Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors

Detalhes bibliográficos
Autor(a) principal: Bensadoun, Jean-Charles
Data de Publicação: 2003
Outros Autores: Pereira de Almeida, Luis, Fine, Eric G., Tseng, Jack L., Déglon, Nicole, Aebischer, Patrick
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5783
https://doi.org/10.1016/S0168-3659(02)00353-X
Resumo: 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.
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spelling Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectorsCNS deliveryNeurotrophic factorsPolymer rodsCell encapsulationLentiviral vectorsGlial 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.http://www.sciencedirect.com/science/article/B6T3D-47903SW-1/1/6e1fe20b6e31450aa7a03ca03fb4fc3f2003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5783http://hdl.handle.net/10316/5783https://doi.org/10.1016/S0168-3659(02)00353-XengJournal of Controlled Release. 87:1-3 (2003) 107-115Bensadoun, Jean-CharlesPereira de Almeida, LuisFine, Eric G.Tseng, Jack L.Déglon, NicoleAebischer, Patrickinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-11-06T16:59:38Zoai:estudogeral.uc.pt:10316/5783Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:47:18.241260Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
title Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
spellingShingle Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
Bensadoun, Jean-Charles
CNS delivery
Neurotrophic factors
Polymer rods
Cell encapsulation
Lentiviral vectors
title_short Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
title_full Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
title_fullStr Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
title_full_unstemmed Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
title_sort Comparative study of GDNF delivery systems for the CNS: polymer rods, encapsulated cells, and lentiviral vectors
author Bensadoun, Jean-Charles
author_facet Bensadoun, Jean-Charles
Pereira de Almeida, Luis
Fine, Eric G.
Tseng, Jack L.
Déglon, Nicole
Aebischer, Patrick
author_role author
author2 Pereira de Almeida, Luis
Fine, Eric G.
Tseng, Jack L.
Déglon, Nicole
Aebischer, Patrick
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Bensadoun, Jean-Charles
Pereira de Almeida, Luis
Fine, Eric G.
Tseng, Jack L.
Déglon, Nicole
Aebischer, Patrick
dc.subject.por.fl_str_mv CNS delivery
Neurotrophic factors
Polymer rods
Cell encapsulation
Lentiviral vectors
topic CNS delivery
Neurotrophic factors
Polymer rods
Cell encapsulation
Lentiviral vectors
description 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.
publishDate 2003
dc.date.none.fl_str_mv 2003
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/5783
http://hdl.handle.net/10316/5783
https://doi.org/10.1016/S0168-3659(02)00353-X
url http://hdl.handle.net/10316/5783
https://doi.org/10.1016/S0168-3659(02)00353-X
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Controlled Release. 87:1-3 (2003) 107-115
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dc.format.none.fl_str_mv aplication/PDF
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