Simultaneous determination of 18α-glycyrrhetinic acid and 18β-glycyrrhetinic acid in Glycyrrhiza glabra root by reversed phase high-performance liquid chromatography

Ambika Chamoli, Makhmur Ahmad, Mojeer Hasan, B. Panda
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引用次数: 2

Abstract

Background: The aim of the present research work is to develop a high-performance liquid chromatography (HPLC) method for simultaneous analysis of 18α-glycyrrhetinic acid (18α-GA) and 18β-GA (18β-GA) of Glycyrrhiza glabra. Materials and Methods: About 20 μL aliquots of each 18α-GA and 18β-GA were analyzed using reversed-phase C-18 column. The mobile phase was acetonitrile:tetrahydrofuran:water (10:80:10, v/v/v). The run time was 10 min at flow rate of 1 ml/min. Ultraviolet detection was carried out at 254 nm. Results: 18α-GA and 18β-GA were well resolved in reversed phase C-18 column using mobile phase acetonitrile: tetrahydrofuran: water (10:80:10, v/v/v, pH 7.9). The Rtof 18α-GA and 18β-GA was detected at 2.091 and 2.377 min, respectively. Conclusion: The developed chromatography method could be extended for potential quantification or simultaneous determination of these markers in plant as well as in herbal formulation.
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反相高效液相色谱法同时测定甘草根中18α-甘草次酸和18β-甘草次酸的含量
背景:建立高效液相色谱(HPLC)同时分析甘草中18α-甘草次酸(18α-GA)和18β-GA (18β-GA)的方法。材料与方法:采用C-18反相色谱柱分析18α-GA和18β-GA各20 μL的含量。流动相为乙腈:四氢呋喃:水(10:80:10,v/v/v)。运行时间为10min,流速为1ml /min。紫外检测波长为254 nm。结果:18α-GA和18β-GA在反相C-18色谱柱中分离良好,流动相乙腈:四氢呋喃:水(10:80:10,v/v/v, pH 7.9)。18α-GA和18β-GA的Rtof分别在2.091和2.377 min检测到。结论:所建立的色谱方法可用于植物及中药制剂中这些标记物的定量或同时测定。
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