去酰胺
化学
粘度
赖氨酸
单克隆抗体
氨基酸
降级(电信)
色谱法
盐(化学)
丝氨酸
药品
肺表面活性物质
组合化学
有机化学
抗体
生物化学
药理学
材料科学
酶
计算机科学
免疫学
复合材料
生物
电信
医学
作者
Arvind K. Srivastava,Courtney O’Dell,Evon Bolessa,Suman McLinden,Lori Fortin,Nandkumar Deorkar
标识
DOI:10.1016/j.xphs.2022.05.011
摘要
Monoclonal antibodies are complex molecules that often require high concentration formulations to meet clinical requirement and bulk drug substance storage. Stability is a common concern in both high and low concentration formulations, however, high concentration formulations are further complicated by an increase in viscosity, leading to manufacturing and administration challenges. To manage stability and viscosity, drug developers typically use salt, amino acids, sugars, polyols, and surfactant. It is possible that excipients control some of the product quality attributes (CQAs), at the cost of several others. In this paper, we have evaluated several amino acid derivatives and identified bis acetyl lysine and propionyl serine to be efficient and superior to commonly used parenteral excipients for minimizing antibody solution viscosity, as well as mitigating physical and chemical degradation by controlling protein-protein interactions and deamidation.
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