通过与 β-环糊精和淀粉络合,提高 α-生育酚和α-生育酚醋酸酯抗氧化、抗光和抗紫外线辐射的稳定性

Hussein M. Ali, Mohamed H. Attia, Khaled M. A. Ramadan, Eman N. Rashed, Eslam S. Bendary
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摘要

尽管生育酚具有极高的抗氧化活性,但由于其在各种条件下的不稳定性,它们在食品工业中的应用受到了限制。研究人员制备了 α-生育酚(α-TQ)或 α-生育酚醋酸酯(α-TQA)与 β-环糊精(β-CD)或淀粉的复合物,并通过紫外-可见光、红外和热分析对其进行了表征。α-TQ和α-TQA对H2O2的氧化稳定性分别为74.7%和88.8%(576小时)。然而,β-CD 和淀粉复合物的稳定性分别提高到了 82.9% 和 100%,淀粉复合物的稳定性分别提高到了 99.2% 和 99.4%。α-TQ和α-TQA在光照条件下的稳定性取决于它们的物理状态;在油中的稳定性分别为55.3%和82.9%,但在溶液(2.21 mM)中的稳定性则分别降至19.4%和76.5%。此外,在紫外线照射下,它们在油中的稳定性分别降至 39.2% 和 85.0%,在溶液中的稳定性分别降至 61.2% 和 89.1%。然而,在光照和紫外线条件下,所有复合物的稳定性仍然高达 99.0%。因此,α-TQ(天然的生物活性形式)可以用作复合物,而不是通常使用的α-TQA,因为其稳定性更高。对接结果显示,这两种形式都适合β-CD,侧链呈 "U "构象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Improving stabilization of α-tocopherol and α-tocopheryl acetate against oxidation, light and UV radiation by complexation with β-cyclodextrin and starch

Despite the remarkably high antioxidant activity of tocopherols, their applications in the food industry are limited because of their instability under various conditions. Complexes of α-tocopherol (α-TQ) or α-tocopheryl acetate (α-TQA) with β-cyclodextrin (β-CD) or starch were prepared and characterized by UV–vis, IR and thermal analysis. Oxidative stability of α-TQ and α-TQA against H2O2 was 74.7 and 88.8% respectively (576 h). However, stability increased to 82.9 and 100% for β-CD and 99.2 and 99.4% for starch complexes respectively, which indicates that starch is an excellent stabilizing host in addition to being an economic material. Stability of α-TQ and α-TQA under light conditions was dependent on their physical state; it was 55.3 and 82.9% (oil) but stability was lowered to 19.4 and 76.5% in solution (2.21 mM). In addition, exposure to UV irradiation decreased their stability to 39.2 and 85.0% as oil and 61.2 and 89.1% in solution respectively. However, the stability of all complexes remained > 99.0% under light and UV conditions. Accordingly, α-TQ, the natural and biologically active form, can be used as complex rather than α-TQA often used because of its higher stability. Docking revealed that both forms fit in β-CD with the side chain taking “U” conformation.

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