生物制药
单克隆抗体
下游加工
过程开发
下游(制造业)
制造工艺
蛋白质稳定性
设计质量
上游(联网)
上游和下游(DNA)
新产品开发
生化工程
化学
制造工程
计算机科学
业务
抗体
生物技术
色谱法
材料科学
工程类
生物化学
生物
免疫学
复合材料
营销
计算机网络
作者
Abdulrahman Tuameh,Stephen E. Harding,Nicholas J. Darton
标识
DOI:10.1002/biot.202200115
摘要
Abstract The high demand for monoclonal antibody (mAb) therapeutics in recent years has resulted in significant efforts to improve their costly manufacturing process. The high cost of manufacturing mAbs derives mainly from the purification process, which contributes to 50%–80% of the total manufacturing cost. One of the main challenges facing industry at the purification stage is the clearance of host cell proteins (HCPs) that are produced and often co‐purified with the desired mAb product. One of the issues HCPs can cause is the degradation of the final mAb protein product. In this review, techniques are considered that can be used at different stages (upstream and downstream) of mAb manufacture to improve HCP clearance. In addition to established techniques, many new approaches for HCP removal are discussed that have the potential to replace current methods for improving HCP reduction and thereby the quality and stability of the final mAb product.
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