Suppr超能文献

皮肤致敏潜力的决定因素。

Determinants of skin sensitisation potential.

作者信息

Roberts David W, Aptula Aynur O

机构信息

School of Pharmacy and Chemistry, Liverpool John Moores University, Byrom Street, Liverpool L3 3AF, England.

出版信息

J Appl Toxicol. 2008 Apr;28(3):377-87. doi: 10.1002/jat.1289.

Abstract

Skin sensitisation is an important toxicological endpoint. The possibility that chemicals used in the workplace and in consumer products might cause skin sensitisation is a major concern for individuals, for employers and for marketing. In European REACH (Registration, Evaluation, and Authorisation of Chemicals) legislation, the sensitising potential should therefore be assessed for chemicals below the 10 ton threshold. Development of methods for prediction of skin sensitisation potential without animal testing has been an active research area for some time, but has received further impetus with the advent of REACH and the EU Cosmetics Directive (EU 2003). This paper addresses the issue of non-animal based prediction of sensitisation by a mechanistic approach. It is known that the sequence of molecular, biomolecular and cellular events between exposure to a skin sensitiser and development of the sensitised state involves several stages, in particular penetration through the stratum corneum, covalent binding to carrier protein, migration of Langerhans cells, presentation of the antigen to naïve T-cells. In this paper each of these stages is considered with respect to the extent to which it is dependent on the chemical properties of the sensitiser. The evidence suggests that, although penetration of the stratum corneum, stimulation of migration and maturation of Langerhans cells, and antigen recognition are important events in the induction of sensitisation, except in certain specific circumstances they can be taken for granted. They are not important factors in determining whether a compound will be a sensitiser or not, nor are they important factors in determining how potent one sensitiser will be relative to another. The ability to bind covalently to carrier protein is the major structure-dependent determinant of skin sensitisation potential. A chemistry-based prediction strategy is proposed involving reaction mechanistic domain assignment, reactivity and hydrophobicity determination, and application of quantitative mechanistic modelling (QMM) or read-across.

摘要

皮肤致敏是一个重要的毒理学终点。 workplace和消费品中使用的化学品可能导致皮肤致敏,这一可能性是个人、雇主和市场营销的主要关注点。 因此,在欧洲化学品注册、评估、授权和限制法规(REACH)中,应评估10吨阈值以下化学品的致敏潜力。 一段时间以来,开发无需动物试验即可预测皮肤致敏潜力的方法一直是一个活跃的研究领域,但随着REACH和欧盟化妆品指令(EU 2003)的出现,这一领域得到了进一步推动。 本文通过一种机制方法探讨了基于非动物的致敏预测问题。 已知接触皮肤致敏剂与致敏状态发展之间的分子、生物分子和细胞事件序列涉及几个阶段,特别是穿透角质层、与载体蛋白共价结合、朗格汉斯细胞迁移、将抗原呈递给未致敏T细胞。 在本文中,将考虑这些阶段中的每一个阶段在多大程度上取决于致敏剂的化学性质。 证据表明,尽管角质层的穿透、朗格汉斯细胞迁移和成熟的刺激以及抗原识别是致敏诱导中的重要事件,但除了某些特定情况外,它们可以被视为理所当然。 它们不是决定一种化合物是否会成为致敏剂的重要因素,也不是决定一种致敏剂相对于另一种致敏剂的效力的重要因素。 与载体蛋白共价结合的能力是皮肤致敏潜力的主要结构依赖性决定因素。 提出了一种基于化学的预测策略,包括反应机理域分配、反应性和疏水性测定以及定量机理建模(QMM)或类推法的应用。

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