6-[18F]氟左旋多巴的产生及其体内代谢综述

A. Luxen , M. Guillaume , W.P. Melega , V.W. Pike , O. Solin , R. Wagner
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引用次数: 77

摘要

本报告批判性地评价了6-[18F]氟-l-3,4-二羟基苯丙氨酸(6- fdopa)的合成方法,这些方法基于非区域选择性亲电氟化、区域选择性氟脱金属或亲核取代的标记。对标签程序的标准化、放射化学产率的优化以及产品质量和安全的保证提出了建议。本文还回顾了6-FDOPA在体内代谢的研究,强调了该示踪剂在正电子发射断层扫描(PET)中开发的生化成分的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of 6-[18F]fluoro-l-DOPA and its metabolism in vivo—a critical review

This report critically appraises methods for the synthesis of 6-[18F]fluoro-l-3,4-dihydroxyphenylalanine (6-FDOPA) that are based on labelling by non-regioselective electrophilic fluorination, regioselective fluorodemetalation or nucleophilic substitution. Recommendations for the standardization of labelling procedures, the optimization of radiochemical yield and the assurance of product quality and safety are given. Studies of the metabolism of 6-FDOPA in vivo are also reviewed to emphasize the importance of the biochemical component of the development of this tracer for positron emission tomography (PET).

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