制药工业
化学
蛋白质聚集
业务
生化工程
纳米技术
药理学
生物化学
材料科学
医学
工程类
作者
Mahdie Rahban,Faizan Ahmad,Mieczyslaw A. Piatyszek,Thomas Haertlé,Luciano Saso,Ali Akbar Saboury
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:13 (51): 35947-35963
被引量:128
摘要
Protein-based therapeutics have revolutionized the pharmaceutical industry and become vital components in the development of future therapeutics. They offer several advantages over traditional small molecule drugs, including high affinity, potency and specificity, while demonstrating low toxicity and minimal adverse effects. However, the development and manufacturing processes of protein-based therapeutics presents challenges related to protein folding, purification, stability and immunogenicity that should be addressed. These proteins, like other biological molecules, are prone to chemical and physical instabilities. The stability of protein-based drugs throughout the entire manufacturing, storage and delivery process is essential. The occurrence of structural instability resulting from misfolding, unfolding, and modifications, as well as aggregation, poses a significant risk to the efficacy of these drugs, overshadowing their promising attributes. Gaining insight into structural alterations caused by aggregation and their impact on immunogenicity is vital for the advancement and refinement of protein therapeutics. Hence, in this review, we have discussed some features of protein aggregation during production, formulation and storage as well as stabilization strategies in protein engineering and computational methods to prevent aggregation.
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