Kus Marta, Ibragimow Izabela, Piotrowska-Kempisty Hanna
Department of Toxicology, Poznan University of Medical Sciences, 30 Dojazd St., 60-631 Poznan, Poland.
Research and Development Department of Ethifarm, Ethifarm Manufacturing Plant, 9 Stefana Zeromskiego St., 60-544 Poznan, Poland.
Pharmaceutics. 2023 Oct 24;15(11):2523. doi: 10.3390/pharmaceutics15112523.
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.
源自人结肠癌细胞的Caco-2细胞系常用于评估化合物在体外条件下的渗透性。近年来,由于使用Caco-2细胞系进行的渗透性研究显著增加,因此似乎有必要对这一生物学模型进行标准化。药物要求仅定义了Caco-2细胞系验证的验收标准,并未指定其实施方案。因此,本研究的目的是回顾现有文献中关于验证指南报道的跨Caco-2单层渗透性研究的条件。我们总结了影响Caco-2细胞系验证过程的主要方面,包括培养条件、细胞毒性、细胞分化过程和单层转运条件,主要结论可能有助于开发用于验证目的及进一步渗透性研究的细胞系制备的个性化方法。
J Pharmacol Toxicol Methods. 2015
Expert Opin Drug Metab Toxicol. 2005-8
J Pharmacol Toxicol Methods. 2010
Acta Medica (Hradec Kralove). 2011
Biochem Biophys Res Commun. 2015-2-13
Pharmaceuticals (Basel). 2025-4-9
Pharmaceutics. 2023-2-1
Toxicol Rep. 2022-5-17
Curr Res Pharmacol Drug Discov. 2022-5-4