Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Juliana S.
Data de Publicação: 2022
Outros Autores: Münchow, Eliseu A., Bordini, Ester A. F. [UNESP], Rodrigues, Nathalie S., Dubey, Nileshkumar, Sasaki, Hajime, Fenno, John C., Schwendeman, Steven, Bottino, Marco C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/ijms23020971
http://hdl.handle.net/11449/223253
Resumo: This study aimed at engineering cytocompatible and injectable antibiotic-laden fibrous microparticles gelatin methacryloyl (GelMA) hydrogels for endodontic infection ablation. Clindamycin (CLIN) or metronidazole (MET) was added to a polymer solution and electrospun into fibrous mats, which were processed via cryomilling to obtain CLIN-or MET-laden fibrous microparticles. Then, GelMA was modified with CLIN-or MET-laden microparticles or by using equal amounts of each set of fibrous microparticles. Morphological characterization of electrospun fibers and cryomilled particles was performed via scanning electron microscopy (SEM). The experimental hydrogels were further examined for swelling, degradation, and toxicity to dental stem cells, as well as antimicrobial action against endodontic pathogens (agar diffusion) and biofilm inhibition, evaluated both quantitatively (CFU/mL) and qualitatively via confocal laser scanning microscopy (CLSM) and SEM. Data were analyzed using ANOVA and Tukey’s test (α = 0.05). The modification of GelMA with antibiotic-laden fibrous microparticles increased the hydrogel swelling ratio and degradation rate. Cell viability was slightly reduced, although without any significant toxicity (cell viability > 50%). All hydrogels containing antibiotic-laden fibrous microparticles displayed antibiofilm effects, with the dentin substrate showing nearly complete elimination of viable bacteria. Altogether, our findings suggest that the engineered injectable antibiotic-laden fibrous microparticles hydrogels hold clinical prospects for endodontic infection ablation.
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spelling Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection AblationAntibioticsBiodegradationCryomillingDentistryElectrospinningEndodonticsFibrous particlesRegenerationThis study aimed at engineering cytocompatible and injectable antibiotic-laden fibrous microparticles gelatin methacryloyl (GelMA) hydrogels for endodontic infection ablation. Clindamycin (CLIN) or metronidazole (MET) was added to a polymer solution and electrospun into fibrous mats, which were processed via cryomilling to obtain CLIN-or MET-laden fibrous microparticles. Then, GelMA was modified with CLIN-or MET-laden microparticles or by using equal amounts of each set of fibrous microparticles. Morphological characterization of electrospun fibers and cryomilled particles was performed via scanning electron microscopy (SEM). The experimental hydrogels were further examined for swelling, degradation, and toxicity to dental stem cells, as well as antimicrobial action against endodontic pathogens (agar diffusion) and biofilm inhibition, evaluated both quantitatively (CFU/mL) and qualitatively via confocal laser scanning microscopy (CLSM) and SEM. Data were analyzed using ANOVA and Tukey’s test (α = 0.05). The modification of GelMA with antibiotic-laden fibrous microparticles increased the hydrogel swelling ratio and degradation rate. Cell viability was slightly reduced, although without any significant toxicity (cell viability > 50%). All hydrogels containing antibiotic-laden fibrous microparticles displayed antibiofilm effects, with the dentin substrate showing nearly complete elimination of viable bacteria. Altogether, our findings suggest that the engineered injectable antibiotic-laden fibrous microparticles hydrogels hold clinical prospects for endodontic infection ablation.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)National Institute of Dental and Craniofacial ResearchNational Institutes of HealthDepartment of Cariology Restorative Sciences and Endodontics School of Dentistry University of MichiganDepartment of Restorative Dentistry School of Dentistry Federal University of Pelotas, Rio Grande do SulDepartment of Conservative Dentistry School of Dentistry Federal University of Rio Grande do Sul, Rio Grande do SulDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University, São PauloDepartment of Biologic and Materials Sciences & Prosthodontics University of Michigan School of DentistryDepartment of Pharmaceutical Sciences and the Biointerfaces Institute University of MichiganDepartment of Biomedical Engineering College of Engineering University of MichiganDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University, São PauloFAPESP: 2016/15674-5FAPESP: 2018/14257-7National Institute of Dental and Craniofacial Research: K08DE023552National Institutes of Health: K08DE023552National Institute of Dental and Craniofacial Research: R01DE026578National Institutes of Health: R01DE026578University of MichiganFederal University of PelotasFederal University of Rio Grande do SulUniversidade Estadual Paulista (UNESP)University of Michigan School of DentistryRibeiro, Juliana S.Münchow, Eliseu A.Bordini, Ester A. F. [UNESP]Rodrigues, Nathalie S.Dubey, NileshkumarSasaki, HajimeFenno, John C.Schwendeman, StevenBottino, Marco C.2022-04-28T19:49:34Z2022-04-28T19:49:34Z2022-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/ijms23020971International Journal of Molecular Sciences, v. 23, n. 2, 2022.1422-00671661-6596http://hdl.handle.net/11449/22325310.3390/ijms230209712-s2.0-85122821177Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Molecular Sciencesinfo:eu-repo/semantics/openAccess2022-04-28T19:49:34Zoai:repositorio.unesp.br:11449/223253Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:42:37.011186Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
title Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
spellingShingle Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
Ribeiro, Juliana S.
Antibiotics
Biodegradation
Cryomilling
Dentistry
Electrospinning
Endodontics
Fibrous particles
Regeneration
title_short Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
title_full Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
title_fullStr Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
title_full_unstemmed Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
title_sort Engineering of Injectable Antibiotic-Laden Fibrous Microparticles Gelatin Methacryloyl Hydrogel for Endodontic Infection Ablation
author Ribeiro, Juliana S.
author_facet Ribeiro, Juliana S.
Münchow, Eliseu A.
Bordini, Ester A. F. [UNESP]
Rodrigues, Nathalie S.
Dubey, Nileshkumar
Sasaki, Hajime
Fenno, John C.
Schwendeman, Steven
Bottino, Marco C.
author_role author
author2 Münchow, Eliseu A.
Bordini, Ester A. F. [UNESP]
Rodrigues, Nathalie S.
Dubey, Nileshkumar
Sasaki, Hajime
Fenno, John C.
Schwendeman, Steven
Bottino, Marco C.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv University of Michigan
Federal University of Pelotas
Federal University of Rio Grande do Sul
Universidade Estadual Paulista (UNESP)
University of Michigan School of Dentistry
dc.contributor.author.fl_str_mv Ribeiro, Juliana S.
Münchow, Eliseu A.
Bordini, Ester A. F. [UNESP]
Rodrigues, Nathalie S.
Dubey, Nileshkumar
Sasaki, Hajime
Fenno, John C.
Schwendeman, Steven
Bottino, Marco C.
dc.subject.por.fl_str_mv Antibiotics
Biodegradation
Cryomilling
Dentistry
Electrospinning
Endodontics
Fibrous particles
Regeneration
topic Antibiotics
Biodegradation
Cryomilling
Dentistry
Electrospinning
Endodontics
Fibrous particles
Regeneration
description This study aimed at engineering cytocompatible and injectable antibiotic-laden fibrous microparticles gelatin methacryloyl (GelMA) hydrogels for endodontic infection ablation. Clindamycin (CLIN) or metronidazole (MET) was added to a polymer solution and electrospun into fibrous mats, which were processed via cryomilling to obtain CLIN-or MET-laden fibrous microparticles. Then, GelMA was modified with CLIN-or MET-laden microparticles or by using equal amounts of each set of fibrous microparticles. Morphological characterization of electrospun fibers and cryomilled particles was performed via scanning electron microscopy (SEM). The experimental hydrogels were further examined for swelling, degradation, and toxicity to dental stem cells, as well as antimicrobial action against endodontic pathogens (agar diffusion) and biofilm inhibition, evaluated both quantitatively (CFU/mL) and qualitatively via confocal laser scanning microscopy (CLSM) and SEM. Data were analyzed using ANOVA and Tukey’s test (α = 0.05). The modification of GelMA with antibiotic-laden fibrous microparticles increased the hydrogel swelling ratio and degradation rate. Cell viability was slightly reduced, although without any significant toxicity (cell viability > 50%). All hydrogels containing antibiotic-laden fibrous microparticles displayed antibiofilm effects, with the dentin substrate showing nearly complete elimination of viable bacteria. Altogether, our findings suggest that the engineered injectable antibiotic-laden fibrous microparticles hydrogels hold clinical prospects for endodontic infection ablation.
publishDate 2022
dc.date.none.fl_str_mv 2022-04-28T19:49:34Z
2022-04-28T19:49:34Z
2022-01-01
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/10.3390/ijms23020971
International Journal of Molecular Sciences, v. 23, n. 2, 2022.
1422-0067
1661-6596
http://hdl.handle.net/11449/223253
10.3390/ijms23020971
2-s2.0-85122821177
url http://dx.doi.org/10.3390/ijms23020971
http://hdl.handle.net/11449/223253
identifier_str_mv International Journal of Molecular Sciences, v. 23, n. 2, 2022.
1422-0067
1661-6596
10.3390/ijms23020971
2-s2.0-85122821177
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Molecular Sciences
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
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