Fully automated analytical method for codeine quantification in human plasma using on-line solid-phase extraction and high-performance liquid chromatography with ultraviolet detection

A simple, sensitive and fully automated analytical method for the analysis of codeine in human plasma is presented. Samples are added with oxycodone, used as internal standard (I.S,), and directly loaded in the autosampler tr ay. An on-line sample clean-up system based on solid-phase extraction (SPE) cartridges (Bond-Elut C-2, 20 mg) and valve switching (Prospekt) is used. Isocratic elution improved reproducibility and allowed the recirculation of the mobile phase. A Hypersil BDS C-18, 3 mu m, 10 x 0.46 cm column was use d and detection was done by UV monitoring at 212 nm. Retention times of nor codeine (codeine metabolite), codeine and oxycodone (I.S.) were 5.5, 6.4 an d 9.1 min, respectively. Morphine was left to elute in the chromatographic front. Detection limit for codeine was 0.5 mu g l(-1) and inter-assay preci sion (expressed as relative standard deviation) and accuracy (expressed as relative error) measured at 2 mu g l(-1) were 5.03% and 1.82%. Calibration range was 2-140 mu g l(-1). (C) 1999 Elsevier Science B.V. All rights reser ved.