Journal
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS
Volume 63, Issue 3, Pages 144-150Publisher
WILEY
DOI: 10.1002/jlcr.3827
Keywords
[F-18]FOMPyD; brain imaging; colony stimulating factor receptor (CSF-1R); copper-mediated F-18-fluorination; fluorine-18; GW2580; PET; positron emission tomography; tropomyosin receptor kinase (Trk)
Funding
- Health Canada
- Brain Canada Foundation
- Montreal Neurological Institute
- Alzheimer Society of Canada [18-05]
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Herein we report an efficient radiolabeling of a F-18-fluorinated derivative of dual inhibitor GW2580, with its subsequent evaluation as a positron emission tomography (PET) tracer candidate for imaging of two neuroreceptor targets implicated in the pathophysiology of neurodegeneration: tropomyosin receptor kinases (TrkB/C) and colony stimulating factor receptor (CSF-1R). [F-18]FOMPyD was synthesized from a boronic acid pinacolate precursor via copper-mediated F-18-fluorination concerted with thermal deprotection of the four Boc groups on a diaminopyrimidine moiety in an 8.7 +/- 2.8% radiochemical yield, a radiochemical purity >99%, and an effective molar activity of 187 +/- 93 GBq/mu mol. [F-18]FOMPyD showed moderate brain permeability in wild-type rats (SUVmax = 0.75) and a slow washout rate. The brain uptake was partially reduced (Delta AUC(40-90) = 11.6%) by administration of the nonradioactive FOMPyD (up to 30 mu g/kg). In autoradiography, [F-18]FOMPyD exhibits ubiquitous distribution in rat and human brain tissues with relatively high nonspecific binding revealed by self-blocking experiment. The binding was blocked by TrkB/C inhibitors, but not with a CSF-1R inhibitor, suggesting selective binding to the former receptor. Although an unfavorable pharmacokinetic profile will likely preclude application of [F-18]FOMPyD as a PET tracer for brain imaging, the concomitant one-pot copper-mediated F-18-fluorination/Boc-deprotection is a practical technique for the automated radiosynthesis of acid-sensitive PET tracers.
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