Fully Automated Synthesis of Novel TSPO PET Imaging Ligand [(18)F]Fluoroethyltemazepam

Introduction: Benzodiazepines, including temazepam are described as TSPO antagonists. In fact, TSPO was initially described as a peripheral benzodiazepine receptor (PBR) with a secondary binding site for diazepam. TSPO is a potential imaging target of neuroinflammation because there is an amplification of the expression of this receptor. Objectives: Herein, we developed a novel fluorinated benzodiazepine ligand, [(18)F]Fluoroethyltemazepam ([(18)F]F-FETEM), for positron emission tomography (PET) imaging of translocator protein (18 kDa). Methods: [(18)F]F-FETEM was radiolabelled with an automated synthesizer via a one-pot procedure. We conducted a [(18)F]F-aliphatic nucleophilic substitution of a tosylated precursor followed by purification on C18 and Alumina N SPE cartridges. Quality control tests was also carried out. Results: We obtained 2.0–3.0% decay-uncorrected radiochemical activity yield (3.7% decay-corrected) within the whole synthesis time about 33 min. The radiochemical purity of [(18)F]F-FETEM was over 90% by TLC analysis. Conclusions: This automated procedure may be used as basis for future production of [(18)F]F-FETEM for preclinical PET imaging studies.