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化学评价皮肤代谢:电化学与液相色谱和质谱联用研究丁香酚和异丁香酚。

In chemico evaluation of skin metabolism: Investigation of eugenol and isoeugenol by electrochemistry coupled to liquid chromatography and mass spectrometry.

机构信息

Westfälische Wilhelms-Universität Münster, Institut für Anorganische und Analytische Chemie, Corrensstraße 30, 48149 Münster, Germany.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Jan 15;913-914:106-12. doi: 10.1016/j.jchromb.2012.12.004. Epub 2012 Dec 11.

Abstract

Skin sensitization is initiated by the modification of proteins located in the skin. After oxidative activation, eugenol and isoeugenol have the potential to modify skin proteins and therefore cause sensitization processes. Despite their known skin sensitizing properties, they are of common use in cosmetic products. According to the European Commission regulation No. 1223/2009, animal tests have to be banned for substances intended for cosmetic use. Therefore, alternative methods of investigation need to be developed for the approval of future substances. For this reason, eugenol and isoeugenol were selected as model substances to be investigated in a purely instrumental approach comprising electrochemistry, liquid chromatography and mass spectrometry. In the present work, reactive oxidation products of eugenol and isoeugenol were electrochemically generated. Reactive quinones and quinone methides were formed. Surprisingly, eugenol and isoeugenol differ significantly in their oxidation behaviour. Isoeugenol exhibits the formation of quinones and quinone methides of an alkylated and dealkylated species, respectively, whereas eugenol shows the formation of quinoid species only after dealkylation. Reactive quinoid species could be trapped with glutathione and the protein β-lactoglobulin A. The results are comparable to the ones with conventional animal studies in literature, which attribute the adverse effects of eugenol and isoeugenol to the formation of reactive quinones or quinone methides, which are reactive intermediates, able to react with proteins. Such species were successfully generated and investigated by the use of electrochemistry coupled to mass spectrometry. Above all, the investigation of adduct formation by the additional use of liquid chromatography allowed the assessment of the mechanism of oxidation, as it might happen in the skin. Both substances were proven to be trapped by the protein β-lactoglobulin A after electrochemical oxidation. However, isoeugenol formed the larger variety of adducts compared to eugenol.

摘要

皮肤致敏作用是由位于皮肤内的蛋白质修饰所引发的。氧化激活后,丁香酚和异丁香酚有可能修饰皮肤蛋白,从而引发致敏过程。尽管它们具有已知的皮肤致敏特性,但它们在化妆品产品中仍被广泛使用。根据欧洲委员会第 1223/2009 号法规,用于化妆品用途的物质必须禁止进行动物测试。因此,需要开发替代方法来研究未来的物质。出于这个原因,选择丁香酚和异丁香酚作为模型物质,采用电化学、液相色谱和质谱学的纯仪器方法进行研究。在本工作中,丁香酚和异丁香酚的反应性氧化产物通过电化学方法生成。形成了反应性醌和醌甲基化物。令人惊讶的是,丁香酚和异丁香酚在氧化行为上存在显著差异。异丁香酚分别表现出烷基化和去烷基化的醌和醌甲基化物的形成,而丁香酚仅在去烷基化后才显示出醌型物质的形成。反应性醌型物质可以与谷胱甘肽和蛋白质β-乳球蛋白 A 结合。这些结果与文献中常规动物研究的结果相当,这些研究将丁香酚和异丁香酚的不良反应归因于反应性醌或醌甲基化物的形成,这些物质是具有反应性的中间产物,能够与蛋白质发生反应。通过使用电化学与质谱联用,可以成功地生成和研究这些活性中间体。此外,通过额外使用液相色谱法研究加合物的形成,可以评估氧化机制,因为它可能会在皮肤中发生。两种物质在电化学氧化后都被蛋白质β-乳球蛋白 A 捕获。然而,与丁香酚相比,异丁香酚形成了更多种类的加合物。

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