Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/5783
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dc.contributor.authorBensadoun, Jean-Charles-
dc.contributor.authorPereira de Almeida, Luis-
dc.contributor.authorFine, Eric G.-
dc.contributor.authorTseng, Jack L.-
dc.contributor.authorDéglon, Nicole-
dc.contributor.authorAebischer, Patrick-
dc.date.accessioned2008-09-26T17:41:41Z-
dc.date.available2008-09-26T17:41:41Z-
dc.date.issued2003en_US
dc.identifier.citationJournal of Controlled Release. 87:1-3 (2003) 107-115en_US
dc.identifier.urihttps://hdl.handle.net/10316/5783-
dc.description.abstractGlial 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.en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6T3D-47903SW-1/1/6e1fe20b6e31450aa7a03ca03fb4fc3fen_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectCNS deliveryen_US
dc.subjectNeurotrophic factorsen_US
dc.subjectPolymer rodsen_US
dc.subjectCell encapsulationen_US
dc.subjectLentiviral vectorsen_US
dc.titleComparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectorsen_US
dc.typearticleen_US
dc.identifier.doi10.1016/S0168-3659(02)00353-X-
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCIBB - Center for Innovative Biomedicine and Biotechnology-
crisitem.author.orcid0000-0001-5831-3307-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
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