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One-step radiosynthesis of [18F]LBT-999: a selective radioligand for the visualization of the dopamine transporter with PET

✍ Scribed by Frédéric Dollé; Julie Helfenbein; Françoise Hinnen; Sylvie Mavel; Zoïa Mincheva; Wadad Saba; Marie-Anne Schöllhorn-Peyronneau; Heric Valette; Lucette Garreau; Sylvie Chalon; Christer Halldin; Jean-Claude Madelmont; Jean-Bernard Deloye; Michel Bottlaender; Joël Le Gailliard; Denis Guilloteau; Patrick Emond


Publisher
John Wiley and Sons
Year
2007
Tongue
French
Weight
153 KB
Volume
50
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

LBT‐999 (8‐((E)‐4‐fluoro‐but‐2‐enyl)‐3‐beta‐p‐tolyl‐8‐aza‐bicyclo[3.2.1]octane‐2‐beta‐carboxylicacid methyl ester) is a recently developed cocaine derivative belonging to a new generation of highly selective dopamine transporter (DAT) ligands (K~D~: 9 nM for the DAT and IC~50~ > 1000 nM for the serotonin and norepinephrine transporter). Initial fluorine‐18‐labelling of LBT‐999 was based on the robust and reliable two‐step radiochemical pathway often reported for such tropane derivatives, involving first the preparation of (E)‐1‐[^18^F]fluoro‐4‐tosyloxybut‐2‐ene followed by a N‐alkylation reaction with the appropriate nor‐tropane moiety. In the present work, a simple one‐step fluorine‐18‐labelling of LBT‐999 is reported, based on a chlorine‐for‐fluorine nucleophilic aliphatic substitution, facilitating as expected both automation and final high‐performance liquid chromatography (HPLC) purification. The process involves: (A) reaction of K[^18^F]F–Kryptofix^®^222 with the chlorinated precursor (3.5–4.5 mg) at 165°C for 10 min in DMSO (0.6 mL) followed by (B) C‐18 PrepSep cartridge pre‐purification and finally (C) semi‐preparative HPLC purification on a Waters Symmetry^®^ C‐18. Typically, 3.70–5.92 GBq of [^18^F]LBT‐999 (> 95% chemically and radiochemically pure) could be obtained with specific radioactivities ranging from 37 to 111 GBq/µmol within 85–90 min (HPLC purification and Sep‐Pak‐based formulation included), starting from a 37.0 GBq [^18^F]fluoride batch (overall radiochemical yields: 10–16%, non‐decay‐corrected). Copyright © 2007 John Wiley & Sons, Ltd.


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