Preparation and optimisation of liposome‐in‐alginate beads containing oyster hydrolysate for sustained release
Summary Oyster ( Crassostrea gigas ) hydrolysate shows antihypertensive effect in our previous study. Oral administration of oyster hydrolysate can loss bioactive peptides due to enzymatic degradation in vivo . To maximise its bioavailability, liposome‐in‐alginate (LA) beads were used to encapsulate...
| Published in: | International Journal of Food Science & Technology |
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| Main Authors: | , , , , |
| Other Authors: | |
| Format: | Article in Journal/Newspaper |
| Language: | English |
| Published: |
Wiley
2016
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| Subjects: | |
| Online Access: | http://dx.doi.org/10.1111/ijfs.13207 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fijfs.13207 |
| Summary: | Summary Oyster ( Crassostrea gigas ) hydrolysate shows antihypertensive effect in our previous study. Oral administration of oyster hydrolysate can loss bioactive peptides due to enzymatic degradation in vivo . To maximise its bioavailability, liposome‐in‐alginate (LA) beads were used to encapsulate the oyster hydrolysates to protect from degradation and obtain sustained release. The preparation conditions of the LA beads were optimised by response surface method using a model peptide of tyrosylalanine (YA). Their characterisation, swelling and release properties were investigated. The optimised conditions for the concentration of calcium chloride, sodium alginate and the amount of ethanol‐dissolved lecithin (EDL) were 0.5 m , 3% and 95.4 mg, respectively. The encapsulation efficiencies of YA and the oyster hydrolysate in the optimised condition were 74.9% and 84.3%, respectively. The release time of the oyster hydrolysate in the simulated gastrointestinal fluid was up to 16 h. The LA beads can be recommended to encapsulate oyster hydrolysate for bioavailability improvement. |
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