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Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition

The dissolution-derived release of bioactive ions from ceramic coatings on metallic implants, despite improving osseointegration, renders a concern on the interfacial breakdown of the metal/coating/bone system during long-term service. Consequently, persistent efforts to seek alternative strategies...

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Detalles Bibliográficos
Autores principales: Yu, Dongmei, Li, Bo, Yu, Meng, Guo, Shuo, Guo, Zheng, Han, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961311/
https://www.ncbi.nlm.nih.gov/pubmed/35387170
http://dx.doi.org/10.1016/j.bioactmat.2022.01.039
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author Yu, Dongmei
Li, Bo
Yu, Meng
Guo, Shuo
Guo, Zheng
Han, Yong
author_facet Yu, Dongmei
Li, Bo
Yu, Meng
Guo, Shuo
Guo, Zheng
Han, Yong
author_sort Yu, Dongmei
collection PubMed
description The dissolution-derived release of bioactive ions from ceramic coatings on metallic implants, despite improving osseointegration, renders a concern on the interfacial breakdown of the metal/coating/bone system during long-term service. Consequently, persistent efforts to seek alternative strategies instead of dissolution-derived activation are pressingly carrying out. Inspired by bone mineral containing ions as Ca(2+), Mg(2+), Sr(2+) and Zn(2+), here we hydrothermally grew the quadruple ions co-doped Na(2)TiO(3) nanorod-like coatings. The co-doped ions partially substitute Na(+) in Na(2)TiO(3), and can be efficiently released from cubic lattice via exchange with Na(+) in fluid rather than dissolution, endowing the coatings superior long-term stability of structure and bond strength. Regulated by the coatings-conditioned extracellular ions, TLR4-NFκB signalling is enhanced to act primarily in macrophages (MΦs) at 6 h while CaSR-PI3K-Akt1 signalling is potentiated to act predominately since 24 h, triggering MΦs in a M1 response early and then in a M2 response to sequentially secrete diverse cytokines. Acting on endothelial and mesenchymal stem cells with the released ions and cytokines, the immunomodulatory coatings greatly promote Type-H (CD31(hi)Emcn(hi)) angiogenesis and osteogenesis in vitro and in vivo, providing new insights into orchestrating insoluble ceramics-coated implants for early vascularized osseointegration in combination with long-term fixation to bone.
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spelling pubmed-89613112022-04-05 Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition Yu, Dongmei Li, Bo Yu, Meng Guo, Shuo Guo, Zheng Han, Yong Bioact Mater Article The dissolution-derived release of bioactive ions from ceramic coatings on metallic implants, despite improving osseointegration, renders a concern on the interfacial breakdown of the metal/coating/bone system during long-term service. Consequently, persistent efforts to seek alternative strategies instead of dissolution-derived activation are pressingly carrying out. Inspired by bone mineral containing ions as Ca(2+), Mg(2+), Sr(2+) and Zn(2+), here we hydrothermally grew the quadruple ions co-doped Na(2)TiO(3) nanorod-like coatings. The co-doped ions partially substitute Na(+) in Na(2)TiO(3), and can be efficiently released from cubic lattice via exchange with Na(+) in fluid rather than dissolution, endowing the coatings superior long-term stability of structure and bond strength. Regulated by the coatings-conditioned extracellular ions, TLR4-NFκB signalling is enhanced to act primarily in macrophages (MΦs) at 6 h while CaSR-PI3K-Akt1 signalling is potentiated to act predominately since 24 h, triggering MΦs in a M1 response early and then in a M2 response to sequentially secrete diverse cytokines. Acting on endothelial and mesenchymal stem cells with the released ions and cytokines, the immunomodulatory coatings greatly promote Type-H (CD31(hi)Emcn(hi)) angiogenesis and osteogenesis in vitro and in vivo, providing new insights into orchestrating insoluble ceramics-coated implants for early vascularized osseointegration in combination with long-term fixation to bone. KeAi Publishing 2022-02-15 /pmc/articles/PMC8961311/ /pubmed/35387170 http://dx.doi.org/10.1016/j.bioactmat.2022.01.039 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yu, Dongmei
Li, Bo
Yu, Meng
Guo, Shuo
Guo, Zheng
Han, Yong
Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title_full Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title_fullStr Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title_full_unstemmed Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title_short Cubic multi-ions-doped Na(2)TiO(3) nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
title_sort cubic multi-ions-doped na(2)tio(3) nanorod-like coatings: structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961311/
https://www.ncbi.nlm.nih.gov/pubmed/35387170
http://dx.doi.org/10.1016/j.bioactmat.2022.01.039
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