Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
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Awortwe, C.
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Univ Stellenbosch, Fac Med & Hlth Sci, Div Clin Pharmacol, Cape Town, South AfricaUniv Stellenbosch, Fac Med & Hlth Sci, Div Clin Pharmacol, Cape Town, South Africa
Awortwe, C.
[1
]
Fasinu, P. S.
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Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, Oxford, MS USAUniv Stellenbosch, Fac Med & Hlth Sci, Div Clin Pharmacol, Cape Town, South Africa
Fasinu, P. S.
[2
]
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Rosenkranz, B.
[1
]
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[1] Univ Stellenbosch, Fac Med & Hlth Sci, Div Clin Pharmacol, Cape Town, South Africa
[2] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, Oxford, MS USA
The Caco-2 model is employed in pre-clinical investigations to predict the likely gastrointestinal permeability of drugs because it expresses cytochrome P450 enzymes transporters microvilli and enterocytes of identical characteristics to the human small intestine. The FDA recommends this model as integral component of the Biopharmaceutics Classification System (BCS). Most dedicated laboratories use the Caco-2 cell line to screen new chemical entities through prediction of its solubility bioavailability and the possibility of drug-drug or herb-drug interactions in the gut lumen. However challenges in the inherent characteristics of Caco-2 cell and inter-laboratory protocol variations have resulted to generation of irreproducible data. These limitations affect the extrapolation of data from pre-clinical research to clinical studies involving drug-drug and herb-drug interactions. This review addresses some of these caveats and enumerates the plausible current and future approaches to reduce the anomalies associated with Caco-2 cell line investigations focusing on its application in herb-drug interactions.
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