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We report the experimental characterization and finite element modeling of magnetic fluid hyperthermia (MFH) in tissue-like media using tetramethyl ammonium hydroxide coated superparamagnetic iron oxide magnetic nanoparticles (MNPs) of size ∼19.6 ± 1.2 nm, prepared using a co-precipitation technique. MFH properties are probed for the MNPs in ∼1 wt. % agar, resembling the tumor and surrounding normal tissues. The field-induced temperature rise (ΔT) is experimentally measured in real-time utilizing an infrared camera. A finite element model (FEM) is utilized to simulate the spatiotemporal variations in the thermal profiles, which are found to be in good agreement with the experimental data. FEM-based parametric studies reveal that the thermal conductivity of the medium is the most significant parameter influencing the thermal profiles. The spatiotemporal variations in the thermal profiles are numerically studied for seven different tissues, and the obtained results indicate the highest ΔT for the breast tissue in the tumor and the surrounding regions, which is due to the lowest volumetric specific heat and the highest thermal conductivity of the breast tissue, respectively. Numerical studies on the thermal profiles for sub-surface tumors with parametrically varying depths indicate a strong exponential correlation between the surface and tumor temperature, where the regression coefficients are found to be correlated with the thermo-physical properties of the tissues. The obtained findings are beneficial for developing a simplistic and easily deployable framework for a priori generation of the thermal profiles for various tissues during MFH, which is useful for appropriate planning and parameter selection for MFH-based therapy. [ABSTRACT FROM AUTHOR]

To realize magnetic hyperthermia as an alternate stand-alone therapeutic procedure for cancer treatment, magnetic nanoparticles with optimal performance, within the biologically safe limits, are to be produced using simple, reproducible and scalable techniques. Herein, we present a simple, one-step approach for synthesis of water-dispersible magnetic nanoclusters (MNCs) of superparamagnetic iron oxide by reducing of Fe 2 (SO 4 ) 3 in sodium acetate (alkali), poly ethylene glycol (capping ligand), and ethylene glycol (solvent and reductant) in a microwave reactor. The average size and saturation magnetization of the MNC’s are tuned from 27 to 52 nm and 32 to 58 emu/g by increasing the reaction time from 10 to 600 s. Transmission electron microscopy images reveal that each MNC composed of large number of primary Fe 3 O 4 nanoparticles. The synthesised MNCs show excellent colloidal stability in aqueous phase due to the adsorbed PEG layer. The highest SAR value of 215 ± 10 W/g Fe observed in 52 nm size MNC at a frequency of 126 kHz and field of 63 kA/m suggest the potential use of these MNC in hyperthermia applications. This study further opens up the possibilities to develop metal ion-doped MNCs with tunable sizes suitable for various biomedical applications using microwave assisted synthesis. [ABSTRACT FROM AUTHOR]