摘要

An automated synthesis procedure of [F-18]Florbetaben ([F-18]BAY94-9172), a radiolabeled imaging agent in phase III study for in vivo mapping of fibrillar amyloid beta (A beta) with PET, was developed using the commercial PET-MF-2V-IT-1 synthesizer. The automated radiosynthesis was carried out via a one-step nucleophilic fluorination of methanesulfonic acid 2-[2-(2{4-[2-(4-methylamino-phenyl)-vinyl]-phenoxy}-ethoxy)-ethoxy]-ethyl ester, as a new precursor, and separation with semi-preparative high performance liquid chromatography (HPLC). The total synthesis time amounted to 50 min with 20-25% yield (uncorrected for decay) and radiochemical purities of more than 95% in all runs. The described automated radiosynthesis allows the production of [F-18]Florbetaben using a commercial radiosynthesis module and enables clinical trials of this compound.