Facile synthesis of multifunctional Fe3O4@SiO2n@Au magneto-plasmonic nanoparticles for MR/CT dual imaging and photothermal therapy

被引:36
|
作者
Hou, Xuemei [1 ,2 ]
Wang, Xuandong [1 ,2 ]
Liu, Rong [1 ,2 ]
Zhang, Huicong [1 ,2 ]
Liu, Xiaolong [3 ]
Zhang, Yun [1 ,2 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Peoples R China
[2] Chinese Acad Sci, Xiamen Inst Rare Earth Mat, Dept Translat Med, Xiamen 361024, Peoples R China
[3] Fujian Med Univ, Mengchao Hepatobiliary Hosp, United Innovat Mengchao Hepatobiliary Technol Key, Fuzhou 350025, Peoples R China
来源
RSC ADVANCES | 2017年 / 7卷 / 31期
基金
中国国家自然科学基金;
关键词
RAY COMPUTED-TOMOGRAPHY; NEAR-INFRARED LIGHT; CONTRAST AGENTS; INORGANIC NANOPARTICLES; GOLD NANOSHELLS; SILICA NANORATTLES; DRUG-DELIVERY; IN-VITRO; CANCER; NANOMATERIALS;
D O I
10.1039/c7ra00925a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magneto-plasmonic nanoparticles have exhibited great potential in cancer diagnosis and therapy because of their excellent magnetic and optically activable plasmonic properties. However, it is still a great challenge to combine these two components in one single-nanoparticle. In this work, we developed a facile method to synthesize monodispersed and uniform theranostic agents of Fe3O4@SiO2@GNSs-PEG (PMGNSs) nanoparticles. The as-synthesized PMGNSs composed of a superparamagnetic Fe3O4 inner core, silica as the midlayer and coated with gold nanoshells at the outside, with uniform size distribution of less than 100 nm. It has been demonstrated to be with excellent magnetic resonance (MR) and computed tomography (CT) imaging contrast abilities at different concentrations. Meanwhile, the as-synthesized PMGNSs exhibited high stability with no significant change of photothermal performance after five laser ON/OFF cycles, and high photothermal conversion ability with temperature increase of 40 degrees C under 808 nm laser irradiation at 2 W cm(-2) for 10 min at the concentration of 160 mu g ml(-1). Furthermore, in vitro photothermal therapy ability has also been demonstrated on HePG2 cancer cells.
引用
收藏
页码:18844 / 18850
页数:7
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