On-demand CO release for amplification of chemotherapy by MOF functionalized magnetic carbon nanoparticles with NIR irradiation

被引:115
作者
Yao, Jizong [1 ,2 ]
Liu, Yao [3 ,4 ]
Wang, Jiawen [1 ,2 ]
Jiang, Qin [5 ,6 ]
She, Dejun [7 ]
Guo, Huishu [4 ]
Sun, Nianrong [1 ,2 ]
Pang, Zhiqing [8 ,9 ]
Deng, Chunhui [1 ,2 ]
Yang, Wuli [5 ,6 ]
Shen, Shun [3 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Genet & Dev, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Collaborat Innovat Ctr Genet & Dev, Inst Biomed Sci, Shanghai 200433, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai East Hosp, Inst Translat Nanomed, Shanghai 200120, Peoples R China
[4] Dalian Med Univ, Inst Coll Integrat Med, Affiliated Hosp 1, Cent Lab, Dalian 116021, Peoples R China
[5] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[6] Fudan Univ, Dept Macromol Sci, Shanghai 200433, Peoples R China
[7] Fudan Univ, Huashan Hosp, Dept Radiol, Shanghai 200040, Peoples R China
[8] Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China
[9] Fudan Univ, Key Lab Smart Drug Delivery, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
CO gas therapy; Carbon nanoparticles; Synergistic treatment; MOFs; Dual-mode imaging; METAL-ORGANIC FRAMEWORKS; IRON-OXIDE NANOPARTICLES; PHOTOTHERMAL THERAPY; DRUG-DELIVERY; MONOXIDE;
D O I
10.1016/j.biomaterials.2018.12.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Carbon monoxide (CO) gas therapy combined with chemotherapy and photothermal therapy (PIT) is a promising treatment mode for malignant tumor. Herein, we firstly reported doxorubicin (DOX) loaded Mn carbonyl modified Fe (III)-based nanoMOFs (MIL-100) coated PEGylated magnetic carbon nanoparticles (denoted as MCM@PEG-CO-DOX NPs) as theranostics nanoplatforms for near-infrared (NIR)-responded CO-DOX combination therapy. MIL-100 as a good nanocarrier of DOX with high loading capacity can also chelate the Mn carbonyl after a smart modification. Meanwhile, magnetic carbon core possessed photothermal effect, which can convert the NIR light to heat by an 808 nm laser irradiation, resulting in the on-demand release of CO and DOX. As a result, combining with PTT, MCM@PEG-CO-DOX NPs killed tumor efficiently. Moreover, our synthesized MCM@PEG-CO-DOX NPs were capable of realizing tumor dual-mode imaging including magnetic resonance imaging (MRI) and photoacoustic imaging (PAI).
引用
收藏
页码:51 / 62
页数:12
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