克隆(Java方法)
效价
生物制药
生产力
校准
克隆选择
拉曼光谱
可转让性
生物
计算生物学
计算机科学
生物技术
生物化学
统计
遗传学
数学
机器学习
免疫学
光学
物理
DNA
宏观经济学
罗伊特
抗体
经济
作者
Rafael Machleid,Marek Hoehse,Steffi Scholze,Kleanthis Mazarakis,David Nilsson,Erik Johansson,Christoph Zehe,Johan Trygg,Christian Grimm,Izabella Surowiec
标识
DOI:10.1002/biot.202300289
摘要
Raman spectroscopy is widely used in monitoring and controlling cell cultivations for biopharmaceutical drug manufacturing. However, its implementation for culture monitoring in the cell line development stage has received little attention. Therefore, the impact of clonal differences, such as productivity and growth, on the prediction accuracy and transferability of Raman calibration models is not yet well described. Raman OPLS models were developed for predicting titer, glucose and lactate using eleven CHO clones from a single cell line. These clones exhibited diverse productivity and growth rates. The calibration models were evaluated for clone-related biases using clone-wise linear regression analysis on cross validated predictions. The results revealed that clonal differences did not affect the prediction of glucose and lactate, but titer models showed a significant clone-related bias, which remained even after applying variable selection methods. The bias was associated with clonal productivity and lead to increased prediction errors when titer models were transferred to cultivations with productivity levels outside the range of their training data. The findings demonstrate the feasibility of Raman-based monitoring of glucose and lactate in cell line development with high accuracy. However, accurate titer prediction requires careful consideration of clonal characteristics during model development.
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