化学
前药
细胞毒性
结合
体内
单克隆抗体
点击化学
治疗指标
体外
药理学
药品
抗体
喜树碱
组合化学
生物化学
免疫学
医学
数学分析
数学
生物技术
生物
作者
Sung-Ju Moon,Serengulam V. Govindan,Thomas M. Cardillo,Christopher D'Souza,Hans J. Hansen,David M. Goldenberg
摘要
CPT-11 is a clinically used cancer drug, and it is a prodrug of the potent topoisomerase I inhibitor, SN-38 (7-ethyl-10-hydroxycamptothecin). To bypass the need for the in vivo conversion of CPT-11 and increase the therapeutic index, bifunctional derivatives of SN-38 were prepared for use in antibody-based targeted therapy of cancer. The general synthetic scheme incorporated an acetylene-azide click cycloaddition step in the design, a short polyethylene glycol spacer for aqueous solubility, and a maleimide group for conjugation. Conjugates of a humanized anti-CEACAM5 monoclonal antibody, hMN-14, prepared using these SN-38 derivatives were evaluated in vitro for stability in buffer and human serum and for antigen-binding and cytotoxicity in a human colon adenocarcinoma cell line. Conjugates of hMN-14 and SN-38 derivatives 16 and 17 were found promising for further development.
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