在 perfusion 生物反应器中开发病毒污染模型,以建立集成连续生物处理的合理控制策略
Takao Ito1, Takashi Nihei2, Koichi Yamamoto3
1Merck Ltd. (An Affiliate of Merck KGaA, Darmstadt, Germany), Koto-ku, Tokyo, Japan.
Biotechnology and bioengineering
|May 14, 2025
概括
一个新的模型评估了连续生物制造中的病毒污染,显示每日取样和9LRV清除确保了产品的安全性,即使在未检测到的病毒.
科学领域:
- 生物技术是生物技术.
- 病毒学 病毒学
- 工艺工程是过程工程.
背景情况:
- 持续的生物制造需要强大的病毒安全策略.
- 评估病毒污染对下游清除的影响至关重要.
研究的目的:
- 为稳定状态 perfusion 细胞培养开发病毒污染模型.
- 评估采样频率和体积对病毒清除因子的影响.
- 评估综合连续生物制造中的病毒风险.
主要方法:
- 细胞和病毒的种群平衡率方程.
- 纳入病毒感染周期和细胞保留装置选.
- 模拟内源性和偶然性病毒污染场景.
主要成果:
- 模型预测可行的细胞密度下降后污染 (例如,MVM从第4天).
- 为了达到99.999%的产品安全,需要总下游清除>15LRV.
- 如果计划去除未检测到的病毒,每日采样和9个LRV清除就足够了.
结论:
- 该模型有效地模拟病毒污染场景.
- 它有助于评估持续生物制造的病毒安全策略.
- 优化的采样和清除策略可以提高生物工艺的安全性.
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