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Multimodal porogen platforms for calcium phosphate cement degradation

Calcium phosphate cements (CPCs) represent excellent bone substitute materials due to their biocompatibility and injectability. However, their poor degradability and lack of macroporosity limits bone regeneration. The addition of poly(d,l‐lactic‐co‐glycolic acid) (PLGA) particles improves macroporos...

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Autores principales: Lodoso‐Torrecilla, Irene, Grosfeld, Eline‐Claire, Marra, Abe, Smith, Brandon T, Mikos, Antonios G, Ulrich, Dietmar JO, Jansen, John A, van den Beucken, Jeroen JJP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618311/
https://www.ncbi.nlm.nih.gov/pubmed/30920119
http://dx.doi.org/10.1002/jbm.a.36686
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author Lodoso‐Torrecilla, Irene
Grosfeld, Eline‐Claire
Marra, Abe
Smith, Brandon T
Mikos, Antonios G
Ulrich, Dietmar JO
Jansen, John A
van den Beucken, Jeroen JJP
author_facet Lodoso‐Torrecilla, Irene
Grosfeld, Eline‐Claire
Marra, Abe
Smith, Brandon T
Mikos, Antonios G
Ulrich, Dietmar JO
Jansen, John A
van den Beucken, Jeroen JJP
author_sort Lodoso‐Torrecilla, Irene
collection PubMed
description Calcium phosphate cements (CPCs) represent excellent bone substitute materials due to their biocompatibility and injectability. However, their poor degradability and lack of macroporosity limits bone regeneration. The addition of poly(d,l‐lactic‐co‐glycolic acid) (PLGA) particles improves macroporosity and therefore late stage material degradation. CPC degradation and hence, bone formation at an early stage remains challenging, due to the delayed onset of PLGA degradation (i.e., after 2–3 weeks). Consequently, we here explored multimodal porogen platforms based on sucrose porogens (for early pore formation) and PLGA porogens (for late pore formation) to enhance CPC degradation and analyzed mechanical properties, dynamic in vitro degradation and in vivo performance in a rat femoral bone defect model. Porogen addition to CPC showed to decrease compressive strength of all CPC formulations; transition of the crystal phase upon in vitro incubation increased compressive strength. Although dynamic in vitro degradation showed rapid sucrose dissolution within 1 week, no additional effects on CPC degradation or bone formation were observed upon in vivo implantation. © 2019 The Authors. journal Of Biomedical Materials Research Part A Published By Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1713–1722, 2019.
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spelling pubmed-66183112019-07-22 Multimodal porogen platforms for calcium phosphate cement degradation Lodoso‐Torrecilla, Irene Grosfeld, Eline‐Claire Marra, Abe Smith, Brandon T Mikos, Antonios G Ulrich, Dietmar JO Jansen, John A van den Beucken, Jeroen JJP J Biomed Mater Res A Original Articles Calcium phosphate cements (CPCs) represent excellent bone substitute materials due to their biocompatibility and injectability. However, their poor degradability and lack of macroporosity limits bone regeneration. The addition of poly(d,l‐lactic‐co‐glycolic acid) (PLGA) particles improves macroporosity and therefore late stage material degradation. CPC degradation and hence, bone formation at an early stage remains challenging, due to the delayed onset of PLGA degradation (i.e., after 2–3 weeks). Consequently, we here explored multimodal porogen platforms based on sucrose porogens (for early pore formation) and PLGA porogens (for late pore formation) to enhance CPC degradation and analyzed mechanical properties, dynamic in vitro degradation and in vivo performance in a rat femoral bone defect model. Porogen addition to CPC showed to decrease compressive strength of all CPC formulations; transition of the crystal phase upon in vitro incubation increased compressive strength. Although dynamic in vitro degradation showed rapid sucrose dissolution within 1 week, no additional effects on CPC degradation or bone formation were observed upon in vivo implantation. © 2019 The Authors. journal Of Biomedical Materials Research Part A Published By Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1713–1722, 2019. John Wiley & Sons, Inc. 2019-04-09 2019-08 /pmc/articles/PMC6618311/ /pubmed/30920119 http://dx.doi.org/10.1002/jbm.a.36686 Text en © 2019 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Lodoso‐Torrecilla, Irene
Grosfeld, Eline‐Claire
Marra, Abe
Smith, Brandon T
Mikos, Antonios G
Ulrich, Dietmar JO
Jansen, John A
van den Beucken, Jeroen JJP
Multimodal porogen platforms for calcium phosphate cement degradation
title Multimodal porogen platforms for calcium phosphate cement degradation
title_full Multimodal porogen platforms for calcium phosphate cement degradation
title_fullStr Multimodal porogen platforms for calcium phosphate cement degradation
title_full_unstemmed Multimodal porogen platforms for calcium phosphate cement degradation
title_short Multimodal porogen platforms for calcium phosphate cement degradation
title_sort multimodal porogen platforms for calcium phosphate cement degradation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618311/
https://www.ncbi.nlm.nih.gov/pubmed/30920119
http://dx.doi.org/10.1002/jbm.a.36686
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