Radiochemical synthesis of 2′-[18F]-labelled and 3′-[18F]-labelled nucleosides for positron emission tomography imaging

被引:7
|
作者
Meyer, Jan-Philip [1 ,2 ]
Probst, Katrin C. [2 ]
Westwell, Andrew D. [1 ]
机构
[1] Cardiff Univ, Sch Pharm & Pharmaceut Sci, Cardiff CF10 3NB, S Glam, Wales
[2] Cardiff Univ, Wales Res & Diagnost PET Imaging Ctr PETIC, Inst Translat Innovat Methodol & Engagement TIME, Sch Med, Cardiff CF14 4XN, S Glam, Wales
关键词
nucleoside analogues; late stage precursor; F-18]-incorporation; radiosynthesis; IN-VIVO; CELLULAR PROLIFERATION; RADIOSYNTHESIS; GEMCITABINE; RATIONALE; F-18-FMAU; LYMPHOMA; PROMISE; TUMORS; PROBE;
D O I
10.1002/jlcr.3197
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This review article considers 2'-labelled and 3'-labelled nucleosides, which are of great importance as positron emission tomography (PET) probes in clinical diagnostics and PET research. Although the radiochemical preparation of several [F-18]-labelled nucleosides such as [F-18]fluorothymidine or [F-18](fluoroarabinofuranosyl) cytosine has been accomplished within the last two decades, a number of potentially interesting nucleoside-based biomarkers are not yet available for automated good manufacturing practice production due to the lack of fast and efficient synthetic methods for late-stage [F-18]-introduction. In order to meet recent demands for new PET-based biomarkers in various clinical applications, appropriate precursors that can easily be fluorinated and deprotected need to be developed.
引用
收藏
页码:333 / 337
页数:5
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