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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9610547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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