质量(理念)
蛋白质聚集
产品(数学)
生化工程
制药工业
风险分析(工程)
设计质量
计算机科学
骨料(复合)
单克隆抗体
蛋白质质量
业务
化学
计算生物学
纳米技术
生物技术
新产品开发
生物
抗体
生物化学
材料科学
营销
工程类
物理
数学
量子力学
免疫学
几何学
作者
Christopher J. Roberts
标识
DOI:10.1016/j.copbio.2014.08.001
摘要
Protein pharmaceutical products are typically active as folded monomers that are composed of one or more protein chains, such as the heavy and light chains in monoclonal antibodies that are a mainstay of current drug pipelines. There are numerous possible aggregated states for a given protein, some of which are potentially useful, while most of which are considered deleterious from the perspective of pharmaceutical product quality and performance. This review provides an overview of how and why different aggregated states of proteins occur, how this potentially impacts product quality and performance, fundamental approaches to control aggregate formation, and the practical approaches that are currently used in the pharmaceutical industry.
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