Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies

A straightforward method for synthesizing at the multigram scale a low molecular weight PCTA-based gadolinium complex bearing an ionizable oxyacetic chain on the pyridine unit was described, together with its encapsulation within a nanohydrogel matrix. The ionic gelation occurred between chitosan an...

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Autores principales: Fabienne Dioury, Maité Callewaert, Cyril Cadiou, Céline Henoumont, Michael Molinari, Sophie Laurent, Christophe Portefaix, Marc Port, Francoise Chuburu
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Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/6c4c5efee7f24c0388493c111a7fc19f
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spelling oai:doaj.org-article:6c4c5efee7f24c0388493c111a7fc19f2021-11-12T04:32:27ZPyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies2211-715610.1016/j.rechem.2021.100237https://doaj.org/article/6c4c5efee7f24c0388493c111a7fc19f2021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2211715621001429https://doaj.org/toc/2211-7156A straightforward method for synthesizing at the multigram scale a low molecular weight PCTA-based gadolinium complex bearing an ionizable oxyacetic chain on the pyridine unit was described, together with its encapsulation within a nanohydrogel matrix. The ionic gelation occurred between chitosan and hyaluronic acid, reinforced by crosslinking with sodium tripolyphosphate. The resulting nanogels are spherical and narrowly monodisperse. They are stable for at least four months at room temperature in water and in media of higher ionic strength (NaCl 0.9%, PBS). They display an enhanced longitudinal relaxivity r1 of 15.9 and 12.1 mM−1.s−1 at 20 MHz and 60 MHz at 37 °C respectively which is at least 4 times higher than that of DOTAREM®.Fabienne DiouryMaité CallewaertCyril CadiouCéline HenoumontMichael MolinariSophie LaurentChristophe PortefaixMarc PortFrancoise ChuburuElsevierarticlePCTA chelating agentGadolinium contrast agentNanohydrogelChemistryQD1-999ENResults in Chemistry, Vol 3, Iss , Pp 100237- (2021)
institution DOAJ
collection DOAJ
language EN
topic PCTA chelating agent
Gadolinium contrast agent
Nanohydrogel
Chemistry
QD1-999
spellingShingle PCTA chelating agent
Gadolinium contrast agent
Nanohydrogel
Chemistry
QD1-999
Fabienne Dioury
Maité Callewaert
Cyril Cadiou
Céline Henoumont
Michael Molinari
Sophie Laurent
Christophe Portefaix
Marc Port
Francoise Chuburu
Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
description A straightforward method for synthesizing at the multigram scale a low molecular weight PCTA-based gadolinium complex bearing an ionizable oxyacetic chain on the pyridine unit was described, together with its encapsulation within a nanohydrogel matrix. The ionic gelation occurred between chitosan and hyaluronic acid, reinforced by crosslinking with sodium tripolyphosphate. The resulting nanogels are spherical and narrowly monodisperse. They are stable for at least four months at room temperature in water and in media of higher ionic strength (NaCl 0.9%, PBS). They display an enhanced longitudinal relaxivity r1 of 15.9 and 12.1 mM−1.s−1 at 20 MHz and 60 MHz at 37 °C respectively which is at least 4 times higher than that of DOTAREM®.
format article
author Fabienne Dioury
Maité Callewaert
Cyril Cadiou
Céline Henoumont
Michael Molinari
Sophie Laurent
Christophe Portefaix
Marc Port
Francoise Chuburu
author_facet Fabienne Dioury
Maité Callewaert
Cyril Cadiou
Céline Henoumont
Michael Molinari
Sophie Laurent
Christophe Portefaix
Marc Port
Francoise Chuburu
author_sort Fabienne Dioury
title Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
title_short Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
title_full Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
title_fullStr Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
title_full_unstemmed Pyclen-based Gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive MRI nanoprobes: Synthesis and relaxation studies
title_sort pyclen-based gd complex with ionisable side-chain as a contrastophore for the design of hypersensitive mri nanoprobes: synthesis and relaxation studies
publisher Elsevier
publishDate 2021
url https://doaj.org/article/6c4c5efee7f24c0388493c111a7fc19f
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