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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.
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页码:4828 / 4833
页数:6
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