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This study presents an analysis of a set of iron oxides nanoparticles (NPs) (γ-Fe2O3, α-FeOOH, δ-FeOOH, 5Fe2O3·9H2O, and Fe3O4) as potential candidates for ferroptosis therapy in terms of a phase state, magnetic characteristics, and the release of Fe2+/Fe3+ as ROS mediators. Due to the values of saturation magnetization for Fe3O4 (31.6 emu/g) and γ-Fe2O3 (33.8 emu/g), as well as the surface area of these particles (130 and 123 m2/g), it is possible to consider them as promising magnetically controlled carriers that can function with various ligands. The evaluation of the release of Fe2+/Fe3+ ions as catalysts for the Fenton reaction showed that the concentration of the released ions increases within first 3 h after suspension and decreases within 24 h, which probably indicates desorption and adsorption of ions from/onto the surface of nanoparticles regardless their nature. The concentration of ions released by all nanoparticles, except α-FeOOH-Fe2+, reached 9.1 mg/L for Fe3+ to 1.7 mg/L for Fe2+, which makes them preferable for controlling the catalysis of the Fenton reaction. In contrast, a high concentration of iron ions to 90 mg/L for Fe3+ and 316 mg/L for Fe2+ released from compound α-FeOOH-Fe2+ allows us to utilize this oxide as an aid therapy agent. Results obtained on iron oxide nanoparticles will provide data for the most prospective candidates that are used in ferroptosis-inducing systems.

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