Authors Cheng, Y. Q.; Zhang, Y. X.; Qi, S. D.; Chen, H. L.; Chen, X. G.
Journal ACTA CHROMATOGRAPHICA , DEC 2010,4:22
DOI 10.1556/AChrom.22.2010.4.12
Abstract 1,7-Dihydroxy-3,8-dimethoxyxanthone (X1) and 1,8-dihydroxy-3,7-dimethoxyxanthone (X2) are two important xanthones of the Tibetan medicinal plant Gentianopsis paludosa (Hook. f.) Ma. They are very similar in structure, the only difference being exchange of OH and OCH3 at the 7 and 8 positions. By calculations based on the geometry of the molecules using the MM+ force field, the different distances between the hydroxyl groups of the two xanthones were obtained (4.64774 angstrom for X2 and 7.19412 angstrom for X1), therefore, the two hydroxyl groups of X1 should freely interact with more water molecules than those of X2 in aqueous solution. In other words, X2 is more hydrophobic than X1. Micellar electrokinetic capillary chromatography (MEKC) was therefore chosen for separation of the compounds. The optimum separation conditions were: 20 mM borate + 20 mM SDS (pH 9.8) as running buffer, 17.5 kV applied potential, and detection wavelength 260 nm. The two xanthones were well separated in 9.0 min, with Gaussian peak shapes. The repeatability of the MEKC method (expressed as RSD) for X1 and X2 was 0.9 and 1.1%, respectively, for migration time, and 3.1 and 1.4% for peak area. The limits of detection (S/N = 3) were 0.41 mu g mL(-1) for X1 and 0.82 mu g mL(-1) for X2. The recovery of the MEKC method for the two xanthones was also satisfactory.
Species covered 湿生扁蕾(原变种) Gentianopsis paludosa
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