PET radioligands for dopamine receptors and re-uptake sites: Chemistry and biochemistry

B Mazière , H.H Coenen , C Halldin , K Någren , V.W Pike
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引用次数: 44

Abstract

This report, based on the past experience of European centres, offers practical guidance on the chemistry and biochemistry of PET radioligands used for the in vivo imaging of dopamine receptors and re-uptake sites. It mainly summarizes methods for the preparation of D1 and D2 receptor ligands labelled with positron-emitting radioisotopes. Some of these ligands (11C-labelled SCH23390, raclopride and nomifensine, 18F-labelled butyrophenones, [76Br]bromolisuride), which have been found useful in PET clinical investigations, have been emphasized. This report is intended as an introduction and guideline for new PET-groups who want to start research in the dopaminergic neurotransmission imaging field.

多巴胺受体和再摄取位点的PET放射配体:化学和生物化学
本报告基于欧洲中心过去的经验,提供了用于多巴胺受体和再摄取部位体内成像的PET放射配体的化学和生物化学的实用指导。主要综述了用正电子放射同位素标记D1和D2受体配体的制备方法。其中一些配体(11c标记的SCH23390, raclopride和nomifenine, 18f标记的butyrophenones, [76Br]bromolisuride)已被发现在PET临床研究中有用,已被强调。本报告旨在为希望在多巴胺能神经传递成像领域开展研究的新pet组提供介绍和指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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