MilliporeSigma, Bedford 01730, MA, USA.
Biotechnol J. 2019 Feb;14(2):e1700718. doi: 10.1002/biot.201700718. Epub 2018 Jun 12.
Viral inactivation plays a critical role in assuring the safety of monoclonal antibody (mAb) therapeutics. Traditional viral inactivation involves large holding tanks in which product is maintained at a target low pH for a defined hold time, typically 30-60 min. The drive toward continuous processing and improved facility utilization has provided motivation for development of a continuous viral inactivation process. To this end, a lab-scale prototype viral inactivation system was designed, built, and characterized. Multiple incubation chamber designs are evaluated to identify the optimal design that enables narrow residence time distributions in continuous flow systems. Extensive analysis is conducted supporting rapid low pH viral inactivation and included evaluations with multiple viruses, a range of pH levels, buffer compositions, mAb concentrations, and temperatures. Multiple test conditions are evaluated using the in-line system and results compared to traditional batch-mode viral inactivation. Comparability in kinetics of virus inactivation suggests equivalency between the two approaches.
病毒灭活在确保单克隆抗体 (mAb) 治疗药物的安全性方面起着至关重要的作用。传统的病毒灭活涉及大型储罐,在该储罐中,产品在目标低 pH 值下保持一定的停留时间,通常为 30-60 分钟。对连续处理和提高设施利用率的推动,为连续病毒灭活工艺的开发提供了动力。为此,设计、构建和表征了实验室规模的原型病毒灭活系统。评估了多种孵育室设计,以确定最佳设计,从而在连续流动系统中实现狭窄的停留时间分布。进行了广泛的分析以支持快速低 pH 值病毒灭活,并使用多种病毒、多种 pH 值、缓冲液组成、mAb 浓度和温度进行了评估。使用在线系统评估了多个测试条件,并将结果与传统的批处理病毒灭活进行了比较。病毒灭活动力学的可比性表明两种方法具有等效性。