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Microenvironmental Enzyme-Responsive Methotrexate Modified Quercetin Micelles for the Treatment of Rheumatoid Arthritis

体内 化学 胶束 类风湿性关节炎 炎症 药理学 细胞毒性 关节炎 免疫学 医学 癌症研究 体外 生物 生物化学 水溶液 生物技术 物理化学
作者
Xiuying Li,Xin Wang,Xiuwu Qu,Ning‐Ning Shi,Qinqing Li,Zhifang Yan,Yandong Li,Yingli Wang
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 19: 3259-3273
标识
DOI:10.2147/ijn.s457004
摘要

Purpose: Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease involving synovial inflammation and joint destruction.Although therapeutic drugs for RA have some efficacy, they usually cause severe side effects and are expensive.RA is characterized by synovial hyperplasia, intra-articular hypoxia, upregulated expression of matrix metalloproteinases, and excessive accumulation of reactive oxygen species.The adverse microenvironment further aggravates activated macrophage infiltration.Therefore, controlling the microenvironment of diseased tissues and targeting the activated macrophages have become new therapeutic targets in RA patients.Methods: Here, microenvironment-targeting micelles (PVGLIG-MTX-Que-Ms) were synthesized using the thin film hydration method.In the inflammatory microenvironment, PVGLIG was cleaved by the highly expressed MMP-2, PEG 5000 was eliminated, MTX was exposed, macrophage activation was targeted, and Que enrichment was enhanced.The cytotoxicity, targeting, antioxidant, and anti-inflammatory properties of drug-loaded micelles were tested in vitro.The drug-loaded micelles were used to treat CIA rats.In vivo targeting, expression of serum inflammatory factors, immunohistochemistry of the articular cartilage, and changes in immunofluorescence staining were observed. Results:The developed micelles had a particle size of (89.62 ±1.33) nm and a zeta potential of (-4.9 ±0.53) mV.The IC 50 value of PVGLIG-MTX-Que-Ms (185.90 ±6.98) μmol/L was significantly lower than that of free Que (141.10 ±6.39) μmol/L.The synthesized micelles exhibited slow-release properties, low cytotoxicity, strong targeting abilities, and significant anti-inflammatory effects in vitro.In vivo, the drug-loaded micelles accumulated at the joint site for a long time.PVGLIG-MTX-Que-Ms significantly reduced joint swelling, improved bone destruction, and decreased the expression of serum inflammatory factors in CIA rats. Conclusion:The smart-targeting micelles PVGLIG-MTX-Que-Ms with strong targeting, anti-inflammatory, cartilage-protective, and other multiple positive effects are a promising new tool for RA treatment.
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