4.8 Article

Mussel-Inspired Bisphosphonated Injectable Nanocomposite Hydrogels with Adhesive, Self-Healing, and Osteogenic Properties for Bone Regeneration

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 28, 页码 32673-32689

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c06058

关键词

injectable hydrogels; tissue adhesive; osteogenesis; nano-hydroxyapatite; poly(L-glutamic acid)

资金

  1. National Natural Science Foundation of China [51873101, 81972076, 51773113]

向作者/读者索取更多资源

Injectable hydrogels mimicking the natural extracellular matrix have advantages such as microinvasive implantation and complex defect repair, but current options for bone repair lack tissue adhesion, self-healing, and osteogenic activity. A new strategy involving mussel-inspired bisphosphonated injectable nanocomposite hydrogels with adhesive, self-healing, and osteogenic properties has been developed, showing excellent biocompatibility and promoting cell viability, proliferation, migration, and osteogenesis differentiation. The hydrogels, dually cross-linked, also demonstrate potential for bone regeneration with the successful healing of a rat cranial defect.
Injectable hydrogels have received much attention because of the advantages of simulation of the natural extracellular matrix, microinvasive implantation, and filling and repairing of complex shape defects. Yet, for bone repair, the current injectable hydrogels have shown significant limitations such as the lack of tissue adhesion, deficiency of self-healing ability, and absence of osteogenic activity. Herein, a strategy to construct mussel-inspired bisphosphonated injectable nanocomposite hydrogels with adhesive, self-healing, and osteogenic properties is developed. The nano-hydroxyapatite/poly(L-glutamic acid)-dextran (nHA/PLGA-Dex) dually cross-linked (DC) injectable hydrogels are fabricated via Schiff base cross-linking and noncovalent nHA-BP chelation. The chelation between bisphosphonate ligands (alendronate sodium, BP) and nHA favors the uniform dispersion of the latter. Moreover, multiple adhesion ligands based on catechol motifs, BP, and aldehyde groups endow the hydrogels with good tissue adhesion. The hydrogels possess excellent biocompatibility and the introduction of BP and nHA both can effectively promote viability, proliferation, migration, and osteogenesis differentiation of MC3T3-E1 cells. The incorporation of BP groups and HA nanoparticles could also facilitate the angiogenic property of endothelial cells. The nHA/PLGA-Dex DC hydrogels exhibited considerable biocompatibility despite the presence of a certain degree of inflammatory response in the early stage. The successful healing of a rat cranial defect further proves the bone regeneration ability of nHA/PLGA-Dex DC injectable hydrogels. The developed tissue adhesive osteogenic injectable nHA/PLGA-Dex hydrogels show significant potential for bone regeneration application.

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