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The Journal of Nuclear Medicine Vol. 31 No. 8 1328-1334
© 1990 by Society of Nuclear Medicine
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Synthesis and Preliminary Evaluation of Carbon-11-Meta-Hydroxyephedrine: A False Transmitter Agent for Heart Neuronal Imaging

Karen C. Rosenspire, Michael S. Haka, Marcian E. Van Dort, Douglas M. Jewett, David L. Gildersleeve, Markus Schwaiger and Donald M. Wieland

Division of Nuclear Medicine, University of Michigan Medical Center, Ann Arbor, Michigan

Correspondence: For reprints contact: Donald M. Wieland, PhD, Division of Nuclear Medicine, University of Michigan Medical Center, 3480 Kresge III, Box 0552, Ann Arbor, MI 48109-0552.

ABSTRACT

Carbon-11-meta-hydroxyephedrine is a new radiotracer developed for mapping the sympathetic nerves of the heart. Carbon-11-meta-hydroxyephedrine is synthesized by direct N-methylation of metaraminol with [11C]methyl iodide in dimethyl formamide/dimethyl sulfoxide and purified by semi-preparative reversed-phase HPLC. Total synthesis time is 45 min from end-of-bombardment. Carbon-11-meta-hydroxyephedrine is produced in 40%–50% corrected radiochemical yield with a specific activity of 900 Ci/mmol. Routine radiochemical and chemical purity are 95% and 98%, respectively. Biodistribution studies in rats show high myocardial uptake. Pretreatment with desipramine, a drug known to selectively block neuronal uptake, results in a 92% decrease in tracer accumulation in the myocardium. Metabolic studies in guinea pigs show <5% metabolites in heart tissue 30 min after intravenous injection suggesting that [11C]meta-hydroxyephedrine is suitable for kinetic modeling. These preliminary results support this new tracer as a clinical agent for neuronal imaging of the heart.




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