Combined effect of zinc oxide nano particle incorporated chitosan for better antimicrobial activity towards wound healing

Aim : The aim of the present study was to characterize the zinc oxide nano particle incorporated Chitosan (ZnO-NP-CS) and its antimicrobial activity. Methodology : Zinc oxide nanoparticles (ZnO-NP) were prepared by sol-gel method and Minimum Inhibitory Concentration (MIC), Minimum bactericidal Conce...

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Veröffentlicht in:Journal of environmental biology 2019-07, Vol.40 (4), p.691-697
Hauptverfasser: Visnuvinayagam, S., Murthy, L.N., Jeyakumari, A., Parvathy, U., Anandan, R., Sivaraman, G.K., Ravishankar, C.N.
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Sprache:eng
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Zusammenfassung:Aim : The aim of the present study was to characterize the zinc oxide nano particle incorporated Chitosan (ZnO-NP-CS) and its antimicrobial activity. Methodology : Zinc oxide nanoparticles (ZnO-NP) were prepared by sol-gel method and Minimum Inhibitory Concentration (MIC), Minimum bactericidal Concentration (MBC) and agar well diffusion method was used for the assessment of antibacterial activity of ZnO-NP and ZnO-NP-CS as well. Results : In UV-spectroscopy, blue shiftin wavelength (~365 nm) corresponding to bulk ZnO particles (~385 nm) indicates the nano size. In SEM image, ZnO-NP appeared as nano flake shape and ZnO-NP treated Methicillin resistant Staphylococcus aureus and Pseudomonas aeruginosa (PA) bacteria illustrates leakage of intracellular content, fusion and shrinkage of bacteria, respectively. The MIC of ZnO-NP for most of food pathogens were between 0.01 to 0.1mg. Lower MIC was observed for Vibrio cholerae and Listeria monocytogenes; higher MIC was observed for Bacillus cereus and Pseudomonas aeruginosa. In antibiogram assay, the zone of inhibition of ZnO-NP-CS was equal to commercial antibiotics against Multiple Drug Resistant bacteria. Interpretation : The combined effect of ZnO-NP and chitosan is better than the individual component, i.e., around 5-15 mm wider zone of inhibition than chitosan. ZnO-NP-CS can be a suitable alternative for the treatment of wound infected by multiple drug resistant bacteria.
ISSN:0254-8704
2394-0379
DOI:10.22438/jeb/40/4/MRN-920