In vitro liver models for toxicological research

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ichiro Fukunaga , Takanori Takebe
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引用次数: 0

Abstract

Drug-induced liver injury (DILI) presents a major challenge not only in new drug development but also in post-marketing withdrawals and the safety of food, cosmetics, and chemicals. Experimental model organisms such as the rodents have been widely used for preclinical toxicological testing. However, the tension exists associated with the ethical and sustainable use of animals in part because animals do not necessarily inform the human-specific ADME (adsorption, dynamics, metabolism and elimination) profiling. To establish alternative models in humans, in vitro hepatic tissue models have been proposed, ranging from primary hepatocytes, immortal hepatocytes, to the development of new cell resources such as stem cell-derived hepatocytes. Given the evolving number of novel alternative methods, understanding possible combinations of cell sources and culture methods will be crucial to develop the context-of-use assays. This review primarily focuses on 3D liver organoid models for conducting. We will review the relevant cell sources, bioengineering methods, selection of training compounds, and biomarkers towards the rationale design of in vitro toxicology testing.
体外肝模型毒理学研究
药物性肝损伤(drug -induced liver injury, DILI)不仅在新药开发中,而且在上市后撤销和食品、化妆品和化学品的安全性方面都是一个重大挑战。实验模式生物如啮齿动物已被广泛用于临床前毒理学试验。然而,这种紧张关系与动物的伦理和可持续利用有关,部分原因是动物不一定能提供人类特异性ADME(吸附、动力学、代谢和消除)分析的信息。为了在人体中建立替代模型,已经提出了体外肝组织模型,范围从原代肝细胞,永生肝细胞,到开发新的细胞资源,如干细胞来源的肝细胞。鉴于不断发展的新颖替代方法的数量,了解细胞来源和培养方法的可能组合对于开发使用环境检测至关重要。本文主要综述了三维肝类器官模型的研究进展。我们将回顾相关的细胞来源、生物工程方法、训练化合物的选择和生物标志物对体外毒理学测试的基本原理设计。
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来源期刊
CiteScore
4.80
自引率
9.50%
发文量
50
审稿时长
69 days
期刊介绍: DMPK publishes original and innovative scientific papers that address topics broadly related to xenobiotics. The term xenobiotic includes medicinal as well as environmental and agricultural chemicals and macromolecules. The journal is organized into sections as follows: - Drug metabolism / Biotransformation - Pharmacokinetics and pharmacodynamics - Toxicokinetics and toxicodynamics - Drug-drug interaction / Drug-food interaction - Mechanism of drug absorption and disposition (including transporter) - Drug delivery system - Clinical pharmacy and pharmacology - Analytical method - Factors affecting drug metabolism and transport - Expression of genes for drug-metabolizing enzymes and transporters - Pharmacogenetics and pharmacogenomics - Pharmacoepidemiology.
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