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Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings

Intravascular catheter related bloodstream infections (CRBSIs) are a leading cause of hospital-acquired infections worldwide, resulting not only in the burden of cost and morbidity for patients but also in the over-consumption of medical resources for hospitals and health care organizations. In this...

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Autores principales: Liu, Hanyang, Shukla, Shashank, Vera-González, Noel, Tharmalingam, Nagendran, Mylonakis, Eleftherios, Fuchs, Beth Burgwyn, Shukla, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403144/
https://www.ncbi.nlm.nih.gov/pubmed/30873389
http://dx.doi.org/10.3389/fcimb.2019.00037
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author Liu, Hanyang
Shukla, Shashank
Vera-González, Noel
Tharmalingam, Nagendran
Mylonakis, Eleftherios
Fuchs, Beth Burgwyn
Shukla, Anita
author_facet Liu, Hanyang
Shukla, Shashank
Vera-González, Noel
Tharmalingam, Nagendran
Mylonakis, Eleftherios
Fuchs, Beth Burgwyn
Shukla, Anita
author_sort Liu, Hanyang
collection PubMed
description Intravascular catheter related bloodstream infections (CRBSIs) are a leading cause of hospital-acquired infections worldwide, resulting not only in the burden of cost and morbidity for patients but also in the over-consumption of medical resources for hospitals and health care organizations. In this study, a novel auranofin releasing antibacterial and antibiofilm polyurethane (PU) catheter coating was developed and investigated for future use in preventing CRBSIs. Auranofin is an antirheumatic drug with recently identified antimicrobial properties. The drug carrier, PU, acts as a barrier surrounding the antibacterial agent, auranofin, to extend the drug release profile and improve its long-term antibacterial and antibiofilm efficacy and potentially the length of catheter implantation within a patient. The PU+auranofin coatings developed here were found to be highly stretchable (exhibiting ~500% percent elongation), which is important for the compliance of the material on a flexible catheter. PU+auranofin coated catheters were able to inhibit the growth of methicillin-resistant Staphylococcus aureus (MRSA) for 8 to 26 days depending on the specific drug concentration utilized during the dip coating process. The PU+auranofin coated catheters were also able to completely inhibit MRSA biofilm formation in vitro, an effect that was not observed with auranofin or PU alone. Lastly, these coatings were found to be hemocompatible with human erythrocytes and maintain liver cell viability.
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spelling pubmed-64031442019-03-14 Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings Liu, Hanyang Shukla, Shashank Vera-González, Noel Tharmalingam, Nagendran Mylonakis, Eleftherios Fuchs, Beth Burgwyn Shukla, Anita Front Cell Infect Microbiol Cellular and Infection Microbiology Intravascular catheter related bloodstream infections (CRBSIs) are a leading cause of hospital-acquired infections worldwide, resulting not only in the burden of cost and morbidity for patients but also in the over-consumption of medical resources for hospitals and health care organizations. In this study, a novel auranofin releasing antibacterial and antibiofilm polyurethane (PU) catheter coating was developed and investigated for future use in preventing CRBSIs. Auranofin is an antirheumatic drug with recently identified antimicrobial properties. The drug carrier, PU, acts as a barrier surrounding the antibacterial agent, auranofin, to extend the drug release profile and improve its long-term antibacterial and antibiofilm efficacy and potentially the length of catheter implantation within a patient. The PU+auranofin coatings developed here were found to be highly stretchable (exhibiting ~500% percent elongation), which is important for the compliance of the material on a flexible catheter. PU+auranofin coated catheters were able to inhibit the growth of methicillin-resistant Staphylococcus aureus (MRSA) for 8 to 26 days depending on the specific drug concentration utilized during the dip coating process. The PU+auranofin coated catheters were also able to completely inhibit MRSA biofilm formation in vitro, an effect that was not observed with auranofin or PU alone. Lastly, these coatings were found to be hemocompatible with human erythrocytes and maintain liver cell viability. Frontiers Media S.A. 2019-02-28 /pmc/articles/PMC6403144/ /pubmed/30873389 http://dx.doi.org/10.3389/fcimb.2019.00037 Text en Copyright © 2019 Liu, Shukla, Vera-González, Tharmalingam, Mylonakis, Fuchs and Shukla. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Liu, Hanyang
Shukla, Shashank
Vera-González, Noel
Tharmalingam, Nagendran
Mylonakis, Eleftherios
Fuchs, Beth Burgwyn
Shukla, Anita
Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title_full Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title_fullStr Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title_full_unstemmed Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title_short Auranofin Releasing Antibacterial and Antibiofilm Polyurethane Intravascular Catheter Coatings
title_sort auranofin releasing antibacterial and antibiofilm polyurethane intravascular catheter coatings
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403144/
https://www.ncbi.nlm.nih.gov/pubmed/30873389
http://dx.doi.org/10.3389/fcimb.2019.00037
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