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Effect of Alginate Composition on Profile Release and Characteristics of Chitosan-alginate Microparticles Loaded with Mangosteen Extract

机译:山氨酸盐组合物对山竹素提取物负荷的壳体藻酸盐微粒的剖面释放及特征

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Preparation of mangostin-loaded chitosan-alginate microparticles, chemical and physical characterization of the particles, and mangostin release profiles, are described herein. Mangostin rich fraction was obtained from Garcinia mangostana L. pericarp by extraction followed by fractionation. Mangostin-loaded chitosan-alginate microparticles were prepared by ionic gelation method using tripolyphosphate as the linking agent and various concentration of alginate. Mangostin was effectively loaded in all microparticle formulations, resulting in ~97% encapsulation efficiencies. The loading of mangostin and the in-vitro release profiles in simulated gastrointestinal fluids were affected by the chitosan to alginate ratios used in the preparation of the microparticles. Increased alginate concentration resulted in lowered release of mangostin from microparticles immersed in simulated gastric fluid (pH 1.2) up to two hours. Low release of mangostin in acidic fluid but high release in simulated colon fluid, indicated that the chitosan-alginate microparticles are prospective carrier for extended release of active compound in gastrointestinal system.
机译:本文描述了甲状腺素的壳聚糖 - 藻酸盐的微粒,化学和物理表征,以及颗粒的化学和物理表征,以及血小蛋白释放曲线。通过提取,然后分馏从Garcinia Mangostana L. Pericarp获得Mangostin富分裂。通过使用三聚磷酸盐作为连接剂和各种浓度的藻酸盐,通过离子凝胶化方法制备Mangostin加载的壳聚糖酸盐微粒。芒果蛋白在所有微粒制剂中有效地装载,导致〜97%的包封效率。模拟胃肠液中的植物加载和体外释放曲线受壳聚糖对微粒的制备中使用的藻酸盐比的影响。在浸入模拟胃液(pH1.2)中,增加海藻酸盐浓度从浸入模拟胃液(pH1.2)中的微粒释放到2小时。在酸性流体中的山竹蛋白酶释放出来,但在模拟结肠流体中释放出高,表明壳聚糖 - 藻酸盐微粒是用于延长胃肠系统中活性化合物的前瞻性载体。

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