槲皮素
锰
巨噬细胞
膜
体内
脂多糖
材料科学
化学
透射电子显微镜
兴奋剂
傅里叶变换红外光谱
肺
药理学
生物物理学
粒径
免疫系统
生物化学
纳米颗粒
细胞生物学
MAPK/ERK通路
细胞膜
生物医学工程
分子生物学
作者
Jing Jiang,Jie Sun,Lu Zhu,Yingzhi Zhou,Chunhua Ma,Xuemei Li
标识
DOI:10.1016/j.matdes.2026.115518
摘要
The mechanism of acute lung injury (ALI) is unclear and its treatment method is unsatisfactory. The aim of this study was to investigate the effects of macrophage membrane encapsulated manganese doped ZIF-8 (Mn@ZIF-8) loaded quercetin (Qu) to form M@Mn@ZIF-8@Qu on ALI. Mn@ZIF-8 was prepared by one-step method and combined with Qu to form M@Mn@ZIF-8@Qu, and macrophage membrane encapsulated Mn@ZIF-8@Qu to form M@Mn@ZIF-8@Qu by extrusion method. Lung tissues from control and ALI mice were used for RNA sequencing for the mechanism of M@Mn@ZIF-8@Qu ALI. The cercal ligation and puncture (CLP) model in vivo and lipopolysaccharide (LPS) models were used to evaluate the effects of M@Mn@ZIF-8@Qu on ALI. M@Mn@ZIF-8@Qu was successfully prepared and verify its good biocompatibility. Transmission electron microscope (TEM), potential and particle size and Fourier Transform Infrared Spectrometer (FT-IR) analysis showed that the construction of M@Mn@ZIF-8@Qu was successful has an encapsulation efficiency of 72.39 ± 3.87 % and a drug loading efficiency of 59.42 ± 3.28 %. The results of RNA-Seq showed Yes associated protein (YAP) was significantly decreased in lung tissues of ALI mice. It was also found that inhibition of YAP, the level of NLRP3 was significantly decreased. M@Mn@ZIF-8@Qu significantly alleviated ALI by inhibition the YAP/ NLRP3 signaling pathway. In conclusion, M@Mn@ZIF-8@Qu was successfully prepared for treating ALI. This study provides a new target and treatment for ALI.
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