首页> 美国卫生研究院文献>Pharmaceutics >Mechanistic Studies on the Absorption-Enhancing Effects of Gemini Surfactant on the Intestinal Absorption of Poorly Absorbed Hydrophilic Drugs in Rats
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Mechanistic Studies on the Absorption-Enhancing Effects of Gemini Surfactant on the Intestinal Absorption of Poorly Absorbed Hydrophilic Drugs in Rats

机译:双子表面活性剂对大鼠吸收不良亲水药物肠道吸收的机制研究

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摘要

Generally, the use of absorption enhancers might be the most effective approaches to ameliorate the enteric absorption of poorly absorbed substances. Among numerous absorption enhancers, we already reported that a gemini surfactant, sodium dilauramidoglutamide lysine (SLG-30) with two hydrophobic and two hydrophilic moieties, is a novel and promising adjuvant with a high potency in improving the absorption safely. Here, we examined and elucidated the absorption-improving mechanisms of SLG-30 in the enteric absorption of substances. SLG-30 increased the intestinal absorption of 5(6)-carboxyfluorescein (CF) to a greater level than the typical absorption enhancers, including sodium glycocholate and sodium laurate, as evaluated by an in situ closed-loop method. Furthermore, SLG-30 significantly lowered the fluorescence anisotropy of dansyl chloride (DNS-Cl), suggesting that it might increase the fluidity of protein sections in the intestinal cell membranes. Moreover, SLG-30 significantly lowered the transepithelial-electrical resistance (TEER) values of Caco-2 cells, suggesting that it might open the tight junctions (TJs) between the enteric epithelial cells. Additionally, the levels of claudin-1 and claudin-4 expression decreased in the presence of SLG-30. These outcomes propose that SLG-30 might improve the enteric transport of poorly absorbed substances through both transcellular and paracellular routes.
机译:通常,使用吸收促进剂可能是改善吸收不良的物质对肠道吸收的最有效方法。在众多吸收促进剂中,我们已经报道了一种双子表面活性剂,具有两个疏水和两个亲水部分的双月桂酰谷氨酰胺赖氨酸钠(SLG-30),是一种新型且有前途的佐剂,具有安全改善吸收的高效能。在这里,我们检查并阐明了SLG-30在物质肠溶吸收中的吸收改善机制。通过原位闭环方法评估,SLG-30将5(6)-羧基荧光素(CF)的肠道吸收水平提高到比典型的吸收促进剂(包括甘醇酸钠和月桂酸钠)更高的水平。此外,SLG-30大大降低了丹酰氯(DNS-Cl)的荧光各向异性,表明它可能会增加肠细胞膜中蛋白质切片的流动性。此外,SLG-30大大降低了Caco-2细胞的跨上皮电阻(TEER)值,表明它可能会打开肠上皮细胞之间的紧密连接(TJ)。此外,在存在SLG-30时,claudin-1和claudin-4的表达水平降低。这些结果表明,SLG-30可能通过跨细胞途径和旁细胞途径改善吸收不良的物质的肠运输。

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