On‐chip chiral and achiral separation of amphetamine and related compounds labeled with 4‐fluoro‐7‐nitrobenzofurazane
On‐chip chiral and achiral separation of amphetamine and related compounds labeled with 4‐fluoro‐7‐nitrobenzofurazane
复制标题
4-氟-7-硝基苯并呋喃标记的安非他明及相关化合物的芯片上手性和非手性分离
作者:
S. Wallenborg;I. Lurie;D. Arnold;C. Bailey
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 γ‐CD (HS‐γ‐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‐γ‐CD and 1.5 mM SDS.