Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity

Bibliographic Details
Main Author: De Paula, Mirian Michelle Machado
Publication Date: 2018
Other Authors: Bassous, Nicole Joy, Afewerki, Samson, Harb, Samarah Vargas [UNESP], Ghannadian, Paria, Marciano, Fernanda Roberta, Viana, Bartolomeu Cruz, Tim, Carla Roberta, Webster, Thomas Jay, Lobo, Anderson Oliveira
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1371/journal.pone.0209386
http://hdl.handle.net/11449/187192
Summary: Herein, we report the design of electrospun ultrathin fibers based on the combination of three different polymers polycaprolactone (PCL), polyethylene glycol (PEG), and gelatin methacryloyl (GelMA), and their potential bactericidal activity against three different bacteria Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa (P. aeruginosa), and Methi-cillin-resistant Staphylococcus aureus (MRSA). We evaluated the morphology, chemical structure and wettability before and after UV photocrosslinking of the produced scaffolds. Results showed that the developed scaffolds presented hydrophilic properties after PEG and GelMA incorporation. Moreover, they were able to significantly reduce gram-positive, negative, and MRSA bacteria mainly after UV photocrosslinking (PCL:PEG:GelMa-UV). Furthermore, we performed a series of study for gaining a better mechanistic understanding of the scaffolds bactericidal activity through protein adsorption study and analysis of the reactive oxygen species (ROS) levels. Furthermore, the in vivo subcutaneous implantation performed in rats confirmed the biocompatibility of our designed scaffolds.
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spelling Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activityHerein, we report the design of electrospun ultrathin fibers based on the combination of three different polymers polycaprolactone (PCL), polyethylene glycol (PEG), and gelatin methacryloyl (GelMA), and their potential bactericidal activity against three different bacteria Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa (P. aeruginosa), and Methi-cillin-resistant Staphylococcus aureus (MRSA). We evaluated the morphology, chemical structure and wettability before and after UV photocrosslinking of the produced scaffolds. Results showed that the developed scaffolds presented hydrophilic properties after PEG and GelMA incorporation. Moreover, they were able to significantly reduce gram-positive, negative, and MRSA bacteria mainly after UV photocrosslinking (PCL:PEG:GelMa-UV). Furthermore, we performed a series of study for gaining a better mechanistic understanding of the scaffolds bactericidal activity through protein adsorption study and analysis of the reactive oxygen species (ROS) levels. Furthermore, the in vivo subcutaneous implantation performed in rats confirmed the biocompatibility of our designed scaffolds.Instituto de Desenvolvimento Sustentável MamirauáFaculty of Medical Sciences State University of CampinasDepartment of Chemical Engineering Northeastern UniversityDepartment of Chemical Engineering Koch Institute for Integrative Cancer Research Massachusetts Institute of TechnologyDivision of Gastroenterology Brigham and Women´s Hospital Harvard Medical SchoolInstitute of Chemistry UNESP-São Paulo State UniversityInstitute of Science and Technology Brasil UniversityLIMAV-Interdisciplinary Laboratory for Advanced Materials PPGCM-Materials Science and Engineering graduate program UFPI-Federal University of PiauíDepartment of Physics UFPI-Federal University of PiauíDepartment of Chemistry Massachusetts Institute of TechnologyInstitute of Chemistry UNESP-São Paulo State UniversityInstituto de Desenvolvimento Sustentável Mamirauá: Serra-1709-19479Universidade Estadual de Campinas (UNICAMP)Northeastern UniversityMassachusetts Institute of TechnologyHarvard Medical SchoolUniversidade Estadual Paulista (Unesp)Brasil UniversityUFPI-Federal University of PiauíDe Paula, Mirian Michelle MachadoBassous, Nicole JoyAfewerki, SamsonHarb, Samarah Vargas [UNESP]Ghannadian, PariaMarciano, Fernanda RobertaViana, Bartolomeu CruzTim, Carla RobertaWebster, Thomas JayLobo, Anderson Oliveira2019-10-06T15:28:17Z2019-10-06T15:28:17Z2018-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1371/journal.pone.0209386PLoS ONE, v. 13, n. 12, 2018.1932-6203http://hdl.handle.net/11449/18719210.1371/journal.pone.02093862-s2.0-85058818901Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPLoS ONEinfo:eu-repo/semantics/openAccess2025-05-28T06:14:51Zoai:repositorio.unesp.br:11449/187192Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-28T06:14:51Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
title Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
spellingShingle Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
De Paula, Mirian Michelle Machado
title_short Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
title_full Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
title_fullStr Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
title_full_unstemmed Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
title_sort Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
author De Paula, Mirian Michelle Machado
author_facet De Paula, Mirian Michelle Machado
Bassous, Nicole Joy
Afewerki, Samson
Harb, Samarah Vargas [UNESP]
Ghannadian, Paria
Marciano, Fernanda Roberta
Viana, Bartolomeu Cruz
Tim, Carla Roberta
Webster, Thomas Jay
Lobo, Anderson Oliveira
author_role author
author2 Bassous, Nicole Joy
Afewerki, Samson
Harb, Samarah Vargas [UNESP]
Ghannadian, Paria
Marciano, Fernanda Roberta
Viana, Bartolomeu Cruz
Tim, Carla Roberta
Webster, Thomas Jay
Lobo, Anderson Oliveira
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Northeastern University
Massachusetts Institute of Technology
Harvard Medical School
Universidade Estadual Paulista (Unesp)
Brasil University
UFPI-Federal University of Piauí
dc.contributor.author.fl_str_mv De Paula, Mirian Michelle Machado
Bassous, Nicole Joy
Afewerki, Samson
Harb, Samarah Vargas [UNESP]
Ghannadian, Paria
Marciano, Fernanda Roberta
Viana, Bartolomeu Cruz
Tim, Carla Roberta
Webster, Thomas Jay
Lobo, Anderson Oliveira
description Herein, we report the design of electrospun ultrathin fibers based on the combination of three different polymers polycaprolactone (PCL), polyethylene glycol (PEG), and gelatin methacryloyl (GelMA), and their potential bactericidal activity against three different bacteria Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa (P. aeruginosa), and Methi-cillin-resistant Staphylococcus aureus (MRSA). We evaluated the morphology, chemical structure and wettability before and after UV photocrosslinking of the produced scaffolds. Results showed that the developed scaffolds presented hydrophilic properties after PEG and GelMA incorporation. Moreover, they were able to significantly reduce gram-positive, negative, and MRSA bacteria mainly after UV photocrosslinking (PCL:PEG:GelMa-UV). Furthermore, we performed a series of study for gaining a better mechanistic understanding of the scaffolds bactericidal activity through protein adsorption study and analysis of the reactive oxygen species (ROS) levels. Furthermore, the in vivo subcutaneous implantation performed in rats confirmed the biocompatibility of our designed scaffolds.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
2019-10-06T15:28:17Z
2019-10-06T15:28:17Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0209386
PLoS ONE, v. 13, n. 12, 2018.
1932-6203
http://hdl.handle.net/11449/187192
10.1371/journal.pone.0209386
2-s2.0-85058818901
url http://dx.doi.org/10.1371/journal.pone.0209386
http://hdl.handle.net/11449/187192
identifier_str_mv PLoS ONE, v. 13, n. 12, 2018.
1932-6203
10.1371/journal.pone.0209386
2-s2.0-85058818901
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv PLoS ONE
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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