首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Separation and identification of water-soluble salvianolic acids from Salvia miltiorrhiza Bunge by high-speed counter-current chromatography and ESI-MS analysis
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Separation and identification of water-soluble salvianolic acids from Salvia miltiorrhiza Bunge by high-speed counter-current chromatography and ESI-MS analysis

机译:高速逆流色谱-ESI-MS分析法分离和鉴定丹参中水溶性丹酚酸

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摘要

High-speed counter-current chromatography (HSCCC) technique in semi-preparative scale has been applied to separate and purify salvianolic acids from the water extract of Danshen, Salvia miltiorrhiza Bunge. High efficiency HSCCC separation was achieved on a two-phase solvent system composed of a mixture of n-hexane-ethyl acetate-water-methanol (1.5:5:5:1.5, v/v) by eluting the lower mobile phase at a flow-rate of 1.7 ml/min and a revolution of 850 rpm. A total of five well separated peaks were obtained in the HSCCC chromatogram, and their purities determined by HPLC-UV absorption. These peaks were characterized by, UV-vis spectra and ESI-MS, and the data compared with the reference standards. Salvianolic acid B was positively identified as one of the major peaks. Three of the remaining four peaks were also tentatively identified as rosmarinic acid, lithospermic acid, and salvianolic acid E, an isomer of salvianolic acid B, all are members of the salvianolic acids group. In a typical run, tens of milligrams of samples can be separated with high efficiency to yield tens of milligrams of purified materials with over 98% purity. HSCCC thus provides a cost-effective alternative to preparative scale HPLC for the semi-preparative scale separation and purification of salvianolic acids in Danshen. With appropriate modifications, the technique should also be applicable to other herbs in general. (c) 2005 Elsevier B.V. All rights reserved.
机译:半制备规模的高速逆流色谱(HSCCC)技术已用于从丹参丹参水提取物中分离和纯化丹酚酸。通过在流动相下洗脱下层流动相,在由正己烷-乙酸乙酯-水-甲醇(1.5:5:5:1.5,v / v)混合物组成的两相溶剂系统上实现了高效的HSCCC分离速率为1.7 ml / min,转速为850 rpm。在HSCCC色谱图中总共获得了五个分离良好的峰,其纯度通过HPLC-UV吸收测定。通过UV-可见光谱和ESI-MS表征这些峰,并将数据与参考标准品进行比较。丹酚酸B被确定为主要峰之一。其余四个峰中的三个也被初步鉴定为迷迭香酸,紫草酸和丹酚酸E(丹酚酸B的异构体),均属于丹酚酸类。在典型的运行中,可以高效分离数十毫克的样品,以产生数十毫克纯度超过98%的纯化材料。因此,HSCCC为制备规模的HPLC提供了一种经济高效的替代品,可用于丹参中丹酚酸的半制备规模的分离和纯化。经过适当的修改,该技术通常也应适用于其他草药。 (c)2005 Elsevier B.V.保留所有权利。

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