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Effects of antibody disulfide bond reduction on purification process performance and final drug substance stability

机译:抗体二硫键降低对纯化工艺性能和最终药物稳定性的影响

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Antibody disulfide bond reduction during monoclonal antibody (mAb) production is a phenomenon that has been attributed to the reducing enzymes from CHO cells acting on the mAb during the harvest process. However, the impact of antibody reduction on the downstream purification process has not been studied. During the production of an IgG(2) mAb, antibody reduction was observed in the harvested cell culture fluid (HCCF), resulting in high fragment levels. In addition, aggregate levels increased during the low pH treatment step in the purification process. A correlation between the level of free thiol in the HCCF (as a result of antibody reduction) and aggregation during the low pH step was established, wherein higher levels of free thiol in the starting sample resulted in increased levels of aggregates during low pH treatment. The elevated levels of free thiol were not reduced over the course of purification, resulting in carry-over of high free thiol content into the formulated drug substance. When the drug substance with high free thiols was monitored for product degradation at room temperature and 2-8 degrees C, faster rates of aggregation were observed compared to the drug substance generated from HCCF that was purified immediately after harvest. Further, when antibody reduction mitigations (e.g., chilling, aeration, and addition of cystine) were applied, HCCF could be held for an extended period of time while providing the same product quality/stability as material that had been purified immediately after harvest. Biotechnol. Bioeng. 2017;114: 1264-1274. (c) 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals Inc.
机译:单克隆抗体(MAB)生产期间的抗体二硫键降低是一种现象,其归因于在收获过程中作用于MAB的CHO细胞的还原酶。然而,尚未研究抗体对下游纯化过程的影响。在产生IgG(2)mAb期间,在收获的细胞培养液(HCCF)中观察到抗体还原,导致高碎片水平。此外,在纯化过程中低pH处理步骤期间聚集水平增加。建立了HCCF中游离硫醇水平之间的相关性(由于抗体还原)和低pH步骤中的聚集,其中起始样品中的较高水平的游离硫醇导致低pH处理期间的聚集水平增加。在纯化过程中,不降低自由硫醇水平的升高,导致高自由硫醇含量延伸到配制的药物物质中。当在室温下监测具有高自由硫醇的药物物质和2-8℃的产物降解时,与从收获后立即纯化的HCCF产生的药物相比,观察到更快的聚集速率。此外,当施加抗体减少(例如,冷却,冷却,曝气和添加胱氨酸)时,HCCF可以延长一段时间,同时提供与收获后立即纯化的材料相同的产品质量/稳定性。 Biotechnol。生物。 2017; 114:1264-1274。 (c)2017作者。 Wiley期刊公司发布的生物技术和生物工程

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