Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization

Detalhes bibliográficos
Autor(a) principal: Gu, L.
Data de Publicação: 2018
Outros Autores: Mazzoni, A., Gou, Y., Pucci, C. [UNESP], Breschi, L., Pashley, D. H., Niu, L., Tay, F. R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1177/0022034517747264
http://hdl.handle.net/11449/176068
Resumo: A chelate-and-rinse extrafibrillar calcium chelation dentin bonding concept has recently been developed and investigated for its effectiveness in improving resin-dentin bonding by bridging the gap between wet and dry dentin bonding. The objective of the present study was to evaluate the gelatinolytic activity of hybrid layers (HLs) created using the chelate-and-rinse bonding technique. Gelatinolytic activity within the HL was examined using in situ zymography and confocal laser-scanning microscopy after 24-h storage or after thermomechanical cycling. Dentin specimens were bonded with Prime&Bond NT (Dentsply Sirona) after conditioning with 15 wt% phosphoric acid for 15 s (control) or 15 wt% polymeric chelators (sodium salt of polyacrylic acid; PAAN) of 2 different molecular weights for 60 s. For each reagent, bonding was performed using dry-bonding and wet-bonding techniques (n = 10). Slices containing the adhesive-dentin interface were covered with fluorescein-conjugated gelatin and examined with a confocal laser-scanning microscope. Fluorescence intensity emitted by the hydrolyzed fluorescein-conjugated gelatin was quantified. Gelatinolytic activity was expressed as the percentage of green fluorescence emitted within the HL. After storage for 24 h, enzymatic activity was only detected within the completely demineralized phosphoric acid–etched dentin, with values derived from dry bonding higher than those from wet bonding (P < 0.05). Almost no fluorescence signals were detected within the HL when dentin was conditioned with PAANs compared with the controls (P < 0.05). After thermomechanical cycling, enzymatic activities significantly increased for the phosphoric acid–conditioned, drying-bonding group compared with 24-h storage (P < 0.05). The present study showed that the use of the chelate-and-rinse bonding concept for both dry-bonding and wet-bonding approaches results in the near absence of matrix-bound collagenolytic activities in the HL even after aging. This may be attributed to fossilization of endogenous proteases via preservation of intrafibrillar minerals within the dentin collagen matrix.
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spelling Zymography of Hybrid Layers Created Using Extrafibrillar Demineralizationbondingchelationdentinenzymologymatrix metalloproteinasesmicroscopyA chelate-and-rinse extrafibrillar calcium chelation dentin bonding concept has recently been developed and investigated for its effectiveness in improving resin-dentin bonding by bridging the gap between wet and dry dentin bonding. The objective of the present study was to evaluate the gelatinolytic activity of hybrid layers (HLs) created using the chelate-and-rinse bonding technique. Gelatinolytic activity within the HL was examined using in situ zymography and confocal laser-scanning microscopy after 24-h storage or after thermomechanical cycling. Dentin specimens were bonded with Prime&Bond NT (Dentsply Sirona) after conditioning with 15 wt% phosphoric acid for 15 s (control) or 15 wt% polymeric chelators (sodium salt of polyacrylic acid; PAAN) of 2 different molecular weights for 60 s. For each reagent, bonding was performed using dry-bonding and wet-bonding techniques (n = 10). Slices containing the adhesive-dentin interface were covered with fluorescein-conjugated gelatin and examined with a confocal laser-scanning microscope. Fluorescence intensity emitted by the hydrolyzed fluorescein-conjugated gelatin was quantified. Gelatinolytic activity was expressed as the percentage of green fluorescence emitted within the HL. After storage for 24 h, enzymatic activity was only detected within the completely demineralized phosphoric acid–etched dentin, with values derived from dry bonding higher than those from wet bonding (P < 0.05). Almost no fluorescence signals were detected within the HL when dentin was conditioned with PAANs compared with the controls (P < 0.05). After thermomechanical cycling, enzymatic activities significantly increased for the phosphoric acid–conditioned, drying-bonding group compared with 24-h storage (P < 0.05). The present study showed that the use of the chelate-and-rinse bonding concept for both dry-bonding and wet-bonding approaches results in the near absence of matrix-bound collagenolytic activities in the HL even after aging. This may be attributed to fossilization of endogenous proteases via preservation of intrafibrillar minerals within the dentin collagen matrix.Department of Operative Dentistry and Endodontics Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology Sun Yat-sen UniversityDepartment of Biomedical and Neuromotor Sciences DIBINEM University of Bologna–Alma Mater StudiorumState Key Laboratory of Oral Diseases West China Hospital of Stomatology Sichuan UniversityDepartment of Restorative Dentistry Institute of Science and Technology São Paulo State University UNESP São Jose dos CamposDepartment of Endodontics The Dental College of Georgia Augusta UniversityState Key Laboratory of Military Stomatology & National Clinical Research Center for Oral Diseases & Shaanxi Key Laboratory of Oral Diseases Department of Prosthodontics School of Stomatology The Fourth Military Medical UniversityDepartment of Restorative Dentistry Institute of Science and Technology São Paulo State University UNESP São Jose dos CamposSun Yat-sen UniversityUniversity of Bologna–Alma Mater StudiorumSichuan UniversityUniversidade Estadual Paulista (Unesp)Augusta UniversityThe Fourth Military Medical UniversityGu, L.Mazzoni, A.Gou, Y.Pucci, C. [UNESP]Breschi, L.Pashley, D. H.Niu, L.Tay, F. R.2018-12-11T17:18:46Z2018-12-11T17:18:46Z2018-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article409-415application/pdfhttp://dx.doi.org/10.1177/0022034517747264Journal of Dental Research, v. 97, n. 4, p. 409-415, 2018.1544-05910022-0345http://hdl.handle.net/11449/17606810.1177/00220345177472642-s2.0-850443934672-s2.0-85044393467.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Dental Research2,302info:eu-repo/semantics/openAccess2023-10-28T06:05:01Zoai:repositorio.unesp.br:11449/176068Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:13:25.292154Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
title Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
spellingShingle Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
Gu, L.
bonding
chelation
dentin
enzymology
matrix metalloproteinases
microscopy
title_short Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
title_full Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
title_fullStr Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
title_full_unstemmed Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
title_sort Zymography of Hybrid Layers Created Using Extrafibrillar Demineralization
author Gu, L.
author_facet Gu, L.
Mazzoni, A.
Gou, Y.
Pucci, C. [UNESP]
Breschi, L.
Pashley, D. H.
Niu, L.
Tay, F. R.
author_role author
author2 Mazzoni, A.
Gou, Y.
Pucci, C. [UNESP]
Breschi, L.
Pashley, D. H.
Niu, L.
Tay, F. R.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Sun Yat-sen University
University of Bologna–Alma Mater Studiorum
Sichuan University
Universidade Estadual Paulista (Unesp)
Augusta University
The Fourth Military Medical University
dc.contributor.author.fl_str_mv Gu, L.
Mazzoni, A.
Gou, Y.
Pucci, C. [UNESP]
Breschi, L.
Pashley, D. H.
Niu, L.
Tay, F. R.
dc.subject.por.fl_str_mv bonding
chelation
dentin
enzymology
matrix metalloproteinases
microscopy
topic bonding
chelation
dentin
enzymology
matrix metalloproteinases
microscopy
description A chelate-and-rinse extrafibrillar calcium chelation dentin bonding concept has recently been developed and investigated for its effectiveness in improving resin-dentin bonding by bridging the gap between wet and dry dentin bonding. The objective of the present study was to evaluate the gelatinolytic activity of hybrid layers (HLs) created using the chelate-and-rinse bonding technique. Gelatinolytic activity within the HL was examined using in situ zymography and confocal laser-scanning microscopy after 24-h storage or after thermomechanical cycling. Dentin specimens were bonded with Prime&Bond NT (Dentsply Sirona) after conditioning with 15 wt% phosphoric acid for 15 s (control) or 15 wt% polymeric chelators (sodium salt of polyacrylic acid; PAAN) of 2 different molecular weights for 60 s. For each reagent, bonding was performed using dry-bonding and wet-bonding techniques (n = 10). Slices containing the adhesive-dentin interface were covered with fluorescein-conjugated gelatin and examined with a confocal laser-scanning microscope. Fluorescence intensity emitted by the hydrolyzed fluorescein-conjugated gelatin was quantified. Gelatinolytic activity was expressed as the percentage of green fluorescence emitted within the HL. After storage for 24 h, enzymatic activity was only detected within the completely demineralized phosphoric acid–etched dentin, with values derived from dry bonding higher than those from wet bonding (P < 0.05). Almost no fluorescence signals were detected within the HL when dentin was conditioned with PAANs compared with the controls (P < 0.05). After thermomechanical cycling, enzymatic activities significantly increased for the phosphoric acid–conditioned, drying-bonding group compared with 24-h storage (P < 0.05). The present study showed that the use of the chelate-and-rinse bonding concept for both dry-bonding and wet-bonding approaches results in the near absence of matrix-bound collagenolytic activities in the HL even after aging. This may be attributed to fossilization of endogenous proteases via preservation of intrafibrillar minerals within the dentin collagen matrix.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:18:46Z
2018-12-11T17:18:46Z
2018-04-01
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/10.1177/0022034517747264
Journal of Dental Research, v. 97, n. 4, p. 409-415, 2018.
1544-0591
0022-0345
http://hdl.handle.net/11449/176068
10.1177/0022034517747264
2-s2.0-85044393467
2-s2.0-85044393467.pdf
url http://dx.doi.org/10.1177/0022034517747264
http://hdl.handle.net/11449/176068
identifier_str_mv Journal of Dental Research, v. 97, n. 4, p. 409-415, 2018.
1544-0591
0022-0345
10.1177/0022034517747264
2-s2.0-85044393467
2-s2.0-85044393467.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Dental Research
2,302
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 409-415
application/pdf
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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