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Automated Radiochemical Synthesis of [(18)F]3F4AP: A Novel PET Tracer for Imaging Demyelinating Diseases

3-[(18)F]fluoro-4-aminopyridine, [(18)F]3F4AP, is a radiofluorinated analog of the FDA-approved drug for multiple sclerosis 4-aminopyridine (4AP). This compound is currently under investigation as a PET tracer for demyelination. We recently described a novel chemical reaction to produce metafluorina...

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Detalles Bibliográficos
Autores principales: Brugarolas, Pedro, Bhuiyan, Mohammed, Kucharski, Anna, Freifelder, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608160/
https://www.ncbi.nlm.nih.gov/pubmed/28605366
http://dx.doi.org/10.3791/55537
Descripción
Sumario:3-[(18)F]fluoro-4-aminopyridine, [(18)F]3F4AP, is a radiofluorinated analog of the FDA-approved drug for multiple sclerosis 4-aminopyridine (4AP). This compound is currently under investigation as a PET tracer for demyelination. We recently described a novel chemical reaction to produce metafluorinated pyridines consisting of direct fluorination of a pyridine N-oxide and the utilization of this reaction for the radiochemical synthesis of [(18)F]3F4AP. In this article, we demonstrate how to produce this tracer using an automated synthesizer and an in-house made flow hydrogenation reactor. We also show the standard quality control procedures performed before releasing the radiotracer for preclinical animal imaging studies. This semi-automated procedure may serve as the basis for future production of [(18)F]3F4AP for clinical studies.