Gel-like pea protein Pickering emulsions at pH 3.0 as a potential intestine-targeted and sustained-release delivery system for β-carotene

被引:120
作者
Shao, Yun [1 ]
Tang, Chuan-He [1 ,2 ]
机构
[1] S China Univ Technol, Dept Food Sci & Technol, Guangzhou 510640, Guangdong, Peoples R China
[2] S China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510640, Guangdong, Peoples R China
关键词
Pea protein isolate (PPI); Pickering emulsion; Emulsion gel; Delivery system; beta-Carotene; IN-VITRO DIGESTION; STRUCTURAL DESIGN PRINCIPLES; XANTHAN GUM CONCENTRATIONS; WATER EMULSIONS; LIPID DIGESTION; RHEOLOGICAL CHARACTERIZATION; EMULSIFYING PROPERTIES; EMULSIFICATION PROCESS; STABILIZED EMULSIONS; OXIDATIVE STABILITY;
D O I
10.1016/j.foodres.2015.11.025
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In recent years, there is increasing interest in the development of food-grade Pickering emulsions as promising delivery systems for bioactive compounds. Our previous work reported that most of the proteins in pea protein isolate (PPI) at pH 3.0, present in the nanoparticle form, can effectively perform as a kind of food-grade Pickering stabilizers for oil-in-water emulsions (LWT, 2014). The purpose of this study was to further report that PPI-stabilized emulsions at pH 3.0 exhibited great potential to act as intestine-targeted and sustained-release delivery systems for beta-carotene. The emulsions were produced by microfluidization at a specific protein concentration of 6.0% (w/v) and varying oil fractions (phi) of 0.2-0.6. The results indicated that increasing phi was favorable for the gel-like network strengthening of these emulsions. The gel formation was largely related to the droplet flocculation as well as inter-floc attractive interactions. The in vitro simulated digestion results showed that the release of beta-carotene during the intestinal digestion of these emulsions could be well modulated by altering phi. The gel-like emulsion at phi = 0.6 exhibited much lower release of beta-carotene, but higher stability towards degradation during the digestion, than that at phi = 0.3. The findings provide important information not only for the design of novel delivery systems for lipophilic bioactive components, but also for the development of plant protein-based formulations. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:64 / 72
页数:9
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