Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats

The purpose of the present study was to prepare glycyrrhizic acid-phospholipid complex (GL-PLC) as to improve the oral bioavailability of glycyrrhizic acid (GL), enhance the drug efficacy and reduce the side effects. The uniform experimental design approach was utilized for the process optimization...

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Autores principales: Liu, Zhen, Chen, Hong, Qiang, Qianqian, Bai, Shufang, Gao, Wenyuan, Zhang, Jingze
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8348
http://www.latamjpharm.org/resumenes/30/8/LAJOP_30_8_1_26.pdf
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id I19-R120-10915-8348
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
anti-inflammatory activity; glycyrrhizic acid-phospholipid complex; oral bioavailability; pharmacokinetics
evaluación comparativa de resultados
spellingShingle Farmacia
anti-inflammatory activity; glycyrrhizic acid-phospholipid complex; oral bioavailability; pharmacokinetics
evaluación comparativa de resultados
Liu, Zhen
Chen, Hong
Qiang, Qianqian
Bai, Shufang
Gao, Wenyuan
Zhang, Jingze
Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
topic_facet Farmacia
anti-inflammatory activity; glycyrrhizic acid-phospholipid complex; oral bioavailability; pharmacokinetics
evaluación comparativa de resultados
description The purpose of the present study was to prepare glycyrrhizic acid-phospholipid complex (GL-PLC) as to improve the oral bioavailability of glycyrrhizic acid (GL), enhance the drug efficacy and reduce the side effects. The uniform experimental design approach was utilized for the process optimization in order to obtain the satisfactory complex. The results of comparison between GL-PLC and free GL indicated that the anti-inflammatory activity of the phospholipid complex was significantly higher than that of free GL at the same dose. The results of pharmacokinetic study displayed that the plasma concentration of glycyrrhetic acid, the metabolite of GL in vivo, increased after oral administration of GL-PLC. The Cmax of GL-PLC was 2.14 times higher than that of free glycyrrhizic acid, while the AUC of GL-PLC was 1.74 times higher than that of free GL. The results proved that GL-PLC improved the lipophilic property of GL, increased the bioavailability and anti-inflammatory activity.
format Articulo
Articulo
author Liu, Zhen
Chen, Hong
Qiang, Qianqian
Bai, Shufang
Gao, Wenyuan
Zhang, Jingze
author_facet Liu, Zhen
Chen, Hong
Qiang, Qianqian
Bai, Shufang
Gao, Wenyuan
Zhang, Jingze
author_sort Liu, Zhen
title Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
title_short Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
title_full Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
title_fullStr Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
title_full_unstemmed Glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
title_sort glycyrrhizic acid-phospholipid complex: preparation process optimization and therapeutic and pharmacokinetic evaluation in rats
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8348
http://www.latamjpharm.org/resumenes/30/8/LAJOP_30_8_1_26.pdf
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