| JOURNAL OF COLLOID AND INTERFACE SCIENCE | 卷:470 |
| Efficient drug delivery using SiO2-layered double hydroxide nanocomposites | |
| Article | |
| Li, Li1  Gu, Zi1,2  Gu, Wenyi1  Liu, Jian3  Xu, Zhi Ping1  | |
| [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; | |
| DOI : 10.1016/j.jcis.2016.02.042 | |
| 来源: Elsevier | |
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【 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.
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| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_jcis_2016_02_042.pdf | 2712KB |
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