Macrophage-Targeted Dextran Sulfate-Dexamethasone Conjugate Micelles for Effective Treatment of Rheumatoid Arthritis.
Jiangfan HanRen NaNingning ZhaoXiaofeng YuanLinke FuJianmei JingAi-Rong QianWei-Liang YePublished in: Molecules (Basel, Switzerland) (2023)
Rheumatoid arthritis (RA) is a chronic, systemic immune disease that causes joint affection and even disability. Activated macrophages play an important role in the pathogenesis and progression of RA by producing pro-inflammatory factors. The use of dexamethasone (DXM) is effective in relieving the intractable pain and inflammatory progression of RA. However, long-term use of DXM is strongly associated with increased rates of diabetes, osteoporosis, bone fractures, and mortality, which hinders its clinical use. In this study, the dextran sulfate-cisaconitic anhydride-dexamethasone (DXM@DS-cad-DXM) micelles were prepared to treat RA by selectively recognizing scavenger receptor (SR) on the activated macrophages. The potent targeting property of DXM@DS-cad-DXM micelles to SR was by fluorescence microscope. Additionally, the effective accumulation and powerful anti-inflammatory activity of DXM@DS-cad-DXM micelles were observed in the inflamed joints of adjuvant-induced arthritis (AIA) rats after intravenous administration. Overall, DXM@DS-cad-DXM micelles are a potentially effective nanomedicine for targeted therapy of RA.
Keyphrases
- rheumatoid arthritis
- cancer therapy
- drug delivery
- disease activity
- coronary artery disease
- drug release
- high dose
- ankylosing spondylitis
- interstitial lung disease
- low dose
- bone mineral density
- type diabetes
- cardiovascular events
- hyaluronic acid
- early stage
- systemic lupus erythematosus
- cardiovascular disease
- chronic pain
- multiple sclerosis
- drug induced
- adipose tissue
- postmenopausal women
- neuropathic pain
- skeletal muscle
- systemic sclerosis
- spinal cord
- metabolic syndrome
- bone loss
- risk factors
- postoperative pain