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A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method

BACKGROUND: In cell-based therapies, in vitro studies on biomimetic cell–scaffold constructs can facilitate the determination of the cell dose, a key factor in guaranteeing the effectiveness of the treatment. However, highly porous scaffolds do not allow a nondestructive evaluation of the cell numbe...

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Detalles Bibliográficos
Autores principales: Divieto, Carla, Sassi, Maria Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137907/
https://www.ncbi.nlm.nih.gov/pubmed/28031911
http://dx.doi.org/10.4155/fso.15.58
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author Divieto, Carla
Sassi, Maria Paola
author_facet Divieto, Carla
Sassi, Maria Paola
author_sort Divieto, Carla
collection PubMed
description BACKGROUND: In cell-based therapies, in vitro studies on biomimetic cell–scaffold constructs can facilitate the determination of the cell dose, a key factor in guaranteeing the effectiveness of the treatment. However, highly porous scaffolds do not allow a nondestructive evaluation of the cell number. Our objective was to develop a nondestructive method for human mesenchymal stem cells dose evaluation in a highly porous scaffold for bone regeneration. MATERIALS & MEASUREMENT METHOD: Proliferation trend of human mesenchymal stem cells on Biocoral(®) scaffolds was measured by a resazurin-based assay here optimized for 3D cultures. The method allows to noninvasively follow the cell proliferation on biocorals over 3 weeks with very high reproducibility. CONCLUSION: This reliable method could be a powerful tool in cell-based therapies for cell dose determination.
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spelling pubmed-51379072016-12-28 A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method Divieto, Carla Sassi, Maria Paola Future Sci OA Research Article BACKGROUND: In cell-based therapies, in vitro studies on biomimetic cell–scaffold constructs can facilitate the determination of the cell dose, a key factor in guaranteeing the effectiveness of the treatment. However, highly porous scaffolds do not allow a nondestructive evaluation of the cell number. Our objective was to develop a nondestructive method for human mesenchymal stem cells dose evaluation in a highly porous scaffold for bone regeneration. MATERIALS & MEASUREMENT METHOD: Proliferation trend of human mesenchymal stem cells on Biocoral(®) scaffolds was measured by a resazurin-based assay here optimized for 3D cultures. The method allows to noninvasively follow the cell proliferation on biocorals over 3 weeks with very high reproducibility. CONCLUSION: This reliable method could be a powerful tool in cell-based therapies for cell dose determination. Future Science Ltd 2015-11-01 /pmc/articles/PMC5137907/ /pubmed/28031911 http://dx.doi.org/10.4155/fso.15.58 Text en © Divieto & Sassi This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Divieto, Carla
Sassi, Maria Paola
A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title_full A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title_fullStr A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title_full_unstemmed A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title_short A first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
title_sort first approach to evaluate the cell dose in highly porous scaffolds by using a nondestructive metabolic method
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137907/
https://www.ncbi.nlm.nih.gov/pubmed/28031911
http://dx.doi.org/10.4155/fso.15.58
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