首页> 外文期刊>Journal of liquid chromatography and related technologies >Separation and purification of triterpene saponins from roots of Radix phytolaccae by high-speed countercurrent chromatography coupled with evaporative light scattering detection.
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Separation and purification of triterpene saponins from roots of Radix phytolaccae by high-speed countercurrent chromatography coupled with evaporative light scattering detection.

机译:通过高速逆流色谱法与蒸发光散射检测耦合的高速逆流色谱法分离和纯化。

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Coupled with evaporative light scattering detection, high-speed countercurrent chromatography was successfully applied for the first time to separation and purification of four triterpene saponins including esculentoside A, B, C and D from roots of Radix Phytolaccae. The separation was performed with an optimized two-phase solvent system composed of chloroform-methanol-water (4:4:2, v/v) using the lower phase as the mobile phase at a flow rate of 1.5 ml/min,. From 150 mg of crude extract 46.3 mg of esculentoside A, 21.8 mg of esculentoside B, 7.3 mg of esculentoside C, and 13.6 mg of esculentoside D were obtained at purities of 96.7%, 99.2%, 96.5% and 97.8%, respectively, as determined by HPLC analysis. The structures of the four triterpene saponins were identified by ESI-MS,(1)H NMR and (13)C NMR.
机译:与蒸发光散射检测相结合,首次成功地应用了高速逆流色谱,以分离和纯化四个三萜皂苷,包括来自植物植物的根源的胰岛素A,B,C和D. 使用较低阶段的氯仿 - 甲醇 - 水(4:4:2,v / v)组成的优化的两相溶剂系统进行分离,其流动率为1.5ml / min。 从150mg的粗提取物46.3mg肝硬化蛋白酶a,21.8mg肝硬化酯B,7.3mg刚血液蚀剂C,以及13.6mg分别获得96.7%,99.2%,96.5%和97.8%的纯度,为 由HPLC分析确定。 通过ESI-MS,(1)H NMR和(13)C NMR鉴定四个三萜皂苷的结构。

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