背景(考古学)
生化工程
计算机科学
鉴定(生物学)
风险分析(工程)
可制造性设计
质量(理念)
表征(材料科学)
药物发现
数据科学
管理科学
计算生物学
纳米技术
工程类
医学
生物
生物信息学
材料科学
认识论
机械工程
哲学
古生物学
植物
作者
Suzanne M. D’Addio,Jameson R. Bothe,Claudia Neri,Paul L. Walsh,Jingtao Zhang,Elizabeth E. Pierson,Yun Mao,Marian E. Gindy,Anthony Leone,Allen C. Templeton
标识
DOI:10.1016/j.xphs.2016.06.011
摘要
Advances in technologies related to the design and manufacture of therapeutic peptides have enabled researchers to overcome the biological and technological challenges that have limited their application in the past. As a result, peptides of increasing complexity have become progressively important against a variety of disease targets. Developing peptide drug products brings with it unique scientific challenges consistent with the unique physicochemical properties of peptide molecules. The identification of the proper characterization tools is required in order to develop peptide formulations with the appropriate stability, manufacturability, and bioperformance characteristics. This knowledge supports the build of critical quality attributes and, ultimately, regulatory specifications. The purpose of this review article is to provide an overview of the techniques that are employed for analytical characterization of peptide drug products. The techniques covered are highlighted in the context of peptide drug product understanding and include chemical and biophysical approaches. Emphasis is placed on summarizing the recent literature experience in the field. Finally, the authors provide regulatory perspective on these characterization approaches and discuss some potential areas for further research in the field.
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