The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kongens, Lyngby, Denmark.
Department of Chemical and Biochemical Engineering, Technical University of Denmark, Kongens, Lyngby, Denmark.
Biotechnol Bioeng. 2022 Apr;119(4):1077-1090. doi: 10.1002/bit.28032. Epub 2022 Jan 21.
The ever-increasing demand for biopharmaceuticals has created the need for improving the overall productivity of culture processes. One such operational concept that is considered is fed-batch operations as opposed to batch operations. However, optimal fed-batch operations require complete knowledge of the cell culture to optimize the culture conditions and the nutrients feeding. For example, when using high-throughput small-scale bioreactors to test multiple clones that do not behave the same, depletion or overfeeding of some key components can occur if the feeding strategy is not individually optimized. Over the recent years, various solutions for real-time measuring of the main cell culture metabolites have been proposed. Still, the complexity in the implementation of these techniques has limited their use. Soft-sensors present an opportunity to overcome these limitations by indirectly estimating these variables in real-time. This manuscript details the development of a new soft-sensor-based fed-batch strategy to maintain substrate concentration (glucose and glutamine) at optimal levels in small-scale multiparallel Chinese Hamster Ovary Cells cultures. Two alternatives to the standard feeding strategy were tested: an OUR soft-sensor-based strategy for glucose and glutamine (Strategy 1) and a dual OUR for glutamine and CO /alkali addition for glucose soft-sensor strategy (Strategy 2). The results demonstrated the applicability of the OUR soft-sensor-based strategy to optimize glucose and glutamine feedings, which yielded a 21% increase in final viable cell density (VCD) and a 31% in erythropoietin titer compared with the reference one. However, CO /alkali addition soft-sensor suffered from insufficient data to relate alkali addition with glucose consumption. As a result, the culture was overfed with glucose resulting in a 4% increase on final VCD, but a 9% decrease in final titer compared with the Reference Strategy.
不断增长的生物制药需求要求提高培养过程的整体生产力。一种被认为是批处理操作的操作概念是补料分批操作。然而,最佳的补料分批操作需要完全了解细胞培养,以优化培养条件和营养物的供给。例如,当使用高通量小型生物反应器测试多个表现不同的克隆时,如果不单独优化进料策略,一些关键成分可能会耗尽或过量。近年来,已经提出了各种用于实时测量主要细胞培养代谢物的解决方案。然而,这些技术的实施复杂性限制了它们的使用。软传感器提供了一个机会,可以通过实时间接估计这些变量来克服这些限制。本文详细介绍了开发一种新的基于软传感器的补料分批策略,以在小型多平行中国仓鼠卵巢细胞培养物中维持基质浓度(葡萄糖和谷氨酰胺)处于最佳水平。测试了两种替代标准进料策略的方法:基于比耗氧速率(OUR)的葡萄糖和谷氨酰胺软传感器策略(策略 1)和用于谷氨酰胺的双 OUR 以及用于葡萄糖软传感器的 CO/碱添加策略(策略 2)。结果表明,基于 OUR 的软传感器策略适用于优化葡萄糖和谷氨酰胺的进料,与参考策略相比,最终活细胞密度(VCD)增加了 21%,促红细胞生成素滴度增加了 31%。然而,CO/碱添加软传感器由于缺乏与葡萄糖消耗相关的数据而受到限制。因此,培养物中葡萄糖过量,最终 VCD 增加了 4%,但最终滴度与参考策略相比下降了 9%。