Wallenborg S R, Lurie I S, Arnold D W, Bailey C G
Sandia National Laboratories, Livermore, CA 94551-0969, USA.
Electrophoresis. 2000 Sep;21(15):3257-63. doi: 10.1002/1522-2683(20000901)21:15<3257::AID-ELPS3257>3.0.CO;2-M.
Amphetamine and analogous compounds have been labeled with 4-fluoro-7-nitrobenzofurazane and analyzed on a microfabricated chip. Separation of norephedrine, ephedrine, cathinone, pseudoephedrine, methcathinone, amphetamine and methamphetamine is demonstrated using micellar electrokinetic capillary chromatography (MEKC) and laser-induced fluorescence (LIF) detection. Chiral separations of individual drugs were studied using neutral and negatively charged cyclodextrins (CDs) with and without the addition of an organic modifier and/or sodium dodecyl sulfate (SDS). The best results were obtained using a highly sulfated gamma-CD (HS-gamm-CD) in combination with a low concentration of SDS. To obtain complete separation of a mixture of (+/-)-norephedrine, (+/-)ephedrine, (+/-)-pseudoephedrine, (+/-)-methcathinone, (+/-)-amphetamine and (+/-)-methamphetamine it was necessary to add a small amount (1.5 mM) of SDS to the separation buffer. Optimized chiral separation was achieved within 7 min using an S-folded separation channel, a separation voltage of 8 kV and a buffer consisting of 50 mM phosphate (pH 7.35), 10 mM HS-gamma-CD and 1.5 mM SDS.
苯丙胺及类似化合物已用4-氟-7-硝基苯并呋喃标记,并在微制造芯片上进行分析。使用胶束电动毛细管色谱法(MEKC)和激光诱导荧光(LIF)检测,实现了去甲麻黄碱、麻黄碱、卡西酮、伪麻黄碱、甲卡西酮、苯丙胺和甲基苯丙胺的分离。使用带中性和负电荷的环糊精(CDs),在添加和不添加有机改性剂和/或十二烷基硫酸钠(SDS)的情况下,研究了各药物的手性分离。使用高度硫酸化的γ-环糊精(HS-γ-CD)与低浓度的SDS相结合,获得了最佳结果。为了实现(±)-去甲麻黄碱、(±)-麻黄碱、(±)-伪麻黄碱、(±)-甲卡西酮、(±)-苯丙胺和(±)-甲基苯丙胺混合物的完全分离,有必要在分离缓冲液中添加少量(1.5 mM)的SDS。使用S形分离通道、8 kV的分离电压以及由50 mM磷酸盐(pH 7.35)、10 mM HS-γ-CD和1.5 mM SDS组成的缓冲液,在7分钟内实现了优化的手性分离。