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Application of Caco-2 Cell Line in Herb-drug Interaction Studies: Current Approaches and Challenges

Overview
Specialties Pharmacology
Pharmacy
Date 2014 Apr 17
PMID 24735758
Citations 30
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Abstract

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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References
1.
Ioannides C . Pharmacokinetic interactions between herbal remedies and medicinal drugs. Xenobiotica. 2002; 32(6):451-78. DOI: 10.1080/00498250210124147. View

2.
Aungst B, Nguyen N, Bulgarelli J . The influence of donor and reservoir additives on Caco-2 permeability and secretory transport of HIV protease inhibitors and other lipophilic compounds. Pharm Res. 2001; 17(10):1175-80. DOI: 10.1023/a:1026402410783. View

3.
Saha P, Kou J . Effect of bovine serum albumin on drug permeability estimation across Caco-2 monolayers. Eur J Pharm Biopharm. 2002; 54(3):319-24. DOI: 10.1016/s0939-6411(02)00089-9. View

4.
Behrens I, Kamm W, Dantzig A, Kissel T . Variation of peptide transporter (PepT1 and HPT1) expression in Caco-2 cells as a function of cell origin. J Pharm Sci. 2004; 93(7):1743-54. DOI: 10.1002/jps.20062. View

5.
Li H, Chung S, Shim C . Characterization of the transport of uracil across Caco-2 and LLC-PK1 cell monolayers. Pharm Res. 2002; 19(10):1495-501. DOI: 10.1023/a:1020456632737. View