理论(学习稳定性)
强制降级
期限(时间)
生物制药
生物信息学
降级(电信)
化学稳定性
生物系统
色谱法
生化工程
化学
计算机科学
环境科学
高效液相色谱法
机器学习
反相色谱法
生物化学
有机化学
物理
生物
工程类
生药学
生物活性
基因
体外
电信
量子力学
作者
Andreas Evers,Didier Clénet,Stefania Pfeiffer‐Marek
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2022-02-08
卷期号:14 (2): 375-375
被引量:32
标识
DOI:10.3390/pharmaceutics14020375
摘要
A crucial aspect of pharmaceutical development is the demonstration of long-term stability of the drug product. Biopharmaceuticals, such as proteins or peptides in liquid formulation, are typically administered via parental routes and should be stable over the shelf life, which generally includes a storing period (e.g., two years at 5 °C) and optionally an in-use period (e.g., 28 days at 30 °C). Herein, we present a case study where chemical degradation of SAR441255, a therapeutic peptide, in different formulations in combination with primary packaging materials was analyzed under accelerated conditions to derive long-term stability predictions for the recommended storing conditions (two years at 5 °C plus 28 days at 30 °C) using advanced kinetic modeling. These predictions served as a crucial decision parameter for the entry into clinical development. Comparison with analytical data measured under long-term conditions during the subsequent development phase demonstrated a high prediction accuracy. These predictions provided stability insights within weeks that would otherwise take years using measurements under long-term stability conditions only. To our knowledge, such in silico studies on stability predictions of a therapeutic peptide using accelerated chemical degradation data and advanced kinetic modeling with comparisons to subsequently measured real-life long-term stability data have not been described in literature before.
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