Development and optimization of biopharmaceutical production processes with cell cultures is cost- and time-consuming and often performed rather empirically. Efficient optimization of multiple-objectives like process time, viable cell density, number of operating steps & cultivation scales, required medium, amount of product as well as product quality depicts a promising approach. This contribution presents a workflow which couples uncertainty-based upstream simulation and Bayes optimization using Gaussian processes. Its application is demonstrated in a simulation case study for a relevant industrial task in process development, the design of a robust cell culture expansion process (seed train), meaning that despite uncertainties and variabilities concerning cell growth, low variations of viable cell density during the seed train are obtained. Compared to a non-optimized reference seed train, the optimized process showed much lower deviation rates regarding viable cell densities (<~10% instead of 41.7%) using 5 or 4 shake flask scales and seed train duration could be reduced by 56 h from 576 h to 520 h. Overall, it is shown that applying Bayes optimization allows for optimization of a multi-objective optimization function with several optimizable input variables and under a considerable amount of constraints with a low computational effort. This approach provides the potential to be used in form of a decision tool, e.g. for the choice of an optimal and robust seed train design or for further optimization tasks within process development.
翻译:高效优化多种目标,例如工艺时间、可行的细胞密度、可行的细胞密度、操作步骤和种植规模的数量、要求的介质、产品数量以及产品质量,体现了一种有希望的方法。这一贡献展示了一种工作流程,即使用高山工艺,同时使用基于不确定性的上游模拟和巴耶斯优化,同时使用高山工艺进行上游和巴耶斯优化;其应用表现为在模拟案例研究中进行相关工业开发,设计强大的细胞文化扩展进程(种子列车),这意味着尽管在细胞增长方面存在着不确定性和变异性,但在种子列期间获取了可行的细胞密度的低变异性。与非优化参考种子列相比,优化流程显示了在可行的细胞密度( ⁇ 10%而不是41.7%)方面的偏差率要低得多,使用5或4个摇动板标标尺和种子列车期限可以减少56小时,从576小时减少到520小时。总体而言,其应用贝耶斯优化使得能够优化多目标的优化开发功能,在种子列列列车期间实现若干优化的种子密度密度变化,在最佳设计努力中可以进一步使用一个最优化的变数。