Paramagnetic water-soluble metallofullerenes having the highest relaxivity for MRI contrast agents
- PMID: 11459454
- DOI: 10.1021/bc000136m
Paramagnetic water-soluble metallofullerenes having the highest relaxivity for MRI contrast agents
Abstract
Water-soluble gadolinium (Gd) endohedral metallofullerenes have been synthesized as polyhydroxyl forms (Gd@C(82)(OH)(n)(), Gd-fullerenols) and their paramagnetic properties were evaluated by in vivo as well as in vitro for the novel magnetic resonance imaging (MRI) contrast agents for next generation. The in vitro water proton relaxivity, R(1) (the effect on 1/T(1)), of Gd-fullerenols is significantly higher (20-folds) than that of the commercial MRI contrast agent, Magnevist (gadolinium-diethylenetriaminepentaacetic acid, Gd-DTPA) at 1.0 T close to the common field of clinical MRI. This unusually high proton relaxivity of Gd-fullerenols leads to the highest signal enhancement at extremely lower Gd concentration in MRI studies. The strong signal was confirmed in vivo MRI at lung, liver, spleen, and kidney of CDF1 mice after i.v. administration of Gd-fullerenols at a dose of 5 micromol Gd/kg, which was 1/20 of the typical clinical dose (100 micromol Gd/kg) of Gd-DTPA.
Similar articles
-
Evaluation of water-soluble metallofullerenes as MRI contrast agents.Acad Radiol. 2002 Aug;9 Suppl 2:S495-7. doi: 10.1016/s1076-6332(03)80274-x. Acad Radiol. 2002. PMID: 12188319 No abstract available.
-
The relaxivity of Gd-EOB-DTPA and Gd-DTPA in liver and kidney of the Wistar rat.Magn Reson Imaging. 1996;14(3):243-53. doi: 10.1016/0730-725x(95)02097-d. Magn Reson Imaging. 1996. PMID: 8725190
-
Water-soluble gadofullerenes: toward high-relaxivity, pH-responsive MRI contrast agents.J Am Chem Soc. 2005 Jan 19;127(2):799-805. doi: 10.1021/ja044688h. J Am Chem Soc. 2005. PMID: 15643906
-
Gd@C82 Fullerenol.2008 Oct 31 [updated 2008 Dec 1]. In: Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004–2013. 2008 Oct 31 [updated 2008 Dec 1]. In: Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004–2013. PMID: 20641737 Free Books & Documents. Review.
-
Cyclen-based Gd3+ complexes as MRI contrast agents: Relaxivity enhancement and ligand design.Bioorg Med Chem. 2016 Nov 15;24(22):5663-5684. doi: 10.1016/j.bmc.2016.09.069. Epub 2016 Oct 1. Bioorg Med Chem. 2016. PMID: 27729196 Review.
Cited by
-
Gain of a 500-fold sensitivity on an intravital MR contrast agent based on an endohedral gadolinium-cluster-fullerene-conjugate: a new chance in cancer diagnostics.Int J Med Sci. 2010 May 28;7(3):136-46. doi: 10.7150/ijms.7.136. Int J Med Sci. 2010. PMID: 20567614 Free PMC article.
-
Synthesis of endohedral metallofullerene glycoconjugates by carbene addition.Molecules. 2011 Nov 14;16(11):9495-504. doi: 10.3390/molecules16119495. Molecules. 2011. PMID: 22083236 Free PMC article.
-
Use of a genetically engineered protein for the design of a multivalent MRI contrast agent.Bioconjug Chem. 2007 Nov-Dec;18(6):1697-700. doi: 10.1021/bc700149u. Epub 2007 Oct 10. Bioconjug Chem. 2007. PMID: 17927227 Free PMC article.
-
Neuroactivity of detonation nanodiamonds: dose-dependent changes in transporter-mediated uptake and ambient level of excitatory/inhibitory neurotransmitters in brain nerve terminals.J Nanobiotechnology. 2016 Mar 31;14:25. doi: 10.1186/s12951-016-0176-y. J Nanobiotechnology. 2016. PMID: 27036406 Free PMC article.
-
Applications of functionalized fullerenes in tumor theranostics.Theranostics. 2012;2(3):238-50. doi: 10.7150/thno.3509. Epub 2012 Mar 1. Theranostics. 2012. PMID: 22509193 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources