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Antibiofilm Activity of PEGylated Branched Polyethylenimine
[Image: see text] Biofilm formation is an adaptive resistance mechanism that pathogens employ to survive in the presence of antimicrobials. Pseudomonas aeruginosa is an infectious Gram-negative bacterium whose biofilm allows it to withstand antimicrobial attack and threaten human health. Chronic wou...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753512/ https://www.ncbi.nlm.nih.gov/pubmed/36530285 http://dx.doi.org/10.1021/acsomega.2c04911 |
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author | Panlilio, Hannah Neel, Andrew Heydarian, Neda Best, William Atkins, Isaac Boris, Andrew Bui, Maggie Dick, Catherine Ferrell, Maya Gu, Tingting Haight, Tristan Roedl, Chase C. Rice, Charles V. |
author_facet | Panlilio, Hannah Neel, Andrew Heydarian, Neda Best, William Atkins, Isaac Boris, Andrew Bui, Maggie Dick, Catherine Ferrell, Maya Gu, Tingting Haight, Tristan Roedl, Chase C. Rice, Charles V. |
author_sort | Panlilio, Hannah |
collection | PubMed |
description | [Image: see text] Biofilm formation is an adaptive resistance mechanism that pathogens employ to survive in the presence of antimicrobials. Pseudomonas aeruginosa is an infectious Gram-negative bacterium whose biofilm allows it to withstand antimicrobial attack and threaten human health. Chronic wound healing is often impeded by P. aeruginosa infections and the associated biofilms. Previous findings demonstrate that 600 Da branched polyethylenimine (BPEI) can restore β-lactam potency against P. aeruginosa and disrupt its biofilms. Toxicity concerns of 600 Da BPEI are mitigated by covalent linkage with low-molecular-weight polyethylene glycol (PEG), and, in this study, PEGylated BPEI (PEG350-BPEI) was found exhibit superior antibiofilm activity against P. aeruginosa. The antibiofilm activity of both 600 Da BPEI and its PEG derivative was characterized with fluorescence studies and microscopy imaging. We also describe a variation of the colony biofilm model that was employed to evaluate the biofilm disruption activity of BPEI and PEG-BPEI. |
format | Online Article Text |
id | pubmed-9753512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97535122022-12-16 Antibiofilm Activity of PEGylated Branched Polyethylenimine Panlilio, Hannah Neel, Andrew Heydarian, Neda Best, William Atkins, Isaac Boris, Andrew Bui, Maggie Dick, Catherine Ferrell, Maya Gu, Tingting Haight, Tristan Roedl, Chase C. Rice, Charles V. ACS Omega [Image: see text] Biofilm formation is an adaptive resistance mechanism that pathogens employ to survive in the presence of antimicrobials. Pseudomonas aeruginosa is an infectious Gram-negative bacterium whose biofilm allows it to withstand antimicrobial attack and threaten human health. Chronic wound healing is often impeded by P. aeruginosa infections and the associated biofilms. Previous findings demonstrate that 600 Da branched polyethylenimine (BPEI) can restore β-lactam potency against P. aeruginosa and disrupt its biofilms. Toxicity concerns of 600 Da BPEI are mitigated by covalent linkage with low-molecular-weight polyethylene glycol (PEG), and, in this study, PEGylated BPEI (PEG350-BPEI) was found exhibit superior antibiofilm activity against P. aeruginosa. The antibiofilm activity of both 600 Da BPEI and its PEG derivative was characterized with fluorescence studies and microscopy imaging. We also describe a variation of the colony biofilm model that was employed to evaluate the biofilm disruption activity of BPEI and PEG-BPEI. American Chemical Society 2022-12-02 /pmc/articles/PMC9753512/ /pubmed/36530285 http://dx.doi.org/10.1021/acsomega.2c04911 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Panlilio, Hannah Neel, Andrew Heydarian, Neda Best, William Atkins, Isaac Boris, Andrew Bui, Maggie Dick, Catherine Ferrell, Maya Gu, Tingting Haight, Tristan Roedl, Chase C. Rice, Charles V. Antibiofilm Activity of PEGylated Branched Polyethylenimine |
title | Antibiofilm Activity
of PEGylated Branched Polyethylenimine |
title_full | Antibiofilm Activity
of PEGylated Branched Polyethylenimine |
title_fullStr | Antibiofilm Activity
of PEGylated Branched Polyethylenimine |
title_full_unstemmed | Antibiofilm Activity
of PEGylated Branched Polyethylenimine |
title_short | Antibiofilm Activity
of PEGylated Branched Polyethylenimine |
title_sort | antibiofilm activity
of pegylated branched polyethylenimine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753512/ https://www.ncbi.nlm.nih.gov/pubmed/36530285 http://dx.doi.org/10.1021/acsomega.2c04911 |
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