Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site

Detalhes bibliográficos
Autor(a) principal: Pires, L
Data de Publicação: 2017
Outros Autores: Lopes, C, Salvador, D, Rocha, DN, Pêgo, AP
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/120735
Resumo: It is now widely accepted that a therapeutic strategy for spinal cord injury (SCI) demands a multi-target approach. Here we propose the use of an easily implantable bilayer polymeric patch based on poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) that combines physical guidance cues provided by electrospun aligned fibres and the delivery of ibuprofen, as a mean to reduce the inhibitory environment at the lesion site by taming RhoA activation. Bilayer patches comprised a solvent cast film onto which electrospun aligned fibres have been deposited. Both layers were loaded with ibuprofen. In vitro release (37°C, in phosphate buffered saline) of the drug from the loaded scaffolds under sink condition was found to occur in the first 24 h. The released ibuprofen was shown to retain its bioactivity, as indicated by the reduction of RhoA activation when the neuronal-like cell line ND7/23 was challenged with lysophosphatidic acid. Ibuprofen-loaded P(TMC-CL) bilayer scaffolds were successfully implanted in vivo in a dorsal hemisection rat SCI model mediating the reduction of RhoA activation after 5 days of implantation in comparison to plain P(TMC-CL) scaffolds. Immunohistochemical analysis of the tissue shows ßIII tubulin positive cells close to the ibuprofen-loaded patches further supporting the use of this strategy in the context of regeneration after a lesion in the spinal cord.
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spelling Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury siteAnimalsCells, CulturedDioxanes/chemistryDrug Carriers/chemistryDrug Delivery Systems/methodsIbuprofen/administration & dosageMiceMicrotechnologyNanofibers/chemistryNerve Regeneration/drug effectsNerve Regeneration/physiologyPolyesters/chemistryPolymers/chemistryRatsSpinal Cord/drug effectsSpinal Cord/physiologySpinal Cord Injuries/therapyTissue EngineeringTissue Scaffolds/chemistryTransdermal PatchIt is now widely accepted that a therapeutic strategy for spinal cord injury (SCI) demands a multi-target approach. Here we propose the use of an easily implantable bilayer polymeric patch based on poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) that combines physical guidance cues provided by electrospun aligned fibres and the delivery of ibuprofen, as a mean to reduce the inhibitory environment at the lesion site by taming RhoA activation. Bilayer patches comprised a solvent cast film onto which electrospun aligned fibres have been deposited. Both layers were loaded with ibuprofen. In vitro release (37°C, in phosphate buffered saline) of the drug from the loaded scaffolds under sink condition was found to occur in the first 24 h. The released ibuprofen was shown to retain its bioactivity, as indicated by the reduction of RhoA activation when the neuronal-like cell line ND7/23 was challenged with lysophosphatidic acid. Ibuprofen-loaded P(TMC-CL) bilayer scaffolds were successfully implanted in vivo in a dorsal hemisection rat SCI model mediating the reduction of RhoA activation after 5 days of implantation in comparison to plain P(TMC-CL) scaffolds. Immunohistochemical analysis of the tissue shows ßIII tubulin positive cells close to the ibuprofen-loaded patches further supporting the use of this strategy in the context of regeneration after a lesion in the spinal cord.Springer Verlag20172017-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/120735eng0957-453010.1007/s10856-017-5967-7Pires, LLopes, CSalvador, DRocha, DNPêgo, APinfo: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:RCAAP2023-11-29T13:54:12Zoai:repositorio-aberto.up.pt:10216/120735Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:50:16.993465Repositório 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 Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
title Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
spellingShingle Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
Pires, L
Animals
Cells, Cultured
Dioxanes/chemistry
Drug Carriers/chemistry
Drug Delivery Systems/methods
Ibuprofen/administration & dosage
Mice
Microtechnology
Nanofibers/chemistry
Nerve Regeneration/drug effects
Nerve Regeneration/physiology
Polyesters/chemistry
Polymers/chemistry
Rats
Spinal Cord/drug effects
Spinal Cord/physiology
Spinal Cord Injuries/therapy
Tissue Engineering
Tissue Scaffolds/chemistry
Transdermal Patch
title_short Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
title_full Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
title_fullStr Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
title_full_unstemmed Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
title_sort Ibuprofen-loaded fibrous patches-taming inhibition at the spinal cord injury site
author Pires, L
author_facet Pires, L
Lopes, C
Salvador, D
Rocha, DN
Pêgo, AP
author_role author
author2 Lopes, C
Salvador, D
Rocha, DN
Pêgo, AP
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pires, L
Lopes, C
Salvador, D
Rocha, DN
Pêgo, AP
dc.subject.por.fl_str_mv Animals
Cells, Cultured
Dioxanes/chemistry
Drug Carriers/chemistry
Drug Delivery Systems/methods
Ibuprofen/administration & dosage
Mice
Microtechnology
Nanofibers/chemistry
Nerve Regeneration/drug effects
Nerve Regeneration/physiology
Polyesters/chemistry
Polymers/chemistry
Rats
Spinal Cord/drug effects
Spinal Cord/physiology
Spinal Cord Injuries/therapy
Tissue Engineering
Tissue Scaffolds/chemistry
Transdermal Patch
topic Animals
Cells, Cultured
Dioxanes/chemistry
Drug Carriers/chemistry
Drug Delivery Systems/methods
Ibuprofen/administration & dosage
Mice
Microtechnology
Nanofibers/chemistry
Nerve Regeneration/drug effects
Nerve Regeneration/physiology
Polyesters/chemistry
Polymers/chemistry
Rats
Spinal Cord/drug effects
Spinal Cord/physiology
Spinal Cord Injuries/therapy
Tissue Engineering
Tissue Scaffolds/chemistry
Transdermal Patch
description It is now widely accepted that a therapeutic strategy for spinal cord injury (SCI) demands a multi-target approach. Here we propose the use of an easily implantable bilayer polymeric patch based on poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) that combines physical guidance cues provided by electrospun aligned fibres and the delivery of ibuprofen, as a mean to reduce the inhibitory environment at the lesion site by taming RhoA activation. Bilayer patches comprised a solvent cast film onto which electrospun aligned fibres have been deposited. Both layers were loaded with ibuprofen. In vitro release (37°C, in phosphate buffered saline) of the drug from the loaded scaffolds under sink condition was found to occur in the first 24 h. The released ibuprofen was shown to retain its bioactivity, as indicated by the reduction of RhoA activation when the neuronal-like cell line ND7/23 was challenged with lysophosphatidic acid. Ibuprofen-loaded P(TMC-CL) bilayer scaffolds were successfully implanted in vivo in a dorsal hemisection rat SCI model mediating the reduction of RhoA activation after 5 days of implantation in comparison to plain P(TMC-CL) scaffolds. Immunohistochemical analysis of the tissue shows ßIII tubulin positive cells close to the ibuprofen-loaded patches further supporting the use of this strategy in the context of regeneration after a lesion in the spinal cord.
publishDate 2017
dc.date.none.fl_str_mv 2017
2017-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/120735
url https://hdl.handle.net/10216/120735
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0957-4530
10.1007/s10856-017-5967-7
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Springer Verlag
publisher.none.fl_str_mv Springer Verlag
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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