Kinetics of the metabolism of four PET radioligands in living minipigs.

N M Gillings, D Bender, L Falborg, K Marthi, O L Munk, P Cumming

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearch

    Abstract

    Most radioligands are substantially metabolised in peripheral organs during the course of positron emission tomography (PET) recordings. Accurate determination of plasma concentrations of unmetabolised radioligands is often important for quantification of data from PET studies. The fractions of untransformed radioligand and radioactive metabolites in plasma extracts must then be measured. Temporal changes in these fractions are influenced by the rate constant of appearance of total radioactive metabolites in plasma (apparent rate constant of metabolism in plasma, k(0)) and the net rate constant of elimination of all radioactive metabolites from plasma (k(-1)). In order to clarify the relationship between radioligand fractions and rate constants, plasma samples collected from Göttingen minipigs during PET recordings using four different binding site ligands were analysed by radio high performance liquid chromatography. The calculated plasma concentrations of parent compounds and their radioactive metabolites were used to calculate k(0) and k(-1) for 11C-labelled NNC 112, NS 2214, PK 11195 and raclopride in minipigs using a novel application of the tissue-slope intercept plot. In general, the apparent rate constant of metabolism in plasma was found to be greater in the minipig than in man. The reported kinetic analysis enables the apparent metabolism of PET radioligands in plasma to be quantified.
    Udgivelsesdato: 2001-Jan
    Original languageEnglish
    JournalNuclear Medicine and Biology
    Volume28
    Issue1
    Pages (from-to)97-104
    Number of pages7
    ISSN0969-8051
    Publication statusPublished - 2001

    Keywords

    • Animals
    • Binding Sites
    • Chromatography, High Pressure Liquid
    • Dopamine Antagonists
    • Molecular Structure
    • Raclopride
    • Swine, Miniature
    • Tissue Distribution
    • Tomography, Emission-Computed

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