DI-UMONS : Dépôt institutionnel de l’université de Mons

Recherche transversale
(titres de publication, de périodique et noms de colloque inclus)
2007-01-01 - Article/Dans un journal avec peer-review - Anglais - 12 page(s)

Laurent Sophie , Vander Elst Luce , Vroman A., Muller Robert , "Synthesis and physicochemical characterization of new C-functionalized derivatives of the gadolinium(III) complex with 3,6,10-tris(carboxymethyl)-3,6,10-triazadodecanedioic acid (H(5)ttda) exhibiting fast water exchange potential paramagnetic reporters fo" in Helvetica Chimica Acta, 90, 3, 562-573

  • Edition : Verlag Helvetica Chimica Acta, Basel (Switzerland)
  • Codes CREF : Résonance magnétique nucléaire (biophysique) (DI131B), Chimie organique (DI1313), Imagerie médicale, radiologie, tomographie (DI3243)
  • Unités de recherche UMONS : Chimie générale, organique et biomédicale (M108)
Texte intégral :

Abstract(s) :

(Anglais) To confirm the observation that [Gd(ttda)] derivatives have a significantly shorter residence time T. of the coordinated H2O molecule than [Gd(dtpa)], four new C-functionalized [Gd(ttda)] complexes, [Gd(4-Me-ttda)] (1), [Gd(4-Ph-ttda)] (2), [Gd(9-Me-ttda)] (3), and [Gd(9-Ph-ttda)] (4), were prepared and characterized (H(5)ttda=3,6,10-tris(carboxymethyl)-3,6,10-triazadodecanedioic acid; H(5)dtpa=3,6,9-tris(carboxymethyl)-3,6,9-triazaundecanedioic acid). The temperature dependence of the proton relaxivity for these complexes at 0.47 T and of the 170 transverse relaxation rate of (H2O)-O-17 at 7.05 T confirm that the proton relaxivity is not limited by the H2O-exchange rate. The residence time of the H2O molecules in the first coordination sphere of the gadolinium complexes at 310 K, as calculated from O-17-NMR data, is 13, 43, 2.9, and 56 ns for 1, 2, 3, and 4, respectively. At 310 K, the longitudinal relaxivity of 2 is higher than for the parent compound [Gd(ttda)] and the other complexes of the series. The stability of the new compounds was studied by transmetallation with Zn2+ ions. All the new complexes are more stable than the parent compound [Gd(ttda)].