• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

二聚体效应:一种使用氨基酸衍生物反应性测定法在化学层面评估皮肤致敏性的优化方法。

The dimer effect: A refinement approach towards skin sensitization assessment in-chemico using Amino acid Derivative Reactivity Assay.

作者信息

Paul Choudhury Ratnadeep, Singh Akanksha, Mathai Eldho, Sudhakar Dgs, Tourneix Fleur, Alépée Nathalie, Gautier Francoise

机构信息

L'Oréal Research & Innovation, Bengaluru, India.

L'Oréal Research & Innovation, Aulnay-sous-Bois, France.

出版信息

J Appl Toxicol. 2024 Nov;44(11):1804-1815. doi: 10.1002/jat.4681. Epub 2024 Aug 2.

DOI:10.1002/jat.4681
PMID:39096042
Abstract

Skin sensitization is a key endpoint for safety assessment, especially for cosmetics and personal care products. The adverse outcome pathway for skin sensitization and the chemical and biological events driving the induction of human skin sensitization are now well understood. Several non-animal test methods have been developed to predict sensitizer potential by measuring the impact of chemical sensitizers on these key events. In this work, we have focused on Key Event 1 (the molecular initiating step), which is based on formation of a covalent adduct between skin sensitizers and endogenous proteins and/or peptides in the skin. There exists three in-chemico assays approved by the Organization for Economic Co-operation and Development-(1) Direct Peptide Reactivity Assay (DPRA), (2) Amino Acid Derivative Reactivity Assay (ADRA), and (3) Kinetic Direct Peptide Reactivity Assay (kDPRA) to quantify peptide/amino acid derivative depletion after incubation with test chemicals. However, overestimated depletion of the cysteine-based peptide/amino acid derivatives is known in such assays because of the dimerization of the thiol group. In this present work, we report the synthesis and structural confirmation of the dimer of N-(2-[1-naphthyl]acetyl)-L-cysteine (NAC) from the ADRA assay to allow simultaneous determination of (a) peptide depletion by quantifying NAC monomer and (b) peptide dimerization by quantifying NAC dimer thereby eliminating the overestimation. We present a case study with three chemicals to demonstrate the importance of this approach. Thus, this simultaneous assay gives a more informed view of the peptide reactivity of chemicals to better identify skin sensitizers.

摘要

皮肤致敏是安全性评估的关键终点,尤其是对于化妆品和个人护理产品而言。目前,人们已经充分了解了皮肤致敏的不良结局途径以及引发人体皮肤致敏的化学和生物学事件。已经开发了几种非动物测试方法,通过测量化学致敏剂对这些关键事件的影响来预测致敏剂潜力。在这项工作中,我们重点关注关键事件1(分子起始步骤),该步骤基于皮肤致敏剂与皮肤中的内源性蛋白质和/或肽之间形成共价加合物。经济合作与发展组织批准了三种体外化学分析方法:(1)直接肽反应性分析(DPRA),(2)氨基酸衍生物反应性分析(ADRA),以及(3)动力学直接肽反应性分析(kDPRA),用于在与测试化学品孵育后量化肽/氨基酸衍生物的消耗。然而,由于硫醇基团的二聚化,在这类分析中,基于半胱氨酸的肽/氨基酸衍生物的消耗被高估是已知的。在本工作中,我们报告了来自ADRA分析的N-(2-[1-萘基]乙酰基)-L-半胱氨酸(NAC)二聚体的合成和结构确认,以便通过量化NAC单体同时测定(a)肽的消耗,并通过量化NAC二聚体同时测定(b)肽的二聚化,从而消除高估。我们用三种化学品进行了案例研究,以证明这种方法的重要性。因此,这种同步分析能更全面地了解化学品的肽反应性,从而更好地识别皮肤致敏剂。

相似文献

1
The dimer effect: A refinement approach towards skin sensitization assessment in-chemico using Amino acid Derivative Reactivity Assay.二聚体效应:一种使用氨基酸衍生物反应性测定法在化学层面评估皮肤致敏性的优化方法。
J Appl Toxicol. 2024 Nov;44(11):1804-1815. doi: 10.1002/jat.4681. Epub 2024 Aug 2.
2
Cause of and countermeasures for oxidation of the cysteine-derived reagent used in the amino acid derivative reactivity assay.用于氨基酸衍生反应性测定的半胱氨酸衍生试剂氧化的原因和对策。
J Appl Toxicol. 2019 Feb;39(2):191-208. doi: 10.1002/jat.3707. Epub 2018 Sep 16.
3
Comparison of in chemico skin sensitization methods and development of an in chemico skin photosensitization assay.比较化学敏化方法和开发化学敏化皮肤光感测定法。
ALTEX. 2019;36(3):373-387. doi: 10.14573/altex.1811011. Epub 2019 Mar 11.
4
Development of a prediction method for skin sensitization using novel cysteine and lysine derivatives.利用新型半胱氨酸和赖氨酸衍生物开发皮肤致敏预测方法。
J Pharmacol Toxicol Methods. 2014 Jul-Aug;70(1):94-105. doi: 10.1016/j.vascn.2014.06.001. Epub 2014 Jun 10.
5
Applicability of amino acid derivative reactivity assay (4 mM) for the prediction of skin sensitization by combining multiple alternative methods to evaluate key events.氨基酸衍生物反应性测定法(4mM)对通过组合多种替代方法评估关键事件预测皮肤致敏性的适用性。
J Appl Toxicol. 2022 Jul;42(7):1159-1167. doi: 10.1002/jat.4283. Epub 2022 Jan 20.
6
Oxidation of a cysteine-derived nucleophilic reagent by dimethyl sulfoxide in the amino acid derivative reactivity assay.半胱氨酸衍生亲核试剂被二甲亚砜氧化在氨基酸衍生物反应性测定中。
J Appl Toxicol. 2020 Jun;40(6):843-854. doi: 10.1002/jat.3948. Epub 2020 Feb 12.
7
Improving predictive capacity of the Amino acid Derivative Reactivity Assay test method for skin sensitization potential with an optimal molar concentration of test chemical solution.优化测试化学物质溶液的最佳摩尔浓度,提高氨基酸衍生物反应性测定法在皮肤致敏性预测能力。
J Appl Toxicol. 2021 Feb;41(2):303-329. doi: 10.1002/jat.4082. Epub 2020 Oct 30.
8
A novel in chemico method to detect skin sensitizers in highly diluted reaction conditions.一种在高稀释反应条件下检测皮肤致敏剂的新型化学方法。
J Appl Toxicol. 2015 Nov;35(11):1348-60. doi: 10.1002/jat.3139. Epub 2015 Mar 25.
9
Amino acid derivative reactivity assay-organic solvent reaction system: A novel alternative test for skin sensitization capable of assessing highly hydrophobic substances.氨基酸衍生物反应性测定-有机溶剂反应系统:一种能够评估高疏水性物质的新型皮肤致敏替代试验。
J Appl Toxicol. 2021 Oct;41(10):1634-1648. doi: 10.1002/jat.4152. Epub 2021 Feb 26.
10
Within- and between-laboratory reproducibility and predictive capacity of amino acid derivative reactivity assay (ADRA) using a 0.5 mg/mL test chemical solution: Results of the study for reproducibility confirmation implemented in five participating laboratories.使用 0.5mg/mL 测试化学溶液的氨基酸衍生物反应性测定(ADRA)的实验室内部和实验室间重现性和预测能力:在五个参与实验室中实施的重现性确认研究结果。
J Appl Toxicol. 2022 Jun;42(6):1078-1090. doi: 10.1002/jat.4279. Epub 2022 Jan 18.

引用本文的文献

1
Limitations and Modifications of Skin Sensitization NAMs for Testing Inorganic Nanomaterials.用于测试无机纳米材料的皮肤致敏NAMs的局限性与改进
Toxics. 2024 Aug 21;12(8):616. doi: 10.3390/toxics12080616.