N. V. Zhdanova, N. Yu. Lotosh, E. A. Kulikov, S. V. Lukashevich, S. N. Malakhov, Yu. A. Koksharov, A. A. Selishcheva
{"title":"有机溶剂中虾青素与铁盐Fe2+和Fe3+的相互作用","authors":"N. V. Zhdanova, N. Yu. Lotosh, E. A. Kulikov, S. V. Lukashevich, S. N. Malakhov, Yu. A. Koksharov, A. A. Selishcheva","doi":"10.3103/S0027131425700348","DOIUrl":null,"url":null,"abstract":"<p>The carotenoid astaxanthin has a variety of biological activities and antioxidant properties. Due to its lipophilic nature, astaxanthin can be used to protect against lipid peroxidation, in which iron ions play an important role. The effect of Fe<sup>2+</sup> ions on the oxidative degradation of astaxanthin in phospholipid liposomes was previously studied. In this paper, we study the interaction of astaxanthin with Fe<sup>3+</sup> and Fe<sup>2+</sup> in organic solvents of various polarities in the absence of lipids. It is shown that in the presence of Fe<sup>3+</sup>, astaxanthin oxidation and degradation occurs in methanol and dichloromethane. The formation of an intermediate product with an absorption maximum at 876 nm is recorded spectrophotometrically. Electron paramagnetic resonance (EPR) proves the radical nature of the intermediate product, whose signal intensity decreased over time, with the signal remaining for up to 3 days. Based on the obtained results, it can be assumed that the radical product formed in the reaction with Fe<sup>3+</sup> is the radical cation of astaxanthin. At the same time, no changes are detected when astaxanthin is incubated with Fe<sup>2+</sup>: the absorption spectrum does not change and no radical product is formed.</p>","PeriodicalId":709,"journal":{"name":"Moscow University Chemistry Bulletin","volume":"80 5","pages":"311 - 320"},"PeriodicalIF":0.5000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interaction of Astaxanthin with Iron Salts Fe2+ and Fe3+ in Organic Solvents\",\"authors\":\"N. V. Zhdanova, N. Yu. Lotosh, E. A. Kulikov, S. V. Lukashevich, S. N. Malakhov, Yu. A. Koksharov, A. A. Selishcheva\",\"doi\":\"10.3103/S0027131425700348\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The carotenoid astaxanthin has a variety of biological activities and antioxidant properties. Due to its lipophilic nature, astaxanthin can be used to protect against lipid peroxidation, in which iron ions play an important role. The effect of Fe<sup>2+</sup> ions on the oxidative degradation of astaxanthin in phospholipid liposomes was previously studied. In this paper, we study the interaction of astaxanthin with Fe<sup>3+</sup> and Fe<sup>2+</sup> in organic solvents of various polarities in the absence of lipids. It is shown that in the presence of Fe<sup>3+</sup>, astaxanthin oxidation and degradation occurs in methanol and dichloromethane. The formation of an intermediate product with an absorption maximum at 876 nm is recorded spectrophotometrically. Electron paramagnetic resonance (EPR) proves the radical nature of the intermediate product, whose signal intensity decreased over time, with the signal remaining for up to 3 days. Based on the obtained results, it can be assumed that the radical product formed in the reaction with Fe<sup>3+</sup> is the radical cation of astaxanthin. At the same time, no changes are detected when astaxanthin is incubated with Fe<sup>2+</sup>: the absorption spectrum does not change and no radical product is formed.</p>\",\"PeriodicalId\":709,\"journal\":{\"name\":\"Moscow University Chemistry Bulletin\",\"volume\":\"80 5\",\"pages\":\"311 - 320\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Moscow University Chemistry Bulletin\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.3103/S0027131425700348\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Moscow University Chemistry Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.3103/S0027131425700348","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Interaction of Astaxanthin with Iron Salts Fe2+ and Fe3+ in Organic Solvents
The carotenoid astaxanthin has a variety of biological activities and antioxidant properties. Due to its lipophilic nature, astaxanthin can be used to protect against lipid peroxidation, in which iron ions play an important role. The effect of Fe2+ ions on the oxidative degradation of astaxanthin in phospholipid liposomes was previously studied. In this paper, we study the interaction of astaxanthin with Fe3+ and Fe2+ in organic solvents of various polarities in the absence of lipids. It is shown that in the presence of Fe3+, astaxanthin oxidation and degradation occurs in methanol and dichloromethane. The formation of an intermediate product with an absorption maximum at 876 nm is recorded spectrophotometrically. Electron paramagnetic resonance (EPR) proves the radical nature of the intermediate product, whose signal intensity decreased over time, with the signal remaining for up to 3 days. Based on the obtained results, it can be assumed that the radical product formed in the reaction with Fe3+ is the radical cation of astaxanthin. At the same time, no changes are detected when astaxanthin is incubated with Fe2+: the absorption spectrum does not change and no radical product is formed.
期刊介绍:
Moscow University Chemistry Bulletin is a journal that publishes review articles, original research articles, and short communications on various areas of basic and applied research in chemistry, including medical chemistry and pharmacology.