Synthesis of Iron Oxide/Gold Composite Nanoparticles Using Polyethyleneimine as a Polymeric Active Stabilizer for Development of a Dual Imaging Probe.

The combination of magnetic and plasmonic properties using iron oxide/gold nanocomposite particles is crucial for the development of multimodal molecular imaging probes. In this study, iron oxide/gold composite nanoparticles (NanoIOGs) were synthesized via the on-site reduction of an Au precursor salt by polyethyleneimine (PEI) molecules attached to iron oxide nanoparticles (IONPs), and they were employed in magnetic resonance and dark-field microscope imaging. PEI is considered as a polymeric active stabilizer (PAS), acting as a reducing agent for the synthesis of Au and a dispersant for nanoparticles. When the IONPs prepared at the PEI concentration of 0.02 wt. % were used for the NanoIOG synthesis, Au nanoseeds were formed around the IONPs. The alloy clusters of IONPs/Au crystals were produced with further reduction depending on PEI concentration. The NanoIOGs exhibited superparamagnetism in a magnetic field and plasmonic response in a dark-field (DF) microscope. The sizes, morphologies, magnetizations, and r2 relaxivities of NanoIOGs were affected significantly by the amount of PEI added during the NanoIOG synthesis. It is suggested that the PAS-mediated synthesis is simple and effective, and can be applied to various nanostructured Au-metal alloys.

Polyethyleneimine-mediated synthesis of superparamagnetic iron oxide nanoparticles with enhanced sensitivity in T2 magnetic resonance imaging.

The development of iron oxide nanoparticles (IONPs) with enhanced r2 relaxivity is important for achieving greater sensitivity in in vivo magnetic resonance (MR) imaging. In this study, it was considered that polyethyleneimine (PEI) could play a role in varying the particle and cluster sizes in IONP synthesis, leading to different r2 relaxivities. To demonstrate this, superparamagnetic IONPs were synthesised in the presence of NH4OH and PEI using a co-precipitation method. PEI acted as an active stabiliser during IONP synthesis, and therefore the particle size, hydrodynamic cluster size, coating layer thickness, saturation magnetisation, and r2 relaxivity were all strongly influenced by the PEI concentration. Monodispersed IONPs with a mean hydrodynamic cluster size of 14.4nm were synthesised at a PEI concentration of 0.05wt% and in this case, the r2 relaxivity was increased up to 227.6mM(-1)s(-1). This confirmed the viability of PEI-mediated synthesis as a means of controlling the particle/cluster size and enhancing the r2 relaxivity. The PEI-IONPs exhibited no significant cytotoxicity up to 132ppm. Rapid and strong uptake of PEI-IONPs was detected in rat liver by in vivo MR imaging. The superparamagnetic PEI-IONPs prepared in this study are considered to be sufficiently sensitive for use as MR imaging contrast agents, which can be used as parent particles for further functional modification.