Semi-automatic synthesis and biodistribution of N-(2- 18 F-fluoropropionyl)-bis(zinc (II)-dipicolylamine) ( 18 F-FP-DPAZn2) for AD model imaging.

BACKGROUND: Phosphatidylserine (PS)-targeting positron emission tomography (PET) imaging with labeled small-molecule tracer is a crucial non-invasive molecule imaging method of apoptosis. In this study, semi-automatic radiosynthesis and biodistribution of N-(2-18 F-fluoropropionyl)-bis(zinc(II)-dipicolylamine) (18 F-FP-DPAZn2), as a potential small-molecule tracer for PET imaging of cell death in Alzheimer's disease (AD) model, were performed.

METHODS: 18 F-FP-DPAZn2 was synthesized on the modified PET-MF-2V-IT-I synthesizer. Biodistribution was determined in normal mice and PET images of AD model were obtained on a micro PET-CT scanner.

RESULTS: With the modified synthesizer, the total decay-corrected radiochemical yield of 18 F-FP-DPAZn2 was 35 ± 6% (n = 5) from 18 F- within 105 ± 10 min. Biodistribution results showed that kidney has the highest uptake of 18 F-FP-DPAZn2. The uptake of radioactivity in brain kept at a relatively low level during the whole observed time. In vivo 18 F-FP-DPAZn2 PET images demonstrated more accumulation of radioactivity in the brain of AD model mice than that in the brain of normal mice.

CONCLUSIONS: The semi-automatic synthetic method provides a slightly higher radiochemical yield and shorter whole synthesis time of 18 F-FP-DPAZn2 than the manual operation method. This improved method can give enough radioactivity and high radiochemical purity of 18 F-FP-DPAZn2 for in vivo PET imaging. The results show that 18 F-FP-DPAZn2 seems to be a potential cell death tracer for AD imaging.