Smart Cu1.75S nanocapsules with high and stable photothermal efficiency for NIR photo-triggered drug release

被引:49
作者
Huang, Sheng [1 ]
Liu, Jing [2 ,3 ]
He, Qian [1 ]
Chen, Hongli [1 ]
Cui, Jiabin [1 ]
Xu, Suying [1 ]
Zhao, Yuliang [2 ,3 ]
Chen, Chunying [2 ,3 ]
Wang, Leyu [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing Key Lab Environm Harmful Chem Anal, Beijing 100029, Peoples R China
[2] Chinese Acad Sci, Natl Ctr Nanosci & Technol China, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
copper sulfides; near infrared light; photothermal therapy; drug release; REDUCED GRAPHENE OXIDE; CANCER-CELLS; IN-VIVO; CONVERSION EFFICIENCY; GENE DELIVERY; GOLD NANORODS; THERAPY; NANOCRYSTALS; AGENT; NANOPARTICLES;
D O I
10.1007/s12274-015-0905-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Thermosensitive drug delivery systems (DDSs) face major challenges, such as remote and repeatable control of in vivo temperature, although these can increase the therapeutic efficacy of drugs. To address this issue, we coated near-infrared (NIR) photothermal Cu1.75S nanocrystals with pH/thermos-sensitive polymer by in situ polymerization. The doxorubicine (DOX) loading content was up to 40 wt.%, with less than 8.2 wt.% of DOX being leaked under normal physiological conditions (pH = 7.4, 37 A degrees C) for almost 48 h in the absence of NIR light. These nanocapsules demonstrate excellent photothermal stability by continuous longterm NIR irradiation. Based on the stable and high photothermal efficiency (55.8%), pre-loaded drugs were released as desired using 808-nm light as a trigger. Both in vitro and in vivo antitumor therapy results demonstrated that this smart nanoplatform is an effective agent for synergistic hyperthermia-based chemotherapy of cancer, demonstrating remote and noninvasive control.
引用
收藏
页码:4038 / 4047
页数:10
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