补骨脂素
类风湿性关节炎
化学
医学
材料科学
纳米技术
生物化学
内科学
DNA
作者
Kexin Wang,Chuanhui Yin,Xiangmin Ye,Quanlin Chen,Jie Wu,Yupeng Chen,Yi Li,Jun Wang,Chuanzhi Duan,Aiping Lü,Daogang Guan
出处
期刊:Small
[Wiley]
日期:2023-03-04
卷期号:19 (21)
被引量:5
标识
DOI:10.1002/smll.202207319
摘要
Abstract Overexpressed matrix metalloproteinases, hypoxia microenvironment, and metabolic abnormality are important pathological signs of rheumatoid arthritis (RA). Designing a delivery carrier according to the pathological characteristics of RA that can control drug release in response to disease severity may be a promising treatment strategy. Psoralen is the main active ingredient isolated from Psoralea corylifolia L. and possesses excellent anti‐inflammatory activities as well as improving bone homeostasis. However, the specific underlying mechanisms, particularly the possible relationships between the anti‐RA effects of psoralen and related metabolic network, remain largely unexplored. Furthermore, psoralen shows systemic side effects and has unsatisfactory solubility. Therefore, it is desirable to develop a novel delivery system to maximize psoralen's therapeutic effect. In this study, a self‐assembled degradable hydrogel platform is developed that delivers psoralen and calcium peroxide to arthritic joints and controls the release of psoralen and oxygen according to inflammatory stimulation, to regulate homeostasis and the metabolic disorder of the anoxic arthritic microenvironment. Therefore, the hydrogel drug delivery system based on the responsiveness of the inflammatory microenvironment and regulation of metabolism provides a new therapeutic strategy for RA treatment.
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