Dual Mg-Reinforced PCL Membrane with a Janus Structure for Vascularized Bone Regeneration and Bacterial Elimination.
Xianli WangPeiqi ShenNannan GuYi ShaoMengmeng LuChunbo TangCheng WangChenglin ChuFeng XueJing BaiPublished in: ACS biomaterials science & engineering (2023)
Commercially available guided bone regeneration (GBR) membranes often exhibit limited mechanical properties or bioactivity, leading to poor performance in repairing bone defects. To surmount this limitation, we developed a Janus structural composite membrane (Mg-MgO/PCL) reinforced by dual Mg (Mg sheets and MgO NPs) by using a combined processing technique involving casting and electrospinning. Results showed that the addition of Mg sheets and MgO NPs enhanced the mechanical properties of the composite membrane for osteogenic space maintenance, specifically tensile strength (from 10.2 ± 1.2 to 50.3 ± 4.5 MPa) and compression force (from 0 to 0.94 ± 0.09 N mm -1 ), through Mg sheet reinforcement and improved crystallization. The dense cast side of the Janus structure membrane displayed better fibroblast barrier capacity than a single fiber structure; meanwhile, the PCL matrix protected the Mg sheet from severe corrosion due to predeformation. The porous microfibers side supported preosteoblast cell adhesion, enhanced osteogenesis, and angiogenesis in vitro, through the biomimetic extracellular matrix and sustainable Mg 2+ release. Furthermore, the Mg-MgO/PCL membrane incorporating 2 wt % MgO NPs exhibited remarkable antimicrobial properties, inducing over 88.75% apoptosis in Staphylococcus aureus . An in vivo experiment using the rat skull defect model (Φ = 5 mm) confirmed that the Mg-MgO/PCL membrane significantly improved new bone formation postsurgery. Collectively, our investigation provides valuable insights into the design of multifunctional membranes for clinical oral GBR application.
Keyphrases
- bone regeneration
- staphylococcus aureus
- extracellular matrix
- oxidative stress
- cell death
- bone marrow
- cell adhesion
- mesenchymal stem cells
- early onset
- cell proliferation
- bone mineral density
- endothelial cells
- escherichia coli
- drug delivery
- biofilm formation
- vascular endothelial growth factor
- cystic fibrosis
- tissue engineering
- single molecule
- bone loss
- wound healing
- pseudomonas aeruginosa
- candida albicans