A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Preparation of [F-18]beta-CFT-FP and [C-11]beta-CFT-FP, selective radioligands for visualisation of the dopamine transporter using positron emission tomography (PET)
Tekijät: Kamarainen EL, Kyllonen T, Airaksinen A, Lundkvist C, Yu MX, Nagren K, Sandell J, Langer O, Vepsalainen J, Hiltunen J, Bergstrom K, Lotjonen S, Jaakkola T, Halldin C
Kustantaja: JOHN WILEY & SONS LTD
Julkaisuvuosi: 2000
Journal: Journal of Labelled Compounds and Radiopharmaceuticals
Tietokannassa oleva lehden nimi: JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS
Lehden akronyymi: J LABELLED COMPD RAD
Vuosikerta: 43
Numero: 12
Aloitussivu: 1235
Lopetussivu: 1244
Sivujen määrä: 10
ISSN: 0362-4803
DOI: https://doi.org/10.1002/1099-1344(20001030)43:12<1235::AID-JLCR411>3.0.CO;2-9
Tiivistelmä
In this study the N-fluoropropyl analogue of the cocaine congener beta -CFT (I), N-(3-fluoropropyl)-2 beta -carbomethoxy-3 beta-(4-fluorophenyl) (beta -CFT-FP, III), was labelled with F-18 or C-11. Syntheses of the precursors nor-beta -CFT (II) and beta -CFT-FP acid (IV) as well as III itself are described. [F-18]beta -CFT-FP was prepared starting from I using two different labelling reagents: [F-18]fluoropropyl bromide (V) and [F-18]fluoropropyl tosylate (VI), A reversed-phase HPLC system proved to be effective in separating the labelled product from precursor II. The radiochemical incorporation of V or VI to yield [F-18]beta -CFT-FP (F-18-III) was in general 30-50% and the radiochemical purity was higher than 99%. [C-11]beta -CFT-FP (C-11-III) was synthesised by esterification of IV using [C-11]methyl triflate (VII). An HPLC-purification system using a reversed-phase column proved to be effective in separating the product from the acid precursor. The radiochemical yield starting from [C-11]carbon dioxide was 30-40% and the radiochemical purity was better than 99%. F-18-III and C-11-III have potential as radioligands for visualisation of the dopamine transporter (DAT) using Positron Emission Tomography (PET).
In this study the N-fluoropropyl analogue of the cocaine congener beta -CFT (I), N-(3-fluoropropyl)-2 beta -carbomethoxy-3 beta-(4-fluorophenyl) (beta -CFT-FP, III), was labelled with F-18 or C-11. Syntheses of the precursors nor-beta -CFT (II) and beta -CFT-FP acid (IV) as well as III itself are described. [F-18]beta -CFT-FP was prepared starting from I using two different labelling reagents: [F-18]fluoropropyl bromide (V) and [F-18]fluoropropyl tosylate (VI), A reversed-phase HPLC system proved to be effective in separating the labelled product from precursor II. The radiochemical incorporation of V or VI to yield [F-18]beta -CFT-FP (F-18-III) was in general 30-50% and the radiochemical purity was higher than 99%. [C-11]beta -CFT-FP (C-11-III) was synthesised by esterification of IV using [C-11]methyl triflate (VII). An HPLC-purification system using a reversed-phase column proved to be effective in separating the product from the acid precursor. The radiochemical yield starting from [C-11]carbon dioxide was 30-40% and the radiochemical purity was better than 99%. F-18-III and C-11-III have potential as radioligands for visualisation of the dopamine transporter (DAT) using Positron Emission Tomography (PET).
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