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首页> 外文期刊>Food Hydrocolloids >Protein-reinforced and chitosan-pectin coated alginate microparticles for delivery of flavan-3-ol antioxidants and caffeine from green tea extract
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Protein-reinforced and chitosan-pectin coated alginate microparticles for delivery of flavan-3-ol antioxidants and caffeine from green tea extract

机译:蛋白质增强和壳聚糖-果胶涂层藻酸盐微粒,用于从绿茶提取物中输送黄烷-3-醇抗氧化剂和咖啡因

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摘要

In this study, potential interactions of alginate-proteins and proteins-polyphenols were utilized for the formulation of microparticles encapsulating green tea flavan-3-ols and caffeine. Electrostatic assisted extrusion of alginate-protein (whey proteins, bovine serum albumine, calcium caseinate, soy proteins, hemp proteins) formulations was performed for the production of microparticles and the effect of chitosan or pectin coating was evaluated. Employing alginate in combination with soy or hemp proteins provided large and hard particles, while reinforcement with whey proteins and bovine serum albumin provided the most spherical and softer particles (lower hardness and elasticity), with average diameters around 700-800 mu m. The combination of alginate and calcium caseinate or whey proteins enabled to retain the highest content of polyphenols and caffeine in the formulated particles (up to 80%). Chitosan or pectin coating did not improve the physical and morphological properties or the encapsulation efficiency, but conferred better (prolongued) release profile of polyphenols from the particles. The release studies in water and simulated gastric and intestinal fluids revealed burst release of polyphenols (over 50% in first 5-10 min) followed by sustained release up to 120 min. An artificial neural network designed based on all physical and bioactive parameters of the formulated particles, revealed that the combination of alginate with calcium caseinate or bovine serum albumin as the delivery formulation and pectin coating would provide particles with the maximum loading efficiency of green tea polyphenols and proteins as the functional components, which may facilitate their functional properties when delivered to specific target media in the organism. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在这项研究中,海藻酸盐-蛋白质和蛋白质-多酚的潜在相互作用被用于制备封装绿茶flavan-3-ols和咖啡因的微粒。进行了藻酸盐蛋白(乳清蛋白,牛血清白蛋白,酪蛋白酸钙,大豆蛋白,大麻蛋白)制剂的静电辅助挤出,以制备微粒,并评估了壳聚糖或果胶涂层的效果。将藻酸盐与大豆或大麻蛋白结合使用可提供大而硬的颗粒,而用乳清蛋白和牛血清白蛋白增强可提供最大的球形和较软的颗粒(较低的硬度和弹性),平均直径约为700-800微米。海藻酸钠和酪蛋白酸钙或乳清蛋白的结合能够在配制的颗粒中保留最高含量的多酚和咖啡因(最高80%)。壳聚糖或果胶涂层没有改善物理和形态特性或包封效率,但是赋予了多酚从颗粒中更好的(延长的)释放特性。在水以及模拟的胃液和肠液中的释放研究表明,多酚突然释放(在最初的5-10分钟内释放超过50%),然后持续释放长达120分钟。基于配方颗粒的所有物理和生物活性参数设计的人工神经网络显示,藻酸盐与酪蛋白酸钙或牛血清白蛋白作为递送配方和果胶涂层的组合将为颗粒提供最大的绿茶多酚和蛋白质作为功能成分,当传递到生物体中的特定目标培养基时,可能有助于其功能特性。 (C)2015 Elsevier Ltd.保留所有权利。

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