Synthesis And In Vivo Characterization Of F-18-Labeled Difluoroboron-Curcumin Derivative For Beta-Amyloid Plaque Imaging
SCIENTIFIC REPORTS(2019)
Abstract
Positron emission tomography imaging of beta-amyloid (A beta) plaques has proven useful in the diagnosis of Alzheimer's disease. A previous study from our group showed that 4'-O-[F-18]fluoropropylcurcumin has poor brain permeability, which is thought to be due to its rapid metabolism. In this study, we synthesized difluoroboron complexes of fluorine-substituted curcumin derivatives (1-4) and selected one of them based on the in vitro binding assays. The selected ligand 2 was found to distinctively stain A beta plaques in APP/PS1 transgenic mouse brain sections. Radioligand [F-18]2 was synthesized via a two-step reaction consisting of [F-18]fluorination and subsequent aldol condensation. Biodistribution and metabolism studies indicated that radioligand [F-18]2 was converted to polar radioactive products and trapped in the normal mouse brain. In contrast, optical images of mice acquired after injection of 2 showed moderate fluorescence signal intensity in the mouse brain at 2 min with a decrease in the signal within 30 min. In the ex vivo optical images, the fluorescence signals in major tissues disappeared within 30 min. Taken together, these results suggest that [F-18]2 may be converted to polarl F-18-labeled blue-shifted fluorescent products. Further structural modifications are thus needed to render the radioligand metabolically stable.
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