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降解产物分析在活性药物成分和药品中的作用。

The role of degradant profiling in active pharmaceutical ingredients and drug products.

作者信息

Alsante Karen M, Ando Akemi, Brown Roland, Ensing Janice, Hatajik Todd D, Kong Wei, Tsuda Yoshiko

机构信息

Pfizer Global Research and Development, Analytical Research and Development, Eastern Point Road, Groton, CT 06340, USA.

出版信息

Adv Drug Deliv Rev. 2007 Jan 10;59(1):29-37. doi: 10.1016/j.addr.2006.10.006. Epub 2006 Nov 15.

Abstract

Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products. In order to fulfill development and regulatory needs, this publication provides a roadmap for when and how to perform studies, helpful tools in designing rugged scientific studies, and guidance on how to record and communicate results.

摘要

强制降解研究用于促进分析方法的开发,更好地了解活性药物成分(API)和药品(DP)的稳定性,并提供有关降解途径和降解产物的信息。为满足开发和监管需求,本出版物提供了何时以及如何进行研究的路线图、设计稳健科学研究的有用工具,以及关于如何记录和传达结果的指南。

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