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Biodegradable mesoporous delivery system for biomineralization precursors

Scaffold supplements such as nanoparticles, components of the extracellular matrix, or growth factors have been incorporated in conventional scaffold materials to produce smart scaffolds for tissue engineering of damaged hard tissues. Due to increasing concerns on the clinical side effects of using...

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Autores principales: Yang, Hong-ye, Niu, Li-na, Sun, Jin-long, Huang, Xue-qing, Pei, Dan-dan, Huang, Cui, Tay, Franklin R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279816/
https://www.ncbi.nlm.nih.gov/pubmed/28182119
http://dx.doi.org/10.2147/IJN.S128792
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author Yang, Hong-ye
Niu, Li-na
Sun, Jin-long
Huang, Xue-qing
Pei, Dan-dan
Huang, Cui
Tay, Franklin R
author_facet Yang, Hong-ye
Niu, Li-na
Sun, Jin-long
Huang, Xue-qing
Pei, Dan-dan
Huang, Cui
Tay, Franklin R
author_sort Yang, Hong-ye
collection PubMed
description Scaffold supplements such as nanoparticles, components of the extracellular matrix, or growth factors have been incorporated in conventional scaffold materials to produce smart scaffolds for tissue engineering of damaged hard tissues. Due to increasing concerns on the clinical side effects of using large doses of recombinant bone-morphogenetic protein-2 in bone surgery, it is desirable to develop an alternative nanoscale scaffold supplement that is not only osteoinductive, but is also multifunctional in that it can perform other significant bone regenerative roles apart from stimulation of osteogenic differentiation. Because both amorphous calcium phosphate (ACP) and silica are osteoinductive, a biodegradable, nonfunctionalized, expanded-pore mesoporous silica nanoparticle carrier was developed for loading, storage, and sustained release of a novel, biosilicification-inspired, polyamine-stabilized liquid precursor phase of ACP for collagen biomineralization and for release of orthosilicic acid, both of which are conducive to bone growth. Positively charged poly(allylamine)-stabilized ACP (PAH-ACP) could be effectively loaded and released from nonfunctionalized expanded-pore mesoporous silica nanoparticles (pMSN). The PAH-ACP released from loaded pMSN still retained its ability to infiltrate and mineralize collagen fibrils. Complete degradation of pMSN occurred following unloading of their PAH-ACP cargo. Because PAH-ACP loaded pMSN possesses relatively low cytotoxicity to human bone marrow-derived mesenchymal stem cells, these nanoparticles may be blended with any osteoconductive scaffold with macro- and microporosities as a versatile scaffold supplement to enhance bone regeneration.
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spelling pubmed-52798162017-02-08 Biodegradable mesoporous delivery system for biomineralization precursors Yang, Hong-ye Niu, Li-na Sun, Jin-long Huang, Xue-qing Pei, Dan-dan Huang, Cui Tay, Franklin R Int J Nanomedicine Original Research Scaffold supplements such as nanoparticles, components of the extracellular matrix, or growth factors have been incorporated in conventional scaffold materials to produce smart scaffolds for tissue engineering of damaged hard tissues. Due to increasing concerns on the clinical side effects of using large doses of recombinant bone-morphogenetic protein-2 in bone surgery, it is desirable to develop an alternative nanoscale scaffold supplement that is not only osteoinductive, but is also multifunctional in that it can perform other significant bone regenerative roles apart from stimulation of osteogenic differentiation. Because both amorphous calcium phosphate (ACP) and silica are osteoinductive, a biodegradable, nonfunctionalized, expanded-pore mesoporous silica nanoparticle carrier was developed for loading, storage, and sustained release of a novel, biosilicification-inspired, polyamine-stabilized liquid precursor phase of ACP for collagen biomineralization and for release of orthosilicic acid, both of which are conducive to bone growth. Positively charged poly(allylamine)-stabilized ACP (PAH-ACP) could be effectively loaded and released from nonfunctionalized expanded-pore mesoporous silica nanoparticles (pMSN). The PAH-ACP released from loaded pMSN still retained its ability to infiltrate and mineralize collagen fibrils. Complete degradation of pMSN occurred following unloading of their PAH-ACP cargo. Because PAH-ACP loaded pMSN possesses relatively low cytotoxicity to human bone marrow-derived mesenchymal stem cells, these nanoparticles may be blended with any osteoconductive scaffold with macro- and microporosities as a versatile scaffold supplement to enhance bone regeneration. Dove Medical Press 2017-01-25 /pmc/articles/PMC5279816/ /pubmed/28182119 http://dx.doi.org/10.2147/IJN.S128792 Text en © 2017 Yang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yang, Hong-ye
Niu, Li-na
Sun, Jin-long
Huang, Xue-qing
Pei, Dan-dan
Huang, Cui
Tay, Franklin R
Biodegradable mesoporous delivery system for biomineralization precursors
title Biodegradable mesoporous delivery system for biomineralization precursors
title_full Biodegradable mesoporous delivery system for biomineralization precursors
title_fullStr Biodegradable mesoporous delivery system for biomineralization precursors
title_full_unstemmed Biodegradable mesoporous delivery system for biomineralization precursors
title_short Biodegradable mesoporous delivery system for biomineralization precursors
title_sort biodegradable mesoporous delivery system for biomineralization precursors
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279816/
https://www.ncbi.nlm.nih.gov/pubmed/28182119
http://dx.doi.org/10.2147/IJN.S128792
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