<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Kinnear, Calum</dc:creator>
  <dc:creator>Burnand, David</dc:creator>
  <dc:creator>Clift, Martin J. D.</dc:creator>
  <dc:creator>Kilbinger, Andreas F. M.</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:date>2014</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The functionalization of gold nanorods (GNRs) with polymers is essential for both their colloidal stability and biocompatibility. However, a bilayer of the toxic cationic surfactant cetyl trimethylammonium bromide (CTAB) adsorbed on the nanorods complicates this process. Herein, we report on a strategy for the biocompatible functionalization of GNRs with a hydrophobic polymeric precursor, polyvinyl acetate, which is then transformed into its hydrophilic analogue, polyvinyl alcohol. This polymer was chosen due to its well-established biocompatibility, tunable “stealth” properties, tunable hydrophobicity, and high degree of functionality. The biocompatibility of the functionalized GNRs was tested by exposing them to primary human blood monocyte derived macrophages; the advantages of tunable hydrophobicity were demonstrated with the long-term stable encapsulation of a model hydrophobic drug molecule.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/304152</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304152/files/pet_pab.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304152/files/pet_pab_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/anie.201404100</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Angewandte Chemie International Edition. - 2014, vol. 53, no. 46, p. 12613–12617</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Colloids</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Cytotoxicity</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Gold</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Nanoparticles</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Polymers</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Polyvinyl alcohol as a biocompatible alternative for the passivation of gold nanorods</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
