Preparation and Release of Antibacterial Na-mica-4/Chlorhexidine Nanocomposites

High charge swelling micas are layered silicates used in adsorption of several inorganic and organic species. In this study, we evaluated the adsorption of chlorhexidine digluconate on highly charge mica Na-mica-4. Drug release and antibacterial action against Staphylococcus aureus (S. aureus) and E...

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Detalles Bibliográficos
Autores: Oliveira, Luís H., de Lima, Idglan S., França, Denise B., Moraes, Alan I.S., Fonseca, Maria G., Barreto, Humberto M., Medina Carrasco, Santiago, Osajima, Josy A., da Silva-Filho, Edson C., Orta Cuevas, María del Mar
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/156971
Acceso en línea:https://hdl.handle.net/11441/156971
https://doi.org/10.1016/j.clay.2024.107373
Access Level:acceso abierto
Palabra clave:Antibacterial activity
Chlorhexidine digluconate
High charge swelling mica
Descripción
Sumario:High charge swelling micas are layered silicates used in adsorption of several inorganic and organic species. In this study, we evaluated the adsorption of chlorhexidine digluconate on highly charge mica Na-mica-4. Drug release and antibacterial action against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) using the direct contact test for mica/chlorhexidine hybrids were evaluated. The hybrids were characterized using X-ray diffraction, Fourier transform infrared spectroscopy, zeta potential measurements, CHN elemental analysis, and scanning electron microscopy. Chlorhexidine interacts successfully with the mica surface. The maximum amount of chlorhexidine incorporated was 583 mg g−1, and the characterizations indicated that electrostatic attraction between the protonated amino group of the drug and the negative surface of clay was predominant in the formation of hybrids. Release kinetics study indicated that 80% of the drug release occurred in the first 12 h. The antibacterial test proved to be dependent on the time of chlorhexidine release, reaching 100% inhibition against S. aureus and E. coli after 0.5 h and 6 h, respectively.