摘要
Electrostatic and hydrogen bonding drove OS-GE-TA ternary complex formation. • The incorporation of GE-TA enhanced the viscoelasticity of OS oleogels. • The ternary oleogels exhibited high oil-holding capacity and oxidative stability. • The ternary oleogels show excellent potential for DHA delivery. In this study, ternary complexes composed of octenyl succinate acetylated starch (OS), gelatin (GE), and tannic acid (TA) were used to fabricate oleogels via an emulsion-template method combined with freeze-drying for algal oil delivery. The results indicated that electrostatic interactions and hydrogen bonding drove the formation of the ternary complex, resulting in a stronger oleogel network and improved viscoelastic properties and storage stability. Under accelerated oxidation, OS-GE-TA oleogels exhibited significantly ( p < 0.05) lower peroxide values than OS oleogels, with reductions of 9.55–12.87 meq/kg oil, and effectively inhibited fishy odor-related volatiles. In vitro digestion results showed that the free fatty acid (FFA) release of OS-GE-TA 0.4 and OS-GE-TA 0.8 oleogels reached 71.17% and 80.42%, respectively, both significantly ( p < 0.05) higher than algal oil (64.28%), indicating enhanced lipid digestion and DHA release under simulated gastrointestinal conditions. Overall, the novel oleogels developed in this study have considerable potential for DHA delivery. Download: Download high-res image (407KB) Download: Download full-size image
危险品化学品经营许可证(带存储)