Understanding the impact of crosslinked PCL/ PEG/GelMA electrospun nanofibers on bactericidal activity
Main Author: | |
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Publication Date: | 2018 |
Other Authors: | , , , , , , , , |
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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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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1834482684843261952 |