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An Openable Artificial Intestinal Tract System Enables the Evaluation of Drug Absorption in Caco-2 Cells through the Reduction in Thickness of the Unstirred Water Layer

机译:可打开的人造肠道系统能够通过减少未经误导的水层的厚度来评估CaCo-2细胞中的药物吸收

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摘要

In drug absorption and permeability experiments, an unstirred water layer (UWL) is known to cause differences in the estimated permeability of drugs between in vitro and in vivo experiments. Therefore, it is necessary to develop a new method to allow for accurate measurements of in vitro drug absorption through the reduction of the UWL effect. Previously, we have developed an artificial intestinal tract that mimics the tubular structure of the human intestine and enables study of drug absorption under flow conditions. In order to determine whether our artificial intestinal tract has the potential to reduce the effect of a UWL on drug absorption, the present study evaluated drug absorption in Caco-2 cells using this artificial system. The viability and tight junction structure of Caco-2 cells on the artificial intestinal tract were intact during perfusion. The cumulative amount of the highly lipophilic drugs imipramine and chlorpromazine accumulated in Caco-2 cells cultured on the cell culture plate was 1.5 times higher under mechanical agitation, whereas that of cells on the artificial intestinal tract was 6.5 times higher when internal flow was applied. In addition, the cumulative amounts of 5-aminosalicylic acid and clonidine, drugs with low lipophilicity, accumulated in Caco-2 cells on the artificial intestinal tract were unchanged by internal flow. These results indicate that the artificial intestinal tract enables effective reduction of the UWL thickness at the Caco-2 cell-surface, and allows evaluation of in vitro drug absorption under conditions similar to those found in vivo.
机译:在药物吸收和渗透性实验中,已知未经误导的水层(UWL)导致体外和体内实验之间的药物估计渗透性的差异。因此,有必要开发一种新方法,以便通过减少UWL效应来准确测量体外药物吸收。以前,我们开发了一种人造肠道,模仿人肠的管状结构,并能够在流动条件下研究吸毒。为了确定我们的人造肠道是否有可能降低UWL对药物吸收的影响,本研究使用该人工系统评估了Caco-2细胞中的吸毒。在灌注期间,人工肠道中的CaCo-2细胞的活力和紧密结合性是完整的。在机械搅拌下,在细胞培养板上培养的CaCO-2细胞中积聚的高亲脂性药物的累积量和氯丙嗪在培养上培养的CaCO-2细胞中的1.5倍,而在施加内部流动时,人工肠道上的细胞的细胞越高。此外,通过内部流动不变,在人造肠道上积聚的5-氨基水杨酸和克隆汀,具有低亲脂性的药物的累积量。这些结果表明,人造肠道使得能够在Caco-2细胞表面上有效地降低UWL厚度,并允许在类似于体内发现的条件下评估体外药物吸收。

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