Cargando…
Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging
The growing concern over the toxicity of Gd-based contrast agents used in magnetic resonance imaging (MRI) motivates the search for less toxic and more effective alternatives. Among these alternatives, iron–iron oxide (Fe@FeOx) core-shell architectures have been long recognized as promising MRI cont...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943426/ https://www.ncbi.nlm.nih.gov/pubmed/31861222 http://dx.doi.org/10.3390/molecules24244629 |
_version_ | 1783484878938963968 |
---|---|
author | Mathieu, Paul Coppel, Yannick Respaud, Marc Nguyen, Quyen T. Boutry, Sébastien Laurent, Sophie Stanicki, Dimitri Henoumont, Céline Novio, Fernando Lorenzo, Julia Montpeyó, David Amiens, Catherine |
author_facet | Mathieu, Paul Coppel, Yannick Respaud, Marc Nguyen, Quyen T. Boutry, Sébastien Laurent, Sophie Stanicki, Dimitri Henoumont, Céline Novio, Fernando Lorenzo, Julia Montpeyó, David Amiens, Catherine |
author_sort | Mathieu, Paul |
collection | PubMed |
description | The growing concern over the toxicity of Gd-based contrast agents used in magnetic resonance imaging (MRI) motivates the search for less toxic and more effective alternatives. Among these alternatives, iron–iron oxide (Fe@FeOx) core-shell architectures have been long recognized as promising MRI contrast agents while limited information on their engineering is available. Here we report the synthesis of 10 nm large Fe@FeOx nanoparticles, their coating with a 11 nm thick layer of dense silica and functionalization by 5 kDa PEG chains to improve their biocompatibility. The nanomaterials obtained have been characterized by a set of complementary techniques such as infra-red and nuclear magnetic resonance spectroscopies, transmission electron microscopy, dynamic light scattering and zetametry, and magnetometry. They display hydrodynamic diameters in the 100 nm range, zetapotential values around −30 mV, and magnetization values higher than the reference contrast agent RESOVIST(®). They display no cytotoxicity against 1BR3G and HCT116 cell lines and no hemolytic activity against human red blood cells. Their nuclear magnetic relaxation dispersion (NMRD) profiles are typical for nanomaterials of this size and magnetization. They display high r(2) relaxivity values and low r(1) leading to enhanced r(2)/r(1) ratios in comparison with RESOVIST(®). All these data make them promising contrast agents to detect early stage tumors. |
format | Online Article Text |
id | pubmed-6943426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69434262020-01-10 Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging Mathieu, Paul Coppel, Yannick Respaud, Marc Nguyen, Quyen T. Boutry, Sébastien Laurent, Sophie Stanicki, Dimitri Henoumont, Céline Novio, Fernando Lorenzo, Julia Montpeyó, David Amiens, Catherine Molecules Article The growing concern over the toxicity of Gd-based contrast agents used in magnetic resonance imaging (MRI) motivates the search for less toxic and more effective alternatives. Among these alternatives, iron–iron oxide (Fe@FeOx) core-shell architectures have been long recognized as promising MRI contrast agents while limited information on their engineering is available. Here we report the synthesis of 10 nm large Fe@FeOx nanoparticles, their coating with a 11 nm thick layer of dense silica and functionalization by 5 kDa PEG chains to improve their biocompatibility. The nanomaterials obtained have been characterized by a set of complementary techniques such as infra-red and nuclear magnetic resonance spectroscopies, transmission electron microscopy, dynamic light scattering and zetametry, and magnetometry. They display hydrodynamic diameters in the 100 nm range, zetapotential values around −30 mV, and magnetization values higher than the reference contrast agent RESOVIST(®). They display no cytotoxicity against 1BR3G and HCT116 cell lines and no hemolytic activity against human red blood cells. Their nuclear magnetic relaxation dispersion (NMRD) profiles are typical for nanomaterials of this size and magnetization. They display high r(2) relaxivity values and low r(1) leading to enhanced r(2)/r(1) ratios in comparison with RESOVIST(®). All these data make them promising contrast agents to detect early stage tumors. MDPI 2019-12-17 /pmc/articles/PMC6943426/ /pubmed/31861222 http://dx.doi.org/10.3390/molecules24244629 Text en © 2019 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 Mathieu, Paul Coppel, Yannick Respaud, Marc Nguyen, Quyen T. Boutry, Sébastien Laurent, Sophie Stanicki, Dimitri Henoumont, Céline Novio, Fernando Lorenzo, Julia Montpeyó, David Amiens, Catherine Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title | Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title_full | Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title_fullStr | Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title_full_unstemmed | Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title_short | Silica Coated Iron/Iron Oxide Nanoparticles as a Nano-Platform for T(2) Weighted Magnetic Resonance Imaging |
title_sort | silica coated iron/iron oxide nanoparticles as a nano-platform for t(2) weighted magnetic resonance imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943426/ https://www.ncbi.nlm.nih.gov/pubmed/31861222 http://dx.doi.org/10.3390/molecules24244629 |
work_keys_str_mv | AT mathieupaul silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT coppelyannick silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT respaudmarc silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT nguyenquyent silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT boutrysebastien silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT laurentsophie silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT stanickidimitri silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT henoumontceline silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT noviofernando silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT lorenzojulia silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT montpeyodavid silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging AT amienscatherine silicacoatedironironoxidenanoparticlesasananoplatformfort2weightedmagneticresonanceimaging |