首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Preparation of salvianolic acid A by the degradation reaction of salvianolic acid B in subcritical water integrated with pH-zone-refining counter-current chromatography
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Preparation of salvianolic acid A by the degradation reaction of salvianolic acid B in subcritical water integrated with pH-zone-refining counter-current chromatography

机译:pH区域精制逆流色谱结合亚临界水中丹酚酸B的降解反应制备丹酚酸A

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Salvianolic acid A is the major bioactive compound in Danshen, however, due to the chemical instability and low content in Danshen, it is difficult to extract amount of salvianolic acid A. Therefore, this study was to establish an effective strategy for obtaining adequate amount of salvianolic acid A, subcritical water extraction was used to degrade salvianolic acid B and prepare salvianolic acid A. Different reaction conditions including temperature, time, concentration and pH value in subcritical water were investigated. Under 40 mg/mL of reactant concentration, 180 degrees C of temperature, 4.0 of pH value and 60 min of reaction time, the highest yield rate of salvianolic acid A reached 34.86%. Then, the degradation products were successfully separated by pH-zone-refining counter-current chromatography with the solvent system Pet-EtAc-n-BuOH-H2O(2:3:1:9, v/v), where 10 mM TFA was added in stationary phase and 10 mM NH3 center dot H2O in mobile phase. As a result, a total of 227.3 mg of salvianolic acid A at 98.2% purity, 38.9 mg of danshensu at 99.3% purity, 9.5 mg of salvianolic acid D at 92.7% purity, and 32.8 mg of protocatechuic aldehyde at 93.1% purity were obtained from 1.2 g degradation products of salvianolic acid B by one-step purification. The results demonstrated that the combinative application of subcritical water and pH zone -refining counter-current chromatography is a potential technique for the preparative separation of salvianolic acid A from salvianolic acid B. (C) 2016 Elsevier B.V. All rights reserved.
机译:丹酚酸A是丹参中主要的生物活性化合物,但由于丹参中的化学不稳定和含量低,很难提取大量的丹参酸A。因此,本研究建立了一个有效的策略以获得足够量的丹参酸A。丹酚酸A,亚临界水萃取法用于降解丹酚酸B,制备丹酚酸A。研究了亚临界水中不同的反应条件,包括温度,时间,浓度和pH值。在40 mg / mL的反应物浓度,180摄氏度的温度,4.0的pH值和60分钟的反应时间下,丹酚酸A的最高收率达到34.86%。然后,使用溶剂系统Pet-EtAc-n-BuOH-H2O(2:3:1:9,v / v)通过pH区域精制逆流色谱法成功分离降解产物,其中10 mM TFA为在固定相中添加10mM NH3中心点H2O在流动相中添加。结果,获得了总计227.3 mg纯度为98.2%的丹酚酸A,38.9 mg丹参素纯度为99.3%,9.5 mg纯度为92.7%的丹酚酸D和32.8 mg纯度为93.1%的原儿茶醛。通过一步纯化从1.2克丹酚酸B的降解产物中分离得到。结果表明,亚临界水和pH区域精制逆流色谱法的组合应用是从丹酚酸B制备分离丹酚酸A的潜在技术。(C)2016 Elsevier B.V.保留所有权利。

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