首页> 美国卫生研究院文献>International Journal of Molecular Sciences >The Development of Hyaluronan/Fucoidan-Based Nanoparticles as Macrophages Targeting an Epigallocatechin-3-Gallate Delivery System
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The Development of Hyaluronan/Fucoidan-Based Nanoparticles as Macrophages Targeting an Epigallocatechin-3-Gallate Delivery System

机译:基于透明质酸/岩藻酮的纳米粒子的发展作为巨噬细胞靶向EPIGALLOCATECHIN-3-Gallate递送系统

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摘要

The aim of this study was to develop a macrophage-targeted nanoparticle composed of hyaluronan/fucoidan complexes with polyethylene glycol-gelatin to encapsulate and deliver epigallocatechin-3-gallate (EGCG), a compound that can regulate macrophage activation and pro-inflammatory mediator production. We show that our nanoparticles can successfully bond to macrophages and deliver more EGCG than an EGCG solution treatment, confirming the anti-inflammatory effects of these nanoparticles in lipopolysaccharide-stimulated macrophages. The prepared nanoparticles were established with a small mean particle size (217.00 ± 14.00 nm), an acceptable polydispersity index (0.28 ± 0.07), an acceptable zeta potential value (−33.60 ± 1.30 mV), and a high EGCG loading efficiency (52.08% ± 5.37%). The targeting abilities of CD44 binding were increased as the hyaluronan concentration increased and decreased by adding a competitor CD44 antibody. Moreover, we found that fucoidan treatment significantly reduced macrophage migration after lipopolysaccharide treatment in a dose-responsive manner. In summary, we successfully created macrophage-targeted nanoparticles for effective targeted delivery of EGCG, which should aid in the development of future anti-inflammatory drugs against macrophage-related diseases.
机译:本研究的目的是开发由透明质酸/岩藻酮配合物组成的巨噬细胞靶向纳米颗粒,其用聚乙二醇 - 明胶与聚乙二醇 - 明胶组成,以包封和递送EPIGALLOCATECHIN-3-Gallate(EGCG),一种可以调节巨噬细胞活化和促炎介质的化合物。我们表明我们的纳米颗粒可以成功地键合成巨噬细胞并提供比EGCG溶液处理更换的EGCG,确认这些纳米颗粒在脂多糖刺激的巨噬细胞中的抗炎作用。制备制备的纳米颗粒,具有小的平均粒度(217.00±14.00nm),可接受的多分散性指数(0.28±0.07),可接受的Zeta电位值(-33.60±1.30mV)和高EGG负载效率(52.08% ±5.37%)。随着透明质酸浓度增加和通过添加竞争对手CD44抗体而增加,CD44结合的靶向能力增加。此外,我们发现岩藻糖治疗在剂量响应方式后脂多糖治疗后显着降低巨噬细胞迁移。总之,我们成功地创建了巨噬细胞靶向纳米粒子,以有效地递送EGCG,这应该有助于开发未来的巨噬细胞相关疾病的抗炎药。

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