青藤碱-没食子酸纳米颗粒对脂多糖致小鼠急性肺损伤的保护作用OA
Protective Effect of Sinomenine-Gallic Acid Nanoparticles on Lipopolysaccharide Induced Acute Lung Injury of Mice
为了探寻急性肺损伤(ALI)的有效特异性药物,采用一步自组装法制备青藤碱-没食子酸自组装纳米颗粒(SGNPs),评价其对 ALI 的保护作用及机制.结果表明:SGNPs 的平均水合粒径为(67.00±3.61)nm,呈球形均一分布;浓度 0.8 mmol·L-1 的 SGNPs 溶血率低于 5%安全阈值,满足静脉注射要求;SGNPs 可减轻肺组织病理损伤,抑制炎性细胞浸润,显著降低血清 IL-1β、IL-6 水平及肺组织 IL-1β、IL-6、iNOS、TNF-α的mRNA 表达;SGNPs 可抑制肺组织中 ERK、IκBα及 NF-κB p65 磷酸化水平,且 SGNPs 在体内外均表现出良好的生物安全性;SGNPs 通过调控 MAPK/NF-κB 信号通路发挥抗炎作用,且制备简便、生物相容性良好.
To explore effective and specific drugs for acute lung injury(ALI),sinomenine-gallic acid self-as-sembled nanoparticles(SGNPs)were prepared using one-step self-assembly method,and their protective effects and mechanisms against ALI were evaluated.The results showed that the average hydrodynamic diame-ter of SGNPs was(67.00±3.61)nm with a uniform spherical morphology.The hemolysis rate of SGNPs at a concentration of 0.8 mmol·L-1 was below the 5% safety threshold.,meeting the requirements for intrave-nous administration.SGNPs alleviated pathological damage in lung tissue,reduced inflammatory cell infiltra-tion,and significantly decreased the levels of serum IL-1β and IL-6,as well as the mRNA expression of IL-1β,IL-6,iNOS,and TNF-α in lung tissue.SGNPs could inhibit the phosphorylation levels of ERK,IκBα and NF-κB p65 in lung tissue,and SGNPs exhibited good biosafety both in vitro and in vivo.SGNPs exerted anti-inflammatory effects by regulating the MAPK/NF-κB signaling pathway,with simple preparation and excellent biocompatibility.
邱依婷;刘玫言;岳智涵;辛书竞;汪淳淳;刁勇;李维娜
华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021华侨大学 医学院,福建 泉州 362021||联勤保障部队第910医院 眼科,福建 泉州 362000
通用工业技术
急性肺损伤炎症青藤碱没食子酸自组装纳米颗粒
acute lung injuryinflammationsinomeninegallic acidself-assembled nanoparticles
《华侨大学学报(自然科学版)》 2026 (4)
482-490,9
国家自然科学基金海峡联合基金资助项目(U1405215)
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