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Synthesis and characterization of Gd-C4-thyroxin-DTPA, a potential new MRI contrast agent. Study of its non covalent interaction with human serum albumin

University of Mons, Department of General, Organic and Biomedical Chemistry, Laboratory of NMR and Molecular Imaging, Mendeleev Building, 19 Avenue Maistriau, 7000 Mons, Belgium;
(This article belongs to the section C. Bioorganic Chemistry and Natural Products)
Cite this paper as: Henoumont, C.; Vander Elst, L.; Laurent, S.; Muller, R. Synthesis and characterization of Gd-C4-thyroxin-DTPA, a potential new MRI contrast agent. Study of its non covalent interaction with human serum albumin. In Proceedings of the 13th Int. Electron. Conf. Synth. Org. Chem., 1-30 November 2009; Sciforum Electronic Conferences Series, 2009, c006:1-3.
Abstract: The synthesis and the physicochemical characterization of a new contrast agent for magnetic resonance imaging (MRI), Gd-C4-thyroxin-DTPA, which has a high affinity for human serum albumin (HSA), are reported. The results show that this chelate is characterized by a relatively high relaxivity, which increases moreover with the concentration. This reflects an aggregation of the molecules in solution. It is also characterized by a better stability versus the transmetallation with the zinc ion than the parent compound, the Gd-DTPA (Magnevist®, Bayer Healthcare). The study of its interaction with human serum albumin was performed by the proton relaxometry technique, which has revealed a relatively high affinity (Ka of the order of 10000 M-1, with 2 binding sites). Finally, competition experiments with ibuprofen and salicylate, of which the binding sites on HSA are known, were performed by the NMR diffusometry method. The results suggest that the chelate shares one of the binding site of ibuprofen.

 

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