4.1 Article

The Gd3+complex of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid mono(p-isothiocyanatoanilide) conjugated to inulin: a potential stable macromolecular contrast agent for MRI

Journal

CONTRAST MEDIA & MOLECULAR IMAGING
Volume 6, Issue 6, Pages 482-491

Publisher

WILEY-BLACKWELL
DOI: 10.1002/cmmi.448

Keywords

gadolinium complexes; contrast agents; relaxivity; magnetic resonance imaging; polysaccharides

Funding

  1. European Union [MEST-CT-2004-7442]
  2. Fonds de la Recherche Scientifique
  3. ARC, French Community of Belgium [05/10-335]
  4. European Community
  5. European Regional Development Fund
  6. Walloon Region (CMMI)
  7. COST Action [D38]
  8. EMIL

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Reaction of DOTANCSA [1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid mono(p-isothiocyanatoanilide)] with O-(aminopropyl)inulin (degree of polymerization 25) provided a chelate that formed a kinetically extremely stable Gd3+ complex. No transmetalation was observed with Zn2+. The conjugate has a relaxivity of 21.7s(-1) m m-1 at 20MHz and 37 degrees C, and each molecule of the inulin carries on average 35 Gd3+ ions. The parameters governing the relaxivity of this material and of a low-molecular-weight model compound prepared by conjugation of DOTANCSA and propylamine were evaluated by investigation of their water 1H longitudinal relaxation rate enhancements at different magnetic fields (NMRD) and by studying variable temperature 17O NMR data. The high relaxivity of the inulin conjugate can be ascribed to the efficient slowing down of the molecular tumbling by this carrier. The rotational correlation time at 37 degrees C of this material is 1460ps, whereas that of the model compound is 84ps. Furthermore, both complexes do not interact significantly with human serum albumin, as shown by their NMRD profiles, and do not undergo transmetallation by zinc ions. The inulin conjugate thus has potential for application as a contrast agent for MRI, particularly as a blood pool agent. Copyright (C) 2011 John Wiley & Sons, Ltd.

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