Structure Properties of Gallic Acid-Enhanced Alginate Hydrogels for Sustainable Food Packaging as Plastic Replacement

IF 6.9 Q1 FOOD SCIENCE & TECHNOLOGY
Food frontiers Pub Date : 2025-07-11 DOI:10.1002/fft2.70072
Francisco Javier Leyva-Jiménez, Carlos Abellán-Dieguez, Rodrigo Oliver-Simancas, Antonio M. Rodríguez-García, M. Elena Alañón
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Abstract

Structure properties of alginate and glycerol hydrogels (93:7 v/v) functionalized with gallic acid (0.1%, 0.5%, and 0.8%) (w/v) were evaluated as plastic alternatives for food packaging. A thorough characterization of these hydrogels was performed, evaluating their physico-mechanical, optical, and functional properties, particularly for potential applications in food packaging. FTIR analysis confirmed interactions between the hydrogel matrix and gallic acid, highlighting the formation of hydrogen bonds. The BET method and high-resolution scanning electron microscopy (HRSEM) further verified the homogeneity of the hydrogel surfaces. The inclusion of gallic acid led to increased thickness, permeability, and swelling capacity. However, ultimate tensile strength and fracture toughness significantly decreased, especially in hydrogels containing the highest gallic acid concentration (0.8%). Functionalized hydrogels exhibited enhanced antioxidant activity, as demonstrated by DPPH and FRAP assays. Hydrogels with 0.5% gallic acid showed a 4.4–4.8-fold increase in antioxidant activity, while those with 0.8% gallic acid achieved a 7.0–7.3-fold enhancement. The release of gallic acid from the hydrogels followed a dose-dependent pattern, with peak release occurring within 1–2 h. These findings suggest that alginate-based hydrogels functionalized with gallic acid offer a promising approach for the controlled release of bioactive compounds, presenting potential applications in innovative packaging solutions.

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替代塑料可持续食品包装用没食子酸增强海藻酸盐水凝胶的结构性能
以没食子酸(0.1%、0.5%和0.8%)(w/v)功能化的海藻酸盐和甘油水凝胶(93:7 v/v)作为食品包装的塑料替代品,对其结构性能进行了评价。对这些水凝胶进行了全面的表征,评估了它们的物理力学、光学和功能特性,特别是在食品包装中的潜在应用。FTIR分析证实了水凝胶基质与没食子酸之间的相互作用,突出了氢键的形成。BET法和高分辨率扫描电镜(HRSEM)进一步验证了水凝胶表面的均匀性。没食子酸的加入增加了厚度、渗透性和溶胀能力。然而,极限拉伸强度和断裂韧性显著降低,特别是在未食子酸浓度最高(0.8%)的水凝胶中。DPPH和FRAP实验表明,功能化水凝胶具有增强的抗氧化活性。添加0.5%没食子酸的水凝胶抗氧化活性提高了4.4 - 4.8倍,添加0.8%没食子酸的水凝胶抗氧化活性提高了7.0 - 7.3倍。水凝胶中没食子酸的释放呈剂量依赖性,在1-2小时内达到峰值。这些发现表明,以没食子酸功能化的海藻酸基水凝胶为控制生物活性化合物的释放提供了一种有前途的方法,在创新包装解决方案中具有潜在的应用前景。
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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来源期刊
CiteScore
10.50
自引率
0.00%
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审稿时长
10 weeks
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