Analysis of Anthraquinones by Micellar Electrokinetic Capillary Chromatography
β Scribed by Junko Koyama; Izumi Toyokuni; Kiyoshi Tagahara
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 171 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0958-0344
No coin nor oath required. For personal study only.
β¦ Synopsis
A micellar electrokinetic capillary chromatographic method for the separation of anthraquinone positional isomers was established. The running electrolytes used in this method were 0.03 M sodium dodecyl sulphate (SDS) in 0.03 M borate buffer (pH 9) containing 10% acetonitrile for dihydroxy-and dihydroxy-methoxy-methylanthraquinones, 0.08 M SDS in 0.03 M borate buffer (pH 9) containing 10% acetonitrile for dimethoxyanthraquinones, and 0.03 M SDS in 0.08 M borate buffer (pH 8) containing 10% acetonitrile for hydroxy-methoxy-and dihydroxymethylanthraquinones, each with an applied voltage of 20 kV. This method is simple, rapid and reproducible.
π SIMILAR VOLUMES
The optimization of the organic modifier concentration in micellar Ε½ . electrokinetic capillary chromatography MECC has been achieved by a uniform design and iterative optimization method, which has been developed for the optimization of composition of the mobile phase in high performance liquid chr
A micellar electrokinetic capillary chromatographic method was set up for the quality control of rhubarb and its preparations. Anthraquinone derivatives were separated successfully within 10 min in the buffer solution of 50 mmol/L H 3 BO 3 -NaOH (pH 11) containing 25 mmol/L sodium deoxycholate. The
A micellar electrokinetic capillary chromatographic method was set up for the separation of five anthraquinone derivatives in rhubarb. Optimization of pH and sodium deoxycholate(SDC) concentrations was studied, which showed that 50 mM H3BO3-NaOH(pH 11) containing 25 mM SDC could separate the five in