Please use this identifier to cite or link to this item: https://doi.org/10.1002/adfm.200901820
Title: Synthesis of PEOlated Fe3O4@SiO2 nanoparticles via bioinspired silification for magnetic resonance imaging
Authors: Tan, H. 
Xue, J.M. 
Shuter, B.
Li, X.
Wang, J. 
Issue Date: 9-Mar-2010
Citation: Tan, H., Xue, J.M., Shuter, B., Li, X., Wang, J. (2010-03-09). Synthesis of PEOlated Fe3O4@SiO2 nanoparticles via bioinspired silification for magnetic resonance imaging. Advanced Functional Materials 20 (5) : 722-731. ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.200901820
Abstract: Inspired by the biosilification process, a highly benign synthesis strategy is successfully developed to synthesize PEOIated Fe3O4@ SiO2 nanoparticles JPEOFSN) at room temperature and near-neutral pH. The success of such a strategy lies in the simultaneous encapsulation of Fe 3O4 nanocrystals and silica precursors into the core of PEO-based polymeric micelles. The encapsulation results in the formation of a silica shell being confined to the interface between the core and corona of the Fe3O4-nanocrystaI-loaded polymeric micelles. Consequently, the surface of the Fe3O4@SiO2 nanoparticle is intrinsically covered by a layer of free PEO chains, which enable the PEOFSN to be colloidally stable not only at room temperature, but also upon incubation in the presence of proteins under physiological conditions. In addition, the silica shell formation does not cause any detrimental effects to the encapsulated Fe3O4 nanocrystals with respect to their size, morphology, crystallinity, and magnetic properties, as shown by their physicochemical behavior. The PEOFSN are shown to be good candidates for magnetic resonance imaging (MRl) contrast agents as demonstrated by the high r2/r 1 ratio with long-term stability under high magnetic field, as well as the lack of cytotoxicity. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA,.
Source Title: Advanced Functional Materials
URI: http://scholarbank.nus.edu.sg/handle/10635/86766
ISSN: 1616301X
DOI: 10.1002/adfm.200901820
Appears in Collections:Staff Publications

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