Pfizer Biopharmaceuticals, 1 Burtt Road, Andover, MA 01810, USA.
Biotechnol Bioeng. 2013 Apr;110(4):1142-52. doi: 10.1002/bit.24781. Epub 2012 Dec 10.
Most mAb platform purification processes consist of an affinity capture step followed by one or two polishing steps. An understanding of the performance linkages between the unit operations can lead to robust manufacturing processes. In this study, a weak-partitioning anion-exchange chromatography polishing step used in a mAb purification process was characterized through high-throughput screening (HTS) experiments, small-scale experiments including a cycling study performed on qualified scale-down models, and large-scale manufacturing runs. When material from a Protein A column that had been cycled <10× was loaded on the AEX resin, early breakthrough of impurities and premature loss of capacity was observed. As the cycle number on the Protein A resin increased, the capacity of the subsequent AEX step increased. Different control strategies were considered for preventing impurity breakthrough and improving AEX resin lifetimes. Depth filtration of the Protein A peak pool significantly improved the AEX resin capacity, robustness, and lifetime. Further, the turbidity of the Protein A pool has the potential for use as an in-process control parameter for monitoring the performance of the AEX step.
大多数 mAb 平台的纯化工艺都包含一个亲和捕获步骤,后面跟着一个或两个抛光步骤。对单元操作之间的性能联系的理解可以带来稳健的制造工艺。在这项研究中,通过高通量筛选 (HTS) 实验、在合格的缩小模型上进行的循环研究等小型实验以及大规模制造运行,对 mAb 纯化工艺中使用的弱分配阴离子交换色谱抛光步骤进行了表征。当从经过 <10× 循环的 Protein A 柱上加载 AEX 树脂时,杂质会早期突破并过早损失容量。随着 Protein A 树脂上的循环次数增加,后续 AEX 步骤的容量也会增加。考虑了不同的控制策略来防止杂质突破并提高 AEX 树脂的寿命。对 Protein A 峰池进行深度过滤显著提高了 AEX 树脂的容量、稳健性和寿命。此外,Protein A 池的浊度有可能作为一个过程控制参数,用于监测 AEX 步骤的性能。