抗坏血酸
化学
催化作用
活性氧
体内
组合化学
芬顿反应
内生
双重角色
生物物理学
还原剂
再生(生物学)
纳米复合材料
氧气
氧化还原
体外
离子
生物化学
水溶液中的金属离子
肿瘤微环境
动力学
选择性
过氧化氢
反应中间体
降级(电信)
癌症研究
核化学
维生素C
作者
Ying Tao,Jiatong Ni,Li Ning Yang,Zhengya Yue,Yue Meng,Neda Anastassova,Tiedong Sun,Lei Wang
标识
DOI:10.1021/acsanm.5c04656
摘要
Chemodynamic therapy (CDT) is a tumor treatment that converts endogenous H 2 O 2 into toxic reactive oxygen species (ROS) via Fenton or Fenton-like reactants. It has received much attention because it does not require external energy and has few side effects. However, the therapeutic efficiency of CDT is inhibited by the insufficient supply of H 2 O 2 inside the tumor, thus making it difficult to achieve a satisfactory therapeutic effect. Herein, we designed and synthesized an ascorbic acid (AA)-loaded polyoxometalate-based metal–organic framework nanocomposite (NENU-5) with Mo and Cu ions for Fenton-like reaction centers. On the one hand, AA converts O 2 to H 2 O 2 in vivo to facilitate enhanced ROS production and accelerates the reaction rate of reducing Mo 6+ and Cu 2+ in cells; on the other hand, the reduced Mo 5+ and Cu + in NENU-5 activate Fenton-like reactions. Therefore, NENU-5@AA nanocomposites exhibit a significant inhibitory effect on the tumor cells. Hence, this work effectively addresses the challenges of insufficient H 2 O 2 supply and poor Fenton-like agent regeneration in the tumor microenvironment, thus providing a promising strategy for self-enhanced CDT with potential for clinical applications.
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