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壳聚糖基油凝胶:橄榄油油凝胶的乳液干燥动力学及物理、流变和质构特性。

Chitosan-Based Oleogels: Emulsion Drying Kinetics and Physical, Rheological, and Textural Characteristics of Olive Oil Oleogels.

机构信息

Department of Chemical Engineering, Universidade de Santiago de Compostela, rúa Lope Gómez de Marzoa, s/n, 15782 Santiago de Compostela, Spain.

出版信息

Mar Drugs. 2024 Jul 17;22(7):318. doi: 10.3390/md22070318.

DOI:10.3390/md22070318
PMID:39057427
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11278251/
Abstract

Oleogels are of high interest as promising substitutes for trans fats in foods. An emulsion-templated method was used to trap olive oil in the chitosan crosslinked with vanillin matrix. Oil in water emulsions (50:50 /) with different chitosan content (0.7 and 0.8% /) with a constant vanillin/chitosan ratio (1.3) were air-dried at different temperatures (50, 60, 70, and 80 °C) and freeze-dried (-26 °C and 0.1 mbar) to produce oleogels. Only falling rate periods were determined during air-drying kinetics and were successfully modeled with empirical and diffusional models. At a drying temperature of 70 °C, the drying kinetics were the fastest. The viscoelasticity of oleogels showed that the elastic modulus significantly increased after drying at 60 and 70 °C, and those dried at 50 °C and freeze-dried were weaker. All oleogels showed high oil binding capacity (>91%), but the highest values (>97%) were obtained in oleogels with a threshold elastic modulus (50,000 Pa). The oleogels' color depended on the drying temperature and chitosan content (independent of the drying method). Significant differences were observed between air-dried and freeze-dried oleogels with respect to oxidative stability. Oxidation increased with the air-drying time regardless of chitosan content. The found results indicated that drying conditions must be carefully selected to produce oleogels with specific features.

摘要

油凝胶作为食品中反式脂肪的替代品备受关注。本研究采用乳液模板法,将橄榄油包埋在壳聚糖与香草醛交联的基质中。以不同壳聚糖含量(0.7%和 0.8%/)的水包油(50:50/)为原料,在不同温度(50、60、70 和 80°C)下空气干燥,以及在-26°C 和 0.1 mbar 下冷冻干燥,制备油凝胶。仅在空气干燥动力学中确定了下降速率期,并成功使用经验和扩散模型进行了模拟。在 70°C 的干燥温度下,干燥动力学最快。油凝胶的粘弹性表明,在 60 和 70°C 下干燥后弹性模量显著增加,而在 50°C 下干燥和冷冻干燥的油凝胶较弱。所有油凝胶均表现出高油结合能力(>91%),但在具有阈值弹性模量(50,000 Pa)的油凝胶中获得了最高值(>97%)。油凝胶的颜色取决于干燥温度和壳聚糖含量(与干燥方法无关)。与冷冻干燥的油凝胶相比,空气干燥的油凝胶在氧化稳定性方面存在显著差异。无论壳聚糖含量如何,氧化都会随着空气干燥时间的增加而增加。结果表明,必须仔细选择干燥条件,以生产具有特定特性的油凝胶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/eb6f4529ef01/marinedrugs-22-00318-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/ec7a84735835/marinedrugs-22-00318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/fbf5df06c12b/marinedrugs-22-00318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/c3276981bfb1/marinedrugs-22-00318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/9483a7ebfef0/marinedrugs-22-00318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/ec21094e91f8/marinedrugs-22-00318-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/eb6f4529ef01/marinedrugs-22-00318-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/ec7a84735835/marinedrugs-22-00318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/fbf5df06c12b/marinedrugs-22-00318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/c3276981bfb1/marinedrugs-22-00318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/9483a7ebfef0/marinedrugs-22-00318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/ec21094e91f8/marinedrugs-22-00318-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ede/11278251/eb6f4529ef01/marinedrugs-22-00318-g006.jpg

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