凝聚
化学
多糖
Zeta电位
脂类消化
大豆蛋白
化学工程
触变性
乳清蛋白
水解
保健品
生物高聚物
相(物质)
吸附
色谱法
黄檀
豌豆蛋白
食品科学
皮克林乳液
双乙烯酮
明胶
十八烷
疏水效应
成分
动力学
分离乳清蛋白粉
流变学
纳米载体
单甘酯
疏水
食品化学
流变仪
润湿
功能性食品
消化(炼金术)
活性成分
增稠剂
胶体
穿心莲内酯
有机化学
作者
Yubo Cao,Donggui Wang,Qi Wang,T. Sun,Haizhao Song
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-10-29
卷期号:41 (44): 29789-29800
被引量:1
标识
DOI:10.1021/acs.langmuir.5c04155
摘要
The development of advanced bioactive delivery systems is critical for enhancing nutraceutical stability, controlled release, and functional food design. This study presented the fabrication of high internal phase Pickering emulsions (HIPPEs) stabilized by soy protein isolate (SPI) and Tremella fuciformis polysaccharide (TFP) complexes. The SPI/TFP complex was comprehensively characterized, revealing pH-responsive electrostatic and hydrophobic interactions that regulated complex coacervation and colloidal stability. Optimized SPI/TFP HIPPEs formed at neutral pH with 0.5% TFP exhibited superior physicochemical properties, including reduced droplet size, increased zeta potential, enhanced viscoelastic moduli, pronounced shear-thinning behavior, rapid thixotropic recovery, and stable microstructures. Incorporation of andrographolide (Andr) into the SPI/TFP HIPPEs significantly enhanced their protection against ultraviolet irradiation, thermal stress, and prolonged storage. In vitro digestion studies demonstrated controlled lipid hydrolysis kinetics and facilitated micellarization, resulting in the superior bioaccessibility of Andr compared to conventional formulations. Furthermore, the SPI/TFP HIPPEs exhibited excellent 3D printability with high shape fidelity and mechanical resilience and were unaffected by Andr loading. These findings elucidated the structure-function relationships in SPI/TFP-stabilized HIPPEs and established their potential as multifunctional platforms for nutraceutical delivery and customizable 3D-printed functional foods.
科研通智能强力驱动
Strongly Powered by AbleSci AI