Cargando…

Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation

Phosphate-based glasses (PBGs) are promising materials for bone repair and regeneration as they can be formulated to be compositionally similar to the inorganic components of bone. Alterations to the PBG formulation can be used to tailor their degradation rates and subsequent release of biotherapeut...

Descripción completa

Detalles Bibliográficos
Autores principales: Milborne, Ben, Murrell, Lauren, Cardillo-Zallo, Ian, Titman, Jeremy, Briggs, Louise, Scotchford, Colin, Thompson, Alexander, Layfield, Robert, Ahmed, Ifty
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687370/
https://www.ncbi.nlm.nih.gov/pubmed/36354522
http://dx.doi.org/10.3390/bioengineering9110611
_version_ 1784835988347944960
author Milborne, Ben
Murrell, Lauren
Cardillo-Zallo, Ian
Titman, Jeremy
Briggs, Louise
Scotchford, Colin
Thompson, Alexander
Layfield, Robert
Ahmed, Ifty
author_facet Milborne, Ben
Murrell, Lauren
Cardillo-Zallo, Ian
Titman, Jeremy
Briggs, Louise
Scotchford, Colin
Thompson, Alexander
Layfield, Robert
Ahmed, Ifty
author_sort Milborne, Ben
collection PubMed
description Phosphate-based glasses (PBGs) are promising materials for bone repair and regeneration as they can be formulated to be compositionally similar to the inorganic components of bone. Alterations to the PBG formulation can be used to tailor their degradation rates and subsequent release of biotherapeutic ions to induce cellular responses, such as osteogenesis. In this work, novel invert-PBGs in the series xP(2)O(5)·(56 − x)CaO·24MgO·20Na(2)O (mol%), where x is 40, 35, 32.5 and 30 were formulated to contain pyro (Q(1)) and orthophosphate (Q(0)) species. These PBGs were processed into highly porous microspheres (PMS) via flame spheroidisation, with ~68% to 75% porosity levels. Compositional and structural analysis using EDX and (31)P-MAS NMR revealed that significant depolymerisation occurred with reducing phosphate content which increased further when PBGs were processed into PMS. A decrease from 50% to 0% in Q(2) species and an increase from 6% to 35% in Q(0) species was observed for the PMS when the phosphate content decreased from 40 to 30 mol%. Ion release studies also revealed up to a four-fold decrease in cations and an eight-fold decrease in phosphate anions released with decreasing phosphate content. In vitro bioactivity studies revealed that the orthophosphate-rich PMS had favourable bioactivity responses after 28 days of immersion in simulated body fluid (SBF). Indirect and direct cell culture studies confirmed that the PMS were cytocompatible and supported cell growth and proliferation over 7 days of culture. The P30 PMS with ~65% pyro and ~35% ortho phosphate content revealed the most favourable properties and is suggested to be highly suitable for bone repair and regeneration, especially for orthobiologic applications owing to their highly porous morphology.
format Online
Article
Text
id pubmed-9687370
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96873702022-11-25 Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation Milborne, Ben Murrell, Lauren Cardillo-Zallo, Ian Titman, Jeremy Briggs, Louise Scotchford, Colin Thompson, Alexander Layfield, Robert Ahmed, Ifty Bioengineering (Basel) Article Phosphate-based glasses (PBGs) are promising materials for bone repair and regeneration as they can be formulated to be compositionally similar to the inorganic components of bone. Alterations to the PBG formulation can be used to tailor their degradation rates and subsequent release of biotherapeutic ions to induce cellular responses, such as osteogenesis. In this work, novel invert-PBGs in the series xP(2)O(5)·(56 − x)CaO·24MgO·20Na(2)O (mol%), where x is 40, 35, 32.5 and 30 were formulated to contain pyro (Q(1)) and orthophosphate (Q(0)) species. These PBGs were processed into highly porous microspheres (PMS) via flame spheroidisation, with ~68% to 75% porosity levels. Compositional and structural analysis using EDX and (31)P-MAS NMR revealed that significant depolymerisation occurred with reducing phosphate content which increased further when PBGs were processed into PMS. A decrease from 50% to 0% in Q(2) species and an increase from 6% to 35% in Q(0) species was observed for the PMS when the phosphate content decreased from 40 to 30 mol%. Ion release studies also revealed up to a four-fold decrease in cations and an eight-fold decrease in phosphate anions released with decreasing phosphate content. In vitro bioactivity studies revealed that the orthophosphate-rich PMS had favourable bioactivity responses after 28 days of immersion in simulated body fluid (SBF). Indirect and direct cell culture studies confirmed that the PMS were cytocompatible and supported cell growth and proliferation over 7 days of culture. The P30 PMS with ~65% pyro and ~35% ortho phosphate content revealed the most favourable properties and is suggested to be highly suitable for bone repair and regeneration, especially for orthobiologic applications owing to their highly porous morphology. MDPI 2022-10-25 /pmc/articles/PMC9687370/ /pubmed/36354522 http://dx.doi.org/10.3390/bioengineering9110611 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Milborne, Ben
Murrell, Lauren
Cardillo-Zallo, Ian
Titman, Jeremy
Briggs, Louise
Scotchford, Colin
Thompson, Alexander
Layfield, Robert
Ahmed, Ifty
Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title_full Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title_fullStr Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title_full_unstemmed Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title_short Developing Porous Ortho- and Pyrophosphate-Containing Glass Microspheres; Structural and Cytocompatibility Characterisation
title_sort developing porous ortho- and pyrophosphate-containing glass microspheres; structural and cytocompatibility characterisation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687370/
https://www.ncbi.nlm.nih.gov/pubmed/36354522
http://dx.doi.org/10.3390/bioengineering9110611
work_keys_str_mv AT milborneben developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT murrelllauren developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT cardillozalloian developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT titmanjeremy developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT briggslouise developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT scotchfordcolin developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT thompsonalexander developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT layfieldrobert developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation
AT ahmedifty developingporousorthoandpyrophosphatecontainingglassmicrospheresstructuralandcytocompatibilitycharacterisation