کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2154617 | 1090243 | 2008 | 6 صفحه PDF | دانلود رایگان |
IntroductionWe developed a new fully automated method for the radiosynthesis of [18F]fluorocholine by modifying the commercial 2-[18F]fluoro-2-d-deoxy-glucose ([18F]FDG) synthesizer module (GE TracerLab MX, formerly Coincidence).Methods[18F]Flurocholine was synthesized by 18F-fluoroalkylation of N,N-dimethylaminoethanol using [18F]fluorobromomethane as fluoromethylating agent. [18F]Fluorobromomethane was produced by reaction of dibromomethane with [18F]fluoride, assisted by Kryptofix 2.2.2.ResultsAfter purification on solid-phase extraction cartridges, the [18F]fluorocholine was obtained in 15–25% radiochemical yields (decay not corrected), with more than 99% radiochemical purity. Specific activity was more than 37 GBq/μmol. Synthesis time was less than 35 min.ConclusionThis new automated synthesis technique provides high and reproducible yields that could be dedicated for routine use with the same [18F]FDG disposable cassette system.
Journal: Nuclear Medicine and Biology - Volume 35, Issue 2, February 2008, Pages 255–260