Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics
Main Author: | |
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Publication Date: | 2025 |
Other Authors: | , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1016/j.bioactmat.2024.12.026 https://hdl.handle.net/11449/300820 |
Summary: | Injectable biomaterials, such as thermosensitive chitosan (CH)-based hydrogels, present a highly translational potential in dentistry due to their minimally invasive application, adaptability to irregular defects/shapes, and ability to carry therapeutic drugs. This work explores the incorporation of azithromycin (AZI) into thermosensitive CH hydrogels for use as an intracanal medication in regenerative endodontic procedures (REPs). The morphological and chemical characteristics of the hydrogel were assessed by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR). The thermosensitivity, gelation kinetics, compressive strength, cytocompatibility, and antibacterial efficacy were evaluated according to well-established protocols. An in vivo model of periapical disease and evoked bleeding in rats' immature permanent teeth was performed to determine disinfection, tissue repair, and root formation. AZI was successfully incorporated into interconnected porous CH hydrogels, which retained their thermosensitivity. The mechanical and rheological findings indicated that adding AZI did not adversely affect the hydrogels’ strength and injectability. Incorporating 3 % and 5 % AZI into the hydrogels led to minimal cytotoxic effects compared to higher concentrations while enhancing the antibacterial response against endodontic bacteria. AZI-laden hydrogel significantly decreased E. faecalis biofilm compared to the controls. Regarding tissue response, the 3 % AZI-laden hydrogel improved mineralized tissue formation and vascularization compared to untreated teeth and those treated with double antibiotic paste. Our findings demonstrate that adding 3 % AZI into CH hydrogels ablates infection and supports neotissue formation in vivo when applied to a clinically relevant model of regenerative endodontics. |
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Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodonticsAntibioticsAzithromycinChitosanHydrogelsInjectableRegenerative endodonticsInjectable biomaterials, such as thermosensitive chitosan (CH)-based hydrogels, present a highly translational potential in dentistry due to their minimally invasive application, adaptability to irregular defects/shapes, and ability to carry therapeutic drugs. This work explores the incorporation of azithromycin (AZI) into thermosensitive CH hydrogels for use as an intracanal medication in regenerative endodontic procedures (REPs). The morphological and chemical characteristics of the hydrogel were assessed by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR). The thermosensitivity, gelation kinetics, compressive strength, cytocompatibility, and antibacterial efficacy were evaluated according to well-established protocols. An in vivo model of periapical disease and evoked bleeding in rats' immature permanent teeth was performed to determine disinfection, tissue repair, and root formation. AZI was successfully incorporated into interconnected porous CH hydrogels, which retained their thermosensitivity. The mechanical and rheological findings indicated that adding AZI did not adversely affect the hydrogels’ strength and injectability. Incorporating 3 % and 5 % AZI into the hydrogels led to minimal cytotoxic effects compared to higher concentrations while enhancing the antibacterial response against endodontic bacteria. AZI-laden hydrogel significantly decreased E. faecalis biofilm compared to the controls. Regarding tissue response, the 3 % AZI-laden hydrogel improved mineralized tissue formation and vascularization compared to untreated teeth and those treated with double antibiotic paste. Our findings demonstrate that adding 3 % AZI into CH hydrogels ablates infection and supports neotissue formation in vivo when applied to a clinically relevant model of regenerative endodontics.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Colorado HumanitiesConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)National Institute of Dental and Craniofacial ResearchNational Institutes of HealthFURTHERMORE grants in publishingDepartment of Cariology Restorative Sciences and Endodontics University of Michigan School of DentistryDepartment of Restorative Dentistry Universidade Federal de Minas Gerais (UFMG) School of Dentistry, MGDepartment of Preventive and Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP) - Araraquara School of Dentistry, SPDepartment of Biologic and Materials Sciences & Prosthodontics University of Michigan School of DentistryDepartment of Biomedical Engineering College of Engineering University of MichiganDepartment of Preventive and Restorative Dentistry School of Dentistry São Paulo State University (UNESP), SPDepartment of Morphology and Pediatric Dentistry São Paulo State University (UNESP) - Araraquara School of Dentistry, SPUniversity of Michigan School of DentistryUniversidade Federal de Minas Gerais (UFMG)Universidade Estadual Paulista (UNESP)University of MichiganReis-Prado, Alexandre Henrique dosRahimnejad, MaedehDal-Fabbro, RenanToledo, Priscila Toninatto Alves de [UNESP]Anselmi, Caroline [UNESP]Oliveira, Pedro Henrique Chaves de [UNESP]Fenno, J. ChristopherCintra, Luciano Tavares Angelo [UNESP]Benetti, FrancineBottino, Marco C.2025-04-29T18:50:41Z2025-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article406-422http://dx.doi.org/10.1016/j.bioactmat.2024.12.026Bioactive Materials, v. 46, p. 406-422.2452-199Xhttps://hdl.handle.net/11449/30082010.1016/j.bioactmat.2024.12.0262-s2.0-85213827716Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBioactive Materialsinfo:eu-repo/semantics/openAccess2025-05-01T05:51:56Zoai:repositorio.unesp.br:11449/300820Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-01T05:51:56Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
title |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
spellingShingle |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics Reis-Prado, Alexandre Henrique dos Antibiotics Azithromycin Chitosan Hydrogels Injectable Regenerative endodontics |
title_short |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
title_full |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
title_fullStr |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
title_full_unstemmed |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
title_sort |
Injectable thermosensitive antibiotic-laden chitosan hydrogel for regenerative endodontics |
author |
Reis-Prado, Alexandre Henrique dos |
author_facet |
Reis-Prado, Alexandre Henrique dos Rahimnejad, Maedeh Dal-Fabbro, Renan Toledo, Priscila Toninatto Alves de [UNESP] Anselmi, Caroline [UNESP] Oliveira, Pedro Henrique Chaves de [UNESP] Fenno, J. Christopher Cintra, Luciano Tavares Angelo [UNESP] Benetti, Francine Bottino, Marco C. |
author_role |
author |
author2 |
Rahimnejad, Maedeh Dal-Fabbro, Renan Toledo, Priscila Toninatto Alves de [UNESP] Anselmi, Caroline [UNESP] Oliveira, Pedro Henrique Chaves de [UNESP] Fenno, J. Christopher Cintra, Luciano Tavares Angelo [UNESP] Benetti, Francine Bottino, Marco C. |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
University of Michigan School of Dentistry Universidade Federal de Minas Gerais (UFMG) Universidade Estadual Paulista (UNESP) University of Michigan |
dc.contributor.author.fl_str_mv |
Reis-Prado, Alexandre Henrique dos Rahimnejad, Maedeh Dal-Fabbro, Renan Toledo, Priscila Toninatto Alves de [UNESP] Anselmi, Caroline [UNESP] Oliveira, Pedro Henrique Chaves de [UNESP] Fenno, J. Christopher Cintra, Luciano Tavares Angelo [UNESP] Benetti, Francine Bottino, Marco C. |
dc.subject.por.fl_str_mv |
Antibiotics Azithromycin Chitosan Hydrogels Injectable Regenerative endodontics |
topic |
Antibiotics Azithromycin Chitosan Hydrogels Injectable Regenerative endodontics |
description |
Injectable biomaterials, such as thermosensitive chitosan (CH)-based hydrogels, present a highly translational potential in dentistry due to their minimally invasive application, adaptability to irregular defects/shapes, and ability to carry therapeutic drugs. This work explores the incorporation of azithromycin (AZI) into thermosensitive CH hydrogels for use as an intracanal medication in regenerative endodontic procedures (REPs). The morphological and chemical characteristics of the hydrogel were assessed by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR). The thermosensitivity, gelation kinetics, compressive strength, cytocompatibility, and antibacterial efficacy were evaluated according to well-established protocols. An in vivo model of periapical disease and evoked bleeding in rats' immature permanent teeth was performed to determine disinfection, tissue repair, and root formation. AZI was successfully incorporated into interconnected porous CH hydrogels, which retained their thermosensitivity. The mechanical and rheological findings indicated that adding AZI did not adversely affect the hydrogels’ strength and injectability. Incorporating 3 % and 5 % AZI into the hydrogels led to minimal cytotoxic effects compared to higher concentrations while enhancing the antibacterial response against endodontic bacteria. AZI-laden hydrogel significantly decreased E. faecalis biofilm compared to the controls. Regarding tissue response, the 3 % AZI-laden hydrogel improved mineralized tissue formation and vascularization compared to untreated teeth and those treated with double antibiotic paste. Our findings demonstrate that adding 3 % AZI into CH hydrogels ablates infection and supports neotissue formation in vivo when applied to a clinically relevant model of regenerative endodontics. |
publishDate |
2025 |
dc.date.none.fl_str_mv |
2025-04-29T18:50:41Z 2025-04-01 |
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/10.1016/j.bioactmat.2024.12.026 Bioactive Materials, v. 46, p. 406-422. 2452-199X https://hdl.handle.net/11449/300820 10.1016/j.bioactmat.2024.12.026 2-s2.0-85213827716 |
url |
http://dx.doi.org/10.1016/j.bioactmat.2024.12.026 https://hdl.handle.net/11449/300820 |
identifier_str_mv |
Bioactive Materials, v. 46, p. 406-422. 2452-199X 10.1016/j.bioactmat.2024.12.026 2-s2.0-85213827716 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Bioactive Materials |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
406-422 |
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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1834482867884785664 |