Synthetic methodology of short half-life radiopharmaceuticals for PET

TANG Ganghua

doi:null

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Synthetic methodology of short half-life radiopharmaceuticals for PET

更新时间：2021-03-12

- Synthetic methodology of short half-life radiopharmaceuticals for PET
- NUCLEAR TECHNIQUES Issue 7, (2003)
- 作者机构：
  
  第一军医大学南方医院南方PET中心,广州,510515
- 作者简介：
- 基金信息：
- DOI：
  CLC： R817
- Published：01 July 2003
- 稿件说明：
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[1]唐刚华.短半衰期正电子发射放射性药物合成方法学及进展[J].核技术,2003(07):551-555.

TANG Ganghua. Synthetic methodology of short half-life radiopharmaceuticals for PET[J]. Nuclear techniques, 2003, (7): 551-555.
[1]唐刚华.短半衰期正电子发射放射性药物合成方法学及进展[J].核技术,2003(07):551-555. DOI：

TANG Ganghua. Synthetic methodology of short half-life radiopharmaceuticals for PET[J]. Nuclear techniques, 2003, (7): 551-555. DOI：

摘要

短半衰期正电子发射放射性药物合成方法学已取得巨大进展。本文主要介绍18F标记药物、11C标记药物、15O标记药物及13N标记药物的合成方法学及进展

并重点对前两者进行分析讨论。

Abstract

Great progress in synthetic methodologies of short half-life radiopharmaceuticals for PET has been made. This article aims to summarize the synthetic methodologies and progress of fluorine-18

carbon-11

oxygen-15 and nitrogen-13 labelled radiopharmaceuticals

with special emphasis on the radiochemistry of those labelled with carbon-11 and fluorine-18.

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