化学
前药
点击化学
硝基还原酶
体内
药物输送
体外
癌症治疗
药品
药理学
小分子
酶
组合化学
肿瘤微环境
输送系统
生物化学
细胞内
癌细胞
抗癌药
常用化疗药物
癌症
癌症治疗
生物活性
共价键
靶向给药
癌症研究
作用机理
治疗指标
生物物理学
作者
Xi Wei,Jian Qiao,Wenjing Wei,Meng Liu,Yan Wang,Tommy Jiang,Jian Zhen Ou,Luwen Zhang,Maolin Pang
标识
DOI:10.1021/acs.bioconjchem.5c00285
摘要
Click reactions exhibit remarkable selectivity within biological systems, making them powerful and useful tools for synthesizing various novel anticancer drugs in biomedical fields. Utilizing the overexpressed enzyme in a tumor microenvironment to trigger click reactions between nontoxic or low-toxicity precursors provides an effective solution to the high toxicity of conventional chemotherapeutic agents. However, small-molecule drugs tend to undergo rapid metabolism within biological environments; therefore, an effective drug delivery system was needed. In this study, a hollow covalent organic framework (HCOF) was introduced, prodrug molecules were loaded, and finally, an anticancer drug was formed via the click reaction with the help of nitroreductase (NTR). Both in vitro and in vivo studies confirmed the excellent antitumor efficacy of the resulting therapeutic platform. This work further expands the biomedical applications of HCOF via click chemistry.
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