喜树碱
连接器
药品
化学
两亲性
组合化学
机制(生物学)
药理学
生物物理学
生物化学
生物
聚合物
有机化学
计算机科学
认识论
哲学
操作系统
共聚物
作者
Andrew G. Cheetham,Yu‐Chuan Ou,Pengcheng Zhang,Honggang Cui
摘要
We report here that the release mechanism of free camptothecin from self-assembling drug amphiphiles can be regulated by use of different linker groups. Our results highlight the significance of the linker group of drug amphiphiles on the drug release efficiency and their consequent in vitro efficacy.
科研通智能强力驱动
Strongly Powered by AbleSci AI