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In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process
We report the synthesis of magnetite nanoparticles (IOMNPs) using the polyol method performed at elevated temperature (300 °C) and high pressure. The ferromagnetic polyhedral IOMNPs exhibited high saturation magnetizations at room temperature (83 emu/g) and a maximum specific absorption rate (SAR) o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285148/ https://www.ncbi.nlm.nih.gov/pubmed/32384665 http://dx.doi.org/10.3390/pharmaceutics12050424 |
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author | Iacovita, Cristian Fizeșan, Ionel Pop, Anca Scorus, Lavinia Dudric, Roxana Stiufiuc, Gabriela Vedeanu, Nicoleta Tetean, Romulus Loghin, Felicia Stiufiuc, Rares Lucaciu, Constantin Mihai |
author_facet | Iacovita, Cristian Fizeșan, Ionel Pop, Anca Scorus, Lavinia Dudric, Roxana Stiufiuc, Gabriela Vedeanu, Nicoleta Tetean, Romulus Loghin, Felicia Stiufiuc, Rares Lucaciu, Constantin Mihai |
author_sort | Iacovita, Cristian |
collection | PubMed |
description | We report the synthesis of magnetite nanoparticles (IOMNPs) using the polyol method performed at elevated temperature (300 °C) and high pressure. The ferromagnetic polyhedral IOMNPs exhibited high saturation magnetizations at room temperature (83 emu/g) and a maximum specific absorption rate (SAR) of 2400 W/g(Fe) in water. The uniform dispersion of IOMNPs in solid matrix led to a monotonous increase of SAR maximum (3600 W/g(Fe)) as the concentration decreased. Cytotoxicity studies on two cell lines (cancer and normal) using Alamar Blues and Neutral Red assays revealed insignificant toxicity of the IOMNPs on the cells up to a concentration of 1000 μg/mL. The cells internalized the IOMNPs inside lysosomes in a dose-dependent manner, with higher amounts of IOMNPs in cancer cells. Intracellular hyperthermia experiments revealed a significant increase in the macroscopic temperatures of the IOMNPs loaded cell suspensions, which depend on the amount of internalized IOMNPs and the alternating magnetic field amplitude. The cancer cells were found to be more sensitive to the intracellular hyperthermia compared to the normal ones. For both cell lines, cells heated at the same macroscopic temperature presented lower viability at higher amplitudes of the alternating magnetic field, indicating the occurrence of mechanical or nanoscale heating effects. |
format | Online Article Text |
id | pubmed-7285148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72851482020-06-18 In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process Iacovita, Cristian Fizeșan, Ionel Pop, Anca Scorus, Lavinia Dudric, Roxana Stiufiuc, Gabriela Vedeanu, Nicoleta Tetean, Romulus Loghin, Felicia Stiufiuc, Rares Lucaciu, Constantin Mihai Pharmaceutics Article We report the synthesis of magnetite nanoparticles (IOMNPs) using the polyol method performed at elevated temperature (300 °C) and high pressure. The ferromagnetic polyhedral IOMNPs exhibited high saturation magnetizations at room temperature (83 emu/g) and a maximum specific absorption rate (SAR) of 2400 W/g(Fe) in water. The uniform dispersion of IOMNPs in solid matrix led to a monotonous increase of SAR maximum (3600 W/g(Fe)) as the concentration decreased. Cytotoxicity studies on two cell lines (cancer and normal) using Alamar Blues and Neutral Red assays revealed insignificant toxicity of the IOMNPs on the cells up to a concentration of 1000 μg/mL. The cells internalized the IOMNPs inside lysosomes in a dose-dependent manner, with higher amounts of IOMNPs in cancer cells. Intracellular hyperthermia experiments revealed a significant increase in the macroscopic temperatures of the IOMNPs loaded cell suspensions, which depend on the amount of internalized IOMNPs and the alternating magnetic field amplitude. The cancer cells were found to be more sensitive to the intracellular hyperthermia compared to the normal ones. For both cell lines, cells heated at the same macroscopic temperature presented lower viability at higher amplitudes of the alternating magnetic field, indicating the occurrence of mechanical or nanoscale heating effects. MDPI 2020-05-06 /pmc/articles/PMC7285148/ /pubmed/32384665 http://dx.doi.org/10.3390/pharmaceutics12050424 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Iacovita, Cristian Fizeșan, Ionel Pop, Anca Scorus, Lavinia Dudric, Roxana Stiufiuc, Gabriela Vedeanu, Nicoleta Tetean, Romulus Loghin, Felicia Stiufiuc, Rares Lucaciu, Constantin Mihai In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title | In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title_full | In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title_fullStr | In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title_full_unstemmed | In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title_short | In Vitro Intracellular Hyperthermia of Iron Oxide Magnetic Nanoparticles, Synthesized at High Temperature by a Polyol Process |
title_sort | in vitro intracellular hyperthermia of iron oxide magnetic nanoparticles, synthesized at high temperature by a polyol process |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285148/ https://www.ncbi.nlm.nih.gov/pubmed/32384665 http://dx.doi.org/10.3390/pharmaceutics12050424 |
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