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肠道体外细胞系统在药物吸收研究中的过去、现在和未来。

The Past, Present and Future of Intestinal In Vitro Cell Systems for Drug Absorption Studies.

机构信息

Department of Physiology and Pharmacology, Karolinska Institutet, 171 77 Stockholm, Sweden.

Department of Physiology and Pharmacology, Karolinska Institutet, 171 77 Stockholm, Sweden.

出版信息

J Pharm Sci. 2021 Jan;110(1):50-65. doi: 10.1016/j.xphs.2020.07.001. Epub 2020 Jul 3.

Abstract

The intestinal epithelium acts as a selective barrier for the absorption of water, nutrients and orally administered drugs. To evaluate the gastrointestinal permeability of a candidate molecule, scientists and drug developers have a multitude of cell culture models at their disposal. Static transwell cultures constitute the most extensively characterized intestinal in vitro system and can accurately categorize molecules into low, intermediate and high permeability compounds. However, they lack key aspects of intestinal physiology, including the cellular complexity of the intestinal epithelium, flow, mechanical strain, or interactions with intestinal mucus and microbes. To emulate these features, a variety of different culture paradigms, including microfluidic chips, organoids and intestinal slice cultures have been developed. Here, we provide an updated overview of intestinal in vitro cell culture systems and critically review their suitability for drug absorption studies. The available data show that these advanced culture models offer impressive possibilities for emulating intestinal complexity. However, there is a paucity of systematic absorption studies and benchmarking data and it remains unclear whether the increase in model complexity and costs translates into improved drug permeability predictions. In the absence of such data, conventional static transwell cultures remain the current gold-standard paradigm for drug absorption studies.

摘要

肠上皮作为水、营养物质和口服药物吸收的选择性屏障。为了评估候选分子的胃肠道通透性,科学家和药物开发者可以利用多种细胞培养模型。静态 Transwell 培养是最广泛特征化的肠体外系统,可以准确地将分子分类为低、中、高通透性化合物。然而,它们缺乏肠道生理学的关键方面,包括肠上皮细胞的复杂性、流动、机械应变,或与肠道黏液和微生物的相互作用。为了模拟这些特征,已经开发了各种不同的培养范例,包括微流控芯片、类器官和肠切片培养。在这里,我们提供了一个更新的肠体外细胞培养系统概述,并批判性地审查了它们在药物吸收研究中的适用性。现有数据表明,这些先进的培养模型为模拟肠道复杂性提供了令人印象深刻的可能性。然而,缺乏系统的吸收研究和基准数据,并且仍不清楚模型复杂性和成本的增加是否转化为改善药物通透性预测。在缺乏这些数据的情况下,传统的静态 Transwell 培养仍然是当前药物吸收研究的黄金标准范例。

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