Programmed surface on poly(aryl-ether-ether-ketone) initiating immune mediation and fulfilling bone regeneration sequentially
The immune responses are involved in every stage after implantation but the reported immune-regulated materials only work at the beginning without fully considering the different phases of bone healing. Here, poly(aryl-ether-ether-ketone) (PEEK) is coated with a programmed surface, which rapidly rel...
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Veröffentlicht in: | Innovation (New York, NY) NY), 2021-08, Vol.2 (3), p.100148-100148, Article 100148 |
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Sprache: | eng |
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Zusammenfassung: | The immune responses are involved in every stage after implantation but the reported immune-regulated materials only work at the beginning without fully considering the different phases of bone healing. Here, poly(aryl-ether-ether-ketone) (PEEK) is coated with a programmed surface, which rapidly releases interleukin-10 (IL-10) in the first week and slowly delivers dexamethasone (DEX) up to 4 weeks. Owing to the synergistic effects of IL-10 and DEX, an aptly weak inflammation is triggered within the first week, followed by significant M2 polarization of macrophages and upregulation of the autophagy-related factors. The suitable immunomodulatory activities pave the way for osteogenesis and the steady release of DEX facilitates bone regeneration thereafter. The sequential immune-mediated process is also validated by an 8-week implementation on a rat model. This is the first attempt to construct implants by taking advantage of both immune-mediated modulation and sequential regulation spanning all bone regeneration phases, which provides insights into the fabrication of advanced biomaterials for tissue engineering and immunological therapeutics.
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•A programed surface is designed and fabricated for immune-mediated osteogenesis•The degradation of PTMC coating enables a sequential release of IL-10 and DEX•Initially, osteoimmunomodulation is achieved by IL-10 and a small amount of DEX•Afterwards, sustained release of DEX fosters the peri-implant bone regeneration |
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ISSN: | 2666-6758 2666-6758 |
DOI: | 10.1016/j.xinn.2021.100148 |