Chitosan–Alginate Microcapsules for Oral Delivery of Egg Yolk Immunoglobulin (IgY): Effects of Chitosan Concentration

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作者
Xiao-Yu Li
Li-Ji Jin
Ya-Nan Lu
Yu-Hong Zhen
Shu-Ying Li
Lin-Hui Wang
Yong-Ping Xu
机构
[1] Dalian University of Technology,Department of Bioscience and Biotechnology
[2] Dalian Medical University,Department of Pharmacy
[3] Dalian SEM Bio-Engineering Technology Co. Ltd.,State Key Laboratory of Fine Chemicals
[4] Ministry of Education Center for Food Safety of Animal Origin,undefined
[5] Dalian University of Technology,undefined
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关键词
Alginate; Chitosan; Chitosan concentration; Egg yolk immunoglobulin (IgY); Gastroresistance; Microcapsules;
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摘要
In our previous study, chitosan–alginate microcapsules were developed to protect egg yolk immunoglobulin (IgY) from gastric inactivation. The present study was undertaken to determine the effect of chitosan concentration (0–0.8%; w/v) on various properties of the microcapsules in order to produce the optimum chitosan–alginate microcapsules for use in the oral delivery of IgY. The properties investigated included microcapsule morphology, loading capacity for IgY (expressed as the IgY loading percentage, w/w, of microcapsules), encapsulation efficiency (EE%), in vitro gastroresistance, and IgY release. IgY loading percentage and EE% were both highest at 0.2% (w/v) chitosan, and, above this level, further increases were not observed. The stability of IgY in simulated gastric fluid (pH 1.2) was significantly improved by encapsulation in alginate microcapsules (IgY retained 43.5% of its activity) and was further improved by including chitosan at any of the chitosan concentrations assessed (IgY retained an average of 69.4% activity) although there was no difference in protection of gastric inactivation among concentrations of chitosan varying from 0.05% to 0.8% (w/v). Higher chitosan concentrations (i.e., ≥0.2%; w/v) prolonged the release of IgY from the microcapsules during simulated intestinal fluid incubation (pH 6.8). However, above the 0.2% (w/v) level, no significant differences were observed. We conclude that the optimum chitosan concentration for microencapsulation is 0.2% (w/v).
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页码:778 / 787
页数:9
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