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Antioxidant Nanocomplexes for Delivery of Epigallocatechin-3-gallate

机译:用于递送表没食子儿茶素-3-没食子酸酯的抗氧化剂纳米复合物

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摘要

Modification of chitosan (CS) through grafting with caffeic acid (CA, CA-g-CS) and ferulic acid (FA, FA-g-CS) significantly improved its solubility under neutral and alkaline environments. Spherical and physicochemically stable nanocomplexes assembled from the phenolic acid grafting CS and caseinophosphopeptide (CPP) were obtained with particle size <300 nm and zeta potential of <+30 mV. The net polymer nanocomplexes composed with the phenolic acid grafting CS and CPP showed strong antioxidant activity. The encapsulation efficiencies of epigallocatechin-3-gallate (EGCG) in the CA-g-CS CPP nanocomplexes and FA-g-CS CPP nanocomplexes were 88.1 +/- 6.7 and 90.4 +/- 4.2%, respectively. Improved delivery properties of EGCG were achieved after loading with the antioxidant nanocomplexes, including controlling release of EGCG under simulated gastric environments and preventing its degradation under neutral and alkaline environments.
机译:通过将咖啡酸(CA,CA-g-CS)和阿魏酸(FA,FA-g-CS)接枝改性壳聚糖(CS),可显着提高其在中性和碱性环境下的溶解度。获得了由酚酸接枝CS和酪蛋白磷酸肽(CPP)组装而成的球形和物理化学稳定的纳米复合物,粒径小于300 nm,ζ电位小于+30 mV。由酚酸接枝CS和CPP组成的净聚合物纳米复合物显示出很强的抗氧化活性。表没食子儿茶素-3-没食子酸酯(EGCG)在CA-g-CS CPP纳米复合物和FA-g-CS CPP纳米复合物中的包封效率分别为88.1 +/- 6.7和90.4 +/- 4.2%。负载抗氧化剂纳米复合物后,EGCG的传递特性得到了改善,包括在模拟的胃环境下控制EGCG的释放并在中性和碱性环境下防止其降解。

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