Gellan Gum-based luminal fillers for peripheral nerve regeneration: an in vivo study in the rat sciatic nerve repair model

Peripheral nerve injuries (PNI) resulting in a gap to be bridged between the transected nerve ends are commonly reconstructed with autologous nerve tissue, but there is a need for valuable alternatives. This experimental work considers the innovative use of the biomaterial Gellan Gum (GG) as a lumin...

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Detalhes bibliográficos
Autor principal: Carvalho, C. R. (author)
Outros Autores: Wrobel, S. (author), Meyer, C. (author), Branderberger, C. (author), Cengiz, I. F. (author), López-Cebral, R. (author), Silva-Correia, J. (author), Ronchi, J. (author), Reis, R. L. (author), Grothe, C. (author), Oliveira, J. M. (author), Haastert-Talini, K. (author)
Formato: article
Idioma:eng
Publicado em: 2018
Assuntos:
Texto completo:https://hdl.handle.net/1822/56319
País:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/56319
Descrição
Resumo:Peripheral nerve injuries (PNI) resulting in a gap to be bridged between the transected nerve ends are commonly reconstructed with autologous nerve tissue, but there is a need for valuable alternatives. This experimental work considers the innovative use of the biomaterial Gellan Gum (GG) as a luminal filler for nerve guidance channels made from chitosan with a 5% degree of acetylation. The engineered constructs should remodel the structural support given to regenerating axons by the so-called bands of Büngner. Four different GG formulations were produced by combining varying amounts of High-Acyl GG (HA-GG) and Methacrylated GG (MA-GG). The effective porosity of the freeze-dried networks was analysed by SEM and micro-CT 3D reconstructions, while the degradation and swelling abilities were characterized in vitro for up to 30 days. The metabolic activity and viability of immortalized Schwann cells seeded onto the freeze-dried networks were also evaluated. Finally, the developed hydrogel formulations were freezedried within the chitosan nerve guides and implanted in a 10 mm rat sciatic nerve defect. Functional and histomorphological analyses after 3, 6, and 12 weeks in vivo revealed that although it did not result in improved nerve regeneration, the NGC25:75 formulations could provide a basis for further development of GG scaffolds as luminal fillers for hollow nerve guidance channels.