Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.

Iron-oxide based contrast agents play an important role in magnetic resonance imaging (MRI) of labelled cells in vivo. Currently, a wide range of such contrast agents is available with sizes varying from several nanometers up to a few micrometers and consisting of single or multiple magnetic cores....

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Autores principales: Arthur Taylor, Anne Herrmann, Diana Moss, Violaine Sée, Karen Davies, Steve R Williams, Patricia Murray
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/7adbfa2f666f468ca1945868906d7eaf
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spelling oai:doaj.org-article:7adbfa2f666f468ca1945868906d7eaf2021-11-11T08:21:49ZAssessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.1932-620310.1371/journal.pone.0100259https://doaj.org/article/7adbfa2f666f468ca1945868906d7eaf2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24959883/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Iron-oxide based contrast agents play an important role in magnetic resonance imaging (MRI) of labelled cells in vivo. Currently, a wide range of such contrast agents is available with sizes varying from several nanometers up to a few micrometers and consisting of single or multiple magnetic cores. Here, we evaluate the effectiveness of these different particles for labelling and imaging stem cells, using a mouse mesenchymal stem cell line to investigate intracellular uptake, retention and processing of nano- and microsized contrast agents. The effect of intracellular confinement on transverse relaxivity was measured by MRI at 7 T and in compliance with the principles of the '3Rs', the suitability of the contrast agents for MR-based cell tracking in vivo was tested using a chick embryo model. We show that for all particles tested, relaxivity was markedly reduced following cellular internalisation, indicating that contrast agent relaxivity in colloidal suspension does not accurately predict performance in MR-based cell tracking studies. Using a bimodal imaging approach comprising fluorescence and MRI, we demonstrate that labelled MSC remain viable following in vivo transplantation and can be tracked effectively using MRI. Importantly, our data suggest that larger particles might confer advantages for longer-term imaging.Arthur TaylorAnne HerrmannDiana MossViolaine SéeKaren DaviesSteve R WilliamsPatricia MurrayPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 6, p e100259 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Arthur Taylor
Anne Herrmann
Diana Moss
Violaine Sée
Karen Davies
Steve R Williams
Patricia Murray
Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
description Iron-oxide based contrast agents play an important role in magnetic resonance imaging (MRI) of labelled cells in vivo. Currently, a wide range of such contrast agents is available with sizes varying from several nanometers up to a few micrometers and consisting of single or multiple magnetic cores. Here, we evaluate the effectiveness of these different particles for labelling and imaging stem cells, using a mouse mesenchymal stem cell line to investigate intracellular uptake, retention and processing of nano- and microsized contrast agents. The effect of intracellular confinement on transverse relaxivity was measured by MRI at 7 T and in compliance with the principles of the '3Rs', the suitability of the contrast agents for MR-based cell tracking in vivo was tested using a chick embryo model. We show that for all particles tested, relaxivity was markedly reduced following cellular internalisation, indicating that contrast agent relaxivity in colloidal suspension does not accurately predict performance in MR-based cell tracking studies. Using a bimodal imaging approach comprising fluorescence and MRI, we demonstrate that labelled MSC remain viable following in vivo transplantation and can be tracked effectively using MRI. Importantly, our data suggest that larger particles might confer advantages for longer-term imaging.
format article
author Arthur Taylor
Anne Herrmann
Diana Moss
Violaine Sée
Karen Davies
Steve R Williams
Patricia Murray
author_facet Arthur Taylor
Anne Herrmann
Diana Moss
Violaine Sée
Karen Davies
Steve R Williams
Patricia Murray
author_sort Arthur Taylor
title Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
title_short Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
title_full Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
title_fullStr Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
title_full_unstemmed Assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for MRI cell tracking.
title_sort assessing the efficacy of nano- and micro-sized magnetic particles as contrast agents for mri cell tracking.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/7adbfa2f666f468ca1945868906d7eaf
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