Literature DB >> 21808225

Preparation, purification, and characterization of lanthanide complexes for use as contrast agents for magnetic resonance imaging.

Derek J Averill1, Joel Garcia, Buddhima N Siriwardena-Mahanama, Sashiprabha M Vithanarachchi, Matthew J Allen.   

Abstract

Polyaminopolycarboxylate-based ligands are commonly used to chelate lanthanide ions, and the resulting complexes are useful as contrast agents for magnetic resonance imaging (MRI). Many commercially available ligands are especially useful because they contain functional groups that allow for fast, high-purity, and high-yielding conjugation to macromolecules and biomolecules via amine-reactive activated esters and isothiocyanate groups or thiol-reactive maleimides. While metalation of these ligands is considered common knowledge in the field of bioconjugation chemistry, subtle differences in metalation procedures must be taken into account when selecting metal starting materials. Furthermore, multiple options for purification and characterization exist, and selection of the most effective procedure partially depends on the selection of starting materials. These subtle differences are often neglected in published protocols. Here, our goal is to demonstrate common methods for metalation, purification, and characterization of lanthanide complexes that can be used as contrast agents for MRI (Figure 1). We expect that this publication will enable biomedical scientists to incorporate lanthanide complexation reactions into their repertoire of commonly used reactions by easing the selection of starting materials and purification methods.

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Year:  2011        PMID: 21808225      PMCID: PMC3346304          DOI: 10.3791/2844

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  16 in total

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Journal:  Dalton Trans       Date:  2006-04-28       Impact factor: 4.390

Review 4.  An overview of responsive MRI contrast agents for molecular imaging.

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Review 5.  Responsive magnetic resonance imaging contrast agents as chemical sensors for metals in biology and medicine.

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Journal:  Chem Soc Rev       Date:  2009-10-07       Impact factor: 54.564

6.  Application of arsenazo III in the preparation and characterization of an albumin-linked, gadolinium-based macromolecular magnetic resonance contrast agent.

Authors:  Tavarekere N Nagaraja; Richard L Croxen; Swayamprava Panda; Robert A Knight; Kelly A Keenan; Stephen L Brown; Joseph D Fenstermacher; James R Ewing
Journal:  J Neurosci Methods       Date:  2006-06-12       Impact factor: 2.390

7.  Comparison of MRI properties between derivatized DTPA and DOTA gadolinium-dendrimer conjugates.

Authors:  K Nwe; M Bernardo; C A S Regino; M Williams; M W Brechbiel
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Review 8.  The synthesis and chelation chemistry of DOTA-peptide conjugates.

Authors:  Luis M De León-Rodríguez; Zoltan Kovacs
Journal:  Bioconjug Chem       Date:  2007-12-12       Impact factor: 4.774

9.  Synthesis, characterization, and biological evaluation of integrin alphavbeta3-targeted PAMAM dendrimers.

Authors:  C Andrew Boswell; Peter K Eck; Celeste A S Regino; Marcelino Bernardo; Karen J Wong; Diane E Milenic; Peter L Choyke; Martin W Brechbiel
Journal:  Mol Pharm       Date:  2008-06-07       Impact factor: 4.939

10.  A new approach in the preparation of dendrimer-based bifunctional diethylenetriaminepentaacetic acid MR contrast agent derivatives.

Authors:  Kido Nwe; Heng Xu; Celeste Aida S Regino; Marcelino Bernardo; Lilia Ileva; Lisa Riffle; Karen J Wong; Martin W Brechbiel
Journal:  Bioconjug Chem       Date:  2009-07       Impact factor: 4.774

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  2 in total

1.  Preparation and In Vitro Characterization of Dendrimer-based Contrast Agents for Magnetic Resonance Imaging.

Authors:  Serhat Gündüz; Tanja Savić; Đorđe Toljić; Goran Angelovski
Journal:  J Vis Exp       Date:  2016-12-04       Impact factor: 1.355

2.  Strategies for Target-Specific Contrast Agents for Magnetic Resonance Imaging.

Authors:  Sashiprabha M Vithanarachchi; Matthew J Allen
Journal:  Curr Mol Imaging       Date:  2012-10-01
  2 in total

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