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载姜黄素的果胶酸钙和透明质酸修饰乳铁蛋白纳米粒的双重靶向治疗溃疡性结肠炎。

Calcium pectinate and hyaluronic acid modified lactoferrin nanoparticles loaded rhein with dual-targeting for ulcerative colitis treatment.

机构信息

State Key Laboratory of Southwestern Chinese Medicine Resources, Pharmacy School, Chengdu University of Traditional Chinese Medicine, Chengdu, 611130, China.

State Key Laboratory of Southwestern Chinese Medicine Resources, Pharmacy School, Chengdu University of Traditional Chinese Medicine, Chengdu, 611130, China; Affiliated Hospital, Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China; Sichuan Provincial Acupuncture School, Chengdu, 611731, China.

出版信息

Carbohydr Polym. 2021 Jul 1;263:117998. doi: 10.1016/j.carbpol.2021.117998. Epub 2021 Mar 27.

Abstract

Herein, dual-bioresponsive of Rhein (RH) in promoting colonic mucous damage repair and controlling inflammatory reactions were combined by the dual-targeting (intestinal epithelial cells and macrophages) oral nano delivery strategy for effective therapy of ulcerative colitis (UC). Briefly, two carbohydrates, calcium pectinate (CP) and hyaluronic acid (HA) were used to modify lactoferrin (LF) nanoparticles (NPs) to encapsulate RH (CP/HA/RH-NPs). CP layer make CP/HA/RH-NPs more stable and protect against the destructive effects of the gastrointestinal environment and then release HA/RH-NPs to colon lesion site. Cellular uptake evaluation confirmed that NPs could specifically target and enhance the uptake rate via LF and HA ligands. in vivo experiments revealed that CP/HA/RH-NPs significantly alleviated inflammation by inhibiting the TLR4/MyD88/NF-κB signaling pathway and accelerated colonic healing. Importantly, with the help of CP, this study was the first to attempt for LF as a targeting nanomaterial in UC treatment and offers a promising food-based nanodrug in anti-UC.

摘要

在此,通过双重靶向(肠上皮细胞和巨噬细胞)口服纳米递药策略,将 Rhein(RH)的双重生物响应性与促进结肠粘膜炎性损伤修复和控制炎症反应相结合,用于溃疡性结肠炎(UC)的有效治疗。简而言之,两种碳水化合物,果胶酸钙(CP)和透明质酸(HA)被用于修饰乳铁蛋白(LF)纳米颗粒(NPs)以包封 RH(CP/HA/RH-NPs)。CP 层使 CP/HA/RH-NPs 更加稳定,并防止胃肠道环境的破坏作用,然后将 HA/RH-NPs 释放到结肠病变部位。细胞摄取评估证实, NPs 可以通过 LF 和 HA 配体特异性靶向并提高摄取率。体内实验表明,CP/HA/RH-NPs 通过抑制 TLR4/MyD88/NF-κB 信号通路显著缓解炎症,并加速结肠愈合。重要的是,在 CP 的帮助下,本研究首次尝试将 LF 作为 UC 治疗中的靶向纳米材料,并为抗 UC 提供了一种有前途的基于食品的纳米药物。

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