Gallic acid liposomes decorated with lactoferrin: Characterization, in vitro digestion and antibacterial activity

•GA-LIP was surface decorated by lactoferrin.•LF-GA-LIP was more stable than GA-LIP.•Lactoferrin interacted with GA-LIP through electrostatic interaction.•LF-GA-LIP displayed a delayed-release effect compared with GA-LIP.•LF-GA-LIP exerted higher antibacterial properties against E. coli and S. aureu...

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Veröffentlicht in:Food chemistry 2019-09, Vol.293, p.315-322
Hauptverfasser: Zhang, Yating, Pu, Chuanfen, Tang, Wenting, Wang, Shiqing, Sun, Qingjie
Format: Artikel
Sprache:eng
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Zusammenfassung:•GA-LIP was surface decorated by lactoferrin.•LF-GA-LIP was more stable than GA-LIP.•Lactoferrin interacted with GA-LIP through electrostatic interaction.•LF-GA-LIP displayed a delayed-release effect compared with GA-LIP.•LF-GA-LIP exerted higher antibacterial properties against E. coli and S. aureus. Gallic acid liposomes (GA-LIP) and gallic acid liposomes decorated with lactoferrin (LF-GA-LIP) were fabricated, and their physiochemical, in vitro digestion and antibacterial activity were analysed. The average particle size of LF-GA-LIP was larger than that of GA-LIP, and the former had a higher encapsulation efficiency and storage stability. Electrostatic interaction existed between lactoferrin and the phospholipid bilayer. Spherical structures of both were observed by transmission electron microscopy and atomic force microscopy. Gallic acid existed in an amorphous form in both liposomes. Hydrogen bond was formed between the hydroxyl groups of gallic acid and the polar head of phospholipid in the liposomes. LF-GA-LIP displayed a delayed-release effect compared with GA-LIP in simulated digestion. It exerted higher antibacterial properties against Escherichia coli and Staphylococcus aureus than GA-LIP. The findings suggested that the liposomes decorated with lactoferrin could be developed as a favourable delivery system for a potential application in the food industry.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2019.04.116