Radiosynthesis of 18F-fluoroethylated tracers via a simplified one-pot 18F-fluoroethylation method using [18F]fluoroethyl tosylate

Recently, a straightforward one-pot method for 18F-fluoroethylation without azeotropic drying of cyclotron-produced [18F]F− was developed. In this study, we have attempted to simplify the automated radiosynthesis of two [18F]fluoroethylated tracers, [18F]FEDAC and [18F]FET, using a desmethyl labelin...

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Veröffentlicht in:Applied radiation and isotopes 2021-03, Vol.169, p.109571-109571, Article 109571
Hauptverfasser: Kawamura, Kazunori, Kumata, Katsushi, Mori, Wakana, Fujinaga, Masayuki, Kurihara, Yusuke, Ogawa, Masanao, Ohkubo, Takayuki, Furutsuka, Kenji, Hashimoto, Hiroki, Nengaki, Nobuki, Zhang, Ming-Rong
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Sprache:eng
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Zusammenfassung:Recently, a straightforward one-pot method for 18F-fluoroethylation without azeotropic drying of cyclotron-produced [18F]F− was developed. In this study, we have attempted to simplify the automated radiosynthesis of two [18F]fluoroethylated tracers, [18F]FEDAC and [18F]FET, using a desmethyl labeling precursor and [18F]fluoroethyl tosylate, based on the above-mentioned method. The radiochemical yields of [18F]FEDAC and [18F]FET were 26 ± 3.7% (n = 5) and 14 ± 2.2% (n = 4), respectively, based on total [18F]F− at the end of irradiation. •The simplified one-pot 18F-fluoroethylation method has developed.•The radiosynthesis of [18F]FEDAC and [18F]FET were simplified.•A lower cost of the precursors for 18F-fluoroethylation is provided.•A shorter synthesis time for 18F-fluoroethylation is provided.•Automated one-pot 18F-fluoroethylation strategy is provided.
ISSN:0969-8043
1872-9800
DOI:10.1016/j.apradiso.2020.109571