结肠炎
医学
药理学
炎症性肠病
口服
溃疡性结肠炎
炎症
药品
苦参
药物输送
促炎细胞因子
免疫学
疾病
化学
内科学
有机化学
苦参碱
精神科
作者
Manqi Zhang,Xichao Xu,Liqian Su,Yuqing Zeng,Jingxiong Lin,Wenwen Li,Yigui Zou,Sicong Li,Boxian Lin,Ziyuan Li,Chen Hu,Yuheng Huang,Quanle Xu,Hongbo Chen,Fang Cheng,Dongling Dai,Fang Cheng,Dongling Dai
标识
DOI:10.1186/s12951-024-02856-z
摘要
Ulcerative colitis (UC) belongs to chronic inflammatory disease with a relapsing characterization. Conventional oral drugs of UC are restricted in clinical by premature degradation in the gastrointestinal tract, modest efficacy, and adverse effects. CX5461 can treat autoimmune disease, immunological rejection, and vascular inflammation. However, low solubility, intravenous administration, and non-inflammatory targeting limited its clinical application. Herein, this work aims to develop Sophora Flavescens-derived exosomes-like nanovesicles carrying CX5461 (SFELNVs@CX5461) for efficient CX5461 oral delivery for UC therapy. We identified SFELNVs as nano-diameter (80 nm) with negative zeta potential (-32mV). Cellular uptake has shown that SFELNVs were targeted uptake by macrophages, thus increasing drug concentration. Additionally, oral SFELNVs@CX5461 exhibited good safety and stability, as well as inflammation-targeting ability in the gastrointestinal tract of dextran sodium sulfate (DSS)-induced colitis mice. In vivo, oral administration of SFELNVs and CX5461 could relieve mice colitis. More importantly, combined SFELNVs and CX5461 alleviated mice colitis by inhibiting pro-inflammatory factors (TNF-α, IL-1β, and IL-6) expression and promoting M2 macrophage polarization. Furthermore, SFELNVs promoted M2 polarization by miR4371c using miRNA sequencing. Our results suggest that SFELNVs@CX5461 represents a novel orally therapeutic drug that can ameliorate colitis, and a promising targeting strategy for safe UC therapy.
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