Automated synthesis and purification of [18F]bromofluoromethane at high specific radioactivity

被引:48
作者
Bergman, J
Eskola, O
Lehikoinen, P
Solin, O
机构
[1] Abo Akad Univ, Turku PET Ctr, Accelerator Lab, FIN-20500 Turku, Finland
[2] Turku PET Ctr, Radiopharmaceut Chem Lab, FIN-20500 Turku, Finland
关键词
F-18]bromofluoromethane; specific radioactivity; LC-MS; F-18;
D O I
10.1016/S0969-8043(00)00358-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
[F-18]Bromofluoromethane was synthesised from dibromomethane by substitution of bromine with [F-18]fluoride. The synthesis and separation of the [F-18]bromofluoromethane were automated. [F-18]Bromofluoromethane was used to convert a phenolic and a thiophenolic precursor into a labelled ether and thioether, respectively. The specific radioactivity of these labelled products was determined with both high-performance liquid chromatography (with UV-absorbance detection) and liquid chromatography (with mass spectrometric detection). The median for the specific radioactivity, corrected at the end of radionuclide production, was 934 GBq/mu mol (range 40-9900 GBq/mu mol; n = 83). (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:927 / 933
页数:7
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