Afficher la notice abrégée

dc.rights.licenseopenen_US
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorDEVREUX, Marie
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierUniversity of Mons [Belgium] [UMONS]
dc.contributor.authorHENOUMONT, Céline
hal.structure.identifierConservatoire National des Arts et Métiers [CNAM] [CNAM]
hal.structure.identifierLaboratoire Génomique, bioinformatique et chimie moléculaire [GBCM]
dc.contributor.authorDIOURY, Fabienne
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierCenter for Microscopy and Molecular Imaging [IBMM - CMMI]
hal.structure.identifierUniversity of Mons [Belgium] [UMONS]
dc.contributor.authorBOUTRY, Sebastien
hal.structure.identifierConservatoire National des Arts et Métiers [CNAM] [CNAM]
hal.structure.identifierLaboratoire Génomique, bioinformatique et chimie moléculaire [GBCM]
dc.contributor.authorVACHER, Olivier
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierUniversity of Mons [Belgium] [UMONS]
dc.contributor.authorELST, Luce Vander
hal.structure.identifierConservatoire National des Arts et Métiers [CNAM] [CNAM]
hal.structure.identifierLaboratoire Génomique, bioinformatique et chimie moléculaire [GBCM]
dc.contributor.authorPORT, Marc
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierCenter for Microscopy and Molecular Imaging [IBMM - CMMI]
hal.structure.identifierUniversity of Mons [Belgium] [UMONS]
dc.contributor.authorMULLER, Robert N.
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSANDRE, Olivier
IDREF: 183876504
hal.structure.identifierUniversité de Mons [UMons]
hal.structure.identifierCenter for Microscopy and Molecular Imaging [IBMM - CMMI]
hal.structure.identifierUniversity of Mons [Belgium] [UMONS]
dc.contributor.authorLAURENT, Sophie
dc.date.accessioned2021-02-26T09:25:39Z
dc.date.available2021-02-26T09:25:39Z
dc.date.issued2021-02-24
dc.identifier.issn0020-1669en_US
dc.identifier.urioai:crossref.org:10.1021/acs.inorgchem.0c03120
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26361
dc.description.abstractEnMagnetic resonance imaging (MRI) has a leading place in medicine as an imaging tool of high resolution for anatomical studies and diagnosis of diseases, in particular for soft tissues that cannot be accessible by other modalities. Many research works are thus focused on improving the images obtained with MRI. This technique has indeed poor sensitivity, which can be compensated by using a contrast agent (CA). Today, the clinically approved CAs on market are solely based on gadolinium complexes that may induce nephrogenic systemic fibrosis for patients with kidney failure, whereas more recent studies on healthy rats also showed Gd retention in the brain. Consequently, researchers try to elaborate other types of safer MRI CAs like manganese-based complexes. In this context, the synthesis of Mn2+ complexes of four 12-membered pyridine-containing macrocyclic ligands based on the pyclen core was accomplished and described herein. Then, the properties of these Mn(II) complexes were studied by two relaxometric methods, 17O NMR spectroscopy and 1H NMR dispersion profiles. The time of residence (τM) and the number of water molecules (q) present in the inner sphere of coordination were determined by these two experiments. The efficacy of the pyclen-based Mn(II) complexes as MRI CAs was evaluated by proton relaxometry at a magnetic field intensity of 1.41 T near those of most medical MRI scanners (1.5 T). Both the 17O NMR and the nuclear magnetic relaxation dispersion profiles indicated that the four hexadentate ligands prepared herein left one vacant coordination site to accommodate one water molecule, rapidly exchanging, in around 6 ns. Furthermore, it has been shown that the presence of an additional amide bond formed when the paramagnetic complex is conjugated to a molecule of interest does not alter the inner sphere of coordination of Mn, which remains monohydrated. These complexes exhibit r1 relaxivities, large enough to be used as clinical MRI CAs (1.7–3.4 mM–1·s–1, at 1.41 T and 37 °C).
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourcecrossref
dc.subjectrelaxometry
dc.subject.enmagnetic resonance imaging
dc.subject.entransition metals
dc.subject.enligands
dc.subject.enmolecules
dc.subject.encations
dc.subject.enMRI contrast agents
dc.subject.enpyclen
dc.subject.enmanganese
dc.subject.enrelaxivity
dc.subject.encomplexes
dc.title.enMn2+ Complexes with Pyclen-Based Derivatives as Contrast Agents for Magnetic Resonance Imaging: Synthesis and Relaxometry Characterization
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.inorgchem.0c03120en_US
dc.subject.halChimie/Chimie inorganiqueen_US
dc.identifier.pubmed33625836en_US
bordeaux.journalInorganic Chemistryen_US
bordeaux.volume60en_US
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03153153
hal.version1
hal.date.transferred2021-02-26T09:25:43Z
hal.exporttrue
workflow.import.sourcedissemin
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Inorganic%20Chemistry&rft.date=2021-02-24&rft.volume=60&rft.eissn=0020-1669&rft.issn=0020-1669&rft.au=DEVREUX,%20Marie&HENOUMONT,%20C%C3%A9line&DIOURY,%20Fabienne&BOUTRY,%20Sebastien&VACHER,%20Olivier&rft.genre=article


Fichier(s) constituant ce document

Thumbnail
Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée