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使用氨基酸衍生物测定法、KeratinoSens™、人细胞系激活试验和计算机结构警报参数的新型人工神经网络皮肤致敏风险评估模型。

New artificial neural network models for risk assessment of skin sensitization using amino acid derivative assay, KeratinoSens™, human cell line activation test and in silico structural alert parameter.

作者信息

Imai Kosuke, Hatakeyama Yuri, Oeda Shiho, Ohtake Toshiyuki, Atobe Tomomi, Hirota Morihiko

机构信息

Brand Value R&D Institute, SHISEIDO CO., LTD, 1-2-11, Takashima, Nishi-ku, Yokohama, Kanagawa, 220-0011, Japan.

Brand Value R&D Institute, SHISEIDO CO., LTD, 1-2-11, Takashima, Nishi-ku, Yokohama, Kanagawa, 220-0011, Japan.

出版信息

Regul Toxicol Pharmacol. 2025 Nov;162:105882. doi: 10.1016/j.yrtph.2025.105882. Epub 2025 Jun 16.

DOI:10.1016/j.yrtph.2025.105882
PMID:40516685
Abstract

In the next-generation risk assessment (NGRA) of skin sensitization, estimating the point of departure (PoD) is crucial. The murine local lymph node assay (LLNA) has been considered the 'gold standard' for evaluating the skin sensitizing potential of chemicals, with the LLNA EC3 values serving as the PoD for dermal quantitative risk assessment (QRA). This study presents artificial neural network (ANN) models that predict EC3 values, enhanced by integrating the Amino Acid Derivative Reactivity Assay (ADRA) to expand the applicability domain. Initially, descriptors derived from ADRA, based on both molar and gravimetric concentrations, showed significant correlations with LLNA EC3 values. We then constructed prediction models using ANN analysis, incorporating parameters from GL497-adopted methods. These models exhibited a strong correlation with LLNA EC3 values. The predicted EC3 values for molar and gravimetric concentrations correlated well with each other and with previous values from an ANN model using DPRA instead of ADRA. Additionally, the prediction accuracy of ANN models combined with "2 out of 3″ negative judgment for GHS classification was comparable to that of ITSv1/v2. Ultimately, this enables QRA for a broader range of substances using predictive EC3 values as PoDs without animal testing, paving the way for more effective risk assessments.

摘要

在皮肤致敏的下一代风险评估(NGRA)中,估计起始点(PoD)至关重要。小鼠局部淋巴结试验(LLNA)被认为是评估化学品皮肤致敏潜力的“金标准”,LLNA EC3值用作皮肤定量风险评估(QRA)的PoD。本研究提出了预测EC3值的人工神经网络(ANN)模型,通过整合氨基酸衍生物反应性试验(ADRA)来扩大适用范围进行了改进。最初,基于摩尔浓度和重量浓度从ADRA得出的描述符与LLNA EC3值显示出显著相关性。然后,我们使用ANN分析构建了预测模型,纳入了GL497采用方法的参数。这些模型与LLNA EC3值表现出很强的相关性。摩尔浓度和重量浓度的预测EC3值相互之间以及与使用直接反应性预测试验(DPRA)而非ADRA的ANN模型的先前值相关性良好。此外,结合GHS分类“三选二”阴性判断的ANN模型的预测准确性与国际试验策略(ITS)v1/v2相当。最终,这使得能够使用预测的EC3值作为PoD对更广泛的物质进行QRA,而无需动物试验,为更有效的风险评估铺平了道路。

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