Hyaluronic Acid Loaded with Cerium Oxide Nanoparticles as Antioxidant in Hydrogen Peroxide Induced Chondrocytes Injury: An In Vitro Osteoarthritis Model.
Yi-Wen LinChih-Hsiang FangFan-Qi MengCherng-Jyh KeFeng-Huei LinPublished in: Molecules (Basel, Switzerland) (2020)
Osteoarthritis (OA) is the most common joint disease type and is accompanied by varying degrees of functional limitation. Both hyaluronic acid (HA) joint injections and pain relievers are efficient treatments for early-stage osteoarthritis. However, for the decomposition by hyaluronidase and free radicals in the knee joint, HA injection treatment has limited effect time. The cerium oxide nanoparticles (CeO2) is a long time free radical scavenger. CeO2 combined with HA expected, may extend the HA decomposition time and have a positive effect on osteoarthritis therapy. In this study, CeO2 was successfully synthesized using the hydrothermal method with a particle size of about 120 nm, which possessed excellent dispersibility in the culture medium. The in vitro OA model was established by cell treated with H2O2 for 30 min. Our study found that the inhibition of chondrocyte proliferation dose-dependently increased with H2O2 concentration but was significantly decreased by supplementation of cerium oxide nanoparticles. COL2a1 and ACAN gene expression in chondrocytes was significantly decreased after H2O2 treatment; however, the tendency was changed after cerium oxide nanoparticles treatment, which suggested that damaged chondrocytes were protected against oxidative stress. These findings suggest that cerium oxide nanoparticles are potential therapeutic applications in the early stage of OA.
Keyphrases
- oxide nanoparticles
- hyaluronic acid
- early stage
- knee osteoarthritis
- hydrogen peroxide
- oxidative stress
- gene expression
- rheumatoid arthritis
- chronic pain
- drug delivery
- nitric oxide
- stem cells
- risk assessment
- spinal cord injury
- combination therapy
- pain management
- replacement therapy
- dna damage
- single cell
- lymph node
- ischemia reperfusion injury
- locally advanced