化学
结合
抗体-药物偶联物
连接器
有效载荷(计算)
色谱法
药品
组合化学
单克隆抗体
抗体
药理学
医学
数学分析
计算机网络
数学
网络数据包
计算机科学
免疫学
生物
操作系统
作者
Ilona Pysz,Paul J. Jackson,David J. Barlow,Khondaker Miraz Rahman,David E. Thurston
标识
DOI:10.1016/j.jchromb.2020.122075
摘要
Antibody-Drug Conjugates (ADCs) consist of antibodies attached to cytotoxic small molecules or biological agents (i.e., payloads) through chemical linkers which may be cleavable or non-cleavable. The development of new ADCs is challenging, particularly the process of attaching the linker-payload construct to the antibody (i.e., the conjugation process). One of the major problems associated with conjugation is high hydrophobicity of the payload which can lead to low yields of the ADC through aggregation and/or lower than desired Drug-Antibody Ratios (DARs). We report here a UPLC-based assay that can be used to study the physicochemical properties of ADC payloads at an early stage of development, and to provide information on whether the hydrophilic-hydrophobic balance is suitable for conjugation or further physicochemical optimization is required. The assay is relatively simple to establish and should be of use to those working in the ADC area.
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