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不同肠上皮作为吸收增强研究模型的比较。

Comparison of different intestinal epithelia as models for absorption enhancement studies.

作者信息

Legen I, Salobir M, Kerc J

机构信息

Lek Pharmaceuticals d.d., Research and Development, Verovskova 57, 1526 Ljubljana, Slovenia.

出版信息

Int J Pharm. 2005 Mar 3;291(1-2):183-8. doi: 10.1016/j.ijpharm.2004.07.055. Epub 2004 Dec 28.

Abstract

In this study we compared the effect of two surfactants (laureth-6 and sodium docusate) on the permeability of a model hydrophilic drug across three different epithelia (Caco-2 cells, stripped porcine jejunum and rat ileo-jejunum). Among the tested epithelia Caco-2 cells are the tightest with the trans-epithelial electrical resistance of 372+/-4 Omega cm2 followed by porcine jejunum (124+/-8 Omega cm2) and rat ileo-jejunum (33+/-2 Omega cm2). Both surfactants decreased the trans-epithelial electrical resistance and increased the permeability of a model drug across Caco-2 cells at concentrations as low as 0.02 mg/ml, with more pronounced effect observed for laureth-6. On the other hand, ten times higher concentrations (0.2 mg/ml) did not affect the permeability of the model drug across the porcine jejunum. Similarly, laureth-6 at this high concentration had no effect on the trans-epithelial electrical resistance of the rat ileo-jejunum and did not increase the permeability of the model drug across this tissue. On the basis of these results we concluded that Caco-2 cells are much more sensitive to the investigated surfactants, that act as permeation enhancers, than the native intestinal tissues. Therefore, the results obtained in the experiments with Caco-2 cells might exaggerate the effects of the surfactants on the permeability compared to in vivo situation.

摘要

在本研究中,我们比较了两种表面活性剂(月桂醇聚醚-6和多库酯钠)对一种模型亲水性药物透过三种不同上皮组织(Caco-2细胞、剥离的猪空肠和大鼠回肠-空肠)的通透性的影响。在所测试的上皮组织中,Caco-2细胞的紧密性最高,其跨上皮电阻为372±4Ω·cm²,其次是猪空肠(124±8Ω·cm²)和大鼠回肠-空肠(33±2Ω·cm²)。两种表面活性剂在低至0.02mg/ml的浓度下,均能降低跨上皮电阻并增加模型药物透过Caco-2细胞的通透性,其中月桂醇聚醚-6的效果更为显著。另一方面,浓度高10倍(0.2mg/ml)时,对模型药物透过猪空肠的通透性没有影响。同样,在此高浓度下,月桂醇聚醚-6对大鼠回肠-空肠的跨上皮电阻没有影响,也未增加模型药物透过该组织的通透性。基于这些结果,我们得出结论,Caco-2细胞对作为渗透促进剂的所研究表面活性剂比天然肠道组织更为敏感。因此,与体内情况相比,在Caco-2细胞实验中获得的结果可能会夸大表面活性剂对通透性的影响。

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