PEGylated Cu3BiS3 hollow nanospheres as a new photothermal agent for 980 nm-laser-driven photothermochemotherapy and a contrast agent for X-ray computed tomography imaging

被引:53
作者
Zhou, Shu-Mei [1 ]
Ma, De-Kun [1 ]
Zhang, Sheng-Hui [2 ]
Wang, Wei [2 ]
Chen, Wei [1 ]
Huang, Shao-Ming [1 ]
Yu, Kang [2 ]
机构
[1] Wenzhou Univ, Nanomat & Chem Key Lab, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Dept Hematol, Affiliated Hosp 1, Wenzhou 325027, Zhejiang, Peoples R China
关键词
COPPER SULFIDE NANOPARTICLES; TRIGGERED DRUG-RELEASE; IN-VIVO; CANCER-CELLS; CONVERSION EFFICIENCY; ORGANIC NANOPARTICLES; GOLD NANOPARTICLES; THERAPY; NANOCRYSTALS; ABLATION;
D O I
10.1039/c5nr06041a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing multifunctional near-infrared (NIR) light-driven photothermal agents is in high demand for efficient cancer therapy. Herein, PEGylated Cu3BiS3 hollow nanospheres (HNSs) with an average diameter of 80 nm were synthesized through a facile ethylene glycol-mediated solvothermal route. The obtained PEGylated Cu3BiS3 HNSs exhibited strong NIR optical absorption with a large molar extinction coefficient of 4.1 x 10(9) cm(-1) M-1 at 980 nm. Under the irradiation of a 980 nm laser with a safe power density of 0.72 W cm(-2), Cu3BiS3 HNSs produced significant photothermal heating with a photothermal transduction efficiency of 27.5%. The Cu3BiS3 HNSs also showed a good antitumoral drug doxorubicin (DOX) loading capacity and pH-and NIR-responsive DOX release behaviors. At a low dosage of 10 mg mL(-1), HeLa cells could be efficiently killed through a synergistic effect of chemo-and photothermo-therapy respectively based on the DOX release and the photothermal effect of Cu3BiS3 HNSs. In addition, Cu3BiS3 HNSs displayed a good X-ray computed tomography (CT) imaging capability. Furthermore, Cu3BiS3 HNSs could be used for efficient in vivo photothermochemotherapy and X-ray CT imaging of mice bearing melanoma skin cancer. This multifunctional theranostic nanomaterial shows potential promise for cancer therapy.
引用
收藏
页码:1374 / 1382
页数:9
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