Optimized process operations reduce product retention and column clogging in ATF-based perfusion cell cultures

中国仓鼠卵巢细胞 保留率 色谱法 粒径 化学工程 体积流量 材料科学 纤维 化学 堵塞 生物医学工程 生物物理学 复合材料 生物化学 生物 工程类 受体 考古 物理 历史 医学 量子力学 计算机科学 计算机安全
作者
Yuning Su,Zhaohui Wei,Yana Miao,Liuliu Sun,Yina Shen,Ziran Tang,Le Li,Yufen Quan,Haiyang Yu,Wei‐Chun Wang,Weichang Zhou,Jun Tian
出处
期刊:Applied Microbiology and Biotechnology [Springer Nature]
卷期号:105 (24): 9125-9136 被引量:10
标识
DOI:10.1007/s00253-021-11662-8
摘要

Product retention in hollow fibers is a common issue in ATF-based cell culture system. In this study, the effects of four major process factors on product (therapeutic antibody/recombinant protein) retention were investigated using Chinese hamster ovary cell. Hollow fibers made of polysulfone presented a product retention rate from 15% ± 8 to 43% ± 18% higher than those made of polyether sulfone varying with specific processes. Higher harvest flowrate and ATF exchange rate increased product retention by 13% ± 10% and up to 31% ± 13%, respectively. Hollow fibers with larger pore sizes (0.65 μm) appeared to have increased product retention by 38% ± 7% compared with smaller ones (0.2 μm) in this study. Further investigation revealed that the effects of pore size on retention could be correlated to the particle size distribution in the cell culture broth. A hollow fiber with a larger pore size (>0.5 μm) may reduce protein retention when small particles (approximately 0.01–0.2 μm in diameter) are dominant in the culture. However, if majority of the particles are larger than 0.2 μm in diameter, hollow fiber with smaller pore sizes (0.2 μm) could be a solution to reducing product retention. Alternatively, process optimization may modulate particle size distribution towards reduced production retention with selected ATF hollow fibers. This study for the first time highlights the importance of matching proper pore sizes of hollow fibers with the cell culture particles distribution and offers methods to reducing product retention and ATF column clogging in perfusion cell cultures.
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