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在复杂生物相关介质存在的情况下,用于研究药物渗透的黏蛋白保护的Caco-2细胞模型实验

Mucin-Protected Caco-2 Assay to Study Drug Permeation in the Presence of Complex Biorelevant Media.

作者信息

Ye Dong, López Mármol Álvaro, Lenz Verena, Muschong Patricia, Wilhelm-Alkubaisi Anita, Weinheimer Manuel, Koziolek Mirko, Sauer Kerstin A, Laplanche Loic, Mezler Mario

机构信息

Drug Metabolism and Pharmacokinetics-Bioanalytical Research, AbbVie Deutschland GmbH & Co. KG, 67061 Ludwigshafen, Germany.

NCE Formulation Sciences, AbbVie Deutschland GmbH & Co. KG, 67061 Ludwigshafen, Germany.

出版信息

Pharmaceutics. 2022 Mar 24;14(4):699. doi: 10.3390/pharmaceutics14040699.

DOI:10.3390/pharmaceutics14040699
PMID:35456533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9032137/
Abstract

The poor solubility and permeability of compounds beyond Lipinski's Rule of Five (bRo5) are major challenges for cell-based permeability assays. Due to their incompatibility with gastrointestinal components in biorelevant media, the exploration of important questions addressing food effects is limited. Thus, we established a robust mucin-protected Caco-2 assay to allow the assessment of drug permeation in complex biorelevant media. To do that, the assay conditions were first optimized with dependence of the concentration of porcine mucin added to the cells. Mucin-specific effects on drug permeability were evaluated by analyzing cell permeability values for 15 reference drugs (BCS class I-IV). Secondly, a sigmoidal relationship between mucin-dependent permeability and fraction absorbed in human () was established. A case study with venetoclax (BCS class IV) was performed to investigate the impact of medium complexity and the prandial state on drug permeation. Luminal fluids obtained from the tiny-TIM system showed a higher solubilization capacity for venetoclax, and a better read-out for the drug permeability, as compared to FaSSIF or FeSSIF media. In conclusion, the mucin-protected Caco-2 assay combined with biorelevant media improves the mechanistic understanding of drug permeation and addresses complex biopharmaceutical questions, such as food effects on oral drug absorption.

摘要

超过Lipinski五规则(bRo5)的化合物溶解性和渗透性较差,这是基于细胞的渗透性测定面临的主要挑战。由于它们与生物相关介质中的胃肠道成分不相容,因此针对食物影响的重要问题的探索受到限制。因此,我们建立了一种强大的粘蛋白保护的Caco-2测定法,以评估药物在复杂生物相关介质中的渗透性。为此,首先根据添加到细胞中的猪粘蛋白浓度依赖性对测定条件进行了优化。通过分析15种参考药物(BCS I-IV类)的细胞渗透性值,评估了粘蛋白对药物渗透性的特异性影响。其次,建立了粘蛋白依赖性渗透性与人体吸收分数之间的S形关系。进行了维奈托克(BCS IV类)的案例研究,以研究介质复杂性和进食状态对药物渗透的影响。与FaSSIF或FeSSIF介质相比,从微小TIM系统获得的肠腔液对维奈托克具有更高的溶解能力,并且对药物渗透性的读出效果更好。总之,粘蛋白保护的Caco-2测定法与生物相关介质相结合,提高了对药物渗透的机理理解,并解决了复杂的生物药剂学问题,例如食物对口服药物吸收的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/9f7e8835ddd6/pharmaceutics-14-00699-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/eecd11239606/pharmaceutics-14-00699-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/dc8a26915271/pharmaceutics-14-00699-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/98b5070d95dd/pharmaceutics-14-00699-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/b0891cec7c14/pharmaceutics-14-00699-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/6c7a0d430aa4/pharmaceutics-14-00699-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/ae7077e5b7a4/pharmaceutics-14-00699-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/9f7e8835ddd6/pharmaceutics-14-00699-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/eecd11239606/pharmaceutics-14-00699-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/dc8a26915271/pharmaceutics-14-00699-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/98b5070d95dd/pharmaceutics-14-00699-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/b0891cec7c14/pharmaceutics-14-00699-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/6c7a0d430aa4/pharmaceutics-14-00699-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/ae7077e5b7a4/pharmaceutics-14-00699-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0843/9032137/9f7e8835ddd6/pharmaceutics-14-00699-g007.jpg

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