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

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...

Full description

Bibliographic Details
Main Authors: Charles Awortwe, P.S. Fasinu, B. Rosenkranz
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-01-01
Series:Journal of Pharmacy & Pharmaceutical Sciences
Online Access:https://journals.library.ualberta.ca/jpps/index.php/JPPS/article/view/20490
_version_ 1797720685354680320
author Charles Awortwe
P.S. Fasinu
B. Rosenkranz
author_facet Charles Awortwe
P.S. Fasinu
B. Rosenkranz
author_sort Charles Awortwe
collection DOAJ
description 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.   This article is open to POST-PUBLICATION REVIEW. Registered readers (see “For Readers”) may comment by clicking on ABSTRACT on the issue’s contents page.
first_indexed 2024-03-12T09:23:02Z
format Article
id doaj.art-39ddf01f45024c1e9c78cfd8cc699fce
institution Directory Open Access Journal
issn 1482-1826
language English
last_indexed 2024-03-12T09:23:02Z
publishDate 2014-01-01
publisher Frontiers Media S.A.
record_format Article
series Journal of Pharmacy & Pharmaceutical Sciences
spelling doaj.art-39ddf01f45024c1e9c78cfd8cc699fce2023-09-02T14:23:03ZengFrontiers Media S.A.Journal of Pharmacy & Pharmaceutical Sciences1482-18262014-01-0117110.18433/J30K63Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and ChallengesCharles Awortwe0P.S. Fasinu1B. Rosenkranz2Division of Clinical Pharmacology, Faculty of Medicine and Health Sciences, University of Stellenbosch, Tygerberg, Cape Town, South AfricaNational Center for Natural Products Research, School of Pharmacy, University of Mississippi, Oxford, USADivision of Clinical Pharmacology, Faculty of Medicine and Health Sciences, University of Stellenbosch, Tygerberg, Cape Town, South AfricaThe 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.   This article is open to POST-PUBLICATION REVIEW. Registered readers (see “For Readers”) may comment by clicking on ABSTRACT on the issue’s contents page.https://journals.library.ualberta.ca/jpps/index.php/JPPS/article/view/20490
spellingShingle Charles Awortwe
P.S. Fasinu
B. Rosenkranz
Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
Journal of Pharmacy & Pharmaceutical Sciences
title Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
title_full Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
title_fullStr Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
title_full_unstemmed Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
title_short Application of Caco-2 Cell Line in Herb-Drug Interaction Studies: Current Approaches and Challenges
title_sort application of caco 2 cell line in herb drug interaction studies current approaches and challenges
url https://journals.library.ualberta.ca/jpps/index.php/JPPS/article/view/20490
work_keys_str_mv AT charlesawortwe applicationofcaco2celllineinherbdruginteractionstudiescurrentapproachesandchallenges
AT psfasinu applicationofcaco2celllineinherbdruginteractionstudiescurrentapproachesandchallenges
AT brosenkranz applicationofcaco2celllineinherbdruginteractionstudiescurrentapproachesandchallenges