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Encapsulation of Active Molecules in Microparticles Based on Natural Polysaccharides

机译:基于天然多糖的微粒中的活性分子封装

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摘要

This mini-review is focused on an engineering approach to produce polysaccharides-based microparticles for nutraceutical and pharmaceutical purposes. A brief introduction about the fundamental properties of polysaccharides and their use as microsystems in food, cosmetics, and pharmaceutics, and a summary of the most important methods of preparation are described. Then, a novel method based on the ultrasonic atomization of solutions of the two most used polysaccharides, alginate and chitosan, followed by ionotropic gelation to produce enteric microsystems for oral administration and, in particular, the basic mechanisms of the encapsulation of molecules with different size and hydrophilicity, are investigated. This mini-review will show therefore the pathway to correctly design a polysaccharide microcarrier for the encapsulation of active molecules with different properties: from the choice of materials features, to the selection and the optimization of production methods with the aim to reduce costs and energy (ionotropic gelation coupled to ultrasonic atomization), to the control of the final carrier size (by purposely developed predictive models), at last to the optimization of encapsulation properties (predicting by model the drug leakage and providing different solutions to avoid it).
机译:该迷你评论专注于生产基于多糖的微粒的工程方法,用于营养保健和药物。简要介绍了多糖的基本性质及其作为食品,化妆品和药物中的微系统的基础特性,并描述了最重要的准备方法的概述。然后,一种基于两种最多使用多糖,海藻酸盐和壳聚糖的溶液的超声雾化的新方法,然后是离子脱离凝胶化,从而产生口服给药的肠溶微体系,特别是封装具有不同尺寸的分子的基本机制和亲水性进行研究。这种迷你评论将显示途径,用于正确设计多糖微载体,用于封装具有不同性质的活性分子:从材料的选择特征,选择和优化生产方法的旨在降低成本和能量(离子孔凝胶耦合到超声雾化),以控制最终载体尺寸(通过故意开发的预测模型),最后通过封装性能的优化(通过模型泄漏预测并提供不同的解决方案来避免它)。

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