Electrospun porous poly(3-hydroxybutyrate- co -4-hydroxybutyrate)/lecithin scaffold for bone tissue engineering.
Wei LiuTiejun JiaoYuran SuRan WeiZheng WangJiacheng LiuNa FuLei SuiPublished in: RSC advances (2022)
Bone tissue engineering has emerged as a promising restorative strategy for bone reconstruction and bone defect repair. It is challenging to establish an appropriate scaffold with an excellent porous microstructure for bone defects and thereby promote bone repair. In this study, electrospinning as a simple and efficient technology was employed to fabricate a porous poly(3-hydroxybutyrate- co -4-hydroxybutyrate) (P34HB) scaffold coated with lecithin. The morphology, phase composition, and physical properties of the electrospun P34HB/lec scaffold were characterized. Meanwhile, cellular behaviors of bone marrow mesenchymal stem cells (BMSCs), including proliferation, adhesion, migration, osteogenic differentiation, and related gene expression, were also investigated. Finally, a rat subcutaneous implant model and a calvarial defect model were used to evaluated the biocompatibility and effect of these scaffolds on bone repair, respectively. The in vitro results demonstrated that these electrospun fibers were interwoven with each other to form the porous P34HB/lec scaffold and the addition of lecithin improved the hydrophilicity of the pure P34HB scaffold, enhanced the efficiency of cell migration, and decreased inflammatory response. Furthermore, the in vivo results showed that P34HB/lec scaffold had excellent biocompatibility, improved the vascularization, and promoted the bone regeneration. All these results indicated that nanofibers of P34HB scaffolds in combination with the lecithin could exert a synergistic effect on promoting osteogenesis and regeneration of bone defects; thus, the P34HB scaffold with lecithin showed great application potential for bone tissue engineering.
Keyphrases
- tissue engineering
- bone regeneration
- bone mineral density
- soft tissue
- gene expression
- bone loss
- inflammatory response
- stem cells
- postmenopausal women
- mesenchymal stem cells
- dna methylation
- bone marrow
- mental health
- multiple sclerosis
- risk assessment
- oxidative stress
- staphylococcus aureus
- climate change
- human health
- single molecule