Abstract

In recent years, bone repair biomaterials that combine cells and bioactive factors are superior to autologous and allogeneic bone implants. However, neither natural nor synthetic biomaterials can possess all desired qualities such as strength, porosity, and biological activity. In this study, we used poly (glycerol sebacate) (PGS), a synthetic material with great osteogenic potential that has attracted more attention in the field of tissue (such as bone tissue) regeneration owing to its good biocompatibility and high elasticity. It also has the advantage of being regulated by material synthesis to match the bone tissue's strength and can be easily modified to become functional. However, pure PGS lacks functional groups and hydrophilicity. Therefore, we used PGS as the substrate to graft the adhesive ligands RGD and vascular endothelial growth factor mimetic peptide. The bone repair scaffold can be prepared through photo crosslinking, as it not only improves hydrophobicity but also promotes vascularization and accelerates osteogenesis. Simultaneously, we improved the preparation method of hydrogels after freeze-drying and crosslinking to form a sponge-like structure and to easily regenerate blood vessels. In summary, a bone repair scaffold was prepared to meet the structural and biological requirements. It proved to serve as a potential bone-mimicking scaffold by enhancing tissue regenerative processes such as cell infiltration and vascularization and subsequent replacement by the native bone tissue.

Highlights

  • Bone repair following bone damage caused by trauma and disease is a complex process necessitating the need to identify better ways to promote bone regeneration (Shen et al, 2016)

  • The results showed that vascular endothelial growth factor (VEGF) was released in a controlled manner, which promoted the growth and the tube formation of human umbilical vein endothelial cells (HUVECs) (Impellitteri et al, 2012)

  • We engineered bio-artificial multiporous hydrogel matrices consisting of RGD adhesive ligands and the VEGF mimetic peptide for better cell invasion and vascularization (Figure 1A)

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Summary

Introduction

Bone repair following bone damage caused by trauma and disease is a complex process necessitating the need to identify better ways to promote bone regeneration (Shen et al, 2016) Various synthetic biomaterials, such as poly (lactic-co-glycolic acid) and polymethyl methacrylate, were designed to fill bone defects and promote bone regeneration, resulting in its repair. These biomaterials are popular because they circumvent the limited bone resources and avoid the immunological rejections associated with autogenic and allogeneic bone transplantations. Many studies combine bioactive factors or cells to design these synthetic biomaterials to compensate for the lack of bioactivity in synthetic biomaterials.

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