首页> 外文会议>Conference on single-use technologies II: bridging polymer science to biotechnology applications >ENHANCING MULTIVARIATE CALIBRATION MODEL REPRODUCIBILITY FOR THE ONLINE MONITORING OF UPSTREAM PROCESSES IN CONTINUOUS BIOMANUFACTURING
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ENHANCING MULTIVARIATE CALIBRATION MODEL REPRODUCIBILITY FOR THE ONLINE MONITORING OF UPSTREAM PROCESSES IN CONTINUOUS BIOMANUFACTURING

机译:连续生物制造中上游过程在线监测的多重标定模型重现性

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The complex mixtures present in biomanufacturing processes have traditionally required slow and expensive experimental assays, as well as time consuming and complicated analyses to be characterized properly. Multivariate Data Analysis (MVDA) can be integrated with spectroscopy to uniquely solve both of these problems simultaneously. Spectroscopic data has been generated in real-time, eliminating the need for offline assays; and MVDA has been used to rapidly analyze the data in a straightforward manner. Prior experiments have shown that this paradigm can be used offline to characterize the raw materials that are used to supplement cell culture media. However, online models that reliably quantify extracellular component concentrations in continuous bioprocesses require additional considerations. Even when the components' absorbance properties are well understood, cellular metabolism ensures that nutrient and product profiles vary collinearly with one another. This work explored supplementation strategies that break this collinearity to ensure that proper multivariate calibration models are constructed, instead of soft sensor models whose performance is inconsistent due to their reliance on component concentration collinearity for accurate predictions. This allows for more robust corrective action to be taken. Furthermore, the advantages of training multivariate calibration models from continuous bioprocesses' data, whose steady-state operation allows for more robust and complete design space coverage relative to batch processes, are explored as a way to guide ongoing and future research in this area. Disclaimer: This article reflects the views of the authors and should not be construed to represent official FDA's views or policies.
机译:传统上,生物制造过程中存在的复杂混合物需要缓慢且昂贵的实验分析,以及费时且复杂的分析才能正确表征。多元数据分析(MVDA)可以与光谱法集成在一起,以独特地同时解决这两个问题。光谱数据是实时生成的,无需进行离线分析。 MVDA已被用于以直接的方式快速分析数据。先前的实验表明,该范例可以离线使用,以表征用于补充细胞培养基的原材料。但是,在连续生物过程中可靠地量化细胞外成分浓度的在线模型需要额外考虑。即使很好地了解了组分的吸收特性,细胞新陈代谢也可以确保营养物和产物的分布在同一直线上变化。这项工作探索了打破这种共线性的补充策略,以确保构建适当的多元校准模型,而不是由于依赖精确度预测而依赖成分浓度共线性而导致性能不一致的软传感器模型。这允许采取更可靠的纠正措施。此外,探索了从连续生物过程的数据训练多元校准模型的优势,该模型的稳态操作相对于批处理过程允许更健壮和完整的设计空间覆盖,以此作为指导该领域正在进行和未来研究的一种方法。免责声明:本文反映了作者的观点,不应解释为代表FDA的正式观点或政策。

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