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VPA/PLGA microfibers produced by coaxial electrospinning for the treatment of central nervous system injury
Reis, K P; Sperling, L E; Teixeira, C; Sommer, L; Colombo, M; Koester, L S; Pranke, P.
  • Reis, K P; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Sperling, L E; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Teixeira, C; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Sommer, L; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Colombo, M; Universidade Federal do Rio Grande do Sul. Programa de Pós-Graduação em Ciências Farmacêuticas. Porto Alegre. BR
  • Koester, L S; Universidade Federal do Rio Grande do Sul. Programa de Pós-Graduação em Ciências Farmacêuticas. Porto Alegre. BR
  • Pranke, P; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
Braz. j. med. biol. res ; 53(4): e8993, 2020. tab, graf
Article in English | LILACS | ID: biblio-1089353
ABSTRACT
The central nervous system shows limited regenerative capacity after injury. Spinal cord injury (SCI) is a devastating traumatic injury resulting in loss of sensory, motor, and autonomic function distal from the level of injury. An appropriate combination of biomaterials and bioactive substances is currently thought to be a promising approach to treat this condition. Systemic administration of valproic acid (VPA) has been previously shown to promote functional recovery in animal models of SCI. In this study, VPA was encapsulated in poly(lactic-co-glycolic acid) (PLGA) microfibers by the coaxial electrospinning technique. Fibers showed continuous and cylindrical morphology, randomly oriented fibers, and compatible morphological and mechanical characteristics for application in SCI. Drug-release analysis indicated a rapid release of VPA during the first day of the in vitro test. The coaxial fibers containing VPA supported adhesion, viability, and proliferation of PC12 cells. In addition, the VPA/PLGA microfibers induced the reduction of PC12 cell viability, as has already been described in the literature. The biomaterials were implanted in rats after SCI. The groups that received the implants did not show increased functional recovery or tissue regeneration compared to the control. These results indicated the cytocompatibility of the VPA/PLGA core-shell microfibers and that it may be a promising approach to treat SCI when combined with other strategies.
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Full text: Available Index: LILACS (Americas) Main subject: Spinal Cord Injuries / Central Nervous System / Valproic Acid / Polylactic Acid-Polyglycolic Acid Copolymer Type of study: Prognostic study Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Rio Grande do Sul/BR

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Full text: Available Index: LILACS (Americas) Main subject: Spinal Cord Injuries / Central Nervous System / Valproic Acid / Polylactic Acid-Polyglycolic Acid Copolymer Type of study: Prognostic study Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2020 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Rio Grande do Sul/BR