Nano-liposomal entrapment of bioactive peptidic fraction from fish gelatin hydrolysate

被引:73
作者
Hosseini, Seyed Fakhreddin [1 ]
Ramezanzade, Leila [1 ]
Nikkhah, Maryam [2 ]
机构
[1] Tarbiat Modares Univ, Fac Marine Sci, Dept Seafood Proc, POB 46414-356, Noor, Iran
[2] Tarbiat Modares Univ, Fac Biol Sci, Dept Nanobiotechnol, POB 14115-175, Tehran, Iran
基金
美国国家科学基金会;
关键词
Liposomal entrapment; Fish gelatin peptide; Physiochemical characteristics; Antioxidant activity; CHITOSAN-COATED LIPOSOMES; IN-VITRO RELEASE; ANTIOXIDANT PROPERTIES; SKIN GELATIN; PHOSPHATIDYLCHOLINE NANOVESICLES; PHYSICOCHEMICAL PROPERTIES; FUNCTIONAL-PROPERTIES; LIPID-COMPOSITION; PROTEIN; STABILITY;
D O I
10.1016/j.ijbiomac.2017.05.141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study guided the potential of nanoliposomal vesicles for the encapsulation of an active peptidic fraction from the fish skin gelatin by enzymatic hydrolysis using alcalase. The average particle size of peptide-loaded nanoliposomes was found to be in the range 134-621 nm, with a zeta-potential of 0.06-8.65 mV and a polydispersity index of 0.27-0.49, when the initial peptide content was 0-10 mg/ml. The FTIR analysis showed that there was an effective hydrophobic interaction as well as hydrogen bonding between phosphatidylcholine and peptidic fraction. The encapsulation efficiency (EE) was remarkably influenced by peptide concentration and the maximum EE (84.5%) was achieved with 1 mg/ml peptide concentration. A prolonged release of peptide from nanoliposomes was also observed as compared to free peptidic fraction. The results showed that the encapsulation of gelatin peptidic fraction using liposomal nanocarrier could represent a useful approach to overcome the issues associated with direct application of these antioxidant peptides in foodstuffs. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1455 / 1463
页数:9
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