Abstract
Isolation of the fluoroquinolones, flumequine and oxolinic acid, from fortified chicken liver was achieved using liquid–liquid extraction, aqueous on-line dialysis and trace enrichment. Dialysis, trace enrichment and column switching were performed using the ASTED system. Separation of the isolated compounds in the tissue extracts was performed using reversed-phase HPLC and fluorescence detection. This procedure yielded excellent mean recoveries at the 50, 25, 10 and 5 ng/g spiking levels for flumequine (94–96%; 4–9% R.S.D.) and at the 25 and 5 ng/g spiking levels for oxolinic acid (98–99%; 4–6% R.S.D.). Clean chromatograms were obtained, allowing detection of 5 ng/g flumequine and 2.5 ng/g oxolinic acid to be easily made. Due to its lower organic solvent consumption, automation and on-line capabilities, this method may be a suitable replacement for conventional chemical extraction techniques for drug residues in animal tissues.
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