首页> 外文期刊>Acta Chromatographica >Simultaneous separation and analysis of two bioactive xanthones in the Tibetan medicinal plant Gentianopsis paludosa (Hook. f.) Ma by micellar electrokinetic capillary chromatography
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Simultaneous separation and analysis of two bioactive xanthones in the Tibetan medicinal plant Gentianopsis paludosa (Hook. f.) Ma by micellar electrokinetic capillary chromatography

机译:胶束电动毛细管色谱法同时分离和分析藏药植物龙胆草中的两种生物活性x吨

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摘要

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 OCH 3 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 ? for X2 and 7.19412 ? 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 m style="font-variant:small- caps">m borate + 20 m style="font-variant:small-caps">m 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 μg mL ~(-1) for X1 and 0.82 μg mL ~(-1) for X2. The recovery of the MEKC method for the two xanthones was also satisfactory.
机译:1,7-二羟基-3,8-二甲氧基黄酮(X1)和1,8-二羟基-3,7-二甲氧基黄酮(X2)是藏族药用植物Gentianopsis paludosa(Hook.f.)Ma的两个重要的氧杂蒽。它们的结构非常相似,唯一的区别是在7位和8位的OH和OCH 3交换。通过使用MM +力场基于分子的几何结构进行计算,得出两个氧杂蒽酮的羟基之间的距离不同(X2为4.64774?,X1为7.19412?),因此X1的两个羟基应自由与X2水溶液中的水分子相互作用的水分子更多。换句话说,X 2比X 1更疏水。因此,选择胶束电动毛细管色谱法(MEKC)分离化合物。最佳分离条件为:20 m style =“ font-variant:small-caps”> m 硼酸盐+ 20 m style =“ font-variant:small-caps “> m SDS(pH 9.8)作为运行缓冲液,施加的电势为17.5 kV,检测波长为260 nm。两种x吨在9.0分钟内被很好地分离,呈高斯峰形。对于迁移时间,X1和X2的MEKC方法(表示为RSD)的重复性分别为0.9%和1.1%,对于峰面积分别为3.1%和1.4%。 X1的检出限(S / N = 3)为0.41μgmL〜(-1),X2为0.82μgmL〜(-1)。两种氧杂蒽的MEKC方法的回收率也令人满意。

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