吸附
果胶
化学
化学工程
乳状液
聚结(物理)
分离乳清蛋白粉
表面张力
色谱法
流变学
脂类消化
油滴
乳清蛋白
石英晶体微天平
脂解
脂肪酶
有机化学
材料科学
食品科学
生物化学
热力学
复合材料
物理
脂肪组织
天体生物学
工程类
酶
作者
Hao Li,Paul Van der Meeren
标识
DOI:10.1021/acs.jafc.3c00443
摘要
This work aims to design gastric-stable emulsions with food-grade biopolymers using a novel multiscale approach. The adsorption layer formation at the oil–water interface was based on opposite charge interactions between whey proteins and pectin (with different esterification levels) at pH 3.0 by a sequential adsorption method. The interfacial assembly and disassembly (interfacial complexation, proteolysis, lipolysis) during in vitro gastric digestion were evaluated using a quartz crystal microbalance with dissipation monitoring, ζ-potential, dynamic interfacial tension, and interfacial dilatational rheology. Besides, the evolution of the particle size and microstructure of bulk emulsions during the digestion was investigated by static light scattering and light microscopy. Compared with whey protein isolate (WPI)-stabilized emulsions, the presence of an additional pectin layer can prevent or at least largely delay gastric destabilization (giving rise to coalescence or/and oiling off). Especially, the esterification degree of the pectin used was found to largely affect the emulsion stability upon gastric digestion.
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