal of pharmaceutical sciences(2023)

引用 2|浏览3
暂无评分
摘要
The performance of pharmaceutical dosage forms relies heavily on the characteristics of the excipients that are incorporated into the drug product during the manufacturing process. Therefore, it is imperative that formulators are able to accurately and completely specify the key chemical and physical properties of those excipients. Current approaches to describing excipients are outdated and inadequate for the needs of the 21 century and in this article we highlight the benefits of a more systematic and comprehensive approach to specifying and controlling excipient properties. We hope that this will prompt the users, suppliers, and manufacturers of excipients to take a careful look at current approaches and develop tangible proposals for attaining an enhanced future state.
更多
查看译文
关键词
Drug standards,Excipient(s),Formulation,Quality by design (QBD),Regulatory science,Standards,US pharmacopeia (USP)
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要