炎症
肺
活性氧
药物输送
促炎细胞因子
化学
吸入
DNA损伤
细胞生物学
免疫学
药理学
医学
癌症研究
DNA
生物
生物化学
解剖
内科学
有机化学
作者
Haiyan Wang,Yunfei Jiao,Shuaijing Ma,Zhuoting Li,Jintao Gong,Qiao Jiang,Yingxu Shang,Hongling Li,Jing Li,Na Li,Robert Chunhua Zhao,Baoquan Ding
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-05-13
卷期号:24 (20): 6102-6111
被引量:4
标识
DOI:10.1021/acs.nanolett.4c01222
摘要
Acute lung injury (ALI) is a severe inflammatory lung disease, with high mortality rates. Early intervention by reactive oxygen species (ROS) scavengers could reduce ROS accumulation, break the inflammation expansion chain in alveolar macrophages (AMs), and avoid irreversible damage to alveolar epithelial and endothelial cells. Here, we reported cell-penetrating R9 peptide-modified triangular DNA origami nanostructures (tDONs-R9) as a novel nebulizable drug that could reach the deep alveolar regions and exhibit an enhanced uptake preference of macrophages. tDONs-R9 suppressed the expression of pro-inflammatory cytokines and drove polarization toward the anti-inflammatory M2 phenotype in macrophages. In the LPS-induced ALI mouse model, treatment with nebulized tDONs-R9 alleviated the overwhelming ROS, pro-inflammatory cytokines, and neutrophil infiltration in the lungs. Our study demonstrates that tDONs-R9 has the potential for ALI treatment, and the programmable DNA origami nanostructures provide a new drug delivery platform for pulmonary disease treatment with high delivery efficiency and biosecurity.
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