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兔皮肤刺激试验的变异性分析。

Analysis of variability in the rabbit skin irritation assay.

机构信息

Integrated Laboratory Systems, LLC, 601 Keystone Park Dr, Suite 800, Morrisville, NC, 27560, USA.

Integrated Laboratory Systems, LLC, 601 Keystone Park Dr, Suite 800, Morrisville, NC, 27560, USA.

出版信息

Regul Toxicol Pharmacol. 2021 Jun;122:104920. doi: 10.1016/j.yrtph.2021.104920. Epub 2021 Mar 20.

DOI:10.1016/j.yrtph.2021.104920
PMID:33757807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8186434/
Abstract

The in vivo rabbit test is the benchmark against which new approach methodologies for skin irritation are usually compared. No alternative method offers a complete replacement of animal use for this endpoint for all regulatory applications. Variability in the animal reference data may be a limiting factor in identifying a replacement. We established a curated data set of 2624 test records, representing 990 substances, each tested at least twice, to characterize the reproducibility of the in vivo assay. Methodological deviations from guidelines were noted, and multiple data sets with differing tolerances for deviations were created. Conditional probabilities were used to evaluate the reproducibility of the in vivo method in identification of U.S. Environmental Protection Agency or Globally Harmonized System hazard categories. Chemicals classified as moderate irritants at least once were classified as mild or non-irritants at least 40% of the time when tested repeatedly. Variability was greatest between mild and moderate irritants, which both had less than a 50% likelihood of being replicated. Increased reproducibility was observed when a binary categorization between corrosives/moderate irritants and mild/non-irritants was used. This analysis indicates that variability present in the rabbit skin irritation test should be considered when evaluating nonanimal alternative methods as potential replacements.

摘要

体内兔试验通常是新的皮肤刺激方法学的基准,与之相比,没有任何替代方法可以完全替代动物用于所有监管应用的这一终点。动物参考数据的变异性可能是识别替代方法的一个限制因素。我们建立了一个经过精心整理的 2624 个测试记录数据集,代表 990 种物质,每种物质至少测试了两次,以描述体内试验的重现性。注意到了与指南的方法学偏差,并创建了多个具有不同偏差容忍度的数据集。条件概率用于评估体内方法在识别美国环境保护署或全球协调系统危害类别中的重现性。至少有一次被归类为中度刺激性的化学品至少有 40%的时间被归类为轻度或非刺激性,当被重复测试时。在轻度和中度刺激性之间,变异性最大,两者的复制可能性都小于 50%。当使用腐蚀性/中度刺激性与轻度/非刺激性之间的二进制分类时,观察到了更高的重现性。这项分析表明,在评估非动物替代方法作为潜在替代品时,应考虑到兔皮肤刺激试验中存在的变异性。