Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Biomater Adv ; 161: 213894, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38796956

RESUMO

Engineering of scaffolds for bone regeneration is often inspired by the native extracellular matrix mimicking its composite fibrous structure. In the present study, we used low loadings of diatomite earth (DE) biosilica to improve the bone regeneration potential of gelatin electrospun fibrillar microenvironments. We explored the effect of increasing the DE content from 1 % to 3 % and 5 %, respectively, on the physico-chemical properties of the fibrous scaffolds denoted FG_DE1, FG_DE3, FG_DE5, regarding the aqueous media affinity, stability under simulated physiological conditions, morphology characteristics, and local mechanical properties at the surface. The presence of biosilica generated composite structures with lower swelling degrees and higher stiffness when compared to gelatin fibers. Increasing DE content led to higher Young modulus, while the stability of the protein matrix in PBS, at 37 °C, over 21 was significantly decreased by the presence of diatomite loadings. The best preosteoblast response was obtained for FG_DE3, with enhanced mineralization during the osteogenic differentiation when compared to the control sample without diatomite. 5 % DE in FG_DE5 proved to negatively influence cells' metabolic activity and morphology. Hence, the obtained composite microfibrillar scaffolds might find application as osteoblast-responsive materials for bone tissue engineering.


Assuntos
Gelatina , Osteoblastos , Engenharia Tecidual , Alicerces Teciduais , Gelatina/química , Osteoblastos/efeitos dos fármacos , Osteoblastos/metabolismo , Alicerces Teciduais/química , Engenharia Tecidual/métodos , Animais , Terra de Diatomáceas/química , Osteogênese/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Camundongos , Regeneração Óssea/efeitos dos fármacos , Linhagem Celular , Microambiente Celular/efeitos dos fármacos , Microfibrilas/química , Microfibrilas/metabolismo , Matriz Extracelular/metabolismo , Matriz Extracelular/química , Matriz Extracelular/efeitos dos fármacos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...