Chiral separation of vinpocetine using cyclodextrin-modified micellar electrokinetic chromatography.

Separation of 1,4-benzodiazepine Derivates by Cyclodextrin Modified Micellar Electrokinetic Chromatography

The electrophoretic separation of electrically neutral benzodiazepines (BZDs) can be achieved by micellar electrokinetic chromatograpy (MEKC). The cyclodextrin (CD)-modified micellar electrokinetic chromatography separation of eight of the most frequently used BZD was obtained within 15 minutes at + 25 kV on a 64.5 cm x 50 μm I.D. silica capillary at 25C, using a 25 mM sodium tetraborate-50 mM ...

Enantioseparation of Penconazole, Myclobutanil and Triadimefon by Cyclodextrin-Modified Micellar Electrokinetic Chromatography

Simultaneous enantioseparation of three chiral triazole fungicides i.e. penconazole, myclobutanil and triadimefon by cyclodextrin-modified micellar electrokinetic chromatography (CD-MEKC) under acidic condition was investigated with different HP-γ-CD concentrations as chiral selector. The three triazole fungicides have an asymmetrically substituted carbon atom respectively, and they all contain...

Enantiomeric separation of primaquine, an anti-malarial drug, by cyclodextrin-modified micellar electrokinetic capillary chromatography.

A Comparative Study of the Separation of Oleanolic Acid and Ursolic Acid in Prunella vulgaris by High-Performance Liquid Chromatography and Cyclodextrin-Modified Micellar Electrokinetic Chromatography

A high-performance liquid chromatographic (HPLC) method and a cyclodextrin-modified micellar electrokinetic chromatographic (CD-MEKC) method were developed to separate and determine oleanolic acid (OA) and ursolic acid (UA) in Prunella vulgaris. HPLC separations were carried out on a Hedera ODS C18 column with methanol -H2Oacetic acid (85:15:0.3, v/v/v) as mobile phase at a flow-rate of 0.8 ml ...

Enantiomer separation of miconazole by capillary electrophoresis with dual cyclodextrin systems.

A cyclodextrin-modified micellar capillary electrophoretic method (MECC) was developed using mixtures of beta, cyclodextrins (beta-CD) and mono-3-O-phenylcarbamoyl-beta-CD as chiral additives for the chiral separation of miconazole with the dual CDs systems. The enantiomers were resolved using a running buffer of 50 mmol/L borate pH 9.5 containing 15 mmol/L beta-CD and 15 mmol/L mono-3-O-phenyl...