Synthesis and preliminary evaluation of a carbon-11-labelled agonist of the α7 nicotinic acetylcholine receptor

被引:25
作者
Dolle, F [1 ]
Valette, H [1 ]
Hinnen, F [1 ]
Vaufrey, F [1 ]
Demphel, S [1 ]
Coulon, C [1 ]
Ottaviani, M [1 ]
Bottlaender, M [1 ]
Crouzel, C [1 ]
机构
[1] CEA, Serv Hosp Frederic Joliot, Dept Rech Med, F-91401 Orsay, France
关键词
C-11]isocyanate; alpha; 7; nAChR; carbon-11; positron emission tomography; PET;
D O I
10.1002/jlcr.504
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The lead compound of a new series of azabicyclic carbamates described by Astra Laboratories as ligands for the alpha7 nicotinic acetylcholine receptor subtype, namely N-(4-bromophenyl)carbamic acid quinuclidin-3-yl ester, has been labelled with carbon-11 using no-carrier-added [C-11]phosgene and the isocyanate pathway. Typically, 25-35 mCi (0.92-1.29 GBq) of the tracer was obtained within 30 min of radiosynthesis (HPLC purification included) with specific radioactivities ranging from 500 to 800 mCi/mu mol (18.5-29.6 GBq/mu mol). Biodistribution studies demonstrated a relatively good brain uptake of the compound (0.8-1.2% I.D./g tissue in various brain regions), but without preferential concentration in brain regions rich in alpha7-subtype nicotinic receptor (e.g. hippocampus, pons and colliculi). No specific binding could be demonstrated in pre-saturation studies performed with both the cold compound and nicotine. Therefore, this ligand is not suitable for further exploration in PET imaging. Copyright (C) 2001 John Wiley & Sons, Ltd.
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页码:785 / 795
页数:11
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