Suppr超能文献

人源体外模型在 REACh 下用于皮肤毒性测试。

Human-Derived In Vitro Models Used for Skin Toxicity Testing Under REACh.

机构信息

BASF SE, Experimental Toxicology and Ecology, Ludwigshafen am Rhein, Germany.

出版信息

Handb Exp Pharmacol. 2021;265:3-27. doi: 10.1007/164_2020_368.

Abstract

In regulatory toxicology, in vivo studies are still prevailing, and human-derived in vitro models are mostly used in testing for local toxicity to the skin and the eyes. A single in vitro model may be limited to address one or few molecular or cellular events leading to adverse outcomes. Hence, in many instances their regulatory use involves the combination of several in vitro models to assess the hazard potential of test substance. A so-called defined approach combines different testing methods and a 'data interpretation procedure' to obtain a comprehensive overall assessment which is used for the regulatory hazard classification of the test substance.Validation is a prerequisite of regulatory acceptance of new testing methods: This chapter provides an overview of the method development from an experimental method to a test guideline via application of GIVIMP (good in vitro method practice), standardization, validation to the regulatory adoption as an OECD test guidelines. Quandaries associated with the validation towards reference data from in vivo animal studies with limited accuracy and limited human relevance are discussed, as well as uncertainty and limitations arising from restricted applicability and technical and biological variance of the in vitro methods.This chapter provides an overview of human-derived in vitro models currently adopted as OECD test guidelines: From the first skin corrosion tests utilizing reconstructed human epidermis models (RhE), to models to test for skin irritation, phototoxicity, eye irritation, and skin sensitization. The latter is using a battery of different methods and defined approaches which are still under discussion for their regulatory adoption. They will be a vanguard of future applications of human-derived models in regulatory toxicology. RhEs for testing of genotoxicity and of dermal penetration and absorption, have been developed, underwent validation studies and may soon be adopted for regulatory use; these are included in this chapter.

摘要

在监管毒理学中,体内研究仍然占主导地位,而人体来源的体外模型主要用于测试皮肤和眼睛的局部毒性。单个体外模型可能仅限于解决导致不良后果的一个或几个分子或细胞事件。因此,在许多情况下,它们的监管用途涉及结合几种体外模型来评估测试物质的危害潜力。所谓的定义方法结合了不同的测试方法和“数据解释程序”,以获得全面的综合评估,用于测试物质的监管危害分类。验证是接受新测试方法的监管的前提:本章通过应用 GIVIMP(良好的体外方法实践)、标准化、验证,概述了从实验方法到测试指南的方法开发,然后将其作为 OECD 测试指南被监管机构采用。讨论了与体内动物研究参考数据的验证相关的难题,这些数据准确性有限,与人类相关性有限,以及体外方法的应用范围有限、技术和生物学差异所带来的不确定性和局限性。本章概述了目前被采纳为 OECD 测试指南的人体来源的体外模型:从利用重建人体表皮模型 (RhE) 的第一个皮肤腐蚀性测试开始,到测试皮肤刺激、光毒性、眼睛刺激和皮肤致敏的模型。后者使用一系列不同的方法和定义方法,这些方法仍在讨论是否被监管机构采用。它们将成为监管毒理学中人体来源模型未来应用的先锋。用于测试遗传毒性和皮肤渗透吸收的 RhE 已经开发出来,经过了验证研究,可能很快就会被用于监管用途;这些都包含在本章中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验