Abstract

Magnetic iron oxide nanoparticles have versatile applications in biomedical science that require control over shape and size distribution. Thermal decomposition is one of the best methods for controlling the size and shape of produced nanoparticles (NPs). The size distribution can be tuned (5–30 nm) by varying the reaction environment such as precursor concentration, amount of solvent used, temperature ramp, and reflux time. Iron oleate was used as a precursor solution and heated up to reflux temperature (310 °C) for 10 min within the oxygen-free environment by applying N2 gas flow. The XRD pattern confirmed the formation of NPs with a crystallite size of 17 ± 2.45 nm. Transmission electron microscope images showed moderately cubic shapes with a mean particle size of 28.67 ± 7.12 nm. Magnetic properties such as saturation magnetization, coercivity, and remanence were calculated at 23.48 emu/gm, 33 Oe, and 0.6 emu/gm, respectively, which indicated the ferromagnetic nature of the NPs. The Verwey transition was identified from the magnetization vs temperature (FC-ZFC) plot. The bondings of the oleic acid surfactant with the produced NPs were confirmed from Fourier transformation infrared spectroscopy (FTIR) data analysis. For the application of hyperthermia, the hydrophobic phase was transferred to the hydrophilic phase using cetyltrimethylammonium bromide, which was assured by the FTIR data analysis. The hyperthermia heating of NPs was measured for different concentrations of NPs (0.25, 0.5, 1, 2, and 4 mg/ml), from which specific loss power (SLP) was calculated. Among them, 0.25 mg/ml produced the most prominent SLP (2149 ± 309 w/g) that can be applied for targeted cancer treatment.

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