Separation and determination of three water-soluble vitamins in pharmaceutical preparations and food by micellar electrokinetic chromatography with amperometric electrochemical detection

A simple, reliable and reproducible method, based on micellar electrokineti c chromatography with amperometric detection, for the separation and determ ination of the three water-soluble vitamins, namely nicotinamide (VPP), pyr idoxine (VBs) and ascorbic acid (VC), in pharmaceutical preparations and fo od is described in this paper. A carbon disk electrode was used as working electrode. The optimal conditions of separation and detection were 0.02 mol /l phosphate-0.005 mol/l berate buffer (pH 8.8) containing 0.03 mol/l sodiu m dodecylsulphate (SDS), 7 kV for the separation voltage, and 1.20 V (versu s Ag/AgCl) for the detection potential. The linear ranges were from 3.0 x 1 0(-4) to 1.0 x 10(-2) mol/l for VPP, 2.5 x 10(-6) to 1.0 x 10(-3) mol/l for VBs, and 2.5 x 10(-6) to 1.0 x 10(-3) mol/l for VC with regression coeffic ients of 0.9900, 0.9998 and 0.9990, respectively. The detection limits for VPP, VBs and VC were 5.0 x 10(-5), 1.0 x 10(-6) and 1.0 x 10(-6) mol/l, res pectively. The method developed in this paper was directly applied to the d etermination of the three water-soluble vitamins in pharmaceutical preparat ions and food, and the assay results were satisfactory. (C) 2001 Elsevier S cience B.V. All rights reserved.