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Article Dans Une Revue Journal of Labelled Compounds and Radiopharmaceuticals Année : 2021

[ 18 F]‐labeled positron emission tomography ligand for the histamine H4 receptor

Sylvie Chalon
Gabrielle Chicheri
  • Fonction : Auteur
Sylvie Bodard
  • Fonction : Auteur
Sophie Sérrière
  • Fonction : Auteur
Johnny Vercouillie

Résumé

We synthesized 5‐[ 18 F]‐fluoro‐1 H ‐indol‐2‐yl)(4‐methyl‐1‐piperazinyl)methanone ([ 18 F] 5 ) via a Suzuki approach starting from a protected pinacol borane precursor followed by acidic hydrolysis of the t ‐Boc protecting group. The non‐optimized radiochemical yield was 5.7 ± 1.35%, radiochemical purity was over 99%, and molar activity was 100.7 ± 34.5 GBq/μmol ( n = 3). [ 18 F] 5 was stable in rat plasma for at least 4 h and was evaluated by μPET imaging and biodistribution using a unilateral quinolinic acid rat model of neuroinflammation. The time‐activity curve showed that [ 18 F] 5 entered the brain immediately after intravenous injection and then left it progressively with a very low level reached from 30 min after injection. The biodistribution study showed no difference in the accumulation of [ 18 F] 5 between the lesioned and intact side of the brain and between control rats and animals pretreated with a saturating dose of JNJ‐7777120 as a specific H4R antagonist. Hence, despite its in vitro nanomolar affinity for H4R, and its ability to cross the blood–brain barrier in rats, [ 18 F] 5 does not appear suitable to image in vivo the receptor by PET.
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Dates et versions

hal-04451426 , version 1 (11-02-2024)

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Agnieszka Zak, Lucas Lemaire, Sylvie Chalon, Gabrielle Chicheri, Hamid Marzag, et al.. [ 18 F]‐labeled positron emission tomography ligand for the histamine H4 receptor. Journal of Labelled Compounds and Radiopharmaceuticals, 2021, 64 (9), pp.363-372. ⟨10.1002/jlcr.3929⟩. ⟨hal-04451426⟩
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