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Insights into Elution of Anion Exchange Cartridges: Opening the Path toward Aliphatic (18)F-Radiolabeling of Base-Sensitive Tracers

[Image: see text] Aliphatic nucleophilic substitution (S(N)2) with [(18)F]fluoride is the most widely applied method to prepare (18)F-labeled positron emission tomography (PET) tracers. Strong basic conditions commonly used during (18)F-labeling procedures inherently limit or prohibit labeling of ba...

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Detalles Bibliográficos
Autores principales: Bratteby, Klas, Shalgunov, Vladimir, Battisti, Umberto Maria, Petersen, Ida Nyman, van den Broek, Sara Lopes, Ohlsson, Tomas, Gillings, Nic, Erlandsson, Maria, Herth, Matthias M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506604/
https://www.ncbi.nlm.nih.gov/pubmed/34661074
http://dx.doi.org/10.1021/acsptsci.1c00133
Descripción
Sumario:[Image: see text] Aliphatic nucleophilic substitution (S(N)2) with [(18)F]fluoride is the most widely applied method to prepare (18)F-labeled positron emission tomography (PET) tracers. Strong basic conditions commonly used during (18)F-labeling procedures inherently limit or prohibit labeling of base-sensitive scaffolds. The high basicity stems from the tradition to trap [(18)F]fluoride on anion exchange cartridges and elute it afterward with basic anions. This sequence is used to facilitate the transfer of [(18)F]fluoride from an aqueous to an aprotic organic, polar reaction medium, which is beneficial for S(N)2 reactions. Furthermore, this sequence also removes cationic radioactive contaminations from cyclotron-irradiated [(18)O]water from which [(18)F]fluoride is produced. In this study, we developed an efficient elution procedure resulting in low basicity that permits S(N)2 (18)F-labeling of base-sensitive scaffolds. Extensive screening of trapping and elution conditions (>1000 experiments) and studying their influence on the radiochemical yield (RCY) allowed us to identify a suitable procedure for this. Using this procedure, four PET tracers and three synthons could be radiolabeled in substantially higher RCYs (up to 2.5-fold) compared to those of previously published procedures, even from lower precursor amounts. Encouraged by these results, we applied our low-basicity method to the radiolabeling of highly base-sensitive tetrazines, which cannot be labeled using state-of-art direct aliphatic (18)F-labeling procedures. Labeling succeeded in RCYs of up to 20%. We believe that our findings facilitate PET tracer development by opening the path toward simple and direct S(N)2 (18)F fluorination of base-sensitive substrates.