蛋白质聚集
蛋白质稳定性
生化工程
纳米技术
粒子聚集
粒子(生态学)
关键质量属性
骨料(复合)
计算机科学
化学
材料科学
粒径
纳米颗粒
工程类
物理化学
地质学
海洋学
生物化学
作者
Marie R. G. Kopp,Fulvio Grigolato,Dominik Zürcher,Tapan K. Das,Danny K. Chou,Klaus Wuchner,Paolo Arosio
标识
DOI:10.1016/j.xphs.2022.10.009
摘要
Protein stability against aggregation is a major quality concern for the production of safe and effective biopharmaceuticals. Amongst the different drivers of protein aggregation, increasing evidence indicates that interactions between proteins and interfaces represent a major risk factor for the formation of protein aggregates in aqueous solutions. Potentially harmful surfaces relevant to biologics manufacturing and storage include air-water and silicone oil-water interfaces as well as materials from different processing units, storage containers, and delivery devices. The impact of some of these surfaces, for instance originating from impurities, can be difficult to predict and control. Moreover, aggregate formation may additionally be complicated by the simultaneous presence of interfacial, hydrodynamic and mechanical stresses, whose contributions may be difficult to deconvolute. As a consequence, it remains difficult to identify the key chemical and physical determinants and define appropriate analytical methods to monitor and predict protein instability at these interfaces. In this review, we first discuss the main mechanisms of surface-induced protein aggregation. We then review the types of contact materials identified as potentially harmful or detected as potential triggers of proteinaceous particle formation in formulations and discuss proposed mitigation strategies. Finally, we present current methods to probe surface-induced instabilities, which represent a starting point towards assays that can be implemented in early-stage screening and formulation development of biologics.
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