Bismuth embedded silica nanoparticles loaded with autophagy suppressant to promote photothermal therapy

被引:75
作者
Chen, Tong [1 ]
Cen, Dong [2 ]
Ren, Zhaohui [1 ]
Wang, Yifan [2 ]
Cai, Xiujun [2 ]
Huang, Jie [3 ]
Di Silvio, Lucy [4 ]
Li, Xiang [1 ]
Han, Gaorong [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Key Lab Endoscop Tech Res Zhejiang Prov, Hangzhou 215123, Zhejiang, Peoples R China
[3] UCL, Dept Mech Engn, Torrington Pl, London, England
[4] Kings Coll London, Fac Dent Oral & Craniofacial Sci, London, England
关键词
Bismuth nanocrystal; Mesoporous silica nanoparticles; Photothermal therapy; Autophagy suppression; THERMAL ABLATION; DRUG-DELIVERY; CHEMOTHERAPY; RESISTANCE; INHIBITION; GRAPHENE; NANORODS; PLATFORM; AGENT; CELLS;
D O I
10.1016/j.biomaterials.2019.119419
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
An unpredicted side effect of photothermal therapy (PTT) is agitated by hyperthermia which results in damage to healthy tissue. Developing PTT platforms, enabling effective tumor ablation under mild irradiation conditions, is of wide interest, but challenging. Here, we investigated bismuth crystals embedded silica (Bi@SiO2) nano particles, loaded with an autophagy inhibitor (chloroquine, CQ). It was found that SiO2 effectively prevented the oxidization of Bi nanocrystals in the physiological environment and could serve as a scatter layer to improve NIR absorption, enabling a high photothermal conversion efficiency (similar to 43%) and excellent photostability. Furthermore, the findings indicated that CQ molecules, delivered intracellularly by the particles, significantly weakened the degradation of autolysosomes by lysosome within the tumor cells, thus inducing suppression effect to autophagy and resistance to photothermia. Both in vitro and in vivo anti-tumor effects were consequently promoted owing to the combined effects enabled by Bi@SiO2-CQ nanoparticles under mild NIR irradiation conditions. This study demonstrates a potential new PIT platform with superior therapeutic efficacy.
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页数:9
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