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Microporous scaffolds from poly(lactide-co-epsilon-caprolactone) composites with hydroxyapatite and tricalcium phosphates using supercritical CO2 for bone tissue engineering

Aydin, HM; Piskin, E; Calimli, A


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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/94137</identifier>
  <creators>
    <creator>
      <creatorName>Aydin, HM</creatorName>
      <givenName>HM</givenName>
      <familyName>Aydin</familyName>
    </creator>
    <creator>
      <creatorName>Piskin, E</creatorName>
      <givenName>E</givenName>
      <familyName>Piskin</familyName>
    </creator>
    <creator>
      <creatorName>Calimli, A</creatorName>
      <givenName>A</givenName>
      <familyName>Calimli</familyName>
    </creator>
  </creators>
  <titles>
    <title>Microporous Scaffolds From Poly(Lactide-Co-Epsilon-Caprolactone) Composites With Hydroxyapatite And Tricalcium Phosphates Using Supercritical Co2 For Bone Tissue Engineering</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2004</publicationYear>
  <dates>
    <date dateType="Issued">2004-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/94137</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1177/0883911504046688</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">A copolymer of L-lactide and epsilon-caprolactone (M-n: 73,523, M-w: 127,990 and PI: 1.74) was synthesized by ring-opening polymerization and confirmed by FTIR, H-1-NMR and DSC. The copolymer ratio of L-lactide to epsilon-caprolactone, determined by H-1-NMR, was 89/11. Specific amounts of hydroxyapatite or tricalcium phosphate were blended in the copolymer matrix to form new composites. Films were made by solvent casting the copolymer and the composite materials. The films were subjected to supercritical CO2 at 3300 psi and 70degreesC to create porous structures. The pore sizes were in the range of 40-80 mum. The porous films (both copolymer and composite) degraded in Ringer solutions much faster than corresponding untreated nonporous films.</description>
  </descriptions>
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