Cargando…

The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells

Biodegradable Mg alloys have the potential to replace currently used metallic medical implant devices, likely eliminating toxicity concerns and the need for secondary surgeries, while also providing a potentially stimulating environment for tissue growth. A recently developed Mg–Ca–Sr alloy possesse...

Descripción completa

Detalles Bibliográficos
Autores principales: Berglund, Ida S., Dirr, Elliott W., Ramaswamy, Vidhya, Allen, Josephine B., Allen, Kyle D., Manuel, Michele V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811831/
https://www.ncbi.nlm.nih.gov/pubmed/28323384
http://dx.doi.org/10.1002/jbm.b.33869
_version_ 1783299928947163136
author Berglund, Ida S.
Dirr, Elliott W.
Ramaswamy, Vidhya
Allen, Josephine B.
Allen, Kyle D.
Manuel, Michele V.
author_facet Berglund, Ida S.
Dirr, Elliott W.
Ramaswamy, Vidhya
Allen, Josephine B.
Allen, Kyle D.
Manuel, Michele V.
author_sort Berglund, Ida S.
collection PubMed
description Biodegradable Mg alloys have the potential to replace currently used metallic medical implant devices, likely eliminating toxicity concerns and the need for secondary surgeries, while also providing a potentially stimulating environment for tissue growth. A recently developed Mg–Ca–Sr alloy possesses advantageous characteristics over other Mg alloys, having a good combination of strength and degradation behavior, while also displaying potentially osteogenic properties. To better understand the effect of alloy degradation products on cellular mechanisms, in vitro studies using human bone marrow‐derived mesenchymal stem cells were conducted. Ionic products of alloy dissolution were found to be nontoxic but changed the proliferation profile of stem cells. Furthermore, their presence changed the progress of osteogenic development, while concentrations of Mg in particular appeared to induce stem cell differentiation. The work presented herein provides a foundation for future alloy design where structures can be tailored to obtain specific implant performance. These potentially bioactive implants would reduce the risks for patients by shortening their healing time, minimizing discomfort and toxicity concerns, while reducing hospital costs. © 2017 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 697–704, 2018.
format Online
Article
Text
id pubmed-5811831
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-58118312018-02-16 The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells Berglund, Ida S. Dirr, Elliott W. Ramaswamy, Vidhya Allen, Josephine B. Allen, Kyle D. Manuel, Michele V. J Biomed Mater Res B Appl Biomater Original Research Reports Biodegradable Mg alloys have the potential to replace currently used metallic medical implant devices, likely eliminating toxicity concerns and the need for secondary surgeries, while also providing a potentially stimulating environment for tissue growth. A recently developed Mg–Ca–Sr alloy possesses advantageous characteristics over other Mg alloys, having a good combination of strength and degradation behavior, while also displaying potentially osteogenic properties. To better understand the effect of alloy degradation products on cellular mechanisms, in vitro studies using human bone marrow‐derived mesenchymal stem cells were conducted. Ionic products of alloy dissolution were found to be nontoxic but changed the proliferation profile of stem cells. Furthermore, their presence changed the progress of osteogenic development, while concentrations of Mg in particular appeared to induce stem cell differentiation. The work presented herein provides a foundation for future alloy design where structures can be tailored to obtain specific implant performance. These potentially bioactive implants would reduce the risks for patients by shortening their healing time, minimizing discomfort and toxicity concerns, while reducing hospital costs. © 2017 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 697–704, 2018. John Wiley and Sons Inc. 2017-03-21 2018-02 /pmc/articles/PMC5811831/ /pubmed/28323384 http://dx.doi.org/10.1002/jbm.b.33869 Text en © 2017 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Reports
Berglund, Ida S.
Dirr, Elliott W.
Ramaswamy, Vidhya
Allen, Josephine B.
Allen, Kyle D.
Manuel, Michele V.
The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title_full The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title_fullStr The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title_full_unstemmed The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title_short The effect of Mg–Ca–Sr alloy degradation products on human mesenchymal stem cells
title_sort effect of mg–ca–sr alloy degradation products on human mesenchymal stem cells
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811831/
https://www.ncbi.nlm.nih.gov/pubmed/28323384
http://dx.doi.org/10.1002/jbm.b.33869
work_keys_str_mv AT berglundidas theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT dirrelliottw theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT ramaswamyvidhya theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT allenjosephineb theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT allenkyled theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT manuelmichelev theeffectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT berglundidas effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT dirrelliottw effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT ramaswamyvidhya effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT allenjosephineb effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT allenkyled effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells
AT manuelmichelev effectofmgcasralloydegradationproductsonhumanmesenchymalstemcells