Engineered Niobium Carbide MXenzyme-Integrated Self-Adaptive Coatings Inhibiting Periprosthetic Osteolysis by Orchestrating Osteogenesis-Osteoclastogenesis Balance.
Shishuo LiXiaoqing LuQihao ChaiBenzhao HuangShimin DaiPeng WangJianing LiuZhibo ZhaoXiao LiBing LiuKangqing ZuoZhentao ManNingbo LiWei LiPublished in: ACS applied materials & interfaces (2024)
Periprosthetic osteolysis induced by the ultrahigh-molecular-weight polyethylene (UHMWPE) wear particles is a major complication associated with the sustained service of artificial joint prostheses and often necessitates revision surgery. Therefore, a smart implant with direct prevention and repair abilities is urgently developed to avoid painful revision surgery. Herein, we fabricate a phosphatidylserine- and polyethylenimine-engineered niobium carbide (Nb 2 C) MXenzyme-coated micro/nanostructured titanium implant (PPN@MNTi) that inhibits UHMWPE particle-induced periprosthetic osteolysis. The specific mechanism by which PPN@MNTi operates involves the bioresponsive release of nanosheets from the MNTi substrate within an osteolysis microenvironment, initiated by the cleavage of a thioketal-dopamine molecule sensitive to reactive oxygen species (ROS). Subsequently, functionalized Nb 2 C MXenzyme could target macrophages and escape from lysosomes, effectively scavenging intracellular ROS through its antioxidant nanozyme-mimicking activities. This further achieves the suppression of osteoclastogenesis by inhibiting NF-κB/MAPK and autophagy signaling pathways. Simultaneously, based on the synergistic effect of MXenzyme-integrated coatings and micro/nanostructured topography, the designed implant promotes the osteogenic differentiation of bone mesenchymal stem cells to regulate bone homeostasis, further achieving advanced osseointegration and alleviable periprosthetic osteolysis in vivo . This study provides a precise prevention and repair strategy of periprosthetic osteolysis, offering a paradigm for the development of smart orthopedic implants.
Keyphrases
- total hip arthroplasty
- signaling pathway
- reactive oxygen species
- total hip
- total knee arthroplasty
- soft tissue
- oxidative stress
- minimally invasive
- pi k akt
- cell death
- mesenchymal stem cells
- coronary artery bypass
- bone loss
- bone mineral density
- dna damage
- diabetic rats
- stem cells
- mental health
- surgical site infection
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- bone regeneration
- high glucose
- cell therapy
- toll like receptor
- percutaneous coronary intervention
- metabolic syndrome
- mass spectrometry
- amino acid
- coronary artery disease
- immune response
- uric acid
- nuclear factor
- umbilical cord
- anti inflammatory
- inflammatory response
- cancer therapy