摘要

[18F]PBR111 and [18F]PBR102 are selective radioligands for imaging of the Peripheral Benzodiazepine Receptor (PBR). We have developed a fully automated method for the radiosynthesis of [18F]PBR111 and [18F]PBR102 in the Tracerlab FXFN (30±2 radiochemical yield non-decay-corrected for both tracers) and Tracerlab MXFDG (25±2 radiochemical yield non-decay-corrected for both tracers) from the corresponding p-toluenesulfonyl precursors. For all tracers, radiochemical purity was 99 and specific activity was 150GBq/μmol after less than 60min of preparation time.

  • 单位
    Royal Prince Alfred Hospital

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