Methods for addressing host cell protein impurities in biopharmaceutical product development

被引:10
作者
Tuameh, Abdulrahman [1 ]
Harding, Stephen E. [1 ]
Darton, Nicholas J. [2 ,3 ]
机构
[1] Univ Nottingham, Natl Ctr Macromol Hydrodynam, Sch Biosci, Loughborough, England
[2] AstraZeneca, Dosage Form Design & Dev, BioPharmaceut R&D, Cambridge, England
[3] AstraZeneca, Granta Pk, Cambridge CB216GH, England
关键词
biopharmaceutical manufacturing; cell line engineering; formulation; host cell protein(s); purification; A CHROMATOGRAPHY; ANTIBODY PURIFICATION; PARTICLE FORMATION; IMMUNOGLOBULIN-G; CHO-CELLS; IDENTIFICATION; DEGRADATION; PERFORMANCE; CHROMATIN; PRECIPITATION;
D O I
10.1002/biot.202200115
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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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页数:13
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