Abstract
[18F]Fluorination is usually carried out by nucleophilic substitution reactions entailing the use of stringent conditions. A number of novel techniques including silicon and boron based fluoride acceptor molecules, [18F]FDG conjugation and chelation of the Al18F complex have been employed recently to achieve [18F]radiolabelling of macromolecules. These approaches are reviewed and their limitations outlined.
Original language | English |
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Pages (from-to) | 281-288 |
Number of pages | 8 |
Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
Volume | 55 |
Issue number | 8 |
DOIs | |
Publication status | Published - 30 Jun 2012 |
Keywords
- FDG
- silicon
- boron
- peptide
- protein
- Al18F