Caco-2 Cell Line Standardization with Pharmaceutical Requirements and In Vitro Model Suitability for Permeability Assays
- PMID: 38004503
- PMCID: PMC10674574
- DOI: 10.3390/pharmaceutics15112523
Caco-2 Cell Line Standardization with Pharmaceutical Requirements and In Vitro Model Suitability for Permeability Assays
Abstract
The Caco-2 cell line derived from human colon carcinoma is commonly used to assess the permeability of compounds in in vitro conditions. Due to the significant increase in permeability studies using the Caco-2 cell line in recent years, the need to standardize this biological model seems necessary. The pharmaceutical requirements define only the acceptance criteria for the validation of the Caco-2 cell line and do not specify the protocol for its implementation. Therefore, the aim of this study is to review the conditions for permeability studies across the Caco-2 monolayer reported in the available literature concerning validation guidelines. We summarized the main aspects affecting the validation process of the Caco-2 cell line, including the culture conditions, cytotoxicity, cell differentiation process, and monolayer transport conditions, and the main conclusions may be useful in developing individual methods for preparing the cell line for validation purposes and further permeability research.
Keywords: Caco-2 cell line; biowaiver; drug permeability; pharmaceutical requirements; validation.
Conflict of interest statement
The authors declare no conflict of interest.
Similar articles
-
Demonstrating suitability of the Caco-2 cell model for BCS-based biowaiver according to the recent FDA and ICH harmonised guidelines.J Pharm Pharmacol. 2019 Aug;71(8):1231-1242. doi: 10.1111/jphp.13111. Epub 2019 Jun 2. J Pharm Pharmacol. 2019. PMID: 31155721
-
Variability of permeability estimation from different protocols of subculture and transport experiments in cell monolayers.J Pharmacol Toxicol Methods. 2015 Jan-Feb;71:21-32. doi: 10.1016/j.vascn.2014.11.004. Epub 2014 Nov 26. J Pharmacol Toxicol Methods. 2015. PMID: 25433164
-
Caco-2 cell permeability assays to measure drug absorption.Expert Opin Drug Metab Toxicol. 2005 Aug;1(2):175-85. doi: 10.1517/17425255.1.2.175. Expert Opin Drug Metab Toxicol. 2005. PMID: 16922635 Review.
-
Defining conditions for the co-culture of Caco-2 and HT29-MTX cells using Taguchi design.J Pharmacol Toxicol Methods. 2010 May-Jun;61(3):334-42. doi: 10.1016/j.vascn.2010.02.004. Epub 2010 Feb 13. J Pharmacol Toxicol Methods. 2010. PMID: 20159047
-
Caco-2 cells, biopharmaceutics classification system (BCS) and biowaiver.Acta Medica (Hradec Kralove). 2011;54(1):3-8. Acta Medica (Hradec Kralove). 2011. PMID: 21542416 Review.
Cited by
-
Computational approach for the evaluation of sesquiterpene lactone as a modulator of cannabinoid receptor type 2 for neurodegenerative disease prophylactics.Mol Divers. 2025 Apr 28. doi: 10.1007/s11030-025-11191-w. Online ahead of print. Mol Divers. 2025. PMID: 40293605
-
Identification and evaluation of bioactive compounds from Azadirachta indica as potential inhibitors of DENV-2 capsid protein: An integrative study utilizing network pharmacology, molecular docking, molecular dynamics simulations, and machine learning techniques.Heliyon. 2025 Feb 12;11(4):e42594. doi: 10.1016/j.heliyon.2025.e42594. eCollection 2025 Feb 28. Heliyon. 2025. PMID: 40051864 Free PMC article.
-
Bioengineering the Human Intestinal Mucosa and the Importance of Stromal Support for Pharmacological Evaluation In Vitro.Cells. 2024 Nov 8;13(22):1859. doi: 10.3390/cells13221859. Cells. 2024. PMID: 39594608 Free PMC article.
-
In silico drug repurposing of potential antiviral inhibitors targeting methyltransferase (2'-O-MTase) domain of Marburg virus.In Silico Pharmacol. 2025 Apr 24;13(2):70. doi: 10.1007/s40203-025-00355-z. eCollection 2025. In Silico Pharmacol. 2025. PMID: 40291443
-
Robust and reproducible human intestinal organoid-derived monolayer model for analyzing drug absorption.Sci Rep. 2025 Apr 3;15(1):11403. doi: 10.1038/s41598-025-95823-z. Sci Rep. 2025. PMID: 40181053 Free PMC article.
References
Publication types
Grants and funding
LinkOut - more resources
Full Text Sources