Synthesis and radiopharmacological evaluation of 2'-(4-fluorophenyl)-21-(18F)fluoro-20-oxo-11beta,17alpha-dihydroxy-pregn-4 -eno(3,2-c)pyrazole as potential glucocorticoid receptor ligand for positron emission tomography (PET).

摘要

The radiosynthesis and the radiopharmacological evaluation of pyrazolo steroid 2'-(4-fluorophenyl)-21-[18F]fluoro-20-oxo-11beta,17alpha-dihydroxy-pregn-4 -eno[3,2-c]pyrazole [18F]-2 is described. The radiolabeling was accomplished in 3-4% decay-corrected radiochemical yield within 80 min at an specific radioactivity of 0.8-1.2 Ci/micromol. Biodistribution studies in male Wistar rats showed an initial brain uptake of 0.25+/-0.03% ID/g after 5 min, which remained constant over 60 min. The radiopharmacological evaluation of compound [18F]-2 was completed with autoradiography using rat brain sections and micro-PET imaging.