Efficient drug delivery using SiO2-layered double hydroxide nanocomposites

被引:64
|
作者
Li, Li [1 ]
Gu, Zi [1 ,2 ]
Gu, Wenyi [1 ]
Liu, Jian [3 ]
Xu, Zhi Ping [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
[2] Univ New S Wales, Sch Chem Engn, Sydney, NSW 2052, Australia
[3] Curtin Univ, Dept Chem Engn, Bentley, WA, Australia
关键词
Layered double hydroxide (LDH); Functionalization; Drug delivery; Nanocomposites; Self-assembly; LAYERED DOUBLE-HYDROXIDE; ANTICANCER DRUG; NANOPARTICLES; NANOMATERIALS; CARRIERS; GENE;
D O I
10.1016/j.jcis.2016.02.042
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MgAl-layered double hydroxide (MgAI-LDH) nanoparticles have great potentials in drug and siRNA delivery. In this work, we used a nanodot-coating strategy to prepare SiO2 dot-coated layered double hydroxide (SiO2@MgAl-LDH) nanocomposites with good dispersibility and controllable size for drug delivery. The optimal SiO2@MgAl-LDH nanocomposite was obtained by adjusting synthetic parameters including the mass ratio of MgAl-LDH to SiO2, the mixing temperature and time. The optimal SiO2@MgAl-LDH nanocomposite was shown to have SiO2 nanodots (10-15 nm in diameter) evenly deposited on the surface of MgAl-LDHs (110 nm in diameter) with the plate-like morphology and the average hydrodynamic diameter of 170 nm. We further employed SiO2@MgAl-LDH nanocomposite as a nanocarrier to deliver methotrexate (MTX), a chemotherapy drug, to the human osteosarcoma cell (U2OS) and found that MTX delivered by SiO2@MgAl-LDH nanocomposite apparently inhibited the U2OS cell growth. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 55
页数:9
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