Influence of surfactants in self-microemulsifying formulations on enhancing oral bioavailability of oxyresveratrol: Studies in Caco-2 cells and in vivo

被引:34
作者
Sangsen, Yaowaporn [1 ,2 ]
Wiwattanawongsa, Kamonthip [2 ,3 ]
Likhitwitayawuid, Kittisak [4 ]
Sritularak, Boonchoo [4 ]
Graidist, Potchanapond [5 ,6 ]
Wiwattanapatapee, Ruedeekorn [1 ,2 ]
机构
[1] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Hat Yai 90112, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Pharmaceut Sci, Phytomed & Pharmaceut Biotechnol Excellence Res C, Hat Yai 90112, Songkhla, Thailand
[3] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Clin Pharm, Hat Yai 90112, Songkhla, Thailand
[4] Chulalongkorn Univ, Fac Pharmaceut Sci, Dept Pharmacognosy & Pharmaceut Bot, Bangkok 10330, Thailand
[5] Prince Songkla Univ, Fac Med, Dept Biomed Sci, Hat Yai 90112, Songkhla, Thailand
[6] Prince Songkla Univ, Excellent Res Lab Canc Mol Biol, Hat Yai 90112, Songkhla, Thailand
关键词
Self-microemulsifying drug delivery system; SMEDDS; Surfactants; Caco-2; cells; Oral absorption; Oxyresveratrol; DRUG-DELIVERY SYSTEMS; CUTANEOUS HSV-1 INFECTION; P-GLYCOPROTEIN SUBSTRATE; PERMEABILITY; ABSORPTION; VITRO; RATS; RESVERATROL; MONOLAYERS; TRANSPORT;
D O I
10.1016/j.ijpharm.2015.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Self-microemulsifying drug delivery systems (SMEDDS) containing two types (Tween80 (R) and Labrasol (R)) and two levels (low; 5% and high; 15%) of co-surfactants were formulated to evaluate the impact of surfactant phase on physical properties and oral absorption of oxyresveratrol (OXY). All formulations showed a very rapid release in the simulated gastric fluid (SGF) pH 1.2. After dilution with different media, the microemulsion droplet sizes of the Tween80 (R)-based (similar to 26 to 36 nm) were smaller than that of the Labrasol (R)-based systems (similar to 34 to 45 nm). Both systems with high levels of surfactant increased the Caco-2 cells permeability of OXY compared to those with low levels of surfactant (1.4-1.7 folds) and the unformulated OXY (1.9-2.0 folds). It was of interest, that there was a reduction (4.4-5.3 folds) in the efflux transport of OXY from both systems compared to the unformulated OXY. The results were in good agreement with the in vivo absorption studies of such OXY-formulations in rats. Significantly greater values of Cmax and AUC(0-10h) (p < 0.05) were obtained from the high levels of Tween80 (R)-based (F-r, (0-10h) 786.32%) compared to those from the Labrasol (R)-based system (F-r,F- 0-10h 218.32%). These finding indicate the importance of formulation variables such as type and quantity of surfactant in the SMEDDS to enhance oral drug bioavailability. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:294 / 303
页数:10
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