4.8 Article

Enhanced tissue infiltration and bone regeneration through spatiotemporal delivery of bioactive factors from polyelectrolytes modified biomimetic scaffold

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MATERIALS TODAY BIO
卷 20, 期 -, 页码 -

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DOI: 10.1016/j.mtbio.2023.100681

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Biomimetic scaffold; Polyelectrolyte modification; Dual-factor delivery; Tissue infiltration; Bone regeneration

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In this study, a polyelectrolytes modified-biomimetic scaffold with macroporous and nanofibrous structures was successfully prepared for efficient bone defect healing. The scaffold incorporated strontium-substituted hydroxyapatite (SrHA) and exhibited sequential release of BMP-2 protein and Sr ions. The polyelectrolytes modification improved the scaffold's hydrophilicity and protein binding efficiency, promoting cell proliferation and tissue infiltration. Additionally, the dual-factor loaded scaffold enhanced bone regeneration through spatiotemporal delivery of BMP-2 and Sr ions, as evidenced by increased vascularization and new bone formation. This biomimetic scaffold as a dual-factor delivery system shows great potential for bone regeneration applications.
Efficient healing of bone defect is closely associated with the structured and functional characters of tissue engineered scaffolds. However, the development of bone implants with rapid tissue ingrowth and favorable osteoinductive properties remains a challenge. Herein, we fabricated polyelectrolytes modified-biomimetic scaffold with macroporous and nanofibrous structures as well as simultaneous delivery of BMP-2 protein and trace element strontium. The hierarchically structured scaffold incorporated with strontium-substituted hy-droxyapatite (SrHA) was coated with polyelectrolyte multilayers of chitosan/gelatin via layer-by-layer assembly technique for BMP-2 immobilization, which endowed the composite scaffold with sequential release of BMP-2 and Sr ions. The integration of SrHA improved the mechanical property of composite scaffold, while the poly -electrolytes modification strongly increased the hydrophilicity and protein binding efficiency. In addition, polyelectrolytes modified-scaffold significantly facilitated cell proliferation in vitro, as well as enhanced tissue infiltration and new microvascular formation in vivo. Furthermore, the dual-factor loaded scaffold significantly enhanced the osteogenic differentiation of bone marrow mesenchymal stem cells. Moreover, both vascularization and new bone formation were significantly increased by the treatment of dual-factor delivery scaffold in the rat calvarial defects model, suggesting a synergistic effect on bone regeneration through spatiotemporal delivery of BMP-2 and Sr ions. Overall, this study demonstrate that the prepared biomimetic scaffold as dual-factor delivery system has great potential for bone regeneration application.

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