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
The slow metabolism of L-[2-18F]-fluorophenylalanine in rat
β Scribed by M. Murakami; K. Takahashi; Y. Kondo; S. Mizusawa; H. Nakamichi; H. Sasaki; E. Hagami; H. Iida; I. Kanno; S. Miura; I. Itoh; K. Uemura
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 405 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
The stability of L-[2-16F]-fluorophenylalanine (2-Il8F]-Phe) was compared with that of natural amino acid, L-[2,6-3H]-Phenylalanine (2,6-[3H]-Phe). The mixture of 2-[18F]-and 2,6-13H]-Phe was injected to Wistar rats. The separated arterial plasma was followed by acid treatment and chromatographical analysis. The plasma [ 'F] -and [3H]-radioactivities decreased with the time and showed the lowest value at 20 min after injection. After that, [3H]-radioactivity increased significantly up to 60 min, while [18F]-radioactivit remained at the lowest level. The [3H]-and rr6F]radioactive macromolecules appeared in the plasma at 1 0 and 20 min, respectively. In the acid s o l uble fractions of the plasma and the brain at 60 min, more than 80 % of [18F]-radioactivity existed as 2-['*F] -Phe, while 2,6-[3H] -Phe was less than 15 % . These data suggest the slow metabolism of 2 -[I8F] -Phe as com ared with that of natural Phe. In conclusion, 2-[78F]-Phe is suitable to the compartment analysis using positron emission tomography especially at the process of amino acid transport to the brain due to its stability for the period necessary to kinetic analysis.
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