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Characterization and antioxidant activity of the complexes of tertiary butylhydroquinone with β-cyclodextrin and its derivatives

机译:叔丁基氢醌与β-环糊精及其衍生物的配合物的表征和抗氧化活性

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摘要

Tertiary butylhydroquinone (TBHQ) is a water-insoluble antioxidant. In this study, three cyclodextrin inclusion complexes were prepared to improve the water solubility of TBHQ and expand its range of application. Analysis of phase solubility indicated that TBHQ can form 1:1 inclusion complex with hydroxypropyl-beta-cyclodextrin (HP-β-CD) and dimethyl-beta-cyclodextrin (DM-β-CD) and 1:2 inclusion complex with beta-cyclodextrin (β-CD). The possible inclusion configuration between TBHQ and CDs was determined through FT-IR, PXRD, DSC, NMR, and SEM analyses. Results were validated by theoretical study of AutoDock molecular docking. The scavenging effects of the inclusion complexes were not effective on DPPH radical but higher on hydroxyl, superoxide and ABTS+ radicals than that of TBHQ monomer. Moreover, the water solubility of TBHQ increased after complexation with HP-β-CD and DM-β-CD. The stability of TBHQ is related to the type of storage materials used, and the stability can be improved by complexation with CDs.
机译:叔丁基氢醌(TBHQ)是水不溶性抗氧化剂。在这项研究中,制备了三种环糊精包合物,以改善TBHQ的水溶性并扩大其应用范围。相溶解度分析表明,TBHQ可与羟丙基-β-环糊精(HP-β-CD)和二甲基-β-环糊精(DM-β-CD)形成1:1包合物,与β-环糊精形成1:2包合物。 (β-CD)。通过FT-IR,PXRD,DSC,NMR和SEM分析确定了TBHQ和CD之间可能的夹杂物构型。通过AutoDock分子对接的理论研究验证了结果。与TBHQ单体相比,包合物的清除作用对DPPH自由基无效,但对羟基,超氧化物和ABTS +自由基的清除效果更高。此外,与HP-β-CD和DM-β-CD络合后,TBHQ的水溶性增加。 TBHQ的稳定性与所用存储材料的类型有关,可以通过与CD络合来提高稳定性。

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