Bioactivity evaluation of nanosized ZnFe2O4 fabricated by hydrothermal method

In this study, we investigated the structural, microstructural, magnetic and cytotoxic properties of encapsulated ZnFe2O4 nanoparticles. The nanoparticles were synthesized using the microwave-assisted hydrothermal method and their surfaces were silanized and later encapsulated with poly-2-hydroxyeth...

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Bibliographic Details
Published in:Processing and Application of Ceramics Vol. 15; no. 4; pp. 374 - 384
Main Authors: Hangai Bruno, Acero Gonny, Ortega Pedro Paulo, Garcia Filiberto G., Simões Alexandre Z.
Format: Journal Article
Language:English
Published: University of Novi Sad 01-01-2021
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Summary:In this study, we investigated the structural, microstructural, magnetic and cytotoxic properties of encapsulated ZnFe2O4 nanoparticles. The nanoparticles were synthesized using the microwave-assisted hydrothermal method and their surfaces were silanized and later encapsulated with poly-2-hydroxyethyl methacrylate (PHEMA). Due to the compatibility of Zn2+ ions with a human body, ZnFe2O4 nanoparticles are preferable among all kinds of ferrites for biomedical applications. Quantitative phase analysis obtained by the Rietveld refinement reveals the formation of a single-phase spinel cubic structure. Magnetic hysteresis loops measured at 2 and 300K reveal a remanent magnetization of 4.427 emu/g and 1.002 emu/g, respectively. Such behaviour was ascribed to change in the inversion degree of the spinel structure. The experimental g-factor (g = 1.897) obtained using electron paramagnetic resonance analysis can be attributed to the microwave heating, which induces more surface-active oxygen species. In addition, we demonstrated that the encapsulated ZnFe2O4 nanoparticles showed an absence of cytotoxicity at concentrations of 1.0, 10 and 20 μg/ml against human embryonic kidney (HEK) cells since no significant changes in cell morphology were observed. Hence, our results indicate the possibility to explore the use of ZnFe2O4 nanoparticles encapsulated with PHEMA for biomedical applications, such as cancer therapies.
ISSN:1820-6131
2406-1034
DOI:10.2298/PAC2104374H