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 in | Stem Cells International Vol. 2015; no. 2015; pp. 467 - 474-041 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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. |
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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 |
AuthorAffiliation_xml | – name: 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 – name: 2 Université Paris 13, Sorbonne Paris Cité, Laboratoire CSPBAT, UMR CNRS 7244, 74 rue Marcel Cachin, 93017 Bobigny, France – name: 4 Ecole du Val de Grâce, 1 place Alphonse Lavéran, 75005 Paris Cedex, France – name: 1 Université Paris 13, Sorbonne Paris Cité, Laboratoire CSPBAT, UMR CNRS 7244, 99 avenue JB Clément, 93430 Villetaneuse, France |
Author_xml | – sequence: 1 fullname: Rohman, Géraldine – sequence: 2 fullname: Lataillade, Jean-Jacques – sequence: 3 fullname: Peltzer, Juliette – sequence: 4 fullname: Poirier, Florence – sequence: 5 fullname: Consalus, Anne – sequence: 6 fullname: Radu Bostan, Gabriela – sequence: 7 fullname: Changotade, Sylvie – sequence: 8 fullname: Lutomski, Didier |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26161094$$D View this record in MEDLINE/PubMed https://hal.science/hal-01216611$$DView record in HAL |
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Cites_doi | 10.1002/pola.10096 10.1039/b803718n 10.1002/jbm.a.30834 10.1016/j.biomaterials.2003.10.086 10.3727/096368912x652968 10.1002/mabi.200500114 10.1016/j.progpolymsci.2010.04.002 10.1016/j.msec.2014.05.056 10.1155/2013/312501 10.1002/jbm.a.30669 10.1016/S1369-7021(10)70014-6 10.1002/jbm.10204 10.1002/(sici)1097-4628(19970502)64:560;957::aid-app1562;3.0.co;2-q 10.3171/2010.9.FOCUS10201 10.1111/j.1582-4934.2010.01224.x 10.1155/2012/980353 10.1002/jbm.a.34490 10.1177/10454411010120010501 10.1016/j.polymdegradstab.2012.04.008 10.1021/bm401911p 10.1002/pola.23744 10.1016/j.porgcoat.2005.11.007 |
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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StartPage | 467 |
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 https://www.proquest.com/docview/1709481979 https://search.proquest.com/docview/1695756987 https://search.proquest.com/docview/1762352636 https://hal.science/hal-01216611 https://pubmed.ncbi.nlm.nih.gov/PMC4464009 https://doaj.org/article/5545f4c3125344cd8d7137b36845481b |
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