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Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles

The interest in the biological synthesis of mono metal nanoparticles has been visible for years. As more attention is also given to the biological methods of synthesizing bimetallic nanoparticles, this work used the Agrimoniae herba extract in order to obtain bimetallic core-shell Cu@Pt nanoparticle...

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Detalles Bibliográficos
Autores principales: Dobrucka, Renata, Dlugaszewska, Jolanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035316/
https://www.ncbi.nlm.nih.gov/pubmed/29991908
http://dx.doi.org/10.1016/j.jsps.2018.02.028
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author Dobrucka, Renata
Dlugaszewska, Jolanta
author_facet Dobrucka, Renata
Dlugaszewska, Jolanta
author_sort Dobrucka, Renata
collection PubMed
description The interest in the biological synthesis of mono metal nanoparticles has been visible for years. As more attention is also given to the biological methods of synthesizing bimetallic nanoparticles, this work used the Agrimoniae herba extract in order to obtain bimetallic core-shell Cu@Pt nanoparticles. The formed core-shell Cu@Pt nanoparticles were characterized by Ultraviolet–Visible (UV–vis), Fourier Transform-Infrared (FT-IR), Scanning electron microscopy (SEM), Transmission Electron Microscopy (TEM) and Atomic Force Microscopy (AFM) measurements. The obtained core-shell Cu@Pt nanoparticles were analysed in terms of their antibacterial activity. It was discovered that the synthesized nanoparticles exhibited maximum activity against gram-negative bacteria E. coli ATCC 25922, S. aureus ATCC 25923, and P. aeruginosa NCTC 6749. The core-shell Cu@Pt nanoparticles also exhibited activity against the yeast C. albicans ATCC 10231 and dermatophytes T. mentagrophytes ATCC 9533.
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spelling pubmed-60353162018-07-10 Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles Dobrucka, Renata Dlugaszewska, Jolanta Saudi Pharm J Original Article The interest in the biological synthesis of mono metal nanoparticles has been visible for years. As more attention is also given to the biological methods of synthesizing bimetallic nanoparticles, this work used the Agrimoniae herba extract in order to obtain bimetallic core-shell Cu@Pt nanoparticles. The formed core-shell Cu@Pt nanoparticles were characterized by Ultraviolet–Visible (UV–vis), Fourier Transform-Infrared (FT-IR), Scanning electron microscopy (SEM), Transmission Electron Microscopy (TEM) and Atomic Force Microscopy (AFM) measurements. The obtained core-shell Cu@Pt nanoparticles were analysed in terms of their antibacterial activity. It was discovered that the synthesized nanoparticles exhibited maximum activity against gram-negative bacteria E. coli ATCC 25922, S. aureus ATCC 25923, and P. aeruginosa NCTC 6749. The core-shell Cu@Pt nanoparticles also exhibited activity against the yeast C. albicans ATCC 10231 and dermatophytes T. mentagrophytes ATCC 9533. Elsevier 2018-07 2018-02-15 /pmc/articles/PMC6035316/ /pubmed/29991908 http://dx.doi.org/10.1016/j.jsps.2018.02.028 Text en © 2018 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Dobrucka, Renata
Dlugaszewska, Jolanta
Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title_full Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title_fullStr Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title_full_unstemmed Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title_short Antimicrobial activity of the biogenically synthesized core-shell Cu@Pt nanoparticles
title_sort antimicrobial activity of the biogenically synthesized core-shell cu@pt nanoparticles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035316/
https://www.ncbi.nlm.nih.gov/pubmed/29991908
http://dx.doi.org/10.1016/j.jsps.2018.02.028
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