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Development of a novel and efficient cell culture flocculation process using a stimulus responsive polymer to streamline antibody purification processes

机译:使用刺激响应性聚合物简化抗体纯化过程的新型高效细胞培养物絮凝过程的开发

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摘要

Recent advances in mammalian cell culture processes have significantly increased product titers, but have also resulted in substantial increases in cell density and cellular debris as well as process and product related impurities. As such, with improvements in titer, corresponding improvements in downstream processing are essential. In this study we have developed an alternative antibody harvest process that incorporates flocculation using a novel stimulus responsive polymer, benzylated poly(allylamine), followed by depth filtration. As tested on multiple antibodies, this process demonstrates high process yield, improved clearance of cells and cell debris, and efficient reduction of aggregates, host cell proteins (HCP) and DNA. A wide operating window was established for this novel flocculation process through design of experiments condition screening and optimization. Residual levels of impurities in the Protein A eluate were achieved that potentially meet requirements of drug substance and thus alleviate the burden for further impurities removal in subsequent chromatography steps. In addition, efficient clearance of residual polymer was demonstrated using a fluorescence tagged polymer in the presence of a stimulus reagent. The mechanism of HCP and aggregates removal during flocculation was also explored. This novel and efficient process can be easily integrated into current mAb purification platforms, and may overcome downstream processing challenges. Biotechnol. Bioeng. 2013;110: 2928–2937. © 2013 Wiley Periodicals, Inc.
机译:哺乳动物细胞培养过程的最新进展显着提高了产品滴度,但也导致细胞密度和细胞碎片以及与过程和产品相关的杂质大量增加。这样,随着滴度的改善,下游加工的相应改善是必不可少的。在这项研究中,我们开发了一种替代的抗体收获方法,该方法包括使用新型刺激反应性聚合物苄基化聚烯丙胺进行絮凝,然后进行深度过滤。如对多种抗体的测试所示,此过程证明了高产率,提高了细胞和细胞碎片的清除率,并有效减少了聚集体,宿主细胞蛋白(HCP)和DNA。通过设计实验条件筛选和优化,为新型絮凝过程建立了广阔的操作窗口。蛋白A洗脱液中残留的杂质水平达到了可能满足原料药要求的水平,从而减轻了后续色谱步骤中进一步去除杂质的负担。另外,在刺激试剂的存在下,使用荧光标记的聚合物证明了残留聚合物的有效清除。还探讨了絮凝过程中HCP和聚集体去除的机理。这种新颖而高效的过程可以轻松地集成到当前的mAb纯化平台中,并且可以克服下游的加工难题。生物技术。生恩2013; 110:2928-2937。 ©2013 Wiley Periodicals,Inc.

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