New radiosynthesis of 2-deoxy-2-[18F]fluoroacetamido-D-glucopyranose and its evaluation as a bacterial infections imaging agent

Introduction: The diagnosis of infection and the ability to distinguish bacterial infection from nonbacterial inflammation by positron emission tomography (PET) have gained interest in recent years, but still few specific radiophaanaceuticals are available for use. In this study, we developed a new radiosynthesis od of 2-deoxy-2[(18)]F]fluoroacetamido-D-glucopyranose ([F-18]FAG) by applying microwave irradiation and demonstrated that [F-18]FAG could be a potential radiophanriaceutical to distinguish bacterial infection from nonbacterial inflammation. Methods: 1,3,4,6-Tetra-O-acety1-2-deoxy-2-bromoacetamido-D-glucopyranose was used as precursor, and labeling was performed under microwave irradiation conditions followed by alkaline hydrolysis and high-performance liquid chromatography (HPLC) purification. In vitro uptake of [F-18]FAG by Escherichia coli was performed. Tissue biodistribution of [F-18]FAG was performed in mice. Moreover, PET imaging acquisition of E. coli infection and nonbacterial inflammation models was performed in rats. Tissue radiotracer-accumulated sites were analyzed by hematoxylin and eosin staining and anti-E.coli immunostaining. Results: The radiosynthesis of [F-18]FAG was achieved with microwave irradiation, and the radiochemical yield was 9.7% 2.8% end of bombardment (EOB); the radiochemical purity was more than 98%, and the total synthesis time was 62 min. Compared with control group, in vitro uptake of [F-18]FAG by E. coli was significantly decrease in inhibition group (P<.05). Biodistribution studies in mice showed rapid clearance of [F-18]FAG from the animal body. [F-18]FAG clearly visualized the infection areas but not nonbacterial inflammation areas in PET studies. Quantitative analysis revealed that the uptake of [F-18]FAG into infection areas was significantly higher than that of [E-18]FAG into inflammation areas (P<.05). Histological analysis demonstrated the presence of bacterial cells at the sites of accumulation of [F-18]FAG. Conclusions: Using 1,3,4,6-tetra-O-acety1-2-deoxy-2-bromoacetamido-D-glucopyranose as a precursor, the new radiosynthesis method of [F-18]FAG was achieved in fewer steps and with a shorter synthesis time than previously reported. Furthermore, [F-18]FAG was able to distinguish bacterial infection from nonbacterial inflammation. (C) 2011 Elsevier Inc. All rights reserved.