雾化器
药物输送
肺
体内
气溶胶化
吸入
脂多糖
核糖核酸
细胞外小泡
药理学
气道
细胞外
生物
化学
细胞生物学
免疫学
医学
麻醉
解剖
生物化学
基因
内科学
有机化学
生物技术
作者
Yohan Han,Yin Zhu,Hannah Youngblood,Sultan Almuntashiri,Timothy W. Jones,Xiaoyun Wang,Yutao Liu,Payaningal R. Somanath,Duo Zhang
标识
DOI:10.1016/j.jconrel.2022.10.052
摘要
Small extracellular vesicles (sEVs) are a group of cell-secreted nanovesicles with a diameter up to 200 nm. A growing number of studies have indicated that sEVs can reflect the pathogenesis of human diseases and mediate intercellular communications. Recently, sEV research has drastically increased due to their drug delivery property. However, a comprehensive method of delivering exogenous small RNAs-loaded sEVs through nebulization has not been reported. The methodology is complicated by uncertainty regarding the integrity of sEVs after nebulization, the delivery efficiency of aerosolized sEVs, their deposition in the lungs/cells, etc. This study demonstrates that sEVs can be delivered to murine lungs through a vibrating mesh nebulizer (VMN). In vivo sEV tracking indicated that inhaled sEVs were distributed exclusively in the lung and localized primarily in lung macrophages and airway epithelial cells. Additionally, sEVs loaded with small RNAs were successfully delivered into the lungs. The administration of siMyd88-loaded sEVs through inhalation reduced lipopolysaccharide (LPS)-induced lung injury in mice, supporting an application of this nebulization methodology to deliver functional small RNAs. Collectively, our study proposes a novel method of sEVs-mediated small RNA delivery into the murine lung through nebulization and presents a potential sEV-based therapeutic strategy for human lung diseases.
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