Magnetic mesoporous silica nanoparticles end-capped with hydroxyapatite for pH-responsive drug release

被引:54
|
作者
Zhao, Chun-Xia [1 ]
Yu, Lei [1 ]
Middelberg, Anton P. J. [1 ]
机构
[1] Univ Queensland, Ctr Biomol Engn, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
TARGETED DRUG; DELIVERY; SYSTEM; MOLECULES;
D O I
10.1039/c3tb20641f
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Mesoporous silica nanoparticles (MSNs) have emerged as one of the most promising vehicles for potential application in drug delivery. In this paper, we report a novel multifunctional nanocomposite composed of a magnetite nanocrystal core and a mesoporous silica shell (Fe3O4@mSiO(2)), end-capped with pH-stimuli-responsive hydroxyapatite (HAp) nanovalves for pH-responsive drug release. Iron oxide core and mesoporous silica shell nanoparticles were synthesized using a microemulsion method, and were then employed as templates for surface coating of hydroxyapatite. The efficient coating of the natural nontoxic component hydroxyapatite was achieved through a biomimetic mineralization process. The pH-responsive release of the model drug ibuprofen showed that the Fe3O4@mSiO(2)@HAp nanoparticles possessed pH-responsive drug-release functionalities. The dissolution of hydroxyapatite in an acidic environment triggers the release of the loaded drugs in Fe3O4@mSiO(2)@HAp nanoparticles.
引用
收藏
页码:4828 / 4833
页数:6
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