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Demonstration of a sucrose-derived contrast agent for magnetic resonance imaging of the GI tract

  • Gary V. Martinez
  • , Suryakiran Navath
  • , Kamini Sewda
  • , Venkataramanarao Rao
  • , Parastou Foroutan
  • , Ramesh Alleti
  • , Valerie E. Moberg
  • , Ali M. Ahad
  • , Domenico Coppola
  • , Mark C. Lloyd
  • , Robert J. Gillies
  • , David L. Morse
  • , Eugene A. Mash

Research output: Contribution to journalArticlepeer-review

Abstract

A scaffold bearing eight terminal alkyne groups was synthesized from sucrose, and copies of an azide-terminated Gd-DOTA complex were attached via copper(I)-catalyzed azide-alkyne cycloaddition. The resulting contrast agent (CA) was administered by gavage to C3H mice. Passage of the CA through the gastrointestinal (GI) tract was followed by T1-weighted magnetic resonance imaging (MRI) over a period of 47 h, by which time the CA had exited the GI tract. No evidence for leakage of the CA from the GI tract was observed. Thus, a new, orally administered CA for MRI of the GI tract has been developed and successfully demonstrated.

Original languageEnglish (US)
Pages (from-to)2061-2064
Number of pages4
JournalBioorganic and Medicinal Chemistry Letters
Volume23
Issue number7
DOIs
StatePublished - Apr 1 2013

Keywords

  • Contrast agent
  • DOTA
  • Gadolinium
  • Gastrointestinal tract
  • Magnetic resonance imaging

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Pharmaceutical Science
  • Drug Discovery
  • Clinical Biochemistry
  • Organic Chemistry

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