Cakrt M, Hercegová A, Lesko J, Polonský J, Sádecká J, Skacáni I
Department of Analytical Chemistry, Faculty of Chemical Technology, Slovak University of Technology, Bratislava, Slovak Republic.
J Chromatogr A. 2001 May 4;916(1-2):207-14. doi: 10.1016/s0021-9673(00)01071-2.
An isotachophoretic method with conductivity detection was developed to determine naproxen in the presence of its metabolite 6-O-desmethylnaproxen in human serum. The leading electrolyte contained 10 mM hydrochloric acid, beta-alanine, pH 4.0 and 0.1% methylhydroxypropylcellulose. The terminating electrolyte was 10 mM 2-(N-morpholino)ethanesulfonic acid-tris(hydroxymethyl)aminomethane, pH 6.9, containing 20% (v/v) of ethanol. Naproxen was determined in serum supernatant after simple deproteination of the sample with ethanol. The isotachophoretic results were compared with those obtained by synchronous fluorescence spectrometry.