Silica Coating of Ferromagnetic Iron Oxide Magnetic Nanoparticles Significantly Enhances Their Hyperthermia Performances for Efficiently Inducing Cancer Cells Death In Vitro

Increasing the biocompatibility, cellular uptake, and magnetic heating performance of ferromagnetic iron-oxide magnetic nanoparticles (F-MNPs) is clearly required to efficiently induce apoptosis of cancer cells by magnetic hyperthermia (MH). Thus, F-MNPs were coated with silica layers of different t...

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Published inPharmaceutics Vol. 13; no. 12; p. 2026
Main Authors Iacoviță, Cristian, Fizeșan, Ionel, Nitica, Stefan, Florea, Adrian, Barbu-Tudoran, Lucian, Dudric, Roxana, Pop, Anca, Vedeanu, Nicoleta, Crisan, Ovidiu, Tetean, Romulus, Loghin, Felicia, Lucaciu, Constantin Mihai
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 27.11.2021
MDPI
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Summary:Increasing the biocompatibility, cellular uptake, and magnetic heating performance of ferromagnetic iron-oxide magnetic nanoparticles (F-MNPs) is clearly required to efficiently induce apoptosis of cancer cells by magnetic hyperthermia (MH). Thus, F-MNPs were coated with silica layers of different thicknesses via a reverse microemulsion method, and their morphological, structural, and magnetic properties were evaluated by multiple techniques. The presence of a SiO layer significantly increased the colloidal stability of F-MNPs, which also enhanced their heating performance in water with almost 1000 W/g as compared to bare F-MNPs. The silica-coated F-MNPs exhibited biocompatibility of up to 250 μg/cm as assessed by Alamar Blues and Neutral Red assays on two cancer cell lines and one normal cell line. The cancer cells were found to internalize a higher quantity of silica-coated F-MNPs, in large endosomes, dispersed in the cytoplasm or inside lysosomes, and hence were more sensitive to in vitro MH treatment compared to the normal ones. Cellular death of more than 50% of the malignant cells was reached starting at a dose of 31.25 μg/cm and an amplitude of alternating magnetic field of 30 kA/m at 355 kHz.
Bibliography:These authors contributed equally to this work.
ISSN:1999-4923
1999-4923
DOI:10.3390/pharmaceutics13122026