Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, Zurich, Switzerland.
Merck Serono S.A. Biotech Process Sciences, Corsier-sur-Vevey, Switzerland.
Biotechnol Bioeng. 2020 May;117(5):1367-1380. doi: 10.1002/bit.27296. Epub 2020 Feb 17.
Integrated continuous manufacturing is entering the biopharmaceutical industry. The main drivers range from improved economics, manufacturing flexibility, and more consistent product quality. However, studies on fully integrated production platforms have been limited due to the higher degree of system complexity, limited process information, disturbance, and drift sensitivity, as well as difficulties in digital process integration. In this study, we present an automated end-to-end integrated process consisting of a perfusion bioreactor, CaptureSMB, virus inactivation (VI), and two polishing steps to produce an antibody from an instable cell line. A supervisory control and data acquisition (SCADA) system was developed, which digitally integrates unit operations and analyzers, collects and centrally stores all process data, and allows process-wide monitoring and control. The integrated system consisting of bioreactor and capture step was operated initially for 4 days, after which the full end-to-end integrated run with no interruption lasted for 10 days. In response to decreasing cell-specific productivity, the supervisory control adjusted the loading duration of the capture step to obtain high capacity utilization without yield loss and constant antibody quantity for subsequent operations. Moreover, the SCADA system coordinated VI neutralization and discharge to enable constant loading conditions on the polishing unit. Lastly, the polishing was sufficiently robust to cope with significantly increased aggregate levels induced on purpose during virus inactivation. It is demonstrated that despite significant process disturbances and drifts, a robust process design and the supervisory control enabled constant (optimum) process performance and consistent product quality.
集成式连续生产正在进入生物制药行业。主要驱动力包括提高经济性、制造灵活性和更一致的产品质量。然而,由于系统复杂性更高、过程信息有限、干扰和漂移敏感以及数字化过程集成困难,对完全集成生产平台的研究一直受到限制。在本研究中,我们提出了一种自动化的端到端集成工艺,该工艺由灌流生物反应器、CaptureSMB、病毒灭活 (VI) 和两个纯化步骤组成,用于从不稳定的细胞系生产抗体。开发了一个监督控制和数据采集 (SCADA) 系统,该系统将单元操作和分析仪进行数字化集成,收集和集中存储所有过程数据,并允许进行全过程监测和控制。由生物反应器和捕获步骤组成的集成系统最初运行了 4 天,然后无中断地进行了 10 天的全端到端集成运行。为了应对细胞特异性生产率的下降,监督控制调整了捕获步骤的加载持续时间,以在不损失产量的情况下实现高容量利用率,并为后续操作提供恒定的抗体数量。此外,SCADA 系统协调了 VI 中和和排放,以在抛光单元上实现恒定的加载条件。最后,抛光足够稳健,可以应对在 VI 过程中故意引入的明显增加的聚集物水平。结果表明,尽管存在显著的过程干扰和漂移,但稳健的过程设计和监督控制实现了恒定(最佳)的过程性能和一致的产品质量。