共 50 条
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.
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页码:333 / 337
页数:5
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