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Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection
The resistance of bacteria to antibiotics is a major problem for anti-bacterial therapy. This problem may be solved by using bacteriophages—viruses that can attack and destroy bacteria, including antibiotic-resistant ones. In this article, the authors compared the efficacy of topical bacteriophage t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453372/ https://www.ncbi.nlm.nih.gov/pubmed/37623080 http://dx.doi.org/10.3390/gels9080625 |
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author | Beschastnov, Vladimir V. Egorikhina, Marfa N. Tulupov, Alexander A. Pogodin, Igor E. Orlinskaya, Natalia Yu. Antoshina, Veronica. V. Shirokova, Irina Yu. Ryabkov, Maksim G. |
author_facet | Beschastnov, Vladimir V. Egorikhina, Marfa N. Tulupov, Alexander A. Pogodin, Igor E. Orlinskaya, Natalia Yu. Antoshina, Veronica. V. Shirokova, Irina Yu. Ryabkov, Maksim G. |
author_sort | Beschastnov, Vladimir V. |
collection | PubMed |
description | The resistance of bacteria to antibiotics is a major problem for anti-bacterial therapy. This problem may be solved by using bacteriophages—viruses that can attack and destroy bacteria, including antibiotic-resistant ones. In this article, the authors compared the efficacy of topical bacteriophage therapy and systemic antibiotic therapy in the treatment of wound infections caused by ESKAPE pathogens in patients with limited (less than 5% of the body surface) full-thickness burns. Patients in the study group (n = 30) were treated with PVA-based hydrogel dressings saturated ex tempore with a bacteriophage suspension characterized by its lytic activity against the bacteria colonizing the wound. Patients in the control group (n = 30) were treated using etiotropic systemic antibiotic therapy, and the wounds were covered with gauze bandages soaked in an aqueous solution of povidone-iodine. An assessment of the decrease in the level of bacterial contamination of the recipient wounds in both groups was conducted after 7 days, and after that, free skin grafting was performed. On day 14 after free skin grafting, patients in both groups underwent incisional biopsy. The study group demonstrated an increase in the indices of proliferative activity (Ki-67), and angiogenesis (CD-31, VEGF) in the area of engraftment of the split-thickness skin grafts. The results indicate that PVA-based hydrogel wound dressings can be used as bacteriophage carriers for local antimicrobial therapy ahead of free skin grafting. |
format | Online Article Text |
id | pubmed-10453372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104533722023-08-26 Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection Beschastnov, Vladimir V. Egorikhina, Marfa N. Tulupov, Alexander A. Pogodin, Igor E. Orlinskaya, Natalia Yu. Antoshina, Veronica. V. Shirokova, Irina Yu. Ryabkov, Maksim G. Gels Article The resistance of bacteria to antibiotics is a major problem for anti-bacterial therapy. This problem may be solved by using bacteriophages—viruses that can attack and destroy bacteria, including antibiotic-resistant ones. In this article, the authors compared the efficacy of topical bacteriophage therapy and systemic antibiotic therapy in the treatment of wound infections caused by ESKAPE pathogens in patients with limited (less than 5% of the body surface) full-thickness burns. Patients in the study group (n = 30) were treated with PVA-based hydrogel dressings saturated ex tempore with a bacteriophage suspension characterized by its lytic activity against the bacteria colonizing the wound. Patients in the control group (n = 30) were treated using etiotropic systemic antibiotic therapy, and the wounds were covered with gauze bandages soaked in an aqueous solution of povidone-iodine. An assessment of the decrease in the level of bacterial contamination of the recipient wounds in both groups was conducted after 7 days, and after that, free skin grafting was performed. On day 14 after free skin grafting, patients in both groups underwent incisional biopsy. The study group demonstrated an increase in the indices of proliferative activity (Ki-67), and angiogenesis (CD-31, VEGF) in the area of engraftment of the split-thickness skin grafts. The results indicate that PVA-based hydrogel wound dressings can be used as bacteriophage carriers for local antimicrobial therapy ahead of free skin grafting. MDPI 2023-08-03 /pmc/articles/PMC10453372/ /pubmed/37623080 http://dx.doi.org/10.3390/gels9080625 Text en © 2023 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 Beschastnov, Vladimir V. Egorikhina, Marfa N. Tulupov, Alexander A. Pogodin, Igor E. Orlinskaya, Natalia Yu. Antoshina, Veronica. V. Shirokova, Irina Yu. Ryabkov, Maksim G. Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title | Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title_full | Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title_fullStr | Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title_full_unstemmed | Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title_short | Immobilization of Bacteriophages in Ex Tempore Hydrogel for the Treatment of Burn Wound Infection |
title_sort | immobilization of bacteriophages in ex tempore hydrogel for the treatment of burn wound infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453372/ https://www.ncbi.nlm.nih.gov/pubmed/37623080 http://dx.doi.org/10.3390/gels9080625 |
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