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Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture

Calcium phosphate cements (CPC) are valuable bone fillers. Recently they have been also considered as the basis for drug-, growth factors- or cells-delivery systems. Broad possibilities to manipulate CPC composition provide a unique opportunity to obtain materials with a wide range of physicochemica...

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Autores principales: Olkowski, Radosław, Kaszczewski, Piotr, Czechowska, Joanna, Siek, Dominika, Pijocha, Dawid, Zima, Aneta, Ślósarczyk, Anna, Lewandowska-Szumieł, Małgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624837/
https://www.ncbi.nlm.nih.gov/pubmed/26511138
http://dx.doi.org/10.1007/s10856-015-5589-x
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author Olkowski, Radosław
Kaszczewski, Piotr
Czechowska, Joanna
Siek, Dominika
Pijocha, Dawid
Zima, Aneta
Ślósarczyk, Anna
Lewandowska-Szumieł, Małgorzata
author_facet Olkowski, Radosław
Kaszczewski, Piotr
Czechowska, Joanna
Siek, Dominika
Pijocha, Dawid
Zima, Aneta
Ślósarczyk, Anna
Lewandowska-Szumieł, Małgorzata
author_sort Olkowski, Radosław
collection PubMed
description Calcium phosphate cements (CPC) are valuable bone fillers. Recently they have been also considered as the basis for drug-, growth factors- or cells-delivery systems. Broad possibilities to manipulate CPC composition provide a unique opportunity to obtain materials with a wide range of physicochemical properties. In this study we show that CPC composition significantly influences cell response. Human bone derived cells were exposed to the several well-characterized different cements based on calcium phosphates, magnesium phosphates and calcium sulfate hemihydrate (CSH). Cell viability assays, live/dead staining and real-time observation of cells in contact with the materials (time-laps) were performed. Although all the investigated materials have successfully passed a standard cytocompatibility assay, cell behavior in a direct contact with the materials varied depending on the material and the experimental system. The most recommended were the α-TCP-based materials which proved suitable as a support for cells in a direct contact. The materials which caused a decrease of calcium ions concentration in culture induced the negative cell response, however this effect might be expected efficiently compensated in vivo. All the materials consisting of CSH had negative impact on the cells. The obtained results strongly support running series of cytocompatibility studies for preclinical evaluation of bone cements.
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spelling pubmed-46248372015-11-03 Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture Olkowski, Radosław Kaszczewski, Piotr Czechowska, Joanna Siek, Dominika Pijocha, Dawid Zima, Aneta Ślósarczyk, Anna Lewandowska-Szumieł, Małgorzata J Mater Sci Mater Med Biocompatibility Studies Calcium phosphate cements (CPC) are valuable bone fillers. Recently they have been also considered as the basis for drug-, growth factors- or cells-delivery systems. Broad possibilities to manipulate CPC composition provide a unique opportunity to obtain materials with a wide range of physicochemical properties. In this study we show that CPC composition significantly influences cell response. Human bone derived cells were exposed to the several well-characterized different cements based on calcium phosphates, magnesium phosphates and calcium sulfate hemihydrate (CSH). Cell viability assays, live/dead staining and real-time observation of cells in contact with the materials (time-laps) were performed. Although all the investigated materials have successfully passed a standard cytocompatibility assay, cell behavior in a direct contact with the materials varied depending on the material and the experimental system. The most recommended were the α-TCP-based materials which proved suitable as a support for cells in a direct contact. The materials which caused a decrease of calcium ions concentration in culture induced the negative cell response, however this effect might be expected efficiently compensated in vivo. All the materials consisting of CSH had negative impact on the cells. The obtained results strongly support running series of cytocompatibility studies for preclinical evaluation of bone cements. Springer US 2015-10-28 2015 /pmc/articles/PMC4624837/ /pubmed/26511138 http://dx.doi.org/10.1007/s10856-015-5589-x Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Biocompatibility Studies
Olkowski, Radosław
Kaszczewski, Piotr
Czechowska, Joanna
Siek, Dominika
Pijocha, Dawid
Zima, Aneta
Ślósarczyk, Anna
Lewandowska-Szumieł, Małgorzata
Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title_full Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title_fullStr Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title_full_unstemmed Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title_short Cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
title_sort cytocompatibility of the selected calcium phosphate based bone cements: comparative study in human cell culture
topic Biocompatibility Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624837/
https://www.ncbi.nlm.nih.gov/pubmed/26511138
http://dx.doi.org/10.1007/s10856-015-5589-x
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