铁蛋白
化学
纳米颗粒
分子
没食子酸表没食子酸酯
生物物理学
化学工程
纳米技术
生物化学
材料科学
有机化学
多酚
生物
工程类
抗氧化剂
作者
Shengnan Chen,Yuqian Liu,Lei Zhu,Demei Meng,Liqun Zhang,Qiaoe Wang,Jiangnan Hu,Desheng Wang,Zhiwei Wang,Zhongkai Zhou,Huanlu Song,Rui Yang
标识
DOI:10.1021/acs.jafc.1c01997
摘要
Phytoferritin has a natural cagelike architecture for carrying bioactive molecules, and it is uniquely suited to function as a carrier due to its multiple interfaces and channels. In this study, a novel approach was proposed to prepare ferritin-salvianolic acid B-epigallocatechin gallate (EGCG) three-layer nanoparticles (FSE) through the steric hindrance of ferritin channels. Urea (30 mM) could expand the ferritin channel size evidenced by the improved iron release rate vo and promote the EGCG penetration into the ferritin cavity without disassembly of the ferritin cage. The encapsulation ratio of EGCG was 16.0 ± 0.14% (w/w). Salvianolic acid B attached to the outer interface of ferritin through weak bonds with a binding constant of (2.91 ± 0.04) × 105 M-1. The FSE maintained a spherical structure with a diameter of 12 nm. Moreover, when subjected to heat (40-70 °C) there was a significant increase in the stability of EGCG in the FSE due to the binding of salvianolic acid B. Through this interesting approach, two molecules are simultaneously attached and encapsulated in ferritin in a multilayer form under moderate conditions, which is conducive to the protection of unstable molecules for potential encapsulation and delivery utilization.
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