活性氧
过氧化氢
胶质瘤
葡萄糖氧化酶
癌症研究
化学
IDH1
异柠檬酸脱氢酶
激进的
生物化学
生物物理学
医学
酶
生物
突变体
基因
作者
Chunying Li,Yilin Wan,Yifan Zhang,Lian‐Hua Fu,Nicholas Thomas Blum,Run Cui,Boda Wu,Rui Zheng,Jing Lin,Zhiming Li,Peng Huang
标识
DOI:10.1002/adma.202103980
摘要
Complete resection of isocitrate dehydrogenase 1 (IDH1) (R132H) glioma is unfeasible and the classic post-surgical chemo/radiotherapy suffers from high recurrence and low survival rate. IDH1 (R132H) cells are sensitive to low concentrations of glucose and high concentrations of reactive oxygen species (ROS) due to inherent metabolism reprograming. Hence, a starvation/chemodynamic therapeutic gel is developed to combat residual IDH1 (R132H) tumor cells after surgery. Briefly, glucose oxidase (GOx) is mineralized with manganese-doped calcium phosphate to form GOx@MnCaP nanoparticles, which are encapsulated into the fibrin gel (GOx@MnCaP@fibrin). After spraying gel in the surgical cavity, GOx catalyzes the oxidation of glucose in residual IDH1 (R132H) cells and produces H2 O2 . The generated H2 O2 is further converted into highly lethal hydroxyl radicals (•OH) by a Mn2+ -mediated Fenton-like reaction to further kill the residual IDH1 (R132H) cells. The as-prepared starvation/chemodynamic therapeutic gel shows much higher therapeutic efficacy toward IDH1 (R132H) cells than IDH1 (WT) cells, and achieves long-term survival.
科研通智能强力驱动
Strongly Powered by AbleSci AI