Encapsulation of β-carotene in high internal phase Pickering emulsions stabilized by soy protein isolate - epigallocatechin-3-gallate covalent composite microgel particles

被引:26
|
作者
Geng, Mengjie [1 ]
Li, Lijia [1 ]
Feng, Xumei [1 ]
Xu, Jingwen [1 ]
Huang, Yuyang [1 ]
Teng, Fei [1 ]
Li, Yang [1 ,2 ]
机构
[1] Northeast Agr Univ, Coll Food Sci, Harbin 150030, Heilongjiang, Peoples R China
[2] Heilongjiang Green Food Sci Res Inst, Harbin 150028, Heilongjiang, Peoples R China
基金
黑龙江省自然科学基金;
关键词
High internal phase Pickering emulsions; beta-carotene; Soy protein isolate; Epigallocatechin-3-gallate; Microgel particles; FUNCTIONAL-EVALUATION; LIPID OXIDATION; POLYPHENOL; EGCG; ANTHOCYANINS; COMPLEXATION; CONJUGATION; RHEOLOGY; DELIVERY; ASSAY;
D O I
10.1016/j.molliq.2022.119511
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the current study, soy protein isolate (SPI) and epigallocatechin-3-gallate (EGCG) covalent composite microgel particles with antioxidant capacity were prepared and the particles was used as beta-carotene-loaded high internal phase Pickering emulsions (HIPPEs) stabilizers. The covalent binding of SPI-EGCG altered the structures of the SPI through an unfolding of the polypeptide chain. Moreover, compared to HIPPEs stabilized by SPI alone, HIPPEs stabilized by SPI-EGCG microgel particles showed smaller particle size, higher apparent viscosity, and better stability. Microstructure of the fabricated HIPPEs results revealed that SPI-EGCG covalent conjugates promoted the formation of a thick and dense protective layer on the surfaces of oil droplets. Furthermore, beta-carotene-loaded HIPPEs stabilized by SPI-2% EGCG microgel particles exhibited a higher retention rate after 42 days of storage and better bioaccessibility (86.6 4 +/- 0.27% and 54.43 +/- 0.50%, respectively) compared to HIPPEs stabilized by SPI (75.80 +/- 0.49% and 38. 31 +/- 0.93%, respectively). The current study illustrated that the design of HIPPEs stabilized with protein-polyphenol composite particles were of great importance for the delivery of lipophilic bioactive compounds. (C) 2022 Elsevier B.V. All rights reserved.
引用
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页数:10
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