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首页> 外文期刊>Journal of separation science. >Combinative application of pH-zone-refining and conventional high-speed counter-current chromatography for preparative separation of caged polyprenylated xanthones from gamboge
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Combinative application of pH-zone-refining and conventional high-speed counter-current chromatography for preparative separation of caged polyprenylated xanthones from gamboge

机译:结合使用pH区域精制和常规高速逆流色谱法从甘博格中制备笼状聚异戊二烯化的氧杂蒽的分离方法

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An efficient method for the preparative separation of four structurally similar caged xanthones from the crude extracts of gamboge was established, which involves the combination of pH-zone-refining counter-current chromatography and conventional highspeed counter-current chromatography for the first time. pH-zone-refining counter-current chromatography was performed with the solvent system composed of n-hexane/ethyl acetate/methanol/water (7:3:8:2, v/v/v/v), where 0.1% trifluoroacetic acid was added to the upper organic stationary phase as a retainer and 0.03% triethylamine was added to the aqueous mobile phase as an eluter. From 3.157 g of the crude extract, 1.134 g of gambogic acid, 180.5 mg of gambogenic acid and 572.9 mg of a mixture of two other caged polyprenylated xanthones were obtained. The mixture was further separated by conventional high-speed counter-current chromatography with a solvent system composed of n-hexane/ethyl acetate/methanol/water (5:5:10:5, v/v/v/v) and n-hexane/methyl tert-butyl ether/acetonitrile/water (8:2:6:4, v/v/v/v), yielding 11.6 mg of isogambogenic acid and 10.4 mg of beta-morellic acid from 218.0 mg of the mixture, respectively. The purities of all four of the compounds were over 95%, as determined by high-performance liquid chromatography, and the chemical structures of the four compounds were confirmed by electro-spray ionizationmass spectrometry and NMR spectroscopy. The combinative application of pH-zone-refining counter-current chromatography and conventional high-speed countercurrent chromatography shows great advantages in isolating and enriching the caged polyprenylated xanthones.
机译:建立了一种从甘博粗制提物中制备分离四种结构相似的笼型氧杂蒽的有效方法,该方法首次涉及将pH区精制逆流色谱法与常规高速逆流色谱法结合使用。用正己烷/乙酸乙酯/甲醇/水(7:3:8:2,v / v / v / v)组成的溶剂体系进行pH区域精制逆流色谱法,其中0.1%三氟乙酸向其中加入作为保留剂的上层有机固定相,并将0.03%的三乙胺作为洗脱剂加入到水相中。从3.157g的粗提物中,获得1.134g的藤黄酸,180.5mg的藤黄酸和572.9mg的另外两种笼中的聚异戊二烯化的氧杂蒽的混合物。通过常规的高速逆流色谱法,使用由正己烷/乙酸乙酯/甲醇/水(5:5:10:5,v / v / v / v)和n-己烷/甲基叔丁基醚/乙腈/水(8:2:6:4,v / v / v / v),从218.0 mg的混合物中生成11.6 mg的异藤酸和10.4 mg的β-偏烯酸,分别。通过高效液相色谱法测定,所有四种化合物的纯度均超过95%,并且通过电喷雾电离质谱和NMR光谱证实了这四种化合物的化学结构。 pH区精制逆流色谱法和常规高速逆流色谱法的组合应用在分离和富集笼状聚戊二烯化的氧杂蒽酮方面显示出巨大的优势。

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