Abstract
In this study, we describe the development of a facile and effective route for the synthesis of Fe3O4-based T1 contrast agent, which can be useful for in vivo magnetic resonance (MR) imaging. Citrate-coated Fe3O4 nanoparticles (6nm) with a narrow size distribution were synthesized by “one-pot green chemistry route” in diethylene glycol (DEG) solvent. The synthesized nanoparticles were characterized by different analytical techniques including XRD, TEM, HRTEM, and FTIR. At room temperature, nanoparticles exhibited superparamagnetic nature with high saturation magnetization. The longitudinal (r1) and transverse (r2) relaxivities were found to be 35.45 and 51.81mM−1s−1, respectively. Contrast agent developed by this method showed a relatively higher longitudinal relaxivity (r1) and the lowest relaxivity ratio (r2/r1=1.46) at 3T MR field. The anionic nature of citric acid facilitated non-specific internalization without impairment of cell viability and functionality. The in vitro studies showed both phagocitic and non-phagocytic uptake of these NPs. In vivo MR imaging of swine showed both T1 and T2 contrast effect.
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