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Synergistic effects of Cu-doped ZnO nanoantibiotic against Gram-positive bacterial strains

A viable hydrothermal technique has been explored for the synthesis of copper doped Zinc oxide nanoparticles (Cu-doped ZnO-NPs) based on the precursor’s mixture of Copper-II chloride dihydrate (CuCl(2).2H(2)O), Zinc chloride (ZnCl(2)), and potassium hydroxide (KOH). X-ray diffraction (XRD) reported...

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Detalles Bibliográficos
Autores principales: Khalid, Awais, Ahmad, Pervaiz, Alharthi, Abdulrahman I., Muhammad, Saleh, Khandaker, Mayeen Uddin, Faruque, Mohammad Rashed Iqbal, Din, Israf Ud, Alotaibi, Mshari A., Khan, Abdulhameed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121369/
https://www.ncbi.nlm.nih.gov/pubmed/33989295
http://dx.doi.org/10.1371/journal.pone.0251082
Descripción
Sumario:A viable hydrothermal technique has been explored for the synthesis of copper doped Zinc oxide nanoparticles (Cu-doped ZnO-NPs) based on the precursor’s mixture of Copper-II chloride dihydrate (CuCl(2).2H(2)O), Zinc chloride (ZnCl(2)), and potassium hydroxide (KOH). X-ray diffraction (XRD) reported the hexagonal wurtzite structure of the synthesized Cu-doped ZnO-NPs. The surface morphology is checked via field emission scanning electron microscopy (FE-SEM), whereas, the elemental compositions of the samples were confirmed by Raman, and X-ray photoelectron spectroscopy (XPS), respectively. The as-obtained ZnO-NPs and Cu-doped ZnO-NPs were then tested for their antibacterial activity against clinical isolates of Gram-positive (Staphylococcus aureus, Streptococcus pyogenes) and Gram-negative (Escherichia coli, Klebsiella pneumonia) bacteria via agar well diffusion method. The zone of inhibition (ZOI) for Cu-doped ZnO-NPs was found to be 24 and 19 mm against S. Aureus and S. pyogenes, and 18 and 11 mm against E. coli and K. pneumoniae, respectively. The synthesized Cu-doped ZnO-NPs can thus be found as a potential nano antibiotic against Gram-positive multi-drug resistant bacterial strains.