连接器
化学
结合
组合化学
前药
药品
有效载荷(计算)
抗体-药物偶联物
药物输送
抗体
生物物理学
药理学
生物化学
单克隆抗体
有机化学
免疫学
计算机科学
生物
操作系统
数学分析
网络数据包
数学
计算机网络
医学
作者
Wei Ding,Yurong Mao,Huihui Wang,Siqi Qu,Jiakang Chen,Jiusheng Li,Biao Jiang,Hongli Chen
标识
DOI:10.1016/j.cclet.2022.108091
摘要
Self-immolative linkers have been widely used to construct prodrugs to improve their efficacy and safety. In this study, we report the use of phenoxysilyl linker as a self-immolative unit to prepare antibody-drug conjugates (ADCs). Phenoxysily based ADC Ate-PPS-CA4 was prepared and its release was systematically investigated by mass spectrometry. Biological evaluation showed that Ate-PPS-CA4 displayed the ability to target delivery and self-immolative release the active payload CA4 on PD-L1 positive cells MDA-MB-231. As the same with its payload CA4, it could arrest the cell cycle to the G2/M phase and induced changes in cell morphology at the dose of its IC50. The development of this linker with novel drug release mechanisms will expand the methodology to construct ADCs, especially for non-internalizing ADCs by extracellular cleavage.
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