@article{oai:kanazawa-u.repo.nii.ac.jp:00013102,
 author = {Noda, Akihiro and Takamatsu, Hiroyuki and Murakami, Yoshihiro and Yajima, Kazuyoshi and Tatsumi, Mitsuyoshi and Ichise, Rikiya and Nishimura, Shintaro},
 issue = {1},
 journal = {Journal of Nuclear Medicine},
 month = {Jan},
 note = {This study used PET to measure the time course of the brain concentration of 18F-labeled N-(4-acetyl-1-piperazinyl)-p-fluorobenzamide monohydrate (FK960), a novel antidementia drug, after oral administration to conscious rhesus monkeys. Methods: Three young-adult male rhesus monkeys were tested. FK960 (0.1 mg/kg) containing about 370 MBq of 18F-FK960 was administered orally to each monkey. Dynamic PET images were acquired for 4 h from 5 min after the administration. Arterial blood samples were withdrawn during PET scanning and were analyzed by an automatic well γ-counter and thin-layer chromatography to determine the time course of authentic 18F-FK960 activity concentration in plasma. FK960 concentrations in brain and plasma were calculated in units of mol/L using the specific activity of FK960 preparations. Results: 18F-FK960 penetrated the blood-brain barrier and underwent perfusion-dependent distribution in the entire brain. Maximal concentrations in the brain and plasma were 1.11 ± 0.30 x 10-7 mol/L (at 3.0 ± 0.6 h after administration) and 4.04 ± 1.29 x 10-7 mol/L (at 2.0 ± 1.1 h after administration), respectively. Conclusion: We succeeded in measuring the FK960 concentration in the brains of conscious monkeys and in plasma after oral administration at a dose of 0.1 mg/kg. The results suggested that this method can measure the FK960 concentration in the human brain, and a potential use of the PET technique in drug development was demonstrated., 金沢大学大学院医学系研究科},
 pages = {105--108},
 title = {Measurement of brain concentration of FK960 for development of a novel antidementia drug : A PET study in conscious rhesus monkeys},
 volume = {44},
 year = {2003}
}