Mesoporous silica-coated gold nanostars with drug payload for combined chemo-photothermal cancer therapy

被引:30
|
作者
Su, Gaoxing [1 ]
Miao, Dandan [1 ]
Yu, Yanyan [1 ]
Zhou, Min [1 ]
Jiao, Peifu [2 ]
Cao, Xiaolong [1 ]
Yan, Bing [3 ]
Zhu, Hongyan [1 ]
机构
[1] Nantong Univ, Sch Pharm, Jiangsu Key Lab Inflammat & Mol Drug Targets, Nantong 226001, Peoples R China
[2] Qilu Normal Univ, Dept Chem, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Combined therapy; drug delivery; gold nanostars; mesoporous silica; photothermal therapy; CELLULAR UPTAKE; DELIVERY; NANORODS; NANOPARTICLES; NANOCARRIERS; GRAPHENE; NANOCOMPOSITES; NANOPLATFORM; COMBINATION; PARTICLES;
D O I
10.1080/1061186X.2018.1499746
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Combined chemo-photothermal therapy is attracting increasing attention in the treatment of cancers. In this work, PEGylated mesoporous SiO2-coated gold nanostars (GNS@mSiO(2)-PEG) were synthesised without using the cytotoxic surfactant cetyltrimethylammonium bromide as the template. Mesoporous nanostructures were obtained by poly(vinylpyrrolidone) protection of the outer silica shell and NaOH etching of the inner shell. GNS@mSiO(2)-PEG exhibited good dispersity in medium and excellent photothermal effects. Loading capacity for the anticancer drug doxorubicin (DOX) was similar to 17.9%, and the drug release profile was pH- and light-responsive. In vitro studies revealed that the as-prepared nanocomposites featured good biocompatibility. Furthermore, the nanocomposites were readily internalised by cancer cells, and a combined chemo-photothermal therapy assay revealed that DOX-loaded GNS@mSiO(2)-PEG have a higher therapeutic efficiency than individual therapies, demonstrating suitable synergistic effects.
引用
收藏
页码:201 / 210
页数:10
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