Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1021/acsami.9b22964 http://hdl.handle.net/11449/196785 |
Resumo: | A photocrosslinkable gelatin methacryloyl (GelMA) hydrogel has been widely examined in regenerative engineering because of its good cell-tissue affinity and degradability in the presence of matrix metalloproteinases. A halloysite aluminosilicate nanotube (HNT) is a known reservoir for the loading and sustained delivery of therapeutics. Here, we formulate injectable chlorhexidine (CHX)-loaded nanotube-modified GelMA hydrogel that is cytocompatible and biodegradable and provides sustained release of CHX for infection ablation while displaying good biocompatibility. The effects of HNTs and CHX on hydrogel degradability and mechanical properties, as well as on the kinetics of CHX release, and on the antimicrobial efficacy against oral pathogens were systematically assessed. Cytocompatibility in stem cells from human exfoliated deciduous teeth and inflammatory response in vivo using a subcutaneous rat model were determined. Our hydrogel system, that is, (CHX)-loaded nanotube-modified GelMA showed minimum localized inflammatory responses, supporting its ability for drug delivery applications. Moreover, we showed that the incorporation of CHX-loaded nanotubes reduces the mechanical properties, increases the swelling ratio, and diminishes the degradation rate of the hydrogels. Importantly, the presence of CHX-loaded nanotubes inhibits bacterial growth with minimal cell toxicity. Our findings provide a new strategy to modify GelMA hydrogel with chlorhexidine-loaded nanotubes for clinical use as an injectable drug delivery strategy for dental infection ablation. |
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Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablationdrug deliveryhydrogelinfectionendodonticsdentistrymatrix metalloproteinasesA photocrosslinkable gelatin methacryloyl (GelMA) hydrogel has been widely examined in regenerative engineering because of its good cell-tissue affinity and degradability in the presence of matrix metalloproteinases. A halloysite aluminosilicate nanotube (HNT) is a known reservoir for the loading and sustained delivery of therapeutics. Here, we formulate injectable chlorhexidine (CHX)-loaded nanotube-modified GelMA hydrogel that is cytocompatible and biodegradable and provides sustained release of CHX for infection ablation while displaying good biocompatibility. The effects of HNTs and CHX on hydrogel degradability and mechanical properties, as well as on the kinetics of CHX release, and on the antimicrobial efficacy against oral pathogens were systematically assessed. Cytocompatibility in stem cells from human exfoliated deciduous teeth and inflammatory response in vivo using a subcutaneous rat model were determined. Our hydrogel system, that is, (CHX)-loaded nanotube-modified GelMA showed minimum localized inflammatory responses, supporting its ability for drug delivery applications. Moreover, we showed that the incorporation of CHX-loaded nanotubes reduces the mechanical properties, increases the swelling ratio, and diminishes the degradation rate of the hydrogels. Importantly, the presence of CHX-loaded nanotubes inhibits bacterial growth with minimal cell toxicity. Our findings provide a new strategy to modify GelMA hydrogel with chlorhexidine-loaded nanotubes for clinical use as an injectable drug delivery strategy for dental infection ablation.National Institutes of Health (NIH, National Institute of Dental and Craniofacial Research/NIDCR)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Michigan, Sch Dent, Dept Cariol Restorat Sci & Endodont, Ann Arbor, MI 48109 USAUniv Fed Pelotas, Sch Dent, Dept Restorat Dent, BR-96010610 Pelotas, RS, BrazilSao Paulo State Univ, Sch Dent, Dept Dent Mat & Prosthodont, BR-01049010 Araraquara, SP, BrazilUniv Michigan, Coll Pharm, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USAUniv Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USAUniv Michigan, Sch Dent, Dept Biol & Mat Sci & Prosthodont, Ann Arbor, MI 48109 USASao Paulo State Univ, Sch Dent, Dept Dent Mat & Prosthodont, BR-01049010 Araraquara, SP, BrazilNational Institutes of Health (NIH, National Institute of Dental and Craniofacial Research/NIDCR): K08DE023552National Institutes of Health (NIH, National Institute of Dental and Craniofacial Research/NIDCR): R01DE026578Amer Chemical SocUniv MichiganUniv Fed PelotasUniversidade Estadual Paulista (Unesp)Ribeiro, Juliana S.Bordini, Ester A. F. [UNESP]Ferreira, Jessica A.Mei, LingDubey, NileshkumarFenno, J. ChristopherPiva, EvandroLund, Rafael G.Schwendeman, AnnaBottino, Marco C.2020-12-10T19:56:09Z2020-12-10T19:56:09Z2020-04-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article16006-16017http://dx.doi.org/10.1021/acsami.9b22964Acs Applied Materials & Interfaces. Washington: Amer Chemical Soc, v. 12, n. 14, p. 16006-16017, 2020.1944-8244http://hdl.handle.net/11449/19678510.1021/acsami.9b22964WOS:000526583500004Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAcs Applied Materials & Interfacesinfo:eu-repo/semantics/openAccess2024-09-27T14:57:18Zoai:repositorio.unesp.br:11449/196785Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:57:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
title |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
spellingShingle |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation Ribeiro, Juliana S. drug delivery hydrogel infection endodontics dentistry matrix metalloproteinases |
title_short |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
title_full |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
title_fullStr |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
title_full_unstemmed |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
title_sort |
Injectable MMP-Responsive Nanotube-Modified Gelatin Hydrogel for Dental Infection Ablation |
author |
Ribeiro, Juliana S. |
author_facet |
Ribeiro, Juliana S. Bordini, Ester A. F. [UNESP] Ferreira, Jessica A. Mei, Ling Dubey, Nileshkumar Fenno, J. Christopher Piva, Evandro Lund, Rafael G. Schwendeman, Anna Bottino, Marco C. |
author_role |
author |
author2 |
Bordini, Ester A. F. [UNESP] Ferreira, Jessica A. Mei, Ling Dubey, Nileshkumar Fenno, J. Christopher Piva, Evandro Lund, Rafael G. Schwendeman, Anna Bottino, Marco C. |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Michigan Univ Fed Pelotas Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Ribeiro, Juliana S. Bordini, Ester A. F. [UNESP] Ferreira, Jessica A. Mei, Ling Dubey, Nileshkumar Fenno, J. Christopher Piva, Evandro Lund, Rafael G. Schwendeman, Anna Bottino, Marco C. |
dc.subject.por.fl_str_mv |
drug delivery hydrogel infection endodontics dentistry matrix metalloproteinases |
topic |
drug delivery hydrogel infection endodontics dentistry matrix metalloproteinases |
description |
A photocrosslinkable gelatin methacryloyl (GelMA) hydrogel has been widely examined in regenerative engineering because of its good cell-tissue affinity and degradability in the presence of matrix metalloproteinases. A halloysite aluminosilicate nanotube (HNT) is a known reservoir for the loading and sustained delivery of therapeutics. Here, we formulate injectable chlorhexidine (CHX)-loaded nanotube-modified GelMA hydrogel that is cytocompatible and biodegradable and provides sustained release of CHX for infection ablation while displaying good biocompatibility. The effects of HNTs and CHX on hydrogel degradability and mechanical properties, as well as on the kinetics of CHX release, and on the antimicrobial efficacy against oral pathogens were systematically assessed. Cytocompatibility in stem cells from human exfoliated deciduous teeth and inflammatory response in vivo using a subcutaneous rat model were determined. Our hydrogel system, that is, (CHX)-loaded nanotube-modified GelMA showed minimum localized inflammatory responses, supporting its ability for drug delivery applications. Moreover, we showed that the incorporation of CHX-loaded nanotubes reduces the mechanical properties, increases the swelling ratio, and diminishes the degradation rate of the hydrogels. Importantly, the presence of CHX-loaded nanotubes inhibits bacterial growth with minimal cell toxicity. Our findings provide a new strategy to modify GelMA hydrogel with chlorhexidine-loaded nanotubes for clinical use as an injectable drug delivery strategy for dental infection ablation. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-10T19:56:09Z 2020-12-10T19:56:09Z 2020-04-08 |
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/10.1021/acsami.9b22964 Acs Applied Materials & Interfaces. Washington: Amer Chemical Soc, v. 12, n. 14, p. 16006-16017, 2020. 1944-8244 http://hdl.handle.net/11449/196785 10.1021/acsami.9b22964 WOS:000526583500004 |
url |
http://dx.doi.org/10.1021/acsami.9b22964 http://hdl.handle.net/11449/196785 |
identifier_str_mv |
Acs Applied Materials & Interfaces. Washington: Amer Chemical Soc, v. 12, n. 14, p. 16006-16017, 2020. 1944-8244 10.1021/acsami.9b22964 WOS:000526583500004 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acs Applied Materials & Interfaces |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
16006-16017 |
dc.publisher.none.fl_str_mv |
Amer Chemical Soc |
publisher.none.fl_str_mv |
Amer Chemical Soc |
dc.source.none.fl_str_mv |
Web of Science 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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1813546494386503680 |