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New microencapsulation system for ascorbic acid using pea protein concentrate as coat protector

机译:以豌豆蛋白浓缩物为涂层保护剂的抗坏血酸微囊化新系统

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摘要

Microencapsulation is essential to preserve biological activity of ascorbic acid (AA) and pea protein has not been used as a carrier in such processes. This work aimed to produce microparticles by a spray-drying process using pea protein (PPC) as wall material of AA and evaluate the retention of the core by HPLC, overall morphology SEM, size distribution by light scattering and release kinetics. Carboxymethylcellulose (CMC) and blends with maltodextrin (M) were produced for comparative analyses. The yields were compatible with the applied technology and the retention was above 84% for all materials. The PPC microparticles presented irregular and rough surfaces, CMC produced a regular and smooth surface and agglomeration was more intense in microparticles with M. Mean particle diameters were all below 8 mu m. The microparticle release rates were lower than those with free AA, being best correlated to the Higuchi kinetic model. These results support the utilization of PPC for microencapsulation of AA.
机译:微囊化对于保持抗坏血酸(AA)的生物活性至关重要,而豌豆蛋白尚未在此类过程中用作载体。这项工作旨在通过使用豌豆蛋白(PPC)作为AA壁材料的喷雾干燥工艺生产微粒,并通过HPLC,整体形貌SEM,通过光散射和释放动力学的尺寸分布评估核心的保留。制备了羧甲基纤维素(CMC)和与麦芽糖糊精(M)的混合物进行比较分析。产率与所应用的技术相容,并且所有材料的保留率均高于84%。 PPC微粒呈现不规则和粗糙的表面,CMC产生规则而光滑的表面,并且在M微粒中团聚更为强烈。平均粒径均在8μm以下。微粒的释放速率低于游离氨基酸的释放速率,与Higuchi动力学模型最相关。这些结果支持了将PPC用于AA的微囊化。

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