4.7 Article

Caftaric acid oxidation in the presence of cell signaling regulator glutathione: Electrochemical and chromatographic analyses

期刊

MICROCHEMICAL JOURNAL
卷 193, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.microc.2023.109045

关键词

Antioxidants; Must browning; White wine; Oxidation; Voltammetry; LC-MS

向作者/读者索取更多资源

New antioxidant materials in biomedical applications are being studied using chromatographic techniques, mass spectroscopy, and electrochemical analyses to understand their reaction mechanism and products with nucleophiles. The oxidation products of CFT and its reaction pathways in the presence and absence of GSH were identified using UPLC-MS analysis.
New antioxidant materials in biomedical applications are an exciting research topic. However, the lack of understanding of the products/intermediates formed and the interaction between nucleophiles and these antioxidants will prevent commercial or industrial applications. To overcome this obstacle, chromatographic techniques, mass spectroscopy, and electrochemical analyses were combined to study the mechanism and products of the expected reaction between antioxidants and nucleophiles. Grape juice contains phenolic compounds such as 2-S-glutathionylcaftaric acid, which is formed as a result of oxidative action. Through UPLC and voltammetric analysis of caftaric acid (CFT) and its quinone with glutathione (GSH), the oxidation and subsequent reactions were monitored. Electrochemical techniques such as cyclic voltammetry (CV) and chronoamperometry (CA) have been used to investigate the electrochemical oxidation characteristics of the investigated CFT in a Britton-Robinson (B-R) buffer electrolyte. As a result of the analysis of ultra-high performance liquid chromatography-mass spectrometry (UHPLC-MS) results, the oxidation products were identified to suggest the optimal mechanism for the oxidation of CFTs both in the presence and absence of GSH. A reversible oxidation process is observed at pH 1.8 for CFT without glutathione (GSH) at E1/2 = 0.52 V against Ag/AgCl 3.0 M KCl) using cyclic voltammetry. During this electrochemical process, two electrons in the CFT molecule were oxidized along with two protons, forming o-quinone. In the presence of GSH, the formed quinone either reacts with glutathione to form mono- and bi-glutathione CFT conjugates or is reduced by GSH to its original state. As a result of the UPLC-MS analysis, the oxidation products of CFT were identified, and the reaction pathways were proposed.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据