PEGylated copper(II)-chelated polydopamine nanocomposites for photothermal-enhanced chemodynamic therapy against tumor cells

被引:12
作者
Zhang, Qiuye [1 ]
Wang, Jingjing [1 ,2 ]
Xu, Luen [1 ]
Lu, Shi-Yu [1 ,2 ]
Yang, Huawei [2 ]
Duan, Yifan [1 ]
Yang, Qiang [1 ]
Qiu, Mengfan [1 ]
Chen, Chunmei [1 ]
Zhao, Sheng [1 ]
Liu, Xiaohong [3 ,4 ]
Liu, Hui [1 ]
机构
[1] Southwest Univ, Sch Mat & Energy, Key Lab Luminescence Anal & Mol Sensing, Minist Educ, Chongqing 400715, Peoples R China
[2] Peking Univ, Beijing Innovat Ctr Engn Sci & Adv Technol, Beijing Key Lab Magnetoelect Mat & Devices, Dept Mat Sci & Engn,Coll Engn, Beijing, Peoples R China
[3] Chongqing Youth Vocat & Tech Coll, Chongqing 400712, Peoples R China
[4] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
biomaterials; nanostructured polymers; thermal properties; self‐ assembly; NANOPARTICLES; NANOPLATFORM; CHEMOTHERAPY; NANOCOMPLEX; GENERATION;
D O I
10.1002/app.51172
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Photothermal-enhanced chemodynamic therapy is a novel and promising strategy for effective tumor treatment. Herein, a kind of polydopamine (PDA)-based nanoplatform is reported for photothermal-enhanced chemodynamic therapy against tumor cells. PDA nanoparticles (NPs) were prepared through the self-polymerization method, which were subsequently chelated with Cu2+ and linked with poly(ethylene glycol) (PEG) chains, finally obtaining PDA-Cu(II)-PEG NPs. The fabricated PDA-Cu(II)-PEG NPs were uniform in shape with a narrow polydispersity. They can firstly react with glutathione (GSH) to generate Cu+, inducing GSH depletion meanwhile. The formed Cu+ could catalyze H2O2 to produce hydroxyl radicals (OH) via a Fenton-like reaction. The formed PDA-Cu(II)-PEG NPs displayed good photothermal conversion efficiency and photothermal stability. They can be internalized by 4T1 cells effectively. Under near-infrared light irradiation, PDA-Cu(II)-PEG NPs can generate hyperthermia and OH for photothermal/chemodynamic therapy against tumor cells.
引用
收藏
页数:9
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