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Antibacterial properties of bacterial nanocellulose functionalized with metal nanoparticles via in situ synthesis

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Resumo:[Excerpt] Wound infections are generally caused by pathogens and multidrug-resistant (MDR) strains that render the administration of antibiotics ineffective. An alternative is to treat infected wounds at the initial stage using a fibrous bionanopolymer, bacterial nanocellulose (BNC), functionalized with antimicrobial metal nanoparticles (MNPs). BNC is a highly promising wound dressing due to its very high-water retention capacity (> 99 %) and high porosity. Such properties enable the absorbance of exudates, whilst maintaining the environment moist allowing the exchange of air. However, BNC is absent of antibacterial properties, thus gold (Au), copper (Cu), and copper oxide (Cu2O) NPs were incorporated within the nanofibrous structure of the biopolymer via in situ synthesis.
Autores principais:Melro, Liliana Sofia Silva Ferreira Pinto
Outros Autores:Mehravani, Behnaz; Silva, Gracinda; Ribeiro, Ana Isabel Ferreira; Nicolau, Talita; Dourado, Fernando; Gama, F. M.; Padrão, Jorge; Zille, Andrea
Ano:2023
País:Portugal
Tipo de documento:póster em conferência
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
Descrição
Resumo:[Excerpt] Wound infections are generally caused by pathogens and multidrug-resistant (MDR) strains that render the administration of antibiotics ineffective. An alternative is to treat infected wounds at the initial stage using a fibrous bionanopolymer, bacterial nanocellulose (BNC), functionalized with antimicrobial metal nanoparticles (MNPs). BNC is a highly promising wound dressing due to its very high-water retention capacity (> 99 %) and high porosity. Such properties enable the absorbance of exudates, whilst maintaining the environment moist allowing the exchange of air. However, BNC is absent of antibacterial properties, thus gold (Au), copper (Cu), and copper oxide (Cu2O) NPs were incorporated within the nanofibrous structure of the biopolymer via in situ synthesis.