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Quantitative Determination of 18-?-Glycyrrhetinic Acid in HepG2 Cell Line by High Performance Liquid Chromatography Method.


ABSTRACT: A reverse phase high performance liquid chromatographic (RP-HPLC) method was developed for identification and estimation of 18-?-glycyrrhetinic acid (GA) in HepG2 cell line. The analysis was carried out using a JASCO HPLC system with a C-18 (3??m) Supelco reversed phase column (150 x 4.7?mm) using a mobile phase of 80% CH3OH and 20% of CH3CN: tetrahydrofuran: water (10:80:10,?v/v/v). The method was linear in the concentration range of 1.5-120??g /mL (n = 5). The LOD and LOQ were determined based on standard deviation of the y-intercept and the slope of the calibration curve. The LOD and LOQ values were found to be 11.46??g/mL and 34.72??g/mL, respectively. The mean percentage recovery by standard addition experiments of GA is 92.4 % ± 5.2%. The intracellular GA concentration value, obtained as mean of five different determinations, was 45.8 ± 7.45??g/mL. We have developed a HPLC-UV method for quantitative determination of GA inside cells, with advantages in the cost reduction and economy of the analytical process.

SUBMITTER: Nocca G 

PROVIDER: S-EPMC6257892 | biostudies-other | 2018

REPOSITORIES: biostudies-other

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Quantitative Determination of 18-<i>β</i>-Glycyrrhetinic Acid in HepG2 Cell Line by High Performance Liquid Chromatography Method.

Nocca Giuseppina G   Callà Cinzia C   Santini Stefano Angelo SA   Amalfitano Adriana A   Marigo Luca L   Rossetti Diana Valeria DV   Spagnuolo Gianrico G   Cordaro Massimo M  

International journal of analytical chemistry 20181113


A reverse phase high performance liquid chromatographic (RP-HPLC) method was developed for identification and estimation of 18-<i>β</i>-glycyrrhetinic acid (GA) in HepG2 cell line. The analysis was carried out using a JASCO HPLC system with a C-18 (3 <i>μ</i>m) Supelco reversed phase column (150 x 4.7 mm) using a mobile phase of 80% CH<sub>3</sub>OH and 20% of CH<sub>3</sub>CN: tetrahydrofuran: water (10:80:10, v/v/v). The method was linear in the concentration range of 1.5-120 <i>μ</i>g /mL (n  ...[more]

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