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首页> 外文期刊>Separation and Purification Technology >Two-step preparation of ginsenoside-Re, Rb1, Rc and Rb2 from the root of Panax ginseng by high-performance counter-current chromatography
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Two-step preparation of ginsenoside-Re, Rb1, Rc and Rb2 from the root of Panax ginseng by high-performance counter-current chromatography

机译:高效逆流色谱法从人参根两步制备人参皂苷-Re,Rb1,Rc和Rb2

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A two-step counter-current chromatography (CCC) method was developed for the preparation of ginsenoside-Re, Rb1, Rc and Rb2 from ginseng with two solvent systems, methylene chloride-methanol-water-isopropanol (6:2:4:3, v/v) and n-hexane-n-butanol-0.1% formic acid (0.7:3:4, v/v). The classical CCC mode was' applied in the first separation step while the elution-extrusion counter-current chromatography (EECCC) in the second separation step. The preparation yielded 76.1 mg, 137.0 mg, 58.8 mg and 85.1 mg of ginsenoside-Re, Rb1, Rc and Rb2 with the purity of 97.5%, 94.4%, 91.6% and 92.2%, respectively, from 1440.0 mg of crude sample. The recoveries of these ginsenosides after the two-step separation were 68.7%, 65.6%, 40.1% and 46.6%, respectively. The process throughput of crude sample was 5.14mg/min while the process efficiencies of ginsenoside-Re, Rb1, Rc and Rb2 were 0.54mg/mL, 0.49mg/min, 0.21 mg/min and 0.30mg/min, respectively. The structures of the targets were characterized by liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) and confirmed with the standards.
机译:开发了一种两步逆流色谱法(CCC),用于从人参中用两种溶剂系统(二氯甲烷:甲醇-水-异丙醇(6:2:4:3)制备人参皂甙Re,Rb1,Rc和Rb2 ,v / v)和正己烷-正丁醇-0.1%甲酸(0.7:3:4,v / v)。在第一个分离步骤中采用了经典的CCC模式,而在第二个分离步骤中则采用了洗脱-挤出逆流色谱法(EECCC)。该制剂从1440.0 mg的粗样品中分别产生76.1 mg,137.0 mg,58.8 mg和85.1 mg的人参皂甙Re,Rb1,Rc和Rb2,纯度分别为97.5%,94.4%,91.6%和92.2%。两步分离后,这些人参皂苷的回收率分别为68.7%,65.6%,40.1%和46.6%。粗样品的处理量为5.14mg / min,人参皂甙Re,Rb1,Rc和Rb2的处理效率分别为0.54mg / mL,0.49mg / min,0.21mg / min和0.30mg / min。通过液相色谱-电喷雾电离质谱(LC-ESI-MS)表征目标的结构,并用标准品确认。

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