Synthesis and biological evaluation of gold nanoparticles drug delivery system for anti-rheumatoid arthritis agents

被引:0
|
作者
Fan, Jiahui [1 ,2 ]
Li, Xuena [1 ]
Jin, Meizi [3 ]
Li, Cheng [1 ]
机构
[1] Yanbian Univ, Coll Pharm, 977 Gongyuan Rd, Yanji 133002, Peoples R China
[2] Changchun GeneSci Pharmaceut Co Ltd, Changchun High Tech Dev Zone, 1718 Yueda Rd, Changchun 130021, Peoples R China
[3] Yanbian Univ Hosp, Dept Pharm, 1327 Juzi St, Yanji 133000, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold nanoparticle; Cysteine; Methotrexate; Biological evaluation; Rheumatoid arthritis; FIBROBLAST-LIKE SYNOVIOCYTES; FOLIC-ACID; METHOTREXATE; INFLAMMATION; PROLIFERATION; INVASION; THERAPY; DMARDS; CELLS; MODEL;
D O I
10.1016/j.jddst.2024.106402
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The gold nanoparticle-cysteine-methotrexate (GNPs-Cys-MTX) drug delivery system was developed for the passive targeted therapy of rheumatoid arthritis (RA) to enhance drug delivery efficiency while minimizing toxicity and side effects. The preparation and characterization of the GNPs-Cys-MTX drug delivery system were successfully achieved using Cys as a coupling agent. An IL-1(3-induced anti-inflammatory study of rheumatoid arthritis fibroblast synoviocytes (RA-FLSs) demonstrated that GNPs-Cys-MTX exhibited dose-dependent antiinflammatory effects and effectively inhibited the expression of TNF-alpha, IL-6, and IL-17. Furthermore, studies involving collagen-induced arthritis rats revealed that GNPs-Cys-MTX demonstrated superior therapeutic efficacy compared to free MTX, even at the same drug dose. In summary, this study demonstrates that the GNPs-Cys-MTX drug delivery system can enhance drug efficacy while reducing toxicity and side effects in the treatment of RA.
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页数:11
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