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Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent

The clinical use of urethral stents is usually complicated by various adverse effects, including dysuria, fever, and urinary tract infection (UTI). Biofilms (formed by bacteria, such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus) adhering to the stent cause UTIs in stented p...

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Autores principales: Maknuna, Luluil, Tran, Van Nam, Lee, Byeong-Il, Kang, Hyun Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995349/
https://www.ncbi.nlm.nih.gov/pubmed/36890147
http://dx.doi.org/10.1038/s41598-023-30280-0
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author Maknuna, Luluil
Tran, Van Nam
Lee, Byeong-Il
Kang, Hyun Wook
author_facet Maknuna, Luluil
Tran, Van Nam
Lee, Byeong-Il
Kang, Hyun Wook
author_sort Maknuna, Luluil
collection PubMed
description The clinical use of urethral stents is usually complicated by various adverse effects, including dysuria, fever, and urinary tract infection (UTI). Biofilms (formed by bacteria, such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus) adhering to the stent cause UTIs in stented patients (approximately 11%). The undesirable consequences of antibiotics use include bacterial resistance, weight gain, and type 1 diabetes, which occur when antibiotics are used for a long time. We aimed to assess the efficacy of a new optical treatment with a 405 nm laser to inhibit bacterial growth in a urethral stent in vitro. The urethral stent was grown in S. aureus broth media for three days to induce biofilm formation under dynamic conditions. Various irradiation times with the 405 nm laser light were tested (5, 10, and 15 min). The efficacy of the optical treatment on biofilms was evaluated quantitatively and qualitatively. The production of reactive oxygen species helped eliminate the biofilm over the urethral stent after 405 nm irradiation. The inhibition rate corresponded to a 2.2 log reduction of colony-forming units/mL of bacteria after 0.3 W/cm(2) of irradiation for 10 min. The treated stent showed a significant reduction in biofilm formation compared with the untreated stent, as demonstrated by SYTO 9 and propidium iodide staining. MTT assays using the CCD-986sk cell line revealed no toxicity after 10 min of irradiation. We conclude that optical treatment with 405 nm laser light inhibits bacterial growth in urethral stents with no or minimal toxicity.
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spelling pubmed-99953492023-03-10 Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent Maknuna, Luluil Tran, Van Nam Lee, Byeong-Il Kang, Hyun Wook Sci Rep Article The clinical use of urethral stents is usually complicated by various adverse effects, including dysuria, fever, and urinary tract infection (UTI). Biofilms (formed by bacteria, such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus) adhering to the stent cause UTIs in stented patients (approximately 11%). The undesirable consequences of antibiotics use include bacterial resistance, weight gain, and type 1 diabetes, which occur when antibiotics are used for a long time. We aimed to assess the efficacy of a new optical treatment with a 405 nm laser to inhibit bacterial growth in a urethral stent in vitro. The urethral stent was grown in S. aureus broth media for three days to induce biofilm formation under dynamic conditions. Various irradiation times with the 405 nm laser light were tested (5, 10, and 15 min). The efficacy of the optical treatment on biofilms was evaluated quantitatively and qualitatively. The production of reactive oxygen species helped eliminate the biofilm over the urethral stent after 405 nm irradiation. The inhibition rate corresponded to a 2.2 log reduction of colony-forming units/mL of bacteria after 0.3 W/cm(2) of irradiation for 10 min. The treated stent showed a significant reduction in biofilm formation compared with the untreated stent, as demonstrated by SYTO 9 and propidium iodide staining. MTT assays using the CCD-986sk cell line revealed no toxicity after 10 min of irradiation. We conclude that optical treatment with 405 nm laser light inhibits bacterial growth in urethral stents with no or minimal toxicity. Nature Publishing Group UK 2023-03-08 /pmc/articles/PMC9995349/ /pubmed/36890147 http://dx.doi.org/10.1038/s41598-023-30280-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Maknuna, Luluil
Tran, Van Nam
Lee, Byeong-Il
Kang, Hyun Wook
Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title_full Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title_fullStr Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title_full_unstemmed Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title_short Inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
title_sort inhibitory effect of 405 nm laser light on bacterial biofilm in urethral stent
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995349/
https://www.ncbi.nlm.nih.gov/pubmed/36890147
http://dx.doi.org/10.1038/s41598-023-30280-0
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