Startseite Post-target produced [18F]F2 in the production of PET radiopharmaceuticals
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Post-target produced [18F]F2 in the production of PET radiopharmaceuticals

  • Sarita Forsback EMAIL logo und Olof Solin
Veröffentlicht/Copyright: 18. Dezember 2014

Abstract

Electrophilic radiofluorination was successfully carried out in the early years of PET radiochemistry due to its ease and fast reaction speed. However, at the present, the use of electrophilic methods is limited due to low specific activity (SA). Post-target produced [18F]F2 has significantly higher SA compared to other electrophilic approaches, and it has been used in the production of clinical PET radiopharmaceuticals at the Turku PET Centre for years. Here, we summarize the synthesis and use of these radiopharmaceuticals, namely [18F]FDOPA, [18F] CFT, [18F]EF5 and [18F]FBPA.

Received: 2014-3-4
Accepted: 2014-10-30
Published Online: 2014-12-18
Published in Print: 2015-3-28

©2014 Walter de Gruyter Berlin/Boston

Heruntergeladen am 20.10.2025 von https://www.degruyterbrill.com/document/doi/10.1515/ract-2014-2334/html
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