Zhai Yayuan, Chen Yue, Gao Ang, Dou Yichen, Gao Yang, Xie Heran
College of Public Health and Health Sciences, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
National Institute of Sports Medicine, Beijing, China.
Front Nutr. 2025 Sep 3;12:1651560. doi: 10.3389/fnut.2025.1651560. eCollection 2025.
This study aimed to develop a glucosamine-magnesium composite (GlcN-Mg) as a novel Pickering emulsion stabilizer for the preparation of GlcN-Mg stabilized Pickering emulsion (GlcN-Mg PE) and systematically characterize its structural properties and emulsification performance. Structural analysis revealed that Mg coordination reduced GlcN⋅HCl particle size from 1,117 ± 222.58 to 393.8 ± 45.42 nm, expanded its crystal lattice, and created a porous structure with a 22.9 ± 1.80 nm pore size. studies have shown that GlcN-Mg exhibits exceptional stability in food matrices and controlled Mg release during gastrointestinal digestion. Then GlcN-Mg composite was employed to prepare water-in-oil (W/O) GlcN-Mg PE under different homogenization speeds (5,000-25,000 rpm), GlcN-Mg concentrations (0.3%-1.3%), and oil-to-water ratios (3:7-8:2). Rheological analysis indicated that GlcN-Mg PE exhibited a distinct threshold effect under varying conditions, while environmental factors significantly influenced emulsion stability. Furthermore, during gastrointestinal digestion, GlcN-Mg PE exhibited controlled-release ability, with the Mg release rate reaching 80.42 ± 1.94% during intestinal digestion. Its stability across a wide range of conditions highlights its potential applications in complex emulsion systems.
本研究旨在开发一种氨基葡萄糖 - 镁复合物(GlcN - Mg)作为新型皮克林乳液稳定剂,用于制备GlcN - Mg稳定的皮克林乳液(GlcN - Mg PE),并系统地表征其结构性质和乳化性能。结构分析表明,镁配位使GlcN⋅HCl粒径从1117±222.58 nm减小至393.8±45.42 nm,扩大了其晶格,并形成了孔径为22.9±1.80 nm的多孔结构。研究表明,GlcN - Mg在食品基质中表现出优异的稳定性,并且在胃肠道消化过程中能够控制镁的释放。然后,采用GlcN - Mg复合物在不同的均质速度(5000 - 25000 rpm)、GlcN - Mg浓度(0.3% - 1.3%)和油水比(3:7 - 8:2)下制备油包水(W/O)型GlcN - Mg PE。流变学分析表明,GlcN - Mg PE在不同条件下表现出明显的阈值效应,而环境因素显著影响乳液稳定性。此外,在胃肠道消化过程中,GlcN - Mg PE表现出控释能力,在肠道消化期间镁的释放率达到80.42±1.94%。其在广泛条件下的稳定性突出了其在复杂乳液体系中的潜在应用。