A multifunctional nanoplatform for cancer chemo-photothermal synergistic therapy and overcoming multidrug resistance

被引:106
作者
Peng, Yunmei [1 ,2 ]
Nie, Junpeng [1 ,2 ]
Cheng, Wei [2 ]
Liu, Gan [3 ]
Zhu, Dunwan [4 ,5 ]
Zhang, Linhua [4 ,5 ]
Liang, Chaoyu
Mei, Lin [3 ]
Huang, Laiqiang [1 ,2 ]
Zeng, Xiaowei [1 ,2 ,3 ]
机构
[1] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
[2] Grad Sch, Div Life & Hlth Sci, Grad Sch Shenzhen, Shenzhen, Peoples R China
[3] Sun Yat Sen Univ, Sch Pharmaceut Sci Shenzhen, Guangzhou 510275, Guangdong, Peoples R China
[4] Chinese Acad Med Sci, Inst Biomed Engn, Tianjin 300192, Peoples R China
[5] Peking Union Med Coll, Tianjin Key Lab Biomed Mat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
MESOPOROUS SILICA NANOPARTICLES; REDUCED GRAPHENE OXIDE; SURFACE MODIFICATION; CERVICAL-CANCER; BREAST-CANCER; FUNCTIONALIZED NANOPARTICLES; DOCETAXEL DELIVERY; ANTITUMOR-ACTIVITY; CARCINOMA-CELL; DRUG-DELIVERY;
D O I
10.1039/c7bm01206c
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The integration of various therapy strategies into a single nanoplatform for synergistic cancer treatment has presented a great prospect. Herein, docetaxel (DTX)-loaded poly lactic-co-glycolic acid (PLGA)coated polydopamine modified with D-alpha-tocopherol polyethylene glycol 1000 succinate (TPGS) was synthesized for chemo-photothermal synergistic therapy against cancer. Firstly, the DTX-loaded PLGA NPs were prepared by a facile and robust nanoprecipitation method. Then, they were coated with dopamine to achieve the photothermal effects and to be further modified with TPGS, which can inhibit the P-glycoprotein-mediated multidrug resistance (MDR). The near-infrared (NIR) laser irradiation triggered DTX release from DTX-loaded PLGA NPs@PDA-TPGS, and then the chemo-photothermal therapy effect could be enhanced. The in vitro experimental results illustrated that DTX-loaded PLGA NPs@PDA-TPGS exhibits excellent photothermal conservation properties and remarkable cell-killing efficiency. In vivo antitumor studies further confirmed that DTX-loaded PLGA NPs@PDA-TPGS could present an outstanding synergistic antitumor efficacy compared with any monotherapy. This work exhibits a novel nanoplatform, which could not only load chemotherapy drugs efficiently, but could also improve the therapeutic effect of chemotherapy drugs by overcoming MDR and light-mediated photothermal cancer therapy.
引用
收藏
页码:1084 / 1098
页数:15
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