血红素
葡萄糖氧化酶
胶束
化学
活性氧
过氧化氢
癌细胞
过氧化物酶
过氧化氢酶
组氨酸
生物化学
组合化学
酶
生物物理学
水溶液
血红素
癌症
有机化学
生物
遗传学
作者
Zhen Jiang,Jiexin Li,Gengqi Liu,Qian Qiu,Jingyu Zhang,Minchao Hao,He Ren,Yumiao Zhang
出处
期刊:Small
[Wiley]
日期:2024-10-04
被引量:2
标识
DOI:10.1002/smll.202407674
摘要
Abstract Chemodynamic therapy (CDT) is an emerging therapeutic paradigm for cancer treatment that utilizes reactive oxygen species (ROS) to induce apoptosis of cancer cells but few biomaterials have been developed to differentiate the cancer cells and normal cells to achieve precise and targeted CDT. Herein, a simple cascade enzyme system is developed, termed hemin–micelles–GOx, based on hemin and glucose oxidase (GOx)‐encapsulated Pluronic F127 (F127) micelles with pH‐sensitive enzymatic activities. Histidine‐tagged GOx can be easily chelated to hemin‐F127 micelles via the coordination of histidine and ferrous ions in the center of hemin by simple admixture in an aqueous solution. In tumor microenvironment (TME), hemin–micelles–GOx exhibits enhanced peroxidase (POD)‐like activities to generate toxic hydroxyl radicals due to the acidic condition, whereas in normal cells the catalase (CAT)‐like, but not POD‐like activity is amplified, resulting in the elimination of hydrogen peroxide to generate oxygen. In a murine melanoma model, hemin–micelles–GOx significantly suppresses tumor growth, demonstrating its great potential as a pH‐mediated enzymatic switch for tumor management by CDT.
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