Towards advanced bioprocess optimization: A multiscale modelling approach

被引:7
作者
Monteiro, Mariana [1 ]
Fadda, Sarah [1 ]
Kontoravdi, Cleo [1 ]
机构
[1] Imperial Coll London, Dept Chem Engn, South Kensington Campus, London SW7 2AZ, England
基金
英国生物技术与生命科学研究理事会;
关键词
Bioprocess control; CHO cells; Metabolic optimization; Process systems; Digital twin; AMINO-ACID-METABOLISM; CONTROL STRATEGIES; BATCH; GLYCOSYLATION; SIMULATION; CELLS; MPC;
D O I
10.1016/j.csbj.2023.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mammalian cells produce up to 80 % of the commercially available therapeutic proteins, with Chinese Hamster Ovary (CHO) cells being the primary production host. Manufacturing involves a train of reactors, the last of which is typically run in fed-batch mode, where cells grow and produce the required protein. The feeding strategy is decided a priori, from either past operations or the design of experiments and rarely considers the current state of the process. This work proposes a Model Predictive Control (MPC) formulation based on a hybrid kinetic-stoichiometric reactor model to provide optimal feeding policies in real-time, which is agnostic to the culture, hence transferable across CHO cell culture systems. The benefits of the proposed controller formulation are demonstrated through a comparison between an open-loop simulation and closed-loop optimization, using a digital twin as an emulator of the process.
引用
收藏
页码:3639 / 3655
页数:17
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