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Preparation and in Vitro Release of Alginate/Chitosan Microparticles Containing α-glucosidase Inhibiting Peptide

机译:含α-葡糖苷酶抑制肽的藻酸盐/壳聚糖微粒的制备和体外释放

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Alginate-chitosan multilayer beads containing α-glucosidase inhibiting peptide (GIP) from Ruditapes philippinarum were prepared to develop stable, non-toxic microcapsules. The optimal conditions were alginate concentration (w/v) 1.0%, alginate/GIP ratio (w/w) 1:5, calcium chloride concentration (w/v) 5% and chitosan concentration (w/v) 2.0%, which were obtained through single factor tests and orthogonal experiments. Under the conditions, the encapsulation efficiency (EE%) was 67.21% and the drug-loading percentage was 33.67%.According to the release study, the release rate of GIP was lower than 30% after incubation in simulated gastric fluid (SGF) for 3h and the rate was higher than 70% after incubation in simulated intestinal fluid (SIF) for 5h. The inhibiting rate was 25.13% after treatment in SIF when the concentration of GIP was 10mg/mL. Accordingly,the microcapsules prepared in this paper are acid resistant and therefore can be given orally.
机译:含有来自Ruditapes Philippinarum的含α-葡萄糖苷酶抑制肽(GIP)的藻酸壳多层珠粒被制备用于开发稳定,无毒的微胶囊。最佳条件是海藻酸盐浓度(w / v)1.0%,藻酸盐/缩略率(w / w)1:5,氯化钙浓度(w / v)5%和壳聚糖浓度(w / v)2.0%,即通过单因素测试和正交实验获得。在条件下,封装效率(EE%)为67.21%,药物载量百分比为33.67%。根据释放研究,妊娠胃肠(SGF)孵育后GIP的释放速率低于30% 3h,在模拟肠液(SIF)中孵育5小时后,速率高于70%。在SIF在仪表浓度为10mg / ml时,在SIF处理后抑制率为25.13%。因此,本文制备的微胶囊是耐酸,因此可以口服给出。

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