Porous hybrid structures based on P(DLLA-co-TMC) and collagen for tissue engineering of small-diameter blood vessels
Poly (D,L‐lactide)‐7co‐(1,3‐trimethylene carbonate) [P(DLLA‐co‐TMC)] (83 mol % DLLA) was used to produce matrices suitable for tissue engineering of small‐diameter blood vessels. The copolymer was processed into tubular structures with a porosity of ∼98% by melt spinning and fiber winding, thus obvi...
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Veröffentlicht in: | Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2006-11, Vol.79B (2), p.425-434 |
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container_title | Journal of biomedical materials research. Part B, Applied biomaterials |
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creator | Buttafoco, Laura Boks, Niels P. Engbers-Buijtenhuijs, Paula Grijpma, Dirk W. Poot, Andre A. Dijkstra, Piet J. Vermes, Istvan Feijen, Jan |
description | Poly (D,L‐lactide)‐7co‐(1,3‐trimethylene carbonate) [P(DLLA‐co‐TMC)] (83 mol % DLLA) was used to produce matrices suitable for tissue engineering of small‐diameter blood vessels. The copolymer was processed into tubular structures with a porosity of ∼98% by melt spinning and fiber winding, thus obviating the need of organic solvents that may compromise subsequent cell culture. Unexpectedly, incubation in culture medium at 37°C resulted in disconnection of the contact points between the polymer fibers. To improve the structural stability of these P(DLLA‐co‐TMC) scaffolds, a collagen microsponge was formed inside the pores of the synthetic matrix by dip coating and freeze drying. Hybrid structures with a porosity of 97% and an average pore size of 102 μm were obtained. Structural stability was preserved during incubation in culture medium at 37°C. Smooth‐muscle cells (SMCs) were seeded in these hybrid scaffolds and cultured under pulsatile flow conditions in a bioreactor (120 beats/min, 80–120 mmHg). After 7 days of culture in a dynamic environment viable SMCs were homogeneously distributed throughout the constructs, which were five times stronger and stiffer than noncultured scaffolds. Values for yield stress (2.8 ± 0.6 MPa), stiffness (1.6 ± 0.4 MPa), and yield strain (120% ± 20%) were comparable to those of the human artery mesenterica. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 |
doi_str_mv | 10.1002/jbm.b.30557 |
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The copolymer was processed into tubular structures with a porosity of ∼98% by melt spinning and fiber winding, thus obviating the need of organic solvents that may compromise subsequent cell culture. Unexpectedly, incubation in culture medium at 37°C resulted in disconnection of the contact points between the polymer fibers. To improve the structural stability of these P(DLLA‐co‐TMC) scaffolds, a collagen microsponge was formed inside the pores of the synthetic matrix by dip coating and freeze drying. Hybrid structures with a porosity of 97% and an average pore size of 102 μm were obtained. Structural stability was preserved during incubation in culture medium at 37°C. Smooth‐muscle cells (SMCs) were seeded in these hybrid scaffolds and cultured under pulsatile flow conditions in a bioreactor (120 beats/min, 80–120 mmHg). After 7 days of culture in a dynamic environment viable SMCs were homogeneously distributed throughout the constructs, which were five times stronger and stiffer than noncultured scaffolds. Values for yield stress (2.8 ± 0.6 MPa), stiffness (1.6 ± 0.4 MPa), and yield strain (120% ± 20%) were comparable to those of the human artery mesenterica. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.30557</identifier><identifier>PMID: 16649175</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Blood Vessel Prosthesis ; Cells, Cultured ; Collagen ; Dioxanes ; Humans ; lactate ; melt spinning ; Myocytes, Smooth Muscle ; Polyesters ; Porosity ; Tissue Engineering ; trimethylene carbonate</subject><ispartof>Journal of biomedical materials research. Part B, Applied biomaterials, 2006-11, Vol.79B (2), p.425-434</ispartof><rights>Copyright © 2006 Wiley Periodicals, Inc.</rights><rights>(c) 2006 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4357-48fb9be1b14e0c211b8aa4d4e2e8aa1059562a21dec7d5d04497996a41623c73</citedby><cites>FETCH-LOGICAL-c4357-48fb9be1b14e0c211b8aa4d4e2e8aa1059562a21dec7d5d04497996a41623c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbm.b.30557$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbm.b.30557$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16649175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Buttafoco, Laura</creatorcontrib><creatorcontrib>Boks, Niels P.</creatorcontrib><creatorcontrib>Engbers-Buijtenhuijs, Paula</creatorcontrib><creatorcontrib>Grijpma, Dirk W.</creatorcontrib><creatorcontrib>Poot, Andre A.</creatorcontrib><creatorcontrib>Dijkstra, Piet J.</creatorcontrib><creatorcontrib>Vermes, Istvan</creatorcontrib><creatorcontrib>Feijen, Jan</creatorcontrib><title>Porous hybrid structures based on P(DLLA-co-TMC) and collagen for tissue engineering of small-diameter blood vessels</title><title>Journal of biomedical materials research. Part B, Applied biomaterials</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Poly (D,L‐lactide)‐7co‐(1,3‐trimethylene carbonate) [P(DLLA‐co‐TMC)] (83 mol % DLLA) was used to produce matrices suitable for tissue engineering of small‐diameter blood vessels. The copolymer was processed into tubular structures with a porosity of ∼98% by melt spinning and fiber winding, thus obviating the need of organic solvents that may compromise subsequent cell culture. Unexpectedly, incubation in culture medium at 37°C resulted in disconnection of the contact points between the polymer fibers. To improve the structural stability of these P(DLLA‐co‐TMC) scaffolds, a collagen microsponge was formed inside the pores of the synthetic matrix by dip coating and freeze drying. Hybrid structures with a porosity of 97% and an average pore size of 102 μm were obtained. Structural stability was preserved during incubation in culture medium at 37°C. Smooth‐muscle cells (SMCs) were seeded in these hybrid scaffolds and cultured under pulsatile flow conditions in a bioreactor (120 beats/min, 80–120 mmHg). After 7 days of culture in a dynamic environment viable SMCs were homogeneously distributed throughout the constructs, which were five times stronger and stiffer than noncultured scaffolds. Values for yield stress (2.8 ± 0.6 MPa), stiffness (1.6 ± 0.4 MPa), and yield strain (120% ± 20%) were comparable to those of the human artery mesenterica. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006</description><subject>Blood Vessel Prosthesis</subject><subject>Cells, Cultured</subject><subject>Collagen</subject><subject>Dioxanes</subject><subject>Humans</subject><subject>lactate</subject><subject>melt spinning</subject><subject>Myocytes, Smooth Muscle</subject><subject>Polyesters</subject><subject>Porosity</subject><subject>Tissue Engineering</subject><subject>trimethylene carbonate</subject><issn>1552-4973</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EoqVw4o58QqAqi-34IzmWBUqrLFTqSj1a_pgsKUnc2gmw_30Nuy03OM0cfvNm3jyEXlKyoISwd9d2WNhFSYRQj9AhFYIVvK7o44delQfoWUrXGZZElE_RAZWS11SJQzRdhBjmhL9tbew8TlOc3TRHSNiaBB6HEV-8-dA0J4ULxXq1fIvN6LELfW82MOI2RDx1Kc2AYdx0I0Dsxg0OLU6D6fvCd2aACSK2fQge_4CUoE_P0ZPW9Ale7OsRWn_6uF5-Lpqvp2fLk6ZwvBSq4FVrawvUUg7EMUptZQz3HBjkhhJRC8kMox6c8sITnq3WtTScSlY6VR6h1zvZmxhuZ0iTHrrkIJ8-QvasZVWLvIj-F2REEFEpmcHjHehiSClCq29iN5i41ZTo32HoHIa2-k8YmX61l53tAP4vu_9-BugO-Nn1sP2Xlj5_v7oXLXYzXZrg18OMid-1VKUS-urLqb4U68tmdc70VXkHls-kDA</recordid><startdate>200611</startdate><enddate>200611</enddate><creator>Buttafoco, Laura</creator><creator>Boks, Niels P.</creator><creator>Engbers-Buijtenhuijs, Paula</creator><creator>Grijpma, Dirk W.</creator><creator>Poot, Andre A.</creator><creator>Dijkstra, Piet J.</creator><creator>Vermes, Istvan</creator><creator>Feijen, Jan</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200611</creationdate><title>Porous hybrid structures based on P(DLLA-co-TMC) and collagen for tissue engineering of small-diameter blood vessels</title><author>Buttafoco, Laura ; Boks, Niels P. ; Engbers-Buijtenhuijs, Paula ; Grijpma, Dirk W. ; Poot, Andre A. ; Dijkstra, Piet J. ; Vermes, Istvan ; Feijen, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4357-48fb9be1b14e0c211b8aa4d4e2e8aa1059562a21dec7d5d04497996a41623c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Blood Vessel Prosthesis</topic><topic>Cells, Cultured</topic><topic>Collagen</topic><topic>Dioxanes</topic><topic>Humans</topic><topic>lactate</topic><topic>melt spinning</topic><topic>Myocytes, Smooth Muscle</topic><topic>Polyesters</topic><topic>Porosity</topic><topic>Tissue Engineering</topic><topic>trimethylene carbonate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buttafoco, Laura</creatorcontrib><creatorcontrib>Boks, Niels P.</creatorcontrib><creatorcontrib>Engbers-Buijtenhuijs, Paula</creatorcontrib><creatorcontrib>Grijpma, Dirk W.</creatorcontrib><creatorcontrib>Poot, Andre A.</creatorcontrib><creatorcontrib>Dijkstra, Piet J.</creatorcontrib><creatorcontrib>Vermes, Istvan</creatorcontrib><creatorcontrib>Feijen, Jan</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buttafoco, Laura</au><au>Boks, Niels P.</au><au>Engbers-Buijtenhuijs, Paula</au><au>Grijpma, Dirk W.</au><au>Poot, Andre A.</au><au>Dijkstra, Piet J.</au><au>Vermes, Istvan</au><au>Feijen, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Porous hybrid structures based on P(DLLA-co-TMC) and collagen for tissue engineering of small-diameter blood vessels</atitle><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2006-11</date><risdate>2006</risdate><volume>79B</volume><issue>2</issue><spage>425</spage><epage>434</epage><pages>425-434</pages><issn>1552-4973</issn><eissn>1552-4981</eissn><abstract>Poly (D,L‐lactide)‐7co‐(1,3‐trimethylene carbonate) [P(DLLA‐co‐TMC)] (83 mol % DLLA) was used to produce matrices suitable for tissue engineering of small‐diameter blood vessels. The copolymer was processed into tubular structures with a porosity of ∼98% by melt spinning and fiber winding, thus obviating the need of organic solvents that may compromise subsequent cell culture. Unexpectedly, incubation in culture medium at 37°C resulted in disconnection of the contact points between the polymer fibers. To improve the structural stability of these P(DLLA‐co‐TMC) scaffolds, a collagen microsponge was formed inside the pores of the synthetic matrix by dip coating and freeze drying. Hybrid structures with a porosity of 97% and an average pore size of 102 μm were obtained. Structural stability was preserved during incubation in culture medium at 37°C. Smooth‐muscle cells (SMCs) were seeded in these hybrid scaffolds and cultured under pulsatile flow conditions in a bioreactor (120 beats/min, 80–120 mmHg). After 7 days of culture in a dynamic environment viable SMCs were homogeneously distributed throughout the constructs, which were five times stronger and stiffer than noncultured scaffolds. Values for yield stress (2.8 ± 0.6 MPa), stiffness (1.6 ± 0.4 MPa), and yield strain (120% ± 20%) were comparable to those of the human artery mesenterica. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16649175</pmid><doi>10.1002/jbm.b.30557</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Blood Vessel Prosthesis Cells, Cultured Collagen Dioxanes Humans lactate melt spinning Myocytes, Smooth Muscle Polyesters Porosity Tissue Engineering trimethylene carbonate |
title | Porous hybrid structures based on P(DLLA-co-TMC) and collagen for tissue engineering of small-diameter blood vessels |
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