葡萄糖氧化酶
化学
过氧化氢
活性氧
体内
葡萄糖酸
酶
阿霉素
生物物理学
癌细胞
体外
和厚朴酚
组合化学
癌症
生物化学
化疗
生物技术
外科
内科学
生物
医学
作者
Zongjun Liu,Tuo Li,Fang Han,You Wang,Yang Gan,Junhui Shi,Tianran Wang,Muhammad Akhtar,Yu Li
摘要
Synergistic cancer starvation/ROS-mediated/chemo-therapy is developed through a cascade reaction with enzyme glucose oxidase (GOX) modified on the surface of an Fe-based metal organic framework (MOF(Fe)) and drug camptothecin (CPT) loaded into the cavities of MOF(Fe). Once internalized by tumor cells, GOX catalyzes endogenous glucose into hydrogen peroxide (H2O2) and gluconic acid (H+) enabling starvation therapy through choking off energy (glucose) supply. Meanwhile, the acidic micro-environment of tumor enhanced by the generated H+ degrades the MOF(Fe) simultaneously releasing CPT for chemotherapy and Fe3+, catalyzing H2O2 into one of the strongest reactive oxygen species (ROS) ˙OH enabling ROS-mediated therapy. Both in vitro and in vivo results show remarkable tri-modal synergistic anticancer effects. This work may shed some light on the development of novel multi-modal cancer therapies without any external intervention.
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