Source:http://linkedlifedata.com/resource/pubmed/id/17305394
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-3-12
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pubmed:abstractText |
Degradable shape-memory polymer networks intended for biomedical applications were synthesized from oligo[(epsilon-hydroxycaproate)-co-glycolate]dimethacrylates with glycolate contents between 0 and 30 mol % using a photopolymerization process. In addition AB copolymer networks were prepared by adding 60 wt % n-butyl acrylate as comonomer. All synthesized polymer networks are semicrystalline at room temperature. A melting transition T(m) between 18 and 53 degrees C which can be used as switching transition for the shape-memory effect can be attributed to the crystalline poly(epsilon-hydroxycaproate) phase. At temperatures below T(m) the elastic properties are dominated by these physical cross-links. At temperatures higher than T(m) the E modulus of the amorphous polymer networks is lowered by up to 2 orders of magnitude, depending on the chemical cross-link density. Copolymer networks based on macrodimethacrylates with a M(n) of up to 13,500 g x mol(-1) and a maximum glycolate content of 21 mol % show quantitative strain recovery rates in stress-controlled cyclic thermomechanical experiments. Hydrolytic degradation experiments of polymer networks performed in phosphate buffer solution at 37 degrees C show that the degradation rate can be accelerated by increasing the glycolate content and decelerated by the incorporation of n-butyl acrylate.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acrylates,
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Gels,
http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances,
http://linkedlifedata.com/resource/pubmed/chemical/Methacrylates,
http://linkedlifedata.com/resource/pubmed/chemical/Polyesters,
http://linkedlifedata.com/resource/pubmed/chemical/Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Water,
http://linkedlifedata.com/resource/pubmed/chemical/n-butyl acrylate
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1525-7797
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1018-27
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pubmed:meshHeading |
pubmed-meshheading:17305394-Acrylates,
pubmed-meshheading:17305394-Biocompatible Materials,
pubmed-meshheading:17305394-Calorimetry, Differential Scanning,
pubmed-meshheading:17305394-Cross-Linking Reagents,
pubmed-meshheading:17305394-Gels,
pubmed-meshheading:17305394-Hydrogen-Ion Concentration,
pubmed-meshheading:17305394-Hydrolysis,
pubmed-meshheading:17305394-Macromolecular Substances,
pubmed-meshheading:17305394-Methacrylates,
pubmed-meshheading:17305394-Models, Statistical,
pubmed-meshheading:17305394-Polyesters,
pubmed-meshheading:17305394-Polymers,
pubmed-meshheading:17305394-Temperature,
pubmed-meshheading:17305394-Water
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pubmed:year |
2007
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pubmed:articleTitle |
Shape-memory polymer networks from oligo[(epsilon-hydroxycaproate)-co-glycolate]dimethacrylates and butyl acrylate with adjustable hydrolytic degradation rate.
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pubmed:affiliation |
GKSS Research Center, Center for Biomaterial Development, Institute of Polymer Research, 14513 Teltow, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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