Title |
Semi-automatic synthesis and biodistribution of N-(2-18F-fluoropropionyl)-bis(zinc (II)-dipicolylamine) (18F-FP-DPAZn2) for AD model imaging
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Published in |
BMC Medical Imaging, April 2017
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DOI | 10.1186/s12880-017-0200-1 |
Pubmed ID | |
Authors |
Fuhua Wen, Dahong Nie, Kongzhen Hu, Ganghua Tang, Shaobo Yao, Caihua Tang |
Abstract |
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. (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. 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. 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. |
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