AbstractThis research aimed to explore the digestion properties of oil embedded in the soybean protein–phospholipid (PC) nanocomposite aggregate particles through gastrointestinal digestion model. Soybean protein isolate (SPI), before and after enzymatically hydrolyzed, was combined with PC to form SPI‐PC and enzymatically hydrolyzed SPI‐PC (EHSPI‐PC) nanocomposite aggregate particles. In the process of stomach dynamic digestion, the zeta potential of SPI‐PC changed from −23.50 to 0.40 mV and the Z‐average particle size reached 1,452.00 nm at 70 min while the zeta potential of EHSPI‐PC changed from −45.63 to 6.13 mV and the Z‐average particle size was 594.77 nm. EHSPI‐PC had larger zeta‐potential absolute value and smaller particle size compared with SPI‐PC. It indicated EHSPI‐PC nanocomposite aggregate particles were good gastrointestinal protective carriers. After adding soybean oil, EHSPI‐PC showed denser and smaller droplet morphologies and more surface charge during the digestion process. Compared with SPI‐PC, it also had better emulsification activity and emulsification stability. In conclusion, EHSPI‐PC is more suitable for embedding soybean oil to release in the small intestine.Practical ApplicationsNano‐aggregate particles are widely used in food, medicine, and chemical industries due to their unique physical and chemical properties and functional properties. However, nano‐aggregate particles have unsatisfactory packaging of emulsifiers and leakage of embedded materials. Enzymatically hydrolyzed soybean protein isolate–phospholipid (EHSPI‐PC) nanocomposite aggregate particles have good emulsification and long‐lasting stability. The results showed that it is feasible for EHSPI‐PC nanocomposite aggregate particles to embed oily substances to ensure that the substances perform their functions in the intestinal tract. Therefore, the delivery system based on the EHSPI‐PC nanocomposite aggregate particles has good development potential in the food and pharmaceutical industries for encapsulation, protection, and release of nonpolar substances.
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