Fluorination with 18F-F2 and 18F-AcOF were compared for the synthesis of 18F-fluorophenylalanines. L-phenylalanine in CF,COOH trapped 18F-AcOF more effectively than 18F-F2. The main product was ortho-18F-fluorophenylalanine when 18F-AcOF was used as a reagent. Lower radiochemical yield of 18F-fluoro
Synthesis of 4-dihydroxyboryl-2-[18F]fluorophenylalanine with relatively high-specific activity
✍ Scribed by Jyrki K. Vähätalo; Olli Eskola; Jörgen Bergman; Sarita Forsback; Pertti Lehikoinen; Juha Jääskeläinen; Olof Solin
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- French
- Weight
- 130 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.600
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✦ Synopsis
Abstract
An alternative procedure to produce 4‐dihydroxyboryl‐2‐[^18^F]fluorophenylalanine ([^18^F]FBPA) for positron emission tomography studies in boron neutron capture therapy is described. Relatively high‐specific activity electrophilic radiofluorine is produced using a post‐target conversion of [^18^F]F^–^ to [^18^F]F~2~. Liquid chromatography with mass spectrometric detection is used to estimate the specific radioactivity of [^18^F]FBPA and to verify the quality control for chemical identity of the target compound. [^18^F]FBPA produced according to this method fulfilled the pharmaceutical quality requirements for an injection in patients. Copyright © 2002 John Wiley & Sons, Ltd.
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