Surface activation of medical grade polyurethane for the covalent immobilization of an anti-adhesive biopolymeric coating
Hospital-acquired infections are still a major concern worldwide, being frequently related to bacterial biofilm formation on medical devices, and thus difficult to eradicate with conventional antimicrobial treatments. Therefore, infection-preventive solutions based on natural polymers are being inve...
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Published in | Journal of materials chemistry. B, Materials for biology and medicine Vol. 9; no. 17; pp. 375 - 3715 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
05.05.2021
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Subjects | |
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Abstract | Hospital-acquired infections are still a major concern worldwide, being frequently related to bacterial biofilm formation on medical devices, and thus difficult to eradicate with conventional antimicrobial treatments. Therefore, infection-preventive solutions based on natural polymers are being investigated. Recently, a marine cyanobacterium-derived polymeric coating (CyanoCoating) has demonstrated great anti-adhesive potential when immobilized onto gold model substrates. In this work, we took this technology a step closer to an industrial application by covalently immobilizing CyanoCoating onto medical grade polyurethane (PU). This immobilization was developed through the introduction of linkable moieties onto a PU inert surface using different pre-treatments. Besides the application of the polydopamine (pDA) linker layer, other processes frequently found in industrial settings, such as atmospheric plasma (using O
2
or N
2
as reactive gases) and ozone surface activations, were evaluated. From all the pre-treatments tested, the ozone activation was the most promising since the obtained coating not only revealed a homogeneous distribution, but also significantly reduced the adhesion of two relevant etiological bacteria in static conditions (the Gram-positive
Staphylococcus aureus
and the Gram-negative
Escherichia coli
). Moreover, it also impaired
E. coli
biofilm formation under simulated urinary tract dynamic conditions, reinforcing the potential of CyanoCoating as an antibiotic-free alternative to mitigate medical device-associated infections, particularly in the urinary tract.
Evaluation of the surface activation of medical grade polyurethane through different processes towards the covalent immobilization of an anti-adhesive biopolymeric coating. |
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AbstractList | Hospital-acquired infections are still a major concern worldwide, being frequently related to bacterial biofilm formation on medical devices, and thus difficult to eradicate with conventional antimicrobial treatments. Therefore, infection-preventive solutions based on natural polymers are being investigated. Recently, a marine cyanobacterium-derived polymeric coating (CyanoCoating) has demonstrated great anti-adhesive potential when immobilized onto gold model substrates. In this work, we took this technology a step closer to an industrial application by covalently immobilizing CyanoCoating onto medical grade polyurethane (PU). This immobilization was developed through the introduction of linkable moieties onto a PU inert surface using different pre-treatments. Besides the application of the polydopamine (pDA) linker layer, other processes frequently found in industrial settings, such as atmospheric plasma (using O
2
or N
2
as reactive gases) and ozone surface activations, were evaluated. From all the pre-treatments tested, the ozone activation was the most promising since the obtained coating not only revealed a homogeneous distribution, but also significantly reduced the adhesion of two relevant etiological bacteria in static conditions (the Gram-positive
Staphylococcus aureus
and the Gram-negative
Escherichia coli
). Moreover, it also impaired
E. coli
biofilm formation under simulated urinary tract dynamic conditions, reinforcing the potential of CyanoCoating as an antibiotic-free alternative to mitigate medical device-associated infections, particularly in the urinary tract. Hospital-acquired infections are still a major concern worldwide, being frequently related to bacterial biofilm formation on medical devices, and thus difficult to eradicate with conventional antimicrobial treatments. Therefore, infection-preventive solutions based on natural polymers are being investigated. Recently, a marine cyanobacterium-derived polymeric coating (CyanoCoating) has demonstrated great anti-adhesive potential when immobilized onto gold model substrates. In this work, we took this technology a step closer to an industrial application by covalently immobilizing CyanoCoating onto medical grade polyurethane (PU). This immobilization was developed through the introduction of linkable moieties onto a PU inert surface using different pre-treatments. Besides the application of the polydopamine (pDA) linker layer, other processes frequently found in industrial settings, such as atmospheric plasma (using O2 or N2 as reactive gases) and ozone surface activations, were evaluated. From all the pre-treatments tested, the ozone activation was the most promising since the obtained coating not only revealed a homogeneous distribution, but also significantly reduced the adhesion of two relevant etiological bacteria in static conditions (the Gram-positive Staphylococcus aureus and the Gram-negative Escherichia coli). Moreover, it also impaired E. coli biofilm formation under simulated urinary tract dynamic conditions, reinforcing the potential of CyanoCoating as an antibiotic-free alternative to mitigate medical device-associated infections, particularly in the urinary tract. Hospital-acquired infections are still a major concern worldwide, being frequently related to bacterial biofilm formation on medical devices, and thus difficult to eradicate with conventional antimicrobial treatments. Therefore, infection-preventive solutions based on natural polymers are being investigated. Recently, a marine cyanobacterium-derived polymeric coating (CyanoCoating) has demonstrated great anti-adhesive potential when immobilized onto gold model substrates. In this work, we took this technology a step closer to an industrial application by covalently immobilizing CyanoCoating onto medical grade polyurethane (PU). This immobilization was developed through the introduction of linkable moieties onto a PU inert surface using different pre-treatments. Besides the application of the polydopamine (pDA) linker layer, other processes frequently found in industrial settings, such as atmospheric plasma (using O 2 or N 2 as reactive gases) and ozone surface activations, were evaluated. From all the pre-treatments tested, the ozone activation was the most promising since the obtained coating not only revealed a homogeneous distribution, but also significantly reduced the adhesion of two relevant etiological bacteria in static conditions (the Gram-positive Staphylococcus aureus and the Gram-negative Escherichia coli ). Moreover, it also impaired E. coli biofilm formation under simulated urinary tract dynamic conditions, reinforcing the potential of CyanoCoating as an antibiotic-free alternative to mitigate medical device-associated infections, particularly in the urinary tract. Evaluation of the surface activation of medical grade polyurethane through different processes towards the covalent immobilization of an anti-adhesive biopolymeric coating. |
Author | Mota, Rita Gomes, Marisa Costa, Fabíola Matinha-Cardoso, Jorge Mergulhão, Filipe J Gomes, Luciana C Tamagnini, Paula Martins, M. Cristina L |
AuthorAffiliation | Universidade do Porto Departamento de Biologia ICBAS - Instituto de Ciências Biomédicas Abel Salazar Rua Jorge de Viterbo Ferreira 228 Faculty of Engineering Faculdade de Ciências University of Porto i3S - Instituto de Investigação e Inovação em Saúde LEPABE - Laboratory for Process Engineering, Environment, Biotechnology and Energy INEB - Instituto de Engenharia Biomédica IBMC - Instituto de Biologia Celular e Molecular Rua do Campo Alegre |
AuthorAffiliation_xml | – name: Universidade do Porto – name: Faculty of Engineering – name: LEPABE - Laboratory for Process Engineering, Environment, Biotechnology and Energy – name: University of Porto – name: INEB - Instituto de Engenharia Biomédica – name: i3S - Instituto de Investigação e Inovação em Saúde – name: Faculdade de Ciências – name: Rua Jorge de Viterbo Ferreira 228 – name: Departamento de Biologia – name: Rua do Campo Alegre – name: IBMC - Instituto de Biologia Celular e Molecular – name: ICBAS - Instituto de Ciências Biomédicas Abel Salazar |
Author_xml | – sequence: 1 givenname: Jorge surname: Matinha-Cardoso fullname: Matinha-Cardoso, Jorge – sequence: 2 givenname: Rita surname: Mota fullname: Mota, Rita – sequence: 3 givenname: Luciana C surname: Gomes fullname: Gomes, Luciana C – sequence: 4 givenname: Marisa surname: Gomes fullname: Gomes, Marisa – sequence: 5 givenname: Filipe J surname: Mergulhão fullname: Mergulhão, Filipe J – sequence: 6 givenname: Paula surname: Tamagnini fullname: Tamagnini, Paula – sequence: 7 givenname: M. Cristina L surname: Martins fullname: Martins, M. Cristina L – sequence: 8 givenname: Fabíola surname: Costa fullname: Costa, Fabíola |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33871523$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_compositesb_2022_109623 crossref_primary_10_1016_j_ijbiomac_2022_10_134 crossref_primary_10_1016_j_cobme_2022_100394 crossref_primary_10_1016_j_fbp_2022_11_003 crossref_primary_10_1007_s44174_022_00055_8 crossref_primary_10_3390_microorganisms9091993 crossref_primary_10_1016_j_algal_2022_102939 crossref_primary_10_1016_j_carbpol_2023_121575 |
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Notes | Electronic supplementary information (ESI) available: Contact angle (CA) measurements of PU surfaces subjected to different pDA incubation periods; CA measurements immediately after coating application and after 30 days storage in argon atmosphere; CA measurements of coatings exposed to accelerated degradation static conditions; XPS high resolution spectra of C1s of uncoated and activated PU; micrographs of bacterial cells adhered to uncoated and coated PU. See DOI 10.1039/d1tb00278c ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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SubjectTerms | Antibiotics Antiinfectives and antibacterials Argon Bacteria Biodegradation Biofilms Coatings Contact angle E coli Etiology Immobilization Industrial applications Infections Medical equipment Natural polymers Nitrogen plasma Nosocomial infections Ozone Photomicrographs Polymer coatings Polymers Polyurethane Polyurethane resins Public health Substrates Surface activation Urinary tract Urogenital system |
Title | Surface activation of medical grade polyurethane for the covalent immobilization of an anti-adhesive biopolymeric coating |
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