Novel fluorine-18 PET radiotracers based on flumazenil for GABA sub(A) imaging in the brain

• Published in: Nuclear medicine and biology Vol. 40; no. 7; pp. 901 - 905
• Main Authors: Rodnick, ME, Hockley, B G, Sherman, P, Quesada, C, Battle, M R, Jackson, A, Linder, KE, Macholl, S, Trigg, W J, Kilbourn, M R, Scott, PJH
• Format: Journal Article
• Language: English
• Published: 01-10-2013
• Subjects: Algorithms; Macaca mulatta
• ISSN: 0969-8051

Introduction: Two 7-fluoroimidazobenzodiazepines (AH114726 and GEH120348), analogs of flumazenil, were labeled with fluorine-18 and evaluated as alternative radioligands for in vivo imaging of the GABA sub(A)/benzodiazepine receptor by comparing them to [ super(11)C]flumazenil in rhesus monkey. Methods: Radiotracers were prepared from the corresponding nitro-precursors in an automated synthesis module, and primate imaging studies were conducted on a Concorde MicroPET P4 scanner. The brain was imaged for 60 (12 x 5 min frames) or 90 min (18x5 min frames), and data was reconstructed using the 3D MAP algorithm. Specificity of [ super(18)F]AH114726 and [ super(18)F]GEH120348 was confirmed by displacement studies using unlabeled flumazenil. Results: [ super(18)F]GEH120348 and [ super(18)F]AH114726 were obtained in 13-24% yields (end of synthesis) with high chemical (>95%) and radiochemical (>99%) purities, and high specific activities (2061 plus or minus 985 Ci/mmol). The in vivo pharmacokinetics of [ super(11)F]AH114726 and [ super(18)F]GEH120348 were determined in a non-human primate and directly compared with [ super(11)C]flumazenil. Both fluorine-18 radioligands showed time-dependent regional brain distributions that correlated with the distribution of [ super(11)C]flumazenil and the known concentrations of GABA sub(A)/benzodiazepine receptors in the monkey brain. [ super(18)F]AH114726 exhibited maximal brain uptake and tissue time-radioactivity curves that were most similar to [ super(11)C]flumazenil. In contrast, [ super(18)F]GEH120348 showed higher initial brain uptake but very different pharmacokinetics with continued accumulation of radioactivity into the cortical regions of high GABA/benzodiazepine receptor concentrations and very little clearance from the regions of low receptor densities. Rapid washout of both radiotracers occurred upon treatment with unlabeled flumazenil. Conclusion: The ease of the radiochemical synthesis, together with in vivo brain pharmacokinetics most similar to [ super(11)C]flumazenil, support that [ super(18)F]AH114726 is a suitable option for imaging the GABA sub(A) receptor.