化学
代谢组学
药理学
黄芪
精氨酸
纳米颗粒
免疫系统
脂多糖
丝氨酸
鞘脂
生物化学
中医药
色谱法
氨基酸
酶
免疫学
纳米技术
医学
材料科学
替代医学
病理
生物
作者
Tingli Qu,Shasha Suo,Liqiu Yan,Liwei Wang,Taigang Liang
标识
DOI:10.1002/cbdv.202402234
摘要
Astragaloside IV (ATS) is an active component of Astragalus membranaceus, which has immune regulation and anti‐inflammatory effects. However, owing to its large molecular weight and poor solubility in water, the therapeutic effects of ATS are limited. We aimed to prepare astragaloside IV‐chitosan (ATS‐CS) nanoparticles and determine their anti‐inflammatory effect and mechanism of action on RAW264.7 cells using metabolomics. The size of the ATS‐CS nanoparticles was 200.3 nm with a zeta potential of 30.5 mV, and the encapsulation rate and drug loading were 69% and 13%, respectively. ATS‐CS nanoparticles not only significantly decreased the increase of NO, IL‐6 and TNF‐α levels induced by LPS, but also exerted an anti‐inflammatory effect by acting on arginine and proline, glutathione, sphingolipid, glycerophospholipid, and glycine, serine, and threonine metabolism. Our findings confirmed that ATS‐CS nanoparticles have good anti‐inflammatory activity and showed that the activity of high molecular weight can be increased by producing nanoparticles. Our study paves the way for exploring the mechanism of nanoparticles through metabolomics.
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