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A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections
The aim of this study was to evaluate the effectiveness of a moxifloxacin-loaded organic–inorganic sol-gel (A50) by locally preventing the catheter-related bloodstream infection (CRBSI) provoked by Staphylococcus epidermidis (S. epidermidis) and the effect resulting from its hydrolytic degradation o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372435/ https://www.ncbi.nlm.nih.gov/pubmed/32630210 http://dx.doi.org/10.3390/ma13132946 |
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author | Aguilera-Correa, John Jairo Vidal-Laso, Rosa Carias-Cálix, Rafael Alfredo Toirac, Beatriz García-Casas, Amaya Velasco-Rodríguez, Diego Llamas-Sillero, Pilar Jiménez-Morales, Antonia Esteban, Jaime |
author_facet | Aguilera-Correa, John Jairo Vidal-Laso, Rosa Carias-Cálix, Rafael Alfredo Toirac, Beatriz García-Casas, Amaya Velasco-Rodríguez, Diego Llamas-Sillero, Pilar Jiménez-Morales, Antonia Esteban, Jaime |
author_sort | Aguilera-Correa, John Jairo |
collection | PubMed |
description | The aim of this study was to evaluate the effectiveness of a moxifloxacin-loaded organic–inorganic sol-gel (A50) by locally preventing the catheter-related bloodstream infection (CRBSI) provoked by Staphylococcus epidermidis (S. epidermidis) and the effect resulting from its hydrolytic degradation on coagulation by using a rabbit in-vivo model. A50 coating can completely inhibit growth and would locally prevent CRBSI provoked by S. epidermidis. None of the coagulation blood parameters showed a significant difference constant over time between the control catheter group and the A50-coated catheter group, despite the visible silica release resulting from physiological A50 sol-gel degradation detected in serum at least during the first week. At pathological level, foreign body reaction was present in both of types of catheter, and it was characterized by the presence of macrophages and foreign body giant cell. However, this reaction was different in each group: the A50-coated catheter group showed a higher inflammation with histiocytes, which were forming granuloma-like aggregates with an amorphous crystalline material inside, accompanied by other inflammatory cells such as plasma cells, lymphocytes and mast cells. In conclusion, A50 coating a venous catheter showed excellent bactericidal anti-biofilm response since it completely inhibited S. epidermidis biofilm development and, far from showing procoagulant effects, showed slightly anticoagulant effects. |
format | Online Article Text |
id | pubmed-7372435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73724352020-08-05 A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections Aguilera-Correa, John Jairo Vidal-Laso, Rosa Carias-Cálix, Rafael Alfredo Toirac, Beatriz García-Casas, Amaya Velasco-Rodríguez, Diego Llamas-Sillero, Pilar Jiménez-Morales, Antonia Esteban, Jaime Materials (Basel) Article The aim of this study was to evaluate the effectiveness of a moxifloxacin-loaded organic–inorganic sol-gel (A50) by locally preventing the catheter-related bloodstream infection (CRBSI) provoked by Staphylococcus epidermidis (S. epidermidis) and the effect resulting from its hydrolytic degradation on coagulation by using a rabbit in-vivo model. A50 coating can completely inhibit growth and would locally prevent CRBSI provoked by S. epidermidis. None of the coagulation blood parameters showed a significant difference constant over time between the control catheter group and the A50-coated catheter group, despite the visible silica release resulting from physiological A50 sol-gel degradation detected in serum at least during the first week. At pathological level, foreign body reaction was present in both of types of catheter, and it was characterized by the presence of macrophages and foreign body giant cell. However, this reaction was different in each group: the A50-coated catheter group showed a higher inflammation with histiocytes, which were forming granuloma-like aggregates with an amorphous crystalline material inside, accompanied by other inflammatory cells such as plasma cells, lymphocytes and mast cells. In conclusion, A50 coating a venous catheter showed excellent bactericidal anti-biofilm response since it completely inhibited S. epidermidis biofilm development and, far from showing procoagulant effects, showed slightly anticoagulant effects. MDPI 2020-07-01 /pmc/articles/PMC7372435/ /pubmed/32630210 http://dx.doi.org/10.3390/ma13132946 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Aguilera-Correa, John Jairo Vidal-Laso, Rosa Carias-Cálix, Rafael Alfredo Toirac, Beatriz García-Casas, Amaya Velasco-Rodríguez, Diego Llamas-Sillero, Pilar Jiménez-Morales, Antonia Esteban, Jaime A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title | A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title_full | A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title_fullStr | A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title_full_unstemmed | A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title_short | A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections |
title_sort | new antibiotic-loaded sol-gel can prevent bacterial intravenous catheter-related infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372435/ https://www.ncbi.nlm.nih.gov/pubmed/32630210 http://dx.doi.org/10.3390/ma13132946 |
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