Studies on Intestinal Transport of Ginsenoside Compatibility with Veratrum nigrum via Caco-2 Cell Monolayer Model Coupled with UPLC-ESI-MS Method

The Caco-2 cells have been recognized as effective tools to be applied to imitating the drug absorption in human intestine for the transport of drug. Herein, Caco-2 cell monolayer model was used to study the transport of the ginsenoside compatibility with Veratrum nigrum in different proportions. A...

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Published in:Chemical research in Chinese universities Vol. 31; no. 6; pp. 914 - 918
Main Authors: Ma, Yinghui, Liu, Yuanyuan, Wei, Mengying, Song, Fengrui, Liu, Zhongying, Pi, Zifeng
Format: Journal Article
Language:English
Published: Changchun Jilin University and The Editorial Department of Chemical Research in Chinese Universities 01-12-2015
College of Pharmacy, Jilin University, Changchun 130021, P.R.China%Changchun Institute of Applied Chemistry, Chinese Academy of Sciences,Changchun 130022, P.R.China
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Summary:The Caco-2 cells have been recognized as effective tools to be applied to imitating the drug absorption in human intestine for the transport of drug. Herein, Caco-2 cell monolayer model was used to study the transport of the ginsenoside compatibility with Veratrum nigrum in different proportions. A specific high performance liquid chro- matography-electrospray ionization-mass spectrometry(HPLC-ESI-MS) method was developed for the semiquantita- tive determination of ginsenoside in intestinal transport with Dioscin as an internal standard. For the Caco-2 model constructed, two influencing factors were investigated, including time and concentration. The results suggest that the absorption of ginsenoside Re, Rgl, Rbl, Rc, Rb2 and Rd are time- and concentration-dependent and the excretions of Rbl, Rc, Rb2 and Rd have a relatronship with some transport proteins. The bioavailability of the ginsenosides has reduced compared to the single Panax ginseng extract when compatibility with a certain amount of Veratrum nigrum.
Bibliography:22-1183/O6
The Caco-2 cells have been recognized as effective tools to be applied to imitating the drug absorption in human intestine for the transport of drug. Herein, Caco-2 cell monolayer model was used to study the transport of the ginsenoside compatibility with Veratrum nigrum in different proportions. A specific high performance liquid chro- matography-electrospray ionization-mass spectrometry(HPLC-ESI-MS) method was developed for the semiquantita- tive determination of ginsenoside in intestinal transport with Dioscin as an internal standard. For the Caco-2 model constructed, two influencing factors were investigated, including time and concentration. The results suggest that the absorption of ginsenoside Re, Rgl, Rbl, Rc, Rb2 and Rd are time- and concentration-dependent and the excretions of Rbl, Rc, Rb2 and Rd have a relatronship with some transport proteins. The bioavailability of the ginsenosides has reduced compared to the single Panax ginseng extract when compatibility with a certain amount of Veratrum nigrum.
High performance liquid chromatography-electrospray ionization-mass spectroscopy(HPLC-ESI-MS);Panax ginseng; Ginsenoside; Veratrum nigrum; Transport; Caco-2 cell monolayer model
ISSN:1005-9040
2210-3171
DOI:10.1007/s40242-015-5207-y