A Multifunctional Polydopamine/genipin/alendronate Nanoparticle Licences Fibrin Hydrogels Osteoinductive and Immunomodulatory Potencies for Repairing Bone Defects
Overview
Affiliations
Here, we fabricated a hybrid nanoparticle composed of polydopamine nanoparticles (pNPs), alendronate (Al) and genipin (GP) for cranial bone defect repair. Al was crosslinked into pNPs via GP (Al@pNPs), after which hybrid nanoparticles were obtained. By embedding these Al@pNPs into the fibrin hydrogels, a multifunctional bone repair scaffold was fabricated (Al@pNPs/Fg). The Al@pNPs/Fg exhibited three synergistic effects on the bone microenvironment: i) enhanced ectomesenchymal stem cell (EMSC) osteogenic differentiation by activating the piezo 1 channel; ii) inhibited the formation and function of osteoclasts related to the NF-κB signaling pathways; and iii) promoted M2 polarization and anti-inflammatory factor expression under normal and simulated inflammatory conditions. Al@pNPs/Fg ultimately promoted cranial bone defect regeneration in an SD rat model. This simple and low-cost technology provides a new approach to constructing an efficient delivery system and has desirable biological properties, providing a tissue-committed niche for the repair of bone defects.
Developing fibrin-based biomaterials/scaffolds in tissue engineering.
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PMID: 39239261 PMC: 11375146. DOI: 10.1016/j.bioactmat.2024.08.006.
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PMID: 39194649 PMC: 11355103. DOI: 10.3390/jfb15080211.