Hydrogen-treated CoCrMo alloy: a novel approach to enhance biocompatibility and mitigate inflammation in orthopedic implants.
Yu-Chien LinChih-Chien HuWai-Ching LiuUdesh DhawanYu-Chieh ChenYueh-Lien LeeHung-Wei YenYi-Jie KuoRen-Jei ChungPublished in: Journal of materials chemistry. B (2024)
In recent decades, orthopedic implants have been widely used as materials to replace human bone tissue functions. Among these, metal implants play a crucial role. Metals with better chemical stability, such as stainless steel, titanium alloys, and cobalt-chromium-molybdenum (CoCrMo) alloy, are commonly used for long-term applications. However, good chemical stability can result in poor tissue integration between the tissue and the implant, leading to potential inflammation risks. This study creates hydrogenated CoCrMo (H-CoCrMo) surfaces, which have shown promise as anti-inflammatory orthopedic implants. Using the electrochemical cathodic hydrogen-charging method, the surface of the CoCrMo alloy was hydrogenated, resulting in improved biocompatibility, reduced free radicals, and an anti-inflammatory response. Hydrogen diffusion to a depth of approximately 106 ± 27 nm on the surface facilitated these effects. This hydrogen-rich surface demonstrated a reduction of 85.2% in free radicals, enhanced hydrophilicity as evidenced by a decrease in a contact angle from 83.5 ± 1.9° to 52.4 ± 2.2°, and an increase of 11.4% in hydroxyapatite deposition surface coverage. The cell study results revealed a suppression of osteosarcoma cell activity to 50.8 ± 2.9%. Finally, the in vivo test suggested the promotion of new bone formation and a reduced inflammatory response. These findings suggest that electrochemical hydrogen charging can effectively modify CoCrMo surfaces, offering a potential solution for improving orthopedic implant outcomes through anti-inflammatory mechanisms.
Keyphrases
- soft tissue
- inflammatory response
- anti inflammatory
- single cell
- oxidative stress
- gold nanoparticles
- human health
- lipopolysaccharide induced
- cell therapy
- healthcare
- endothelial cells
- metabolic syndrome
- type diabetes
- visible light
- biofilm formation
- stem cells
- escherichia coli
- staphylococcus aureus
- bone marrow
- adipose tissue
- body composition
- big data
- bone mineral density
- reduced graphene oxide
- climate change
- molecularly imprinted
- artificial intelligence
- mesenchymal stem cells
- insulin resistance
- toll like receptor
- label free
- postmenopausal women
- drinking water
- tissue engineering
- health insurance
- bone loss