蛋白质聚集
单克隆抗体
盐(化学)
稀释
降级(电信)
化学
肺表面活性物质
钠
生物物理学
抗体
生物化学
医学
免疫学
计算机科学
生物
有机化学
电信
物理
热力学
作者
Justin K. Y. Hong,Wei Liu,Kai Zheng
出处
期刊:Pda Journal of Pharmaceutical Science and Technology
[Parenteral Drug Association, Inc.]
日期:2024-01-01
卷期号:78 (4): 465-474
标识
DOI:10.5731/pdajpst.2023.012860
摘要
Monoclonal antibodies (mAbs) are a successful class of biotherapeutics, but their development can be challenging due to the risk of degradation that could happen at different stages of manufacturing and supply chain. One of the common causes of degradation is the agitation during transportation and clinical handling. It poses interfacial stress to the mAbs which can in turn induce protein aggregation. Moreover, the preparation of the intravenous infusion bags requires diluting the mAbs with saline solution, which could affect the extent of the agitation-induced aggregation because the level of protective surfactant is significantly reduced and salt is introduced into the mAbs solution. To better understand the complex interplay between dilution, interfacial stress and salt, we investigated the impact of sodium chloride (NaCl) on the aggregation of model antibodies from different IgG subclasses induced by agitation. We found that the presence of NaCl accelerates the aggregation for both IgG1 and IgG4 antibodies, but the aggregation mechanism, morphology, and reversibility are very different. Our results clearly highlight the impact of salt on the stability of therapeutic mAbs at the clinical in-use condition. We believe this study furthers our understanding of interfacially-mediated protein aggregation and could improve the formulation development of mAb formulations for patients.
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