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首页> 外文期刊>Journal of separation science. >Counter-current chromatographic method for preparative scale isolation of picrosides from traditional Chinese medicine Picrorhiza scrophulariiflora
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Counter-current chromatographic method for preparative scale isolation of picrosides from traditional Chinese medicine Picrorhiza scrophulariiflora

机译:逆流色谱法从中药玄参中制备除垢剂

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Apocynin, androsin, together with picroside I, II and III from crude extracts of Picrorhiza scrophulariiflora were isolated by means of high-speed counter-current chromatography (CCC) combining elution-extrusion (EE) and cycling-elution (CE) approach. The EECCC took full advantages of the liquid nature of the stationary phase for a complete sample recovery and extended the solute hydrophobicity window, while CECCC showed its unique advantage in achieving effective separation of special compounds through preventing stationary phase loss. In the present work, the biphasic liquid system composed of n-hexane/ethyl acetate/methanol/water (1:2:1:2, v/v/v/v) was used for separation of apocynin and androsin, ethyl acetate-butanol/water/formic acid (4:1:5:0.005, v/v/v/v) for picroside I, II and III. However, due to the extremely similar K values (K _1/K _2≈1.2), picroside I and III were always eluted together by several biphasic solvent systems. In this case, the CECCC exhibited great superiority and baseline separated in the sixth cycle using ethyl acetate/water (1:1, v/v) as biphasic liquid system. Each fraction was analyzed by UPLC-UV and ESI-MS analysis, and identified by comparing with the data of reference substances. Compared with classical elution, the combination of EE and CE approach exhibits strong separation efficiency and great potential to be a high-throughput separation technique in the case of complex samples.
机译:通过高速逆流色谱法(CCC)结合洗脱-挤压(EE)和循环-洗脱(CE)方法,分离了刺槐皮粗提取物中的芹菜素,雄激素以及苦瓜苷I,II和III。 EECCC充分利用了固定相的液体性质,可以完全回收样品,并扩展了溶质疏水性窗口,而CECCC则显示出其独特的优势,可以通过防止固定相损失来有效分离特殊化合物。在本工作中,使用由正己烷/乙酸乙酯/甲醇/水(1:2:1:2,v / v / v / v)组成的双相液体系统分离载脂蛋白和雄激素,乙酸乙酯/山梨糖苷I,II和III的正丁醇/水/甲酸(4:1:5:0.005,v / v / v / v)。但是,由于K值极为相似(K _1 / K_2≈1.2),因此,苦瓜苷I和III总是被几种双相溶剂系统一起洗脱。在这种情况下,CECCC表现出极大的优越性,并且在第六个循环中使用乙酸乙酯/水(1:1,v / v)作为双相液体系统分离了基线。通过UPLC-UV和ESI-MS分析对每个馏分进行分析,并与参考物质的数据进行比较进行鉴定。与经典洗脱相比,EE和CE方法的结合显示出强大的分离效率,并且在复杂样品的情况下具有成为高通量分离技术的巨大潜力。

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