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用于动态灌注细胞培养过程计算机模拟优化的混合建模

Hybrid modeling for in silico optimization of a dynamic perfusion cell culture process.

作者信息

Agarwal Piyush, McCready Chris, Ng Say Kong, Ng Jake Chng, van de Laar Jeroen, Pennings Maarten, Zijlstra Gerben

机构信息

Sartorius Corporate Research, Oakville, Ontario, Canada.

Bioprocessing Technology Institute (BTI), A*STAR, Biopolis Way, Singapore.

出版信息

Biotechnol Prog. 2025 Jan-Feb;41(1):e3503. doi: 10.1002/btpr.3503. Epub 2024 Sep 18.

DOI:10.1002/btpr.3503
PMID:39291457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11831417/
Abstract

The bio-pharmaceutical industry heavily relies on mammalian cells for the production of bio-therapeutic proteins. The complexity of implementing and high cost-of-goods of these processes are currently limiting more widespread patient access. This is driving efforts to enhance cell culture productivity and cost reduction. Upstream process intensification (PI), using perfusion approaches in the seed train and/or the main bioreactor, has shown substantial promise to enhance productivity. However, developing optimal process conditions for perfusion-based processes remain challenging due to resource and time constraints. Model-based optimization offers a solution by systematically screening process parameters like temperature, pH, and culture media to find the optimum conditions in silico. To our knowledge, this is the first experimentally validated model to explain the perfusion dynamics under different operating conditions and scales for process optimization. The hybrid model accurately describes Chinese hamster ovary (CHO) cell culture growth dynamics and a neural network model explains the production of mAb, allowing for optimization of media exchange rates. Results from six perfusion runs in Ambr® 250 demonstrated high accuracy, confirming the model's utility. Further, the implementation of dynamic media exchange rate schedule determined through model-based optimization resulted in 50% increase in volumetric productivity. Additionally, two 5 L-scale experiments validated the model's reliable extrapolation capabilities to large bioreactors. This approach could reduce the number of wet lab experiments needed for culture process optimization, offering a promising avenue for improving productivity, cost-of-goods in bio-pharmaceutical manufacturing, in turn improving patient access to pivotal medicine.

摘要

生物制药行业严重依赖哺乳动物细胞来生产生物治疗蛋白。这些工艺实施的复杂性和高昂的生产成本目前限制了更多患者的可及性。这推动了提高细胞培养生产力和降低成本的努力。上游过程强化(PI),即在种子培养和/或主生物反应器中采用灌注方法,已显示出提高生产力的巨大潜力。然而,由于资源和时间限制,为基于灌注的工艺开发最佳工艺条件仍然具有挑战性。基于模型的优化提供了一种解决方案,通过系统地筛选温度、pH值和培养基等工艺参数,在计算机上找到最佳条件。据我们所知,这是第一个经过实验验证的模型,用于解释不同操作条件和规模下的灌注动力学以进行工艺优化。该混合模型准确描述了中国仓鼠卵巢(CHO)细胞培养的生长动力学,神经网络模型解释了单克隆抗体的产生,从而能够优化培养基交换率。在Ambr® 250中进行的六次灌注运行结果显示出高精度,证实了该模型的实用性。此外,通过基于模型的优化确定的动态培养基交换率时间表的实施使体积生产力提高了50%。此外,两个5升规模的实验验证了该模型对大型生物反应器的可靠外推能力。这种方法可以减少培养工艺优化所需的湿实验室实验数量,为提高生物制药生产的生产力、降低成本提供了一条有前景的途径,进而改善患者获得关键药物的机会。

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本文引用的文献

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Biotechnol J. 2024 Jul;19(7):e2400092. doi: 10.1002/biot.202400092.
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Hybrid deep modeling of a CHO-K1 fed-batch process: combining first-principles with deep neural networks.CHO-K1 补料分批培养过程的混合深度建模:将第一性原理与深度神经网络相结合。
Front Bioeng Biotechnol. 2023 Sep 8;11:1237963. doi: 10.3389/fbioe.2023.1237963. eCollection 2023.
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Progress in fed-batch culture for recombinant protein production in CHO cells.
补料分批培养 CHO 细胞生产重组蛋白的进展。
Appl Microbiol Biotechnol. 2023 Feb;107(4):1063-1075. doi: 10.1007/s00253-022-12342-x. Epub 2023 Jan 17.
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Comparison of mechanistic and hybrid modeling approaches for characterization of a CHO cultivation process: Requirements, pitfalls and solution paths.用于表征中国仓鼠卵巢细胞(CHO)培养过程的机理建模方法与混合建模方法的比较:要求、陷阱及解决途径。
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Model-based intensification of CHO cell cultures: One-step strategy from fed-batch to perfusion.基于模型的CHO细胞培养强化:从补料分批培养到灌注培养的一步式策略。
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