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Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer

Gramicidin (Gr) nanoparticles (NPs) and poly (diallyl dimethyl ammonium) chloride (PDDA) water dispersions were characterized and evaluated against Gram-positive and Gram-negative bacteria and fungus. Dynamic light scattering for sizing, zeta potential analysis, polydispersity, and colloidal stabili...

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Autores principales: Pérez-Betancourt, Yunys, Zaia, Rachel, Evangelista, Marina Franchi, Ribeiro, Rodrigo Tadeu, Roncoleta, Bruno Murillo, Mathiazzi, Beatriz Ideriha, Carmona-Ribeiro, Ana Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610547/
https://www.ncbi.nlm.nih.gov/pubmed/36297488
http://dx.doi.org/10.3390/pharmaceutics14102053
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author Pérez-Betancourt, Yunys
Zaia, Rachel
Evangelista, Marina Franchi
Ribeiro, Rodrigo Tadeu
Roncoleta, Bruno Murillo
Mathiazzi, Beatriz Ideriha
Carmona-Ribeiro, Ana Maria
author_facet Pérez-Betancourt, Yunys
Zaia, Rachel
Evangelista, Marina Franchi
Ribeiro, Rodrigo Tadeu
Roncoleta, Bruno Murillo
Mathiazzi, Beatriz Ideriha
Carmona-Ribeiro, Ana Maria
author_sort Pérez-Betancourt, Yunys
collection PubMed
description Gramicidin (Gr) nanoparticles (NPs) and poly (diallyl dimethyl ammonium) chloride (PDDA) water dispersions were characterized and evaluated against Gram-positive and Gram-negative bacteria and fungus. Dynamic light scattering for sizing, zeta potential analysis, polydispersity, and colloidal stability over time characterized Gr NPs/PDDA dispersions, and plating and colony-forming units counting determined their microbicidal activity. Cell viabilities of Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans in the presence of the combinations were reduced by 6, 7, and 7 logs, respectively, at 10 μM Gr/10 μg·mL(−1) PDDA, 0.5 μM Gr/0. 5μg·mL(−1) PDDA, and 0.5 μM Gr/0.5 μg·mL(−1) PDDA, respectively. In comparison to individual Gr doses, the combinations reduced doses by half (S. aureus) and a quarter (C. albicans); in comparison to individual PDDA doses, the combinations reduced doses by 6 times (P. aeruginosa) and 10 times (C. albicans). Gr in supported or free cationic lipid bilayers reduced Gr activity against S. aureus due to reduced Gr access to the pathogen. Facile Gr NPs/PDDA disassembly favored access of each agent to the pathogen: PDDA suctioned the pathogen cell wall facilitating Gr insertion in the pathogen cell membrane. Gr NPs/PDDA differential cytotoxicity suggested the possibility of novel systemic uses for the combination.
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spelling pubmed-96105472022-10-28 Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer Pérez-Betancourt, Yunys Zaia, Rachel Evangelista, Marina Franchi Ribeiro, Rodrigo Tadeu Roncoleta, Bruno Murillo Mathiazzi, Beatriz Ideriha Carmona-Ribeiro, Ana Maria Pharmaceutics Article Gramicidin (Gr) nanoparticles (NPs) and poly (diallyl dimethyl ammonium) chloride (PDDA) water dispersions were characterized and evaluated against Gram-positive and Gram-negative bacteria and fungus. Dynamic light scattering for sizing, zeta potential analysis, polydispersity, and colloidal stability over time characterized Gr NPs/PDDA dispersions, and plating and colony-forming units counting determined their microbicidal activity. Cell viabilities of Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans in the presence of the combinations were reduced by 6, 7, and 7 logs, respectively, at 10 μM Gr/10 μg·mL(−1) PDDA, 0.5 μM Gr/0. 5μg·mL(−1) PDDA, and 0.5 μM Gr/0.5 μg·mL(−1) PDDA, respectively. In comparison to individual Gr doses, the combinations reduced doses by half (S. aureus) and a quarter (C. albicans); in comparison to individual PDDA doses, the combinations reduced doses by 6 times (P. aeruginosa) and 10 times (C. albicans). Gr in supported or free cationic lipid bilayers reduced Gr activity against S. aureus due to reduced Gr access to the pathogen. Facile Gr NPs/PDDA disassembly favored access of each agent to the pathogen: PDDA suctioned the pathogen cell wall facilitating Gr insertion in the pathogen cell membrane. Gr NPs/PDDA differential cytotoxicity suggested the possibility of novel systemic uses for the combination. MDPI 2022-09-27 /pmc/articles/PMC9610547/ /pubmed/36297488 http://dx.doi.org/10.3390/pharmaceutics14102053 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pérez-Betancourt, Yunys
Zaia, Rachel
Evangelista, Marina Franchi
Ribeiro, Rodrigo Tadeu
Roncoleta, Bruno Murillo
Mathiazzi, Beatriz Ideriha
Carmona-Ribeiro, Ana Maria
Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title_full Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title_fullStr Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title_full_unstemmed Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title_short Characterization and Differential Cytotoxicity of Gramicidin Nanoparticles Combined with Cationic Polymer or Lipid Bilayer
title_sort characterization and differential cytotoxicity of gramicidin nanoparticles combined with cationic polymer or lipid bilayer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610547/
https://www.ncbi.nlm.nih.gov/pubmed/36297488
http://dx.doi.org/10.3390/pharmaceutics14102053
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