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An optimized radiosynthesis of [18F]DK222, a PET radiotracer for imaging PD-L1
DanielPHolt,DhirajKumar,SridharNimmagadda,RobertFDannals
Journal of Labelled Compounds and Radiopharmaceuticals Pub Date : 01/10/2023 00:00:00 , DOI:10.1002/jlcr.4012
Abstract
A radiochemical synthesis of [18F]DK222, a peptide binder of programmed death ligand 1 protein, suitable for human PET studies is described, and results from validation productions are presented. The high specific activity radiotracer product is prepared as a sterile, apyrogenic solution that conforms to current Good Manufacturing Practice (cGMP) requirements. In addition, the production is extended to use a commercial synthesizer platform (General Electric FASTlab 2).
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