Microemulsion electrokinetic chromatography in suppressed electroosmotic flow environment -: Separation of fat-soluble vitamins

被引:69
作者
Pedersen-Bjergaard, S [1 ]
Næss, O [1 ]
Moestue, S [1 ]
Rasmussen, KE [1 ]
机构
[1] Univ Oslo, Sch Pharm, N-0316 Oslo, Norway
关键词
microemulsion electrokinetic chromatography; electroosmotic flow; buffer composition; vitamins;
D O I
10.1016/S0021-9673(00)00117-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microemulsion electrokinetic chromatography (MEEKC) was carried out in a pH 2.5 phosphate buffer to effectively suppress the electroosmotic flow (EOF). With 66.6% (w/w) 25 mM phosphate buffer pH 2.5, 20.0% (w/w) 2-propanol, 6.6% (w/w) l-butanol, 6.0% (w/w) sodium lauryl sulphate (SDS), and 0.8% (w/w) n-octane as the separation medium, the fat-soluble vitamins ii palmitate, E acetate, and D-3 were baseline separated within II min. With strongly suppressed EOF, the polarity of the separation voltage was reversed (positive electrode at the outlet); the n-octane micro droplets surrounded by negatively charged SDS molecules migrated towards the detector. The aqueous part of the microemulsion was modified with 20% (w/w) 2-propanol to improve partition between the n-octane phase and the surrounding aqueous medium. The fat-soluble vitamins were separated in order of decreasing hydrophobicity with a high migration time stability (repeatable within 0.1% RSD). Excellent accuracy and precision were obtained when the system was applied for the determination of vitamin E acetate in commercial vitamin tablets; quantitative data corresponded to 97.0% of label claim, intra-day results varied within 1.72% RSD (n=6), and inter-day results varied within 3.22% RSD (n=5). (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:201 / 211
页数:11
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