Preliminary In Vitro Assessment of Stem Cell Compatibility with Cross-Linked Poly( -caprolactone urethane) Scaffolds Designed through High Internal Phase Emulsions

By using a high internal phase emulsion process, elastomeric poly(ε-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 μm to 1800 μm and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excel...

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Published inStem Cells International Vol. 2015; no. 2015; pp. 467 - 474-041
Main Authors Rohman, Géraldine, Lataillade, Jean-Jacques, Peltzer, Juliette, Poirier, Florence, Consalus, Anne, Radu Bostan, Gabriela, Changotade, Sylvie, Lutomski, Didier
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Limiteds 01.01.2015
Hindawi Publishing Corporation
John Wiley & Sons, Inc
Hindawi Limited
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Abstract By using a high internal phase emulsion process, elastomeric poly(ε-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 μm to 1800 μm and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
AbstractList By using a high internal phase emulsion process, elastomeric poly(ε-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 μm to 1800 μm and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
By using a high internal phase emulsion process, elastomeric poly([straight epsilon]-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 μm to 1800 μm and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
By using a high internal phase emulsion process, elastomeric poly( ε -caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150  μ m to 1800  μ m and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
By using a high internal phase emulsion process, elastomeric poly (ζ-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 µm to 1800 µm and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
By using a high internal phase emulsion process, elastomeric poly( epsilon -caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below 150 [mu] m to 1800 [mu] m and a porosity of 86% making them suitable for bone tissue engineering applications. Moreover, the pores appeared to be excellently interconnected, promoting cellularization and future bone ingrowth. This study evaluated the in vitro cytotoxicity of the PCLU scaffolds towards human mesenchymal stem cells (hMSCs) through the evaluation of cell viability and metabolic activity during extract test and indirect contact test at the beginning of the scaffold lifetime. Both tests demonstrated that PCLU scaffolds did not induce any cytotoxic response. Finally, direct interaction of hMSCs and PCLU scaffolds showed that PCLU scaffolds were suitable for supporting the hMSCs adhesion and that the cells were well spread over the pore walls. We conclude that PCLU scaffolds may be a good candidate for bone tissue regeneration applications using hMSCs.
Audience Academic
Author Radu Bostan, Gabriela
Lutomski, Didier
Changotade, Sylvie
Poirier, Florence
Peltzer, Juliette
Lataillade, Jean-Jacques
Rohman, Géraldine
Consalus, Anne
AuthorAffiliation 3 Institut de Recherche Biomédicale des Armées, Unité de Thérapie Cellulaire et Réparation Tissulaire, Site du Centre de Transfusion Sanguine des Armées “Jean Julliard” de Clamart, BP 73 91223 Brétigny-sur-Orge Cedex, France
4 Ecole du Val de Grâce, 1 place Alphonse Lavéran, 75005 Paris Cedex, France
1 Université Paris 13, Sorbonne Paris Cité, Laboratoire CSPBAT, UMR CNRS 7244, 99 avenue JB Clément, 93430 Villetaneuse, France
2 Université Paris 13, Sorbonne Paris Cité, Laboratoire CSPBAT, UMR CNRS 7244, 74 rue Marcel Cachin, 93017 Bobigny, France
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– name: 2 Université Paris 13, Sorbonne Paris Cité, Laboratoire CSPBAT, UMR CNRS 7244, 74 rue Marcel Cachin, 93017 Bobigny, France
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ContentType Journal Article
Copyright Copyright © 2015 Sylvie Changotade et al.
COPYRIGHT 2015 John Wiley & Sons, Inc.
Copyright © 2015 Sylvie Changotade et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Distributed under a Creative Commons Attribution 4.0 International License
Copyright © 2015 Sylvie Changotade et al. 2015
Copyright_xml – notice: Copyright © 2015 Sylvie Changotade et al.
– notice: COPYRIGHT 2015 John Wiley & Sons, Inc.
– notice: Copyright © 2015 Sylvie Changotade et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
– notice: Distributed under a Creative Commons Attribution 4.0 International License
– notice: Copyright © 2015 Sylvie Changotade et al. 2015
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Snippet By using a high internal phase emulsion process, elastomeric poly(ε-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below...
By using a high internal phase emulsion process, elastomeric poly( ε -caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below...
By using a high internal phase emulsion process, elastomeric poly (ζ-caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from below...
By using a high internal phase emulsion process, elastomeric poly([straight epsilon]-caprolactone urethane) (PCLU) scaffolds were designed with pores size...
By using a high internal phase emulsion process, elastomeric poly( epsilon -caprolactone urethane) (PCLU) scaffolds were designed with pores size ranging from...
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SubjectTerms Biomedical materials
Bone marrow
Bone surgery
Chemical Sciences
Cytotoxicity
Defects
Emulsions
Joint replacement surgery
Mechanical properties
Polyesters
Polymers
Pores
Porosity
Stem cells
Tissue engineering
Urethanes
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Title Preliminary In Vitro Assessment of Stem Cell Compatibility with Cross-Linked Poly( -caprolactone urethane) Scaffolds Designed through High Internal Phase Emulsions
URI https://www.airitilibrary.com/Article/Detail/P20150730003-201512-201612270025-201612270025-467-474-041
https://search.emarefa.net/detail/BIM-1076179
https://dx.doi.org/10.1155/2015/283796
https://www.ncbi.nlm.nih.gov/pubmed/26161094
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https://hal.science/hal-01216611
https://pubmed.ncbi.nlm.nih.gov/PMC4464009
https://doaj.org/article/5545f4c3125344cd8d7137b36845481b
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