Determination of 18 β-Glycyrrhetinic Acid in Glycyrrhiza glabra L. Extract by HPLC

Authors

Somayeh Esmaeili1, Farzaneh Naghibi1,*, Mahmoud Mosaddegh1, Nazli Nader1
1Traditional Medicine & Materia Medica Research Center, School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services, Tehran, Iran
*Corresponding Author: Traditional Medicine & Materia Medica Research Center, School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services, Tehran, Iran. Email:[email protected]

IJ Pharmaceutical Research:Vol. 5, issue 2; 137-141
Published online:Nov 20, 2010
Article type:Research Article
Received:Feb 21, 2006
Accepted:Jun 21, 2006
How to Cite:Esmaeili S, Naghibi F, Mosaddegh M, Nader N. Determination of 18 β-Glycyrrhetinic Acid in Glycyrrhiza glabra L. Extract by HPLC. Iran J Pharm Res. 2022;5(2):e128276. doi: https://doi.org/10.22037/ijpr.2010.666

Abstract

A high performance liquid chromatography method was studied for determination of 18 β-glycyrrhetinic acid in Glycyrrhiza glabra L. (licorice) extract. The operating condition were C-18 reversed phase column (VP-ODS, (250×4.6 mm, 5 mm)) at room temperature, acetonitril/phosphoric acid (3/1) as mobile phase, at flow rate of 0.6ml/min (0-8min), 0.4ml/min (8-20min) and UV detection at 230 nm. The recoveries were %99.60-%102.81 with relative standard deviation between %0.01-%1.58. The relative standard deviation of the repeatability test was %2.96. The method is simple, rapid, safe, accurate, economical and useful for standardization of the licorice products.

 

 

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Copyright

© 2022, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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