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在丙烯酸共聚物存在下ABCB1表达和活性降低。

Reduced ABCB1 Expression and Activity in the Presence of Acrylic Copolymers.

作者信息

Mohammadzadeh Ramin, Baradaran Behzad, Valizadeh Hadi, Yousefi Bahman, Zakeri-Milani Parvin

机构信息

Drug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran. ; Students Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

Immunology Research Center and School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Adv Pharm Bull. 2014;4(3):219-24. doi: 10.5681/apb.2014.032. Epub 2014 Feb 7.

Abstract

PURPOSE

P-glycoprotein (P-gp; ABCB1), an integral membrane protein in the apical surface of human intestinal epithelial cells, plays a crucial role in the intestinal transport and efflux leading to changes in the bioavailability of oral pharmaceutical compounds. This study was set to examine the potential effects of three Eudragits RL100, S100 and L100 on the intestinal epithelial membrane transport of rhodammine-123 (Rho-123), a substrate of P-gp using a monolayer of human colon cancer cell line (Caco-2).

METHODS

The least non-cytotoxic concentrations of the excipients were assessed in Caco-2 cells by the MTT assay. Then the transepithelial transport of Rho-123 across Caco-2 monolayers was determined with a fluorescence spectrophotometer. Besides, the expression of the P-gp in cells exposed to the polymers was demonstrated using Western-blotting analysis.

RESULTS

Treatment of cells with Eudragit RL100 and L100 led to a very slight change while Eudragit S100 showed 61% increase in Rho-123 accumulation (P<0.001) and also reduced transporter expression.

CONCLUSION

Our studies suggest that using proper concentrations of the Eudragit S100 in drug formulation would improve intestinal permeability and absorption of p-gp substrate drugs.

摘要

目的

P-糖蛋白(P-gp;ABCB1)是人类肠上皮细胞顶端表面的一种整合膜蛋白,在肠道转运和外排过程中起关键作用,会导致口服药物化合物的生物利用度发生变化。本研究旨在使用人结肠癌细胞系(Caco-2)单层细胞,研究三种丙烯酸树脂RL100、S100和L100对P-gp底物罗丹明-123(Rho-123)肠道上皮膜转运的潜在影响。

方法

通过MTT法在Caco-2细胞中评估辅料的最低无细胞毒性浓度。然后用荧光分光光度计测定Rho-123跨Caco-2单层细胞的跨上皮转运。此外,使用蛋白质免疫印迹分析来证明暴露于聚合物的细胞中P-gp的表达。

结果

用丙烯酸树脂RL100和L100处理细胞导致变化非常轻微,而丙烯酸树脂S100使Rho-123蓄积增加61%(P<0.001),并降低转运蛋白表达。

结论

我们的研究表明,在药物制剂中使用适当浓度的丙烯酸树脂S100将提高P-gp底物药物的肠道通透性和吸收。

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