Enhanced Cartilage and Subchondral Bone Repair Using Carbon Nanotube-Doped Peptide Hydrogel-Polycaprolactone Composite Scaffolds.
Jiayi LvYilun WuZhicheng CaoXu LiuYuzhi SunPo ZhangXin ZhangKexin TangMin ChengQingqiang YaoYishen ZhuPublished in: Pharmaceutics (2023)
A carbon nanotube-doped octapeptide self-assembled hydrogel (FEK/C) and a hydrogel-based polycaprolactone PCL composite scaffold (FEK/C 3 -S) were developed for cartilage and subchondral bone repair. The composite scaffold demonstrated modulated microstructure, mechanical properties, and conductivity by adjusting CNT concentration. In vitro evaluations showed enhanced cell proliferation, adhesion, and migration of articular cartilage cells, osteoblasts, and bone marrow mesenchymal stem cells. The composite scaffold exhibited good biocompatibility, low haemolysis rate, and high protein absorption capacity. It also promoted osteogenesis and chondrogenesis, with increased mineralization, alkaline phosphatase (ALP) activity, and glycosaminoglycan (GAG) secretion. The composite scaffold facilitated accelerated cartilage and subchondral bone regeneration in a rabbit knee joint defect model. Histological analysis revealed improved cartilage tissue formation and increased subchondral bone density. Notably, the FEK/C 3 -S composite scaffold exhibited the most significant cartilage and subchondral bone formation. The FEK/C 3 -S composite scaffold holds great promise for cartilage and subchondral bone repair. It offers enhanced mechanical support, conductivity, and bioactivity, leading to improved tissue regeneration. These findings contribute to the advancement of regenerative strategies for challenging musculoskeletal tissue defects.
Keyphrases
- tissue engineering
- bone regeneration
- carbon nanotubes
- extracellular matrix
- bone mineral density
- cell proliferation
- stem cells
- quantum dots
- drug delivery
- bone loss
- soft tissue
- cell death
- mesenchymal stem cells
- multiple sclerosis
- postmenopausal women
- body composition
- small molecule
- cell cycle arrest
- visible light
- endoplasmic reticulum stress
- pi k akt