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Solid-phase extraction of 18 beta-glycyrrhetinic acid from plasma and subsequent analysis by high-performance liquid chromatography

机译:从血浆中固相萃取18β-甘草次酸,并通过高效液相色谱进行后续分析

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摘要

A new method is described for the solid-phase extraction of 18 beta-glycyrrhetinic acid from plasma or serum, with subsequent analysis by HPLC. New aspects of the method include the use of commercially available 18 alpha-glycyrrhetinic acid as the internal standard and the use of a Bond Elut C-2 (ethyl) extraction column, to avoid the need to use large volumes of organic solvent to elute the isolates from the columns. Separation was achieved on a Shandon Hypersil BDS C-18 analytical column, with a mobile phase consisting of acetonitrile-0.02 M phosphate buffer, pH 5.7 (55:35, v/v). The column effluent was monitored at 248 nm. Compared with previous methods, the procedure is much easier to carry out, whereas the sensitivity (limit of detection, 10 ng/ml, and limit of quantitation, 50 ng/ml), the precision (0.3-6.2%) and the accuracy (97.2-101.9%) are of the same order of magnitude. (C) 1998 Elsevier Science B.V. All rights reserved. [References: 14]
机译:描述了一种从血浆或血清中固相萃取18β-甘草次酸的新方法,随后通过HPLC分析。该方法的新方面包括使用市售的18α-甘草次酸作为内标,以及使用Bond Elut C-2(乙基)萃取柱,从而避免了使用大量有机溶剂洗脱溶剂的麻烦。与列隔离。在Shandon Hypersil BDS C-18分析柱上实现分离,流动相由pH 5.7(55:35,v / v)的乙腈-0.02 M磷酸盐缓冲液组成。在248 nm处监测柱流出物。与以前的方法相比,该过程更容易执行,而灵敏度(检测限为10 ng / ml,定量限为50 ng / ml),精度(0.3-6.2%)和准确性( 97.2-101.9%)的数量级相同。 (C)1998 Elsevier Science B.V.保留所有权利。 [参考:14]

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