The
synthesis of highly water-dispersible iron oxide nanoparticles
with surface functional groups and precisely controlled sizes is essential
for biomedical application. In this paper, we report a one-pot strategy
for versatile surface functionalization. The iron oxide nanoparticles
are first synthesized by thermal decomposition of iron(III) acetylacetonate
(Fe(acac)3) in diethylene glycol (DEG), and their surfaces
are modified by adding the surface ligands at the end of the reaction.
The size of iron oxide nanoparticles can be precisely controlled in
nanometer scale by continuous growth. This facile synthesis method
enables the surface modification with different coating materials
such as dopamine (DOPA), polyethylene glycol with thiol end group
(thiol-PEG), and poly(acrylic acid) (PAA) onto the iron oxide nanoparticles,
introducing new surface functionalities for future biomedical application.
From transmission electron microscopy (TEM) and X-ray diffraction
(XRD), the morphology and crystal structure are not changed during
surface functionalization. The attachment of surface ligands is studied
by Fourier transform infrared spectroscopy (FTIR) and Thermogravimetric
Analysis (TGA). The surface functional groups are confirmed by X-ray
Photoelectron Spectroscopy (XPS). In correlation with the change of
hydrodynamic size, PAA coated nanoparticles are found to exhibit outstanding
stability in aqueous solution. Furthermore, we demonstrate that the
functional groups are available for conjugating with other molecules
such as fluorescent dye, showing potential biological applications.
Lastly, the magnetic resonance phantom studies demonstrate that iron
oxide nanoparticles with PAA coating can be used as T
1 and T
2 dual-modality contrast
agents. Both r
1 and r
2 relaxivities significantly increase after surface functionalization
with PAA, indicating improved sensitivity.