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Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment
Iron oxide particles (IOP) are commonly used for Cellular Magnetic Resonance Imaging (MRI) and in combination with several treatments, like Magnetic Fluid Hyperthermia (MFH), due to the rise in temperature they provoke under an Alternating Magnetic Field (AMF). Micrometric IOP have a high sensitivit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870900/ https://www.ncbi.nlm.nih.gov/pubmed/33558583 http://dx.doi.org/10.1038/s41598-021-82095-6 |
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author | Dallet, Laurence Stanicki, Dimitri Voisin, Pierre Miraux, Sylvain Ribot, Emeline J. |
author_facet | Dallet, Laurence Stanicki, Dimitri Voisin, Pierre Miraux, Sylvain Ribot, Emeline J. |
author_sort | Dallet, Laurence |
collection | PubMed |
description | Iron oxide particles (IOP) are commonly used for Cellular Magnetic Resonance Imaging (MRI) and in combination with several treatments, like Magnetic Fluid Hyperthermia (MFH), due to the rise in temperature they provoke under an Alternating Magnetic Field (AMF). Micrometric IOP have a high sensitivity of detection. Nevertheless, little is known about their internalization processes or their potential heat power. Two micrometric commercial IOP (from Bangs Laboratories and Chemicell) were characterized by Transmission Electron Microscopy (TEM) and their endocytic pathways into glioma cells were analyzed. Their Specific Absorption Rate (SAR) and cytotoxicity were evaluated using a commercial AMF inductor. T2-weighted imaging was used to monitor tumor growth in vivo after MFH treatment in mice. The two micron-sized IOP had similar structures and r(2) relaxivities (100 mM(−1) s(−1)) but involved different endocytic pathways. Only ScreenMAG particles generated a significant rise in temperature following AMF (SAR = 113 W g(−1) Fe). After 1 h of AMF exposure, 60% of ScreenMAG-labeled cells died. Translated to a glioma model, 89% of mice responded to the treatment with smaller tumor volume 42 days post-implantation. Micrometric particles were investigated from their characterization to their intracellular internalization pathways and applied in one in vivo cancer treatment, i.e. MFH. |
format | Online Article Text |
id | pubmed-7870900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78709002021-02-10 Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment Dallet, Laurence Stanicki, Dimitri Voisin, Pierre Miraux, Sylvain Ribot, Emeline J. Sci Rep Article Iron oxide particles (IOP) are commonly used for Cellular Magnetic Resonance Imaging (MRI) and in combination with several treatments, like Magnetic Fluid Hyperthermia (MFH), due to the rise in temperature they provoke under an Alternating Magnetic Field (AMF). Micrometric IOP have a high sensitivity of detection. Nevertheless, little is known about their internalization processes or their potential heat power. Two micrometric commercial IOP (from Bangs Laboratories and Chemicell) were characterized by Transmission Electron Microscopy (TEM) and their endocytic pathways into glioma cells were analyzed. Their Specific Absorption Rate (SAR) and cytotoxicity were evaluated using a commercial AMF inductor. T2-weighted imaging was used to monitor tumor growth in vivo after MFH treatment in mice. The two micron-sized IOP had similar structures and r(2) relaxivities (100 mM(−1) s(−1)) but involved different endocytic pathways. Only ScreenMAG particles generated a significant rise in temperature following AMF (SAR = 113 W g(−1) Fe). After 1 h of AMF exposure, 60% of ScreenMAG-labeled cells died. Translated to a glioma model, 89% of mice responded to the treatment with smaller tumor volume 42 days post-implantation. Micrometric particles were investigated from their characterization to their intracellular internalization pathways and applied in one in vivo cancer treatment, i.e. MFH. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870900/ /pubmed/33558583 http://dx.doi.org/10.1038/s41598-021-82095-6 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dallet, Laurence Stanicki, Dimitri Voisin, Pierre Miraux, Sylvain Ribot, Emeline J. Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title | Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title_full | Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title_fullStr | Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title_full_unstemmed | Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title_short | Micron-sized iron oxide particles for both MRI cell tracking and magnetic fluid hyperthermia treatment |
title_sort | micron-sized iron oxide particles for both mri cell tracking and magnetic fluid hyperthermia treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870900/ https://www.ncbi.nlm.nih.gov/pubmed/33558583 http://dx.doi.org/10.1038/s41598-021-82095-6 |
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