In Vivo And In Vitro Characterization Of A Novel Mao-B Inhibitor Radioligand, F-18-Labeled Deuterated Fluorodeprenyl

The aim of this study was to radiolabel a novel bis-deuterium substituted L-deprenyl analog (fluorodeprenyl-D-2) with F-18 and to evaluate its potential to visualize and quantify monoamine oxidase (MAO) B activity in vivo. Methods: The precursor compound (5a + 5b) and reference standard (6) were synthesized in multistep syntheses. Recombinant human MAO-B and MAO-A enzyme preparations were used to determine inhibitory concentrations of 50%. Radiolabeling was accomplished by a nucleophilic substitution reaction. Whole-hemisphere autoradiography was performed with F-18-fluorodeprenyl-D-2. A PET study was performed on a cynomolgus monkey. Radiometabolites were measured in monkey plasma using high-performance liquid chromatography. Results: The 50% inhibitory concentration of compound 6 for MAO-B was 227 +/- 36.8 nM. Radiolabeling was accomplished with high radiochemical yield, purity, and specific radioactivity. The autoradiography binding density of F-18-fluorodeprenyl-D-2 was consistent with known MAO-B expression in the human brain. In vivo, F-18-fluorodeprenyl-D-2 showed favorable kinetic properties, with relatively fast washout from the brain. Regional time activity curves were better described by the 2-tissue-compartment model. Administration of a 1 mg/kg dose of L-deprenyl yielded 70% inhibition of MAO-B in all regions. Radiometabolite studies demonstrated 20% unchanged radioligand at 120 min after injection. F-18-fluorodeprenyl-D-2 showed less irreversibility than did previously reported MAO-B radioligands. Conclusion: The results suggest that F-18-fluorodeprenyl-D-2 is a suitable PET radioligand for visualization of MAO-B activity in the human brain.