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

Author:

Nocca Giuseppina12ORCID,Callà Cinzia3ORCID,Santini Stefano Angelo3,Amalfitano Adriana1,Marigo Luca4,Rossetti Diana Valeria1,Spagnuolo Gianrico56ORCID,Cordaro Massimo4

Affiliation:

1. Istituto di Biochimica e Biochimica Clinica, Università Cattolica del Sacro Cuore Rome, Italy

2. Istituto di Chimica del Riconoscimento Molecolare, CNR, c/o Università Cattolica del Sacro Cuore, L.go F. Vito 1, I-00168 Rome, Italy

3. UOC Chimica, Biochimica e Biologia Molecolare, Dip. Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Università Cattolica del Sacro Cuore Rome, Italy

4. UOC Odontoiatria Generale e Ortodonzia, Dip Scienze dell’Invecchiamento, Neurologiche, Ortopediche e della Testa Collo. Fondazione Policlinico Universitario A. Gemelli, IRCCS, Università Cattolica del Sacro Cuore Rome, Italy

5. Department of Neurosciences, Reproductive and Odontostomatological Sciences University of Naples “Federico II”, Italy

6. I.M. Sechenov First Moscow State Medical University, Institute of Dentistry, Moscow, Russia

Abstract

A reverse phase high performance liquid chromatographic (RP-HPLC) method was developed for identification and estimation of 18-β-glycyrrhetinic acid (GA) in HepG2 cell line. The analysis was carried out using a JASCO HPLC system with a C-18 (3 μm) 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 μg /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 μg/mL and 34.72 μg/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 μg/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.

Publisher

Hindawi Limited

Subject

Analytical Chemistry

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