期刊
BIOMATERIALS
卷 33, 期 3, 页码 970-978出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2011.10.001
关键词
Magnetic-silica nanocomposites; Mesoporous materials; Cellular uptake; CpG DNA adsorption; Large nanopores
资金
- Australian Research Council (ARC) [LP0882681]
- Discovery Project program [DP1094070, DP1095861]
- Australian Institute for Bioengineering and Nanotechnology Challenge Project Initiative
- National Health and Medical Research Council of Australia [NHMRC526663]
- Australian Institute of Nuclear Science and Technology LtD (AINSE)
Template assisted fabrication of magnetic silica nanospheres with large nanopores (MSNLP) and their adsorption and delivery of nucleic acids are reported in this paper. Silica spheres with controlled particle diameter (similar to 400 nm) and large nanopore size (13-24 nm) are prepared by using Brij56 as a template of mesopore, enabling incorporation of magnetic nanocrystals into the particles under mild neutral synthesis conditions. High resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and field-dependent magnetisation measurements confirm that the magnetic nanocrystals have been encapsulated into the silica spheres. The saturation magnetisation values of the resulted magneticsilica nanocomposites are tunable by adjusting the amount of Fe(3)O(4) magnetic nanocrystals used in the synthesis process. The nitrogen sorption analysis reveals that mesopores with large pore size exist in the silica matrix. After functionalisation of the silica surface with poly-(L-lysine) (PLL), the nanoparticles show strong adsorption capacity (q(m) ranging from 10 to 22.5 mu g/mg) for CpG DNA. We have further demonstrated successful delivery of miRNA into rat proximal tubular epithelial cells, facilitated by efficient cellular uptake of the nanocomposites. This work provides a convenient strategy to prepare MSNLP which can offer a versatile platform for biological applications such as simultaneous drug delivery and magnetic resonance imagining under external magnetic field. (C) 2011 Elsevier Ltd. All rights reserved.
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