表征(材料科学)
关键质量属性
计算生物学
单克隆抗体
化学
遗传变异
抗体
组合化学
生物化学
生物
纳米技术
材料科学
遗传学
基因型
基因
物理化学
粒径
作者
Y. Diana Liu,Lance Cadang,Karenna Bol,Xiao Pan,Katherine Tschudi,Mansour Jazayri,Julien Camperi,David A. Michels,John T. Stults,Reed J. Harris,Feng Yang
出处
期刊:Bioengineering
[MDPI AG]
日期:2022-11-03
卷期号:9 (11): 641-641
被引量:8
标识
DOI:10.3390/bioengineering9110641
摘要
Heterogeneity of therapeutic Monoclonal antibody (mAb) drugs are due to protein variants generated during the manufacturing process. These protein variants can be critical quality attributes (CQAs) depending on their potential impact on drug safety and/or efficacy. To identify CQAs and ensure the drug product qualities, a thorough characterization is required but challenging due to the complex structure of biotherapeutics. Past characterization studies for basic and acidic variants revealed that full characterizations were limited to the basic charge variants, while the quantitative measurements of acidic variants left gaps. Consequently, the characterization and quantitation of acidic variants are more challenging. A case study of a therapeutic mAb1 accounted for two-thirds of the enriched acidic variants in the initial characterization study. This led to additional investigations, closing the quantification gaps of mAb1 acidic variants. This work demonstrates that a well-designed study with the right choices of analytical methods can play a key role in characterization studies. Thus, the updated strategies for more complete antibody charge variant characterization are recommended.
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