Core/Shell Structured Hollow Mesoporous Nanocapsules: A Potential Platform for Simultaneous Cell Imaging and Anticancer Drug Delivery

被引:600
作者
Chen, Yu [1 ]
Chen, Hangrong [1 ]
Zeng, Deping [2 ]
Tian, Yunbo [2 ]
Chen, Feng [1 ]
Feng, Jingwei [1 ]
Shi, Jianlin
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Lab High Performance Ceram & Superfine Micr, Shanghai 200050, Peoples R China
[2] Chongqing Med Univ, Dept Biomed Engn, Chongqing 400016, Peoples R China
基金
中国博士后科学基金;
关键词
mesoporous silica; nanocapsules; drug delivery; MRI; Fe3O4; Au; SILICA NANOPARTICLES; CORE-SHELL; CARBON NANOTUBES; POLYMER SHELLS; SPHERES; RELEASE; FABRICATION; PARTICLES; CAPSULES; MICROCAPSULES;
D O I
10.1021/nn1015117
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A potential platform for simultaneous anticancer drug delivery and MRI cell imaging has been demonstrated by uniform hollow inorganic core/shell structured multifunctional mesoporous nanocapsules, which are composed of functional inorganic (Fe3O4, Au, etc.) nanocrystals as cores, a thin mesoporous silica shell, and a huge cavity in between. The synthetic strategy for the creation of huge cavities between functional core and mesoporous silica shell is based on a structural difference based selective etching method, by which solid silica middle layer of Fe2O3@SiO2@mSiO(2) (or Au@SiO2@mSiO(2)) composite nanostructures was selectively etched away while the mesoporous silica shell could be kept relatively intact. The excellent biocompatibility of obtained multifunctional nanocapsules (Fe3O4@mSiO(2)) was demonstrated by very low cytotoxicity against various cell lines, low hemolyticity against human blood red cells and no significant coagulation effect against blood plasma. The cancer cell uptake and intracellular location of the nanocapsules were observed by confocal laser scanning microscopy and bio-TEM. Importantly, the prepared multifunctional inorganic mesoporous nanocapsules show both high loading capacity (20%) and efficiency (up to 100%) for doxorubicin simultaneously because of the formation of the cavity, enhanced surface area/pore volume and the electrostatic interaction between DOX molecules and mesoporous silica surface. Besides, the capability of Fe3O4@mSiO(2) nanocapsules as contrast agents of MRI was demonstrated both in vitro and in vivo, indicating the simultaneous imaging and therapeutic multifunctionalities of the composite nanocapsules. Moreover, the concept of multifunctional inorganic nanocapsules was extended to design and prepare Gd-Si-DTPA grafted Au@mSiO(2) nanocapsules for nanomedical applications, further demonstrating the generality of this strategy for the preparation of various multifunctional mesoporous nanocapsules.
引用
收藏
页码:6001 / 6013
页数:13
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