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An adaptive modeling approach using spiking-augmentation method to improve chemometric model performance in bioprocess monitoring
Authors:Yuxiang Zhao  Yawen Tang  Dhanuka Wasalathanthri  Jianlin Xu  Julia Ding
Institution:1. Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, Massachusetts, USA;2. Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, Massachusetts, USA

Contribution: Data curation (supporting), Methodology (supporting), Resources (lead);3. Global Product Development and Supply, Bristol-Myers Squibb Company, Devens, Massachusetts, USA

Contribution: Funding acquisition (equal), Project administration (equal), Supervision (equal), Writing - review & editing (equal)

Abstract:Intensified and continuous processes require fast and robust methods and technologies to monitor product titer for faster analytical turnaround time, process monitoring, and process control. The current titer measurements are mostly offline chromatography-based methods which may take hours or even days to get the results back from the analytical labs. Thus, offline methods will not meet the requirement of real time titer measurements for continuous production and capture processes. FTIR and chemometric based multivariate modeling are promising tools for real time titer monitoring in clarified bulk (CB) harvests and perfusate lines. However, empirical models are known to be vulnerable to unseen variability, specifically a FTIR chemometric titer model trained on a given biological molecule and process conditions often fails to provide accurate predictions of titer in another molecule under different process conditions. In this study, we developed an adaptive modeling strategy: the model was initially built using a calibration set of available perfusate and CB samples and then updated by augmenting spiking samples of the new molecules to the calibration set to make the model robust against perfusate or CB harvest of the new molecule. This strategy substantially improved the model performance and significantly reduced the modeling effort for new molecules.
Keywords:adaptive modeling  data augmentation  Fourier transform infrared (FTIR) spectroscopy  monoclonal antibody  partial least squares regression  process analytical technology (PAT)  titer
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