Trombino Sonia, Cassano Roberta, Bloise Ermelinda, Muzzalupo Rita, Leta Sonia, Puoci Francesco, Picci Nevio
Department of Pharmaceutical Sciences, University of Calabria, 87036 Arcavacata di Rende, Cosenza, Italy.
Macromol Biosci. 2008 Jan 9;8(1):86-95. doi: 10.1002/mabi.200700110.
In this study we report the synthesis and characterisation of cellulose ferulate, lipoate and alpha-tocopherulate, and their ability to inhibit lipid peroxidation in rat-liver microsomal membranes, induced in vitro by two different sources of free radicals: tert-butyl hydroperoxide and 2,2'-azobis-(2-amidinopropane). We also compared the antioxidant efficiency of the ferulate derivatives obtained through two different synthetic runs, and of a tocopherulate derivative prepared from 6-carboxycellulose. This study showed that the designed systems, preserving the antioxidant activity of the free substrates, are more effective in protecting from tert-butyl hydroperoxide than from 2,2'-azobis-(2-amidinopropane). Moreover, the cellulose ferulate with the higher degree of substitution acted as the best antioxidant.
在本研究中,我们报告了阿魏酸纤维素、硫辛酸纤维素和生育酚纤维素的合成与表征,以及它们抑制大鼠肝微粒体膜脂质过氧化的能力,该脂质过氧化是由两种不同的自由基源在体外诱导产生的:叔丁基过氧化氢和2,2'-偶氮二(2-脒基丙烷)。我们还比较了通过两种不同合成路线得到的阿魏酸衍生物以及由6-羧基纤维素制备的生育酚衍生物的抗氧化效率。本研究表明,所设计的体系在保留游离底物抗氧化活性的同时,对叔丁基过氧化氢的防护作用比对2,2'-偶氮二(2-脒基丙烷)更有效。此外,取代度较高的阿魏酸纤维素是最佳的抗氧化剂。