<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>Bensadoun JC</dc:creator>
  <dc:creator>Pereira de Almeida L</dc:creator>
  <dc:creator>Fine EG</dc:creator>
  <dc:creator>Tseng JL</dc:creator>
  <dc:creator>Déglon N</dc:creator>
  <dc:creator>Aebischer P</dc:creator>
  <dc:date>2003</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Glial cell line-derived neurotrophic factor (GDNF) holds great promise for the treatment of Parkinson's disease. In humans, its intracerebroventricular administration leads to limiting side effects. Direct parenchymal delivery using mechanical means, or cell and gene therapy represent potential alternatives. In the present study, a representative of each of these three approaches, i.e. polymer rods, genetically modified encapsulated cells and lentiviral vectors was analyzed for its ability to release GDNF in the striatum of rats. One week post-surgery, GDNF was detected over a distance of 4 mm with all three methods. At 4 weeks GDNF staining diminished with rods and to a lesser extent with encapsulated cells, whereas it increased with lentiviral vectors. Nanogram range of GDNF was measured with all methods at 1 week. At 4 weeks, GDNF levels decreased significantly with rods, whereas they remained stable with encapsulated cells and lentiviral vectors. We conclude that all three methods investigated allow striatal delivery of GDNF, but the time during which it needs to be released will determine the approach chosen for clinical application.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/278954</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/s0168-3659(02)00353-x</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/12618027</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Journal of controlled release : official journal of the Controlled Release Society. - 2003</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Central Nervous System</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Corpus Striatum</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Drug Delivery Systems</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Genetic Vectors</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Glial Cell Line-Derived Neurotrophic Factor</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Lentivirus</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Nerve Growth Factors</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Polymers</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Rats</dc:subject>
  <dc:title xmlns:ns12="xml" ns12:lang="en">Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
