Cargando…

Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing

Two types of completely densified β-TCP tablets were synthesized from a stoichiometric β-TCP powder. The first ones (TCP) were conventionally sintered, while the second ones (TCP-T) were sintered and treated by hot isostatic process (HIP). The HIP produced completely densified materials with relativ...

Descripción completa

Detalles Bibliográficos
Autores principales: Mateescu, Mihaela, Rguitti, Emmanuelle, Ponche, Arnaud, Descamps, Michel, Anselme, Karine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549863/
https://www.ncbi.nlm.nih.gov/pubmed/23507861
http://dx.doi.org/10.4161/biom.21377
_version_ 1782256487740997632
author Mateescu, Mihaela
Rguitti, Emmanuelle
Ponche, Arnaud
Descamps, Michel
Anselme, Karine
author_facet Mateescu, Mihaela
Rguitti, Emmanuelle
Ponche, Arnaud
Descamps, Michel
Anselme, Karine
author_sort Mateescu, Mihaela
collection PubMed
description Two types of completely densified β-TCP tablets were synthesized from a stoichiometric β-TCP powder. The first ones (TCP) were conventionally sintered, while the second ones (TCP-T) were sintered and treated by hot isostatic process (HIP). The HIP produced completely densified materials with relative densities greater than 99.9% and a transparent appearance of tablets. Samples were immersed in culture medium with (CM) or without serum (NCM) in static and dynamic conditions for a biomimetic evaluation. Similarly, SaOs-2 cells were cultured on samples in a static or dynamic flow perfusion system. The results of surface transformation in absence of cells showed that the dynamic condition increased the speed of calcium phosphate precipitations compared with the static condition. The morphology of precipitates was different with nature of tablets. The immersion in CM did impede this precipitation. XPS analysis of TCP-T tablets showed the presence of hydroxyapatite (HA) precipitates after incubation in NCM while octacalcium phosphate (OCP) precipitates were formed after incubation in CM. The analysis of the response of SaOs-2 cells on surfaces showed that the two types of materials are biocompatible. However, the dynamic mode of culture stimulated the differentiation of cells. Finally, it appears that the HIP treatment of TCP produces highly densified and transparent samples that display a good in vitro biocompatibility in static and dynamic culture conditions. Moreover, an interesting result of this work is the relationship between the presence of proteins in the immersion medium and the quality of precipitates formed on hipped TCP surface.
format Online
Article
Text
id pubmed-3549863
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Landes Bioscience
record_format MEDLINE/PubMed
spelling pubmed-35498632013-05-22 Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing Mateescu, Mihaela Rguitti, Emmanuelle Ponche, Arnaud Descamps, Michel Anselme, Karine Biomatter Report Two types of completely densified β-TCP tablets were synthesized from a stoichiometric β-TCP powder. The first ones (TCP) were conventionally sintered, while the second ones (TCP-T) were sintered and treated by hot isostatic process (HIP). The HIP produced completely densified materials with relative densities greater than 99.9% and a transparent appearance of tablets. Samples were immersed in culture medium with (CM) or without serum (NCM) in static and dynamic conditions for a biomimetic evaluation. Similarly, SaOs-2 cells were cultured on samples in a static or dynamic flow perfusion system. The results of surface transformation in absence of cells showed that the dynamic condition increased the speed of calcium phosphate precipitations compared with the static condition. The morphology of precipitates was different with nature of tablets. The immersion in CM did impede this precipitation. XPS analysis of TCP-T tablets showed the presence of hydroxyapatite (HA) precipitates after incubation in NCM while octacalcium phosphate (OCP) precipitates were formed after incubation in CM. The analysis of the response of SaOs-2 cells on surfaces showed that the two types of materials are biocompatible. However, the dynamic mode of culture stimulated the differentiation of cells. Finally, it appears that the HIP treatment of TCP produces highly densified and transparent samples that display a good in vitro biocompatibility in static and dynamic culture conditions. Moreover, an interesting result of this work is the relationship between the presence of proteins in the immersion medium and the quality of precipitates formed on hipped TCP surface. Landes Bioscience 2012-07-01 /pmc/articles/PMC3549863/ /pubmed/23507861 http://dx.doi.org/10.4161/biom.21377 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Report
Mateescu, Mihaela
Rguitti, Emmanuelle
Ponche, Arnaud
Descamps, Michel
Anselme, Karine
Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title_full Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title_fullStr Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title_full_unstemmed Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title_short Biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
title_sort biomimetic evaluation of β tricalcium phosphate prepared by hot isostatic pressing
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549863/
https://www.ncbi.nlm.nih.gov/pubmed/23507861
http://dx.doi.org/10.4161/biom.21377
work_keys_str_mv AT mateescumihaela biomimeticevaluationofbtricalciumphosphatepreparedbyhotisostaticpressing
AT rguittiemmanuelle biomimeticevaluationofbtricalciumphosphatepreparedbyhotisostaticpressing
AT ponchearnaud biomimeticevaluationofbtricalciumphosphatepreparedbyhotisostaticpressing
AT descampsmichel biomimeticevaluationofbtricalciumphosphatepreparedbyhotisostaticpressing
AT anselmekarine biomimeticevaluationofbtricalciumphosphatepreparedbyhotisostaticpressing