Exploration of the GARD™skin applicability domain: Indirectly acting haptens, hydrophobic substances and UVCBs.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Andy Forreryd, Robin Gradin, Charles Humfrey, Len Sweet, Henrik Johansson
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引用次数: 3

Abstract

Hazard assessments of skin sensitizers are increasingly performed using new approach methodologies (NAMs), with several in chemico, in vitro, and most recently, also defined approaches accepted for regulatory use. However, keeping track of potential limitations of each method to define applicability domains remains a crucial component to ensure adequate predictivity and to facilitate the appropriate selection of method(s) for each hazard assessment task. The objective of this report is to share test results generated with the GARD™skin assay on chemicals that have traditionally been considered difficult to test in some of the conventional in vitro and in chemico OECD Test Guidelines for skin sensitization. Such compounds may include, for example, indirectly acting haptens, hydrophobic substances, and substances of unknown or variable composition, complex reaction products or biological substances (UVCBs). Based on the results of this study, the sensitivity for prediction of skin sensitizing hazard of indirectly acting haptens was 92.4% and 87.5% when compared with local lymph node assay (LLNA) (n = 25) and human data (n = 8), respectively. Similarly, the sensitivity for prediction of skin sensitizing hazard of hydrophobic substances was 85.1% and 100% when compared with LLNA (n = 24) and human data (n = 9), respectively. Lastly, a case study involving assessment of a set of hydrophobic UVCBs (n = 7) resulted in a sensitivity of 100% compared to available reference data. These data provide support for the inclusion of such chemistries in the GARD™skin applicability domain without an increased risk of false negative classifications.

探索GARD™皮肤适用领域:间接作用半抗原,疏水物质和uvcb。
皮肤致敏剂的危害评估越来越多地使用新的方法方法(NAMs)进行,其中有几种化学方法、体外方法和最近也定义了用于监管使用的方法。然而,跟踪每种方法的潜在局限性以确定适用领域仍然是确保充分的预测性和促进为每个危害评估任务适当选择方法的关键组成部分。本报告的目的是分享GARD™皮肤试验对传统上被认为难以在一些常规体外和OECD皮肤致敏化学测试指南中测试的化学品产生的测试结果。这些化合物可以包括,例如,间接作用的半抗原、疏水物质、未知或可变组成的物质、复杂反应产物或生物物质(UVCBs)。根据本研究结果,与局部淋巴结测定法(LLNA) (n = 25)和人体数据(n = 8)相比,间接作用半抗原预测皮肤致敏危害的敏感性分别为92.4%和87.5%。同样,与LLNA (n = 24)和人类数据(n = 9)相比,该方法预测疏水物质皮肤致敏危害的敏感性分别为85.1%和100%。最后,一项涉及一组疏水uvcb评估的案例研究(n = 7)与现有参考数据相比,其灵敏度为100%。这些数据为将这些化学物质纳入GARD™皮肤适用性领域提供了支持,而不会增加假阴性分类的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Altex-Alternatives To Animal Experimentation
Altex-Alternatives To Animal Experimentation MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
7.70
自引率
8.90%
发文量
89
审稿时长
2 months
期刊介绍: ALTEX publishes original articles, short communications, reviews, as well as news and comments and meeting reports. Manuscripts submitted to ALTEX are evaluated by two expert reviewers. The evaluation takes into account the scientific merit of a manuscript and its contribution to animal welfare and the 3R principle.
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