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자료유형
학술저널
저자정보
Kamath, Amrita V. (Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute) Morrison, Richard A. (Schering Plough Research Institute) Mathias, Neil R. (Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute) Dando, Sandra A. (Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute) Marino, Anthony M. (Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute) Chong, Sae-Ho (Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제30권 제8호
발행연도
2007.1
수록면
1,002 - 1,007 (6page)

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Permeability estimates using Caco-2 cells do not accurately predict the absorption of hydrophilic drugs that are primarily absorbed via the paracellular pathway. The objective of this study was to investigate whether modulation of tight junctions would help differentiation of paracellularly absorbed compounds. Tight junctions in Caco-2 cell monolayers were manipulated using calcium depletion approaches to decrease the transepithelial electrical resistance (TEER) of the monolayers, and permeability of hydrophilic compounds were measured under these conditions. Permeability of these compounds were also measured in Calu-3 cells, which have tighter junctions than Caco-2 cells. Calcium depletion loosened the tight junctions of Caco-2 cells to varying levels as measured by the decrease in TEER values of the monolayers. While the absolute permeability of all the model compounds increased as the tight junctions were loosened, the ratios of their permeability relative to mannitol permeability were similar. The permeability of these compounds in the tighter Calu-3 cells were also found to be similar to each other. Altering the tight junctions of Caco-2 cells to obtain leakier cell monolayers, or using a cell line with tighter junctions like Calu-3 cells, did not improve differentiation between well absorbed and poorly absorbed hydrophilic drugs. Mere manipulation of the tight junctions to increase or decrease transepithelial electrical resistance does not appear to be a viable approach to predict human absorption for hydrophilic compounds that are primarily absorbed via the paracellular pathway.

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