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Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial Activity
[Image: see text] The rational approach motivated the design of novel antimicrobial silver and silver–copper bimetallic nanoparticles contained within zeolitic imidazolate framework-8 supported on graphene oxide (GO), Ag@ZIF-8@GO, and AgCu@ZIF8@GO. In the resultant composites, ZIF-8 was able to prev...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203699/ https://www.ncbi.nlm.nih.gov/pubmed/32391448 http://dx.doi.org/10.1021/acsomega.9b03215 |
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author | Makhetha, Thollwana Andretta Ray, Sekhar Chandra Moutloali, Richard Motlhaletsi |
author_facet | Makhetha, Thollwana Andretta Ray, Sekhar Chandra Moutloali, Richard Motlhaletsi |
author_sort | Makhetha, Thollwana Andretta |
collection | PubMed |
description | [Image: see text] The rational approach motivated the design of novel antimicrobial silver and silver–copper bimetallic nanoparticles contained within zeolitic imidazolate framework-8 supported on graphene oxide (GO), Ag@ZIF-8@GO, and AgCu@ZIF8@GO. In the resultant composites, ZIF-8 was able to prevent the stacking of GO sheets and also acted as a carrier for the nanoparticles within its cavities. GO, on the other hand, acted as an anchoring support enabling uniform dispersion of the nanocomposites, thus eliminating their aggregation. The morphological and physicochemical properties of the composites were determined through a variety of characterization techniques, for example, transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectroscopy, p-X-ray diffraction (XRD), nitrogen sorption, and X-ray photoelectron spectroscopy (XPS). The energy-dispersive system and XPS supplied evidence of the presence of all expected components in the composites. The XRD provided proof of a crystalline, distorted ZIF-8 structure. Ag@ZIF8@GO and Ag–Cu@ZIF-8@GO composites were effective against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria as determined by the disc diffusion method. The role of silver nanoparticles (AgNPs) in the antibacterial activity of both Ag@ZIF8@GO and AgCu@ZIF8@GO was highlighted as crucial in the probable pathway in the antimicrobial activity of the composites. |
format | Online Article Text |
id | pubmed-7203699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-72036992020-05-08 Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial Activity Makhetha, Thollwana Andretta Ray, Sekhar Chandra Moutloali, Richard Motlhaletsi ACS Omega [Image: see text] The rational approach motivated the design of novel antimicrobial silver and silver–copper bimetallic nanoparticles contained within zeolitic imidazolate framework-8 supported on graphene oxide (GO), Ag@ZIF-8@GO, and AgCu@ZIF8@GO. In the resultant composites, ZIF-8 was able to prevent the stacking of GO sheets and also acted as a carrier for the nanoparticles within its cavities. GO, on the other hand, acted as an anchoring support enabling uniform dispersion of the nanocomposites, thus eliminating their aggregation. The morphological and physicochemical properties of the composites were determined through a variety of characterization techniques, for example, transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectroscopy, p-X-ray diffraction (XRD), nitrogen sorption, and X-ray photoelectron spectroscopy (XPS). The energy-dispersive system and XPS supplied evidence of the presence of all expected components in the composites. The XRD provided proof of a crystalline, distorted ZIF-8 structure. Ag@ZIF8@GO and Ag–Cu@ZIF-8@GO composites were effective against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria as determined by the disc diffusion method. The role of silver nanoparticles (AgNPs) in the antibacterial activity of both Ag@ZIF8@GO and AgCu@ZIF8@GO was highlighted as crucial in the probable pathway in the antimicrobial activity of the composites. American Chemical Society 2020-04-24 /pmc/articles/PMC7203699/ /pubmed/32391448 http://dx.doi.org/10.1021/acsomega.9b03215 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Makhetha, Thollwana Andretta Ray, Sekhar Chandra Moutloali, Richard Motlhaletsi Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial Activity |
title | Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle
of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial
Activity |
title_full | Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle
of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial
Activity |
title_fullStr | Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle
of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial
Activity |
title_full_unstemmed | Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle
of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial
Activity |
title_short | Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle
of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial
Activity |
title_sort | zeolitic imidazolate framework-8-encapsulated nanoparticle
of ag/cu composites supported on graphene oxide: synthesis and antibacterial
activity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203699/ https://www.ncbi.nlm.nih.gov/pubmed/32391448 http://dx.doi.org/10.1021/acsomega.9b03215 |
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