Reactive Oxygen Species-Triggered Curcumin Release from Hollow Mesoporous Silica Nanoparticles for PM2.5-Induced Acute Lung Injury Treatment

活性氧 姜黄素 细胞内 牛血清白蛋白 氧化应激 材料科学 炎症 介孔二氧化硅 生物物理学 介孔材料 化学 生物化学 免疫学 生物 催化作用
作者
Guanting Sun,Xirui Wu,Huanhuan Zhu,Kangzhi Yuan,Yifan Zhang,Cai Zhang,Zheng Deng,Meiyu Zhou,Zhengdong Zhang,Guangbao Yang,Haiyan Chu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (28): 33504-33513 被引量:7
标识
DOI:10.1021/acsami.3c07361
摘要

Exposure to fine particulate matter with a diameter ≤2.5 μm (PM2.5) can result in serious inflammation and oxidative stress in lung tissue. However, there is presently very few effective treatments for PM2.5-induced many pulmonary diseases, such as acute lung injury (ALI). Herein, curcumin-loaded reactive oxygen species (ROS)-responsive hollow mesoporous silica nanoparticles (Cur@HMSN-BSA) are proposed for scavenging the intracellular ROS and suppressing inflammatory responses against PM2.5-induced ALI. The prepared nanoparticles were coated with bovine serum albumin (BSA) via an ROS-sensitive thioketal (TK)-containing linker, in which the TK-containing linker would be cleaved by the excessive amounts of ROS in inflammatory sites to induce the detachment of BSA from the nanoparticles surface and thus triggering release of loaded curcumin. The Cur@HMSN-BSA nanoparticles could be used as ROS scavengers because of their excellent ROS-responsiveness, which were able to efficiently consume high concentrations of intracellular ROS. Furthermore, it was also found that Cur@HMSN-BSA downregulated the secretion of several important pro-inflammatory cytokines and promoted the polarization from M1 phenotypic macrophages to M2 phenotypic macrophages for eliminating PM2.5-induced inflammatory activation. Therefore, this work provided a promising strategy to synergistically scavenge intracellular ROS and suppress the inflammation responses, which may serve as an ideal therapeutic platform for pneumonia treatment.
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