类风湿性关节炎
肿瘤坏死因子α
细胞因子
医学
兰克尔
免疫学
破骨细胞
促炎细胞因子
炎症
受体
内科学
激活剂(遗传学)
作者
Ajay Kumar,Aneesh Ali,Kanika,Akshay Vyawahare,Anas Ahmad,Rakesh K. Mishra,Md. Meraj Ansari,Ahmed Nadeem,Nahid Siddiqui,Syed Shadab Raza,Rehan Khan
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2023-08-18
卷期号:9 (9): 5312-5321
被引量:6
标识
DOI:10.1021/acsbiomaterials.3c00514
摘要
Rheumatoid arthritis (RA) is a chronic inflammatory disease that severely affects joints and restricts locomotion. Various treatment regimens are available for RA, providing short-term relief from pain, but long-term relief from the disease is still not available. Evidently, cytokines play a crucial role in the pathophysiology of the disease. However, aberrant immune responses, genetic dispositions, viral infections, or toxicants are some possible causative mediators of RA. The synovial fluid of rheumatoid arthritis patients encompass cytokines, especially osteoclastogenic cytokines, and invasion factors such as macrophage colony-stimulating factor (M-CSF) and the receptor activator of NF-κB ligand (RANKL). Moreover, tumor necrosis factor-α (TNF-α) and interleukins (IL-1, 6, and 17) intensify osteoclast differentiation and activation. Therefore, in order to restrict the cytokine expression, we used budesonide as a therapeutic lead and encapsulated it into a highly biocompatible hydrogel system. The hydrogel system developed by us is enzyme-responsive and provides sustained drug release flow over an extended period of time. This hydrogel is characterized by ζ-potential analysis, field-emission scanning electron microscopy (FE-SEM), and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, and it is further encapsulated with budesonide (glucocorticoids) for therapeutic purposes. Evidently, Bud-loaded ER-hydrogel showed improvement in joint physiology compared to the disease group and downregulated the inflammatory markers.
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