小分子的氟-18标记:使用无载体添加[18F]氟化物衍生的18F标记的芳基氟化物作为标记前体。

F Wuest
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引用次数: 14

摘要

有利的长半衰期,易于生产和发射的正电子能量低,使18F成为PET成像的理想放射性核素。18F的放射化学基本上依赖于两种不同类型的反应:亲核反应和亲电反应。所有18F标记的放射性示踪剂的合成都是基于[18F]氟离子或[18F]氟气体作为直接从回旋加速器获得的简单初级标记前体。它们既可以直接应用于放射性合成,也可以转化为更复杂的标记前体,从而实现有机示踪分子的多步骤构建。本文综述了几种18F标记的芳基氟化物作为无载体添加(n.c.a) [18F]氟化物的组成部分,通过多步合成方法构建具有高比放射性的小单体PET放射性示踪剂的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fluorine-18 labeling of small molecules: the use of 18F-labeled aryl fluorides derived from no-carrier-added [18F]fluoride as labeling precursors.

The favourable long-half life, the ease of production and the low energy of the emitted positron make 18F an ideal radionuclide for PET imaging. Radiochemistry of 18F basically relies on two distinctive types of reactions: nucleophilic and electrophilic reactions. All syntheses of 18F-labeled radiotracers are based on either [18F]fluoride ion or [18F]fluorine gas as simple primary labeling precursors which are obtained directly from the cyclotron. They can be applied either directly to the radiosynthesis or they can be transformed into more complex labeling precursors enabling the multi-step build-up of organic tracer molecules. The topic of this review is a survey on the application of several 18F-labeled aryl fluorides as building blocks derived from no-carrier-added (n.c.a.) [18F] fluoride to build up small monomeric PET radiotracers at high specific radioactivity by multi-step synthesis procedures.

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