黄芩苷
炎症
药物输送
核酸
药品
纳米技术
药理学
医学
化学
材料科学
生物化学
免疫学
色谱法
高效液相色谱法
作者
Mi Zhou,Yuanlin Tang,Yifei Lu,Tianxu Zhang,Shunhao Zhang,Xiaoxiao Cai,Yunfeng Lin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-16
标识
DOI:10.1021/acsnano.4c12917
摘要
Targeted drug delivery is a promising strategy for treating inflammatory diseases, with recent research focusing on the combination of neutrophils and nanomaterials. In this study, a targeted nanodrug delivery platform (Ac-PGP-tFNA, APT) was developed using tetrahedral framework nucleic acid (tFNA) along with a neutrophil hitchhiking mechanism to achieve precise delivery and anti-inflammatory effects. The tFNA structure, known for its excellent drug-loading capacity and cellular uptake efficiency, was used to carry a therapeutic agent─baicalin. The results demonstrate that the development of this drug delivery platform not only considerably enhances the bioavailability and effective concentration of the drug (baicalin) but also promotes the polarization of pro-inflammatory M1 macrophages to anti-inflammatory M2 macrophages by modulating the interactions between the neutrophils and macrophages. This targeted therapeutic method effectively treats inflammatory conditions such as sepsis and introduces a strategy for managing inflammatory diseases characterized by neutrophil infiltration.
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