Assessment of coenzyme Q10 absorption using an in vitro digestion-Caco-2 cell model

被引:47
作者
Bhagavan, Hemmi N.
Chopra, Raj K.
Craft, Neal E.
Chitchumroonchokchai, Chureeporn
Failla, Mark L.
机构
[1] Tishcon Corp, Westbury, NY 11590 USA
[2] Craft Technol Inc, Wilson, NC 27892 USA
[3] Ohio State Univ, Dept Human Nutr, Columbus, OH 43210 USA
关键词
coenzyme Q10; ubiquinone; Caco-2; cells; intestinal absorption; in vitro models; bioavailability;
D O I
10.1016/j.ijpharm.2006.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The feasibility of using a coupled in vitro digestion-Caco-2 cell uptake as a model for examining the digestive stability and absorption of coenzyme Q10 (CoQ10) from a variety of commercially available CoQ10 products was examined. The products were first subjected to simulated digestion to mimic their passage through. the GI tract to generate micelles containing CoQ10, and the micelle fractions added to monolayers of Caco-2 cells to determine CoQ10 uptake. The data demonstrate enhanced uptake of CoQ10 from formulations containing solubilized forms of CoQ10 and also from a CoQ10-gamma-cyclodextrin complex as compared with pure CoQ10 powder or tablets based on CoQ10 powder. The CoQ10 uptake by the cells was correlated with the extent of micellarization of CoQ10 during simulated digestion. Most of CoQ10 taken up-by the cells was converted to ubiquinol either during or following uptake. The data also indicate a correlation between in vitro dissolution of CoQ10 products and uptake of CoQ10 by Caco-2 cells. Thus, this study demonstrates the utility of coupled in vitro digestion-Caco-2 cell model as a cost-effective screening tool that will provide useful information for the optimal design of human trials to assess the bioavailability of CoQ10 and also other bioactive compounds. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 117
页数:6
相关论文
共 27 条
[1]   DISTRIBUTION AND REDOX STATE OF UBIQUINONES IN RAT AND HUMAN TISSUES [J].
ABERG, F ;
APPELKVIST, EL ;
DALLNER, G ;
ERNSTER, L .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 295 (02) :230-234
[2]   Coenzyme Q10 as a possible treatment for neurodegenerative diseases [J].
Beal, MF .
FREE RADICAL RESEARCH, 2002, 36 (04) :455-460
[3]   Hydrolysis of zeaxanthin esters by carboxyl ester lipase during digestion facilitates micellarization and uptake of the xanthophyll by Caco-2 human intestinal cells [J].
Chitchumroonchokcai, C ;
Failla, ML .
JOURNAL OF NUTRITION, 2006, 136 (03) :588-594
[4]   Assessment of lutein bioavailability from meals and a supplement using simulated digestion and Caco-2 human intestinal cells [J].
Chitchumroonchokchai, C ;
Schwartz, SJ ;
Failla, ML .
JOURNAL OF NUTRITION, 2004, 134 (09) :2280-2286
[5]  
Chopra RK, 1998, INT J VITAM NUTR RES, V68, P109
[6]  
Craft NE, 2005, FASEB J, V19, pA449
[7]   Biochemical functions of coenzyme Q10 [J].
Crane, FL .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2001, 20 (06) :591-598
[8]   Cyclodextrin-based pharmaceutics: Past, present and future [J].
Davis, ME ;
Brewster, ME .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (12) :1023-1035
[9]  
Delie F, 1997, CRIT REV THER DRUG, V14, P221
[10]   BIOCHEMICAL, PHYSIOLOGICAL AND MEDICAL ASPECTS OF UBIQUINONE FUNCTION [J].
ERNSTER, L ;
DALLNER, G .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :195-204