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TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells

Scalable expansion of cells for regenerative cell therapy or to produce large quantities for high-throughput screening remains a challenge for bioprocess engineers. Laboratory scale cell expansion using t-flasks requires frequent passaging that exposes cells to many poorly defined bioprocess forces...

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Autores principales: Guedes, Joana C, Park, Jeong-Hui, Lakhkar, Nilay J, Kim, Hae-Won, Knowles, Jonathan C, Wall, Ivan B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107757/
https://www.ncbi.nlm.nih.gov/pubmed/22935537
http://dx.doi.org/10.1177/0885328212459093
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author Guedes, Joana C
Park, Jeong-Hui
Lakhkar, Nilay J
Kim, Hae-Won
Knowles, Jonathan C
Wall, Ivan B
author_facet Guedes, Joana C
Park, Jeong-Hui
Lakhkar, Nilay J
Kim, Hae-Won
Knowles, Jonathan C
Wall, Ivan B
author_sort Guedes, Joana C
collection PubMed
description Scalable expansion of cells for regenerative cell therapy or to produce large quantities for high-throughput screening remains a challenge for bioprocess engineers. Laboratory scale cell expansion using t-flasks requires frequent passaging that exposes cells to many poorly defined bioprocess forces that can cause damage or alter their phenotype. Microcarriers offer a potential solution to scalable production, lending themselves to cell culture processes more akin to fermentation, removing the need for frequent passaging throughout the expansion period. One main problem with microcarrier expansion, however, is the difficulty in harvesting cells at the end of the process. Therefore, therapies that rely on cell delivery using biomaterial scaffolds could benefit from a microcarrier expansion system whereby the cells and microcarriers are transplanted together. In the current study, we used bioactive glass microcarriers doped with 5% TiO(2) that display a controlled rate of degradation and conducted experiments to assess biocompatibility and growth of primary fibroblast cells as a model for cell therapy products. We found that the microcarriers are highly biocompatible and facilitate cell growth in a gradual controlled manner. Therefore, even without additional biofunctionalization methods, Ti-doped bioactive glass microcarriers offer potential as a cell expansion platform.
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spelling pubmed-41077572014-07-28 TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells Guedes, Joana C Park, Jeong-Hui Lakhkar, Nilay J Kim, Hae-Won Knowles, Jonathan C Wall, Ivan B J Biomater Appl Articles Scalable expansion of cells for regenerative cell therapy or to produce large quantities for high-throughput screening remains a challenge for bioprocess engineers. Laboratory scale cell expansion using t-flasks requires frequent passaging that exposes cells to many poorly defined bioprocess forces that can cause damage or alter their phenotype. Microcarriers offer a potential solution to scalable production, lending themselves to cell culture processes more akin to fermentation, removing the need for frequent passaging throughout the expansion period. One main problem with microcarrier expansion, however, is the difficulty in harvesting cells at the end of the process. Therefore, therapies that rely on cell delivery using biomaterial scaffolds could benefit from a microcarrier expansion system whereby the cells and microcarriers are transplanted together. In the current study, we used bioactive glass microcarriers doped with 5% TiO(2) that display a controlled rate of degradation and conducted experiments to assess biocompatibility and growth of primary fibroblast cells as a model for cell therapy products. We found that the microcarriers are highly biocompatible and facilitate cell growth in a gradual controlled manner. Therefore, even without additional biofunctionalization methods, Ti-doped bioactive glass microcarriers offer potential as a cell expansion platform. SAGE Publications 2013-07 /pmc/articles/PMC4107757/ /pubmed/22935537 http://dx.doi.org/10.1177/0885328212459093 Text en © The Author(s) 2012 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle Articles
Guedes, Joana C
Park, Jeong-Hui
Lakhkar, Nilay J
Kim, Hae-Won
Knowles, Jonathan C
Wall, Ivan B
TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title_full TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title_fullStr TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title_full_unstemmed TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title_short TiO(2)-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells
title_sort tio(2)-doped phosphate glass microcarriers: a stable bioactive substrate for expansion of adherent mammalian cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107757/
https://www.ncbi.nlm.nih.gov/pubmed/22935537
http://dx.doi.org/10.1177/0885328212459093
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