Anti-ESBL investigation of chitosan/silver nanocomposites against carbapenem resistant Pseudomonas aeruginosa
Abstract
In the present investigation functional chitosan/silver nanocomposites (CS/Ag NCs) were successfully synthesized and found to possess favorable antibacterial activity against extended spectrum beta-lactasame (ESBL) producing Pseudomonas aeruginosa. Powder X-ray diffraction showed that the obtained CS/Ag NCs are constituted of highly crystalline Ag nanoparticles (NPs) embedded in an amorphous CS matrix material. Transmission electron microscopy (TEM) analysis provided structural information about CS/Ag NCs, revealing the formation of spherical cluster structures constituted of Ag NPs with size ranging from 6 to 18 nm embedded in the amorphous CS matrix. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of Ag NPs and CS/Ag NCs were found to inhibit the ESBL producing P. aeruginosa at 80 mu g/mL (76%) and 50 mu g/mL (92%), respectively. Confocal laser scanning microscope (CLSM) and scanning electron microscopy (SEM) images revealed that P. aeruginosa experienced reduced cell viability and morphological cell membrane damage at desired MIC. The in vivo toxicity effect of Ag NPs and CS/Ag NCs suggested an increased mortality rate when Artemis franciscana were exposed for 24 h to increasing concentrations of Ag NPs and CS/Ag NCs. Anti-ESBL activity and toxicity effect of CS/Ag NCs revealed that these NCs possess promising antibacterial properties to overcome numerous communicable bacterial strains. (C) 2019 Elsevier B.V. All rights reserved.
Más información
Título según WOS: | Anti-ESBL investigation of chitosan/silver nanocomposites against carbapenem resistant Pseudomonas aeruginosa |
Título según SCOPUS: | Anti-ESBL investigation of chitosan/silver nanocomposites against carbapenem resistant Pseudomonas aeruginosa |
Título de la Revista: | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES |
Volumen: | 132 |
Editorial: | Elsevier |
Fecha de publicación: | 2019 |
Página de inicio: | 1221 |
Página final: | 1234 |
Idioma: | English |
DOI: |
10.1016/j.ijbiomac.2019.03.238 |
Notas: | ISI, SCOPUS |