Improving the performance of dextran-whey protein isolation microcapsules for the encapsulation of selenium-enriched peptide by Maillard reaction

被引:1
|
作者
Zhou, Jiaojiao [1 ]
Wei, Lingfeng [1 ]
Wang, Zhenyu [1 ,2 ]
Din, Zia-ud [3 ]
Lv, Xuqin [1 ,2 ]
Gui, Yue [1 ]
Xie, Fang [1 ]
Cai, Jie [1 ,2 ]
机构
[1] Wuhan Polytech Univ, Natl R&D Ctr Se Rich Agr Prod Proc, Hubei Engn Res Ctr Deep Proc Green Se Rich Agr Pro, Sch Modern Ind Selenium Sci & Engn, Wuhan 430023, Peoples R China
[2] Wuhan Polytech Univ, Key Lab Deep Proc Major Grain & Oil, Hubei Key Lab Proc & Transformat Agr Prod, Minist Educ, Wuhan 430023, Peoples R China
[3] Women Univ Swabi, Dept Food Sci & Nutr, Swabi, Khyber Pakhtunk, Pakistan
关键词
Selenium-enriched peptide; Stabilization; Maillard reaction; Encapsulation; Electrostatic spray; ANTIOXIDANT ACTIVITY; MICROENCAPSULATION; DIGESTIBILITY; STABILITY; EMULSIONS;
D O I
10.1016/j.lwt.2023.115645
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Selenium-enriched peptide (SP) is a new type of selenium supplement with unique bioactivities; however, its instability jeopardizes its industrial applications. Hence, a system stabilizing and delivering SP is a prerequisite to overcome this defect. This study developed a microcapsule, dextran-whey protein isolate-selenium-enriched peptide (DX-WPI-SP), encapsulating SP within the WPI-DX glycation product via electrospraying technology, and its properties were characterized. Results showed that DX-WPI-SP considerably surpassed the physical mixture of WPI, DX, and SP, with respect to antioxidant capacity, thermal stability, and cell cytotoxicity. The in vitro gastrointestinal digestion results showed that over 42% of the SP in DX-WPI-SP survived the gastric fluids and was then released in the intestinal phase. The stability of SP in long-term storage was also observed after its encapsulation in DX-WPI-SP, signifying its stability in this delivery system. This study demonstrated that the DX-WPI-SP microcapsule is a valid strategy to stabilize SP in intestinal delivery.
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页数:8
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    Wei, Lingfeng
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    Din, Zia-ud
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