Alternative solvents for electrophilic synthesis of 6-[18F]fluoro-L-DOPA

被引:14
|
作者
Forsback, Sarita [1 ,2 ]
Eskola, Olli [1 ,2 ]
Bergman, Joergen [1 ,2 ]
Haaparanta, Merja [3 ]
Solin, Olof [1 ,2 ]
机构
[1] Turku PET Ctr, Radiopharmaceut Chem Lab, FI-20500 Turku, Finland
[2] Turku PET Ctr, Accelerator Lab, FI-20500 Turku, Finland
[3] Turku PET Ctr, MediCity PET Preclin Imaging, FI-20520 Turku, Finland
来源
基金
芬兰科学院;
关键词
F-18]FDOPA; electrophilic fluorodestannylation; F-18]F-2; Freon-11; ELEMENTAL FLUORINE; ORGANIC-CHEMISTRY; RADIOFLUORODESTANNYLATION; 6-<F-18>FLUORO-L-DOPA; PRECURSOR;
D O I
10.1002/jlcr.1599
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Owing to the ozone layer-depleting properties of chlorofluorocarbon compounds, alternative solvents for electrophilic fluorination reactions are desirable. Chloroform, dichloromethane, acetone or their deuterated analogues were examined as substitutes for Freon-11 in the electrophilic synthesis of 6-[F-18]fluoro-L-DOPA ([F-18]FDOPA). CDCl3, CD2Cl2 and C3D6O were found to be suitable solvents in this reaction, with the deuterated solvents providing significantly higher yields than Freon-11. There were no differences among the solvents in the specific radioactivity, the radiochemical purity, the chemical purity or the microbiological quality of the final product. However, the radiochemical yield of [F-18]FDOPA was increased when acetic acid was added to the precursor solution prior to the fluorination reaction.
引用
收藏
页码:286 / 288
页数:3
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