结合
连接器
药品
化学
组合化学
抗体
抗体-药物偶联物
单克隆抗体
纳米技术
药理学
计算机科学
材料科学
医学
免疫学
数学
数学分析
操作系统
作者
Jonathan D. Bargh,Albert Isidro‐Llobet,Jeremy S. Parker,David R. Spring
摘要
Antibody-Drug Conjugates (ADCs) are now established as a major class of therapeutics for the clinical treatment of cancer. The properties of the linker between the antibody and the payload are proven to be critical to the success of an ADC. Although ADC linkers can be 'non-cleavable', the vast majority of ADCs in clinical development have specific release mechanisms to allow controlled linker cleavage at the target site and are thus termed 'cleavable'. In recent years, the development of new methods of drug release from ADCs has continued in parallel to the deepening understanding of the biological processes underlying the mechanisms of action of pre-existing technologies. This review summarises the advances in the field of cleavable linker technologies for ADCs.
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