碳酸钙-2
并行传输
基质(水族馆)
跨细胞
化学
吸收(声学)
二肽
计算机科学
药理学
生物化学
细胞
医学
材料科学
生物
氨基酸
磁导率
复合材料
膜
生态学
作者
F. Ingels,S. Deferme,N. Delbar,M. Oth,Patrick Augustijns
出处
期刊:PubMed
日期:2003-02-25
卷期号:57 (6): 153-8
被引量:6
摘要
The Caco-2 cell culture model is widely used during drug development and lead optimization as a predictive tool for the oral absorption of drugs. In order to improve the reliability and quality of the results of Caco-2 experiments and to ensure that the system being used is functionally and enzymatically representative for the intestinal mucosa, it is important to perform a validation of the implemented Caco-2 system. In this paper, we summarize evaluation techniques to guarantee the in-house validity of the model. Theophyllin and sodium fluorescein are used as model compounds to evaluate passive transcellular and passive paracellular transport, respectively. Phenylalanine serves as a substrate to demonstrate active carrier mechanisms. Aminopeptidase and dipeptidyl peptidase are two brush border enzymes present in an active form in the Caco-2 culture model. The presence of an active efflux carrier mechanism is demonstrated with cyclosporin A as a substrate.
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