Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.22/3882
Título: Ibuprofen-loaded poly(trimethylene carbonate-co-ϵ- caprolactone) electrospun fibres for nerve regeneration
Autor: Pires, Liliana
Guarino, Vincenzo
Oliveira, Maria J.
Ribeiro, Cristina C.
Barbosa, Mário A.
Ambrosio, Luigi
Pêgo, A. P.
Palavras-chave: Confocal Raman microscopy
Drug delivery
Electrospinning
Ibuprofen
Inflammation
Nerve guide
Data: 2013
Editora: Wiley-Blackwell
Relatório da Série N.º: Journal of Tissue Engineering and Regenerative Medicine; Vol. 8, Issue 3
Resumo: The development of scaffolds that combine the delivery of drugs with the physical support provided by electrospun fibres holds great potential in the field of nerve regeneration. Here it is proposed the incorporation of ibuprofen, a well-known non-steroidal anti-inflammatory drug, in electrospun fibres of the statistical copolymer poly(trimethylene carbonate-co-ε-caprolactone) [P(TMC-CL)] to serve as a drug delivery system to enhance axonal regeneration in the context of a spinal cord lesion, by limiting the inflammatory response. P(TMC-CL) fibres were electrospun from mixtures of dichloromethane (DCM) and dimethylformamide (DMF). The solvent mixture applied influenced fibre morphology, as well as mean fibre diameter, which decreased as the DMF content in solution increased. Ibuprofen-loaded fibres were prepared from P(TMC-CL) solutions containing 5% ibuprofen (w/w of polymer). Increasing drug content to 10% led to jet instability, resulting in the formation of a less homogeneous fibrous mesh. Under the optimized conditions, drug-loading efficiency was above 80%. Confocal Raman mapping showed no preferential distribution of ibuprofen in P(TMC-CL) fibres. Under physiological conditions ibuprofen was released in 24h. The release process being diffusion-dependent for fibres prepared from DCM solutions, in contrast to fibres prepared from DCM-DMF mixtures where burst release occurred. The biological activity of the drug released was demonstrated using human-derived macrophages. The release of prostaglandin E2 to the cell culture medium was reduced when cells were incubated with ibuprofen-loaded P(TMC-CL) fibres, confirming the biological significance of the drug delivery strategy presented. Overall, this study constitutes an important contribution to the design of a P(TMC-CL)-based nerve conduit with anti-inflammatory properties.
Peer review: yes
URI: http://hdl.handle.net/10400.22/3882
ISSN: 1932-6254
1932-7005
Versão do Editor: http://onlinelibrary.wiley.com/doi/10.1002/term.1792/abstract
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