Photothermal-reinforced and glutathione-triggered in Situ cascaded nanocatalytic therapy

被引:89
作者
An, Peijing [1 ]
Fan, Fengying [2 ]
Gu, Dihai [1 ]
Gao, Zhiguo [1 ]
Hossain, Abul Monsur Showkot [3 ]
Sun, Baiwang [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 210089, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, 501 Haike Rd, Shanghai 201210, Peoples R China
[3] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanocatalytic medicine; Synergistic therapy; Chemodynamic therapy; Photothermal-enhanced GSH depletion; GSH-triggered ROS generation; NEAR-INFRARED WINDOW; COPPER; OXIDATION;
D O I
10.1016/j.jconrel.2020.03.007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tumor microenvironment (TME)-responsive nanoformulations that catalyze a cascade of intracellular redox reactions showed promise for tumor treatment with high specificity and efficiency. In this study, we report Cu2+-doped zeolitic imidazolate frameworks-coated polydopamine nanoparticles (PDA@Cu/ZIF-8 NPs) for glutathione-triggered and photothermal-reinforced sequential catalytic therapy against breast cancer. In the TME, the PDA@Cu/ZIF-8 NPs could initially react with antioxidant glutathione (GSH), inducing GSH depletion and Cu+ generation. Whereafter, the generated Cu+ would catalyze local H2O2 to produce highly toxic hydroxyl radicals (center dot OH) through an efficient Fenton-like reaction even in weakly acidity. Importantly, the PDA could exert excellent photothermal conversion effect to simultaneously accelerate GSH consumption and improve the Fenton-like reaction for further expanding the intracellular oxidative stress, which innovatively achieves a synergistic photothermal-chemodynamic therapy for highly efficient anticancer treatment.
引用
收藏
页码:734 / 743
页数:10
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