Shaheen Nusrat, Lu Yanzhen, Geng Ping, Shao Qian, Wei Yun
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 15 3rd North East Road, Chaoyang District, Beijing 100029, China.
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 15 3rd North East Road, Chaoyang District, Beijing 100029, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Mar 1;1046:211-217. doi: 10.1016/j.jchromb.2017.01.018. Epub 2017 Jan 15.
Two-step high speed countercurrent chromatography method, following normal phase and elution-extrusion mode of operation by using selected solvent systems, was introduced for phenolic compounds separation. Phenolic compounds including gallic acid, ethyl gallate, ethyl digallate and ellagic acid were separated from the ethanol extract of mango (Mangifera indica L.) flowers for the first time. In the first step, gallic acid of 3.7mg and ethyl gallate of 3.9mg with the purities of 98.87% and 99.55%, respectively, were isolated by using hexane-ethylacetate-methanol-water (4:6:4:6, v/v) in normal phase high speed countercurrent chromatography from 200mg of crude extract, while ethyl digallate and ellagic acid were collected in the form of mixture fraction. In the second step, further purification of the mixture was carried out with the help of another selected solvent system of dichloromethane-methanol-water (4:3:2, v/v) following elusion-extrusion mode of operation. Ethyl digallate of 3.8mg and ellagic acid of 5.7mg were separated well with high purities of 98.68% and 99.71%, respectively. The separated phenolic compounds were identified and confirmed by HPLC, UPLC-QTOF/ESI-MS, H and C NMR spectrometric analysis.
介绍了一种两步高速逆流色谱法,该方法采用选定的溶剂系统,按照正相和洗脱-挤出操作模式,用于酚类化合物的分离。首次从芒果(Mangifera indica L.)花的乙醇提取物中分离出包括没食子酸、没食子酸乙酯、二没食子酸乙酯和鞣花酸在内的酚类化合物。第一步,在正相高速逆流色谱中,使用己烷-乙酸乙酯-甲醇-水(4:6:4:6,v/v)从200mg粗提取物中分离出3.7mg纯度为98.87%的没食子酸和3.9mg纯度为99.55%的没食子酸乙酯,而二没食子酸乙酯和鞣花酸则以混合馏分的形式收集。第二步,借助另一种选定的二氯甲烷-甲醇-水(4:3:2,v/v)溶剂系统,按照洗脱-挤出操作模式对混合物进行进一步纯化。分离出3.8mg纯度为98.