Transport evaluation of alendronate across Caco-2 cell monolayers

被引:7
|
作者
Karamustafa, F. [1 ]
Celebi, N. [1 ]
Degim, Z. [1 ]
Unal, N. [2 ]
机构
[1] Gazi Univ, Dept Pharmaceut Technol, Fac Pharm, TR-06330 Ankara, Turkey
[2] Food & Mouth Dis Inst, Ankara, Turkey
来源
PHARMAZIE | 2009年 / 64卷 / 02期
关键词
INTESTINAL-ABSORPTION; MICELLAR SYSTEMS; DELIVERY-SYSTEMS; BILE-SALT; INSULIN; PERMEABILITY; ACID; BISPHOSPHONATES; CYCLODEXTRINS; CYTOTOXICITY;
D O I
10.1691/ph.2008.8201
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The transport of alendronate through Caco-2 monolayers in the absence and presence of absorption enhancers (sodium taurocholate-STC and dimethyl-beta-cyclodextrin-DM-beta-CD) was studied. The viability of Caco-2 cells was determined by MTT assay. The effects of the experiment period and serum existence in Dubelco's Modified Eagle's Medium (DMEM) on cell viability were examined. The least toxic concentrations of alendronate, STC and DM-beta-CD were found as 0.2% (w/v), 5 mM and 0.3% (w/v), respectively. Transport experiments were performed with these concentrations in DMEM supplemented with serum for an 8 h period. DM-beta-CD increased the transport of alendronate through Caco-2 monolayers significantly. No significance was observed with STC. Cell integrity was determined by measuring the electrical resistance values at the end of the transport experiments and found to be decreased to a greater extent with DM-beta-CD. These results indicate that DM-beta-CD is a promising agent for improving the transport of alendronate.
引用
收藏
页码:98 / 103
页数:6
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