Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays

Detalhes bibliográficos
Autor(a) principal: Prakki, Anuradha
Data de Publicação: 2018
Outros Autores: Xiong, Yaoyang, Bortolatto, Janaína, Gonçalves, Lucélia Lemes [UNESP], Bafail, Arwa, Anderson, Greg, Stavroullakis, Alexander Terry
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.dental.2018.08.297
http://hdl.handle.net/11449/228590
Resumo: Objectives: We investigated the biostability of dentin organic matrices treated with epigallocatechin gallate (EGCG) in comparison to chlorhexidine (CHX), both extracted from functionalized copolymers. Methods: Copolymers were prepared with bis-GMA:TEGDMA and incorporated with 1% of EGCG or CHX (w/w). Blank copolymers were used as control. Copolymer samples were individually stored in 1 mL deionized water to produce copolymer extracts. Dentin matrices were obtained by demineralization of dentin disks in 10% phosphoric acid solution. Matrices were individually treated with 1 mL of the copolymer extracts or distilled water for 48 h. Collected extracts were analyzed by high-performance liquid chromatography (HPLC) for the presence and quantification of EGCG, CHX, and copolymer by-products. Treated dentin matrices were tested for ultimate tensile strength, gravimetric changes, and swelling ratio. The treatment media were tested for total protein concentration, and dentin protease activity through solubilized telopeptide (ICTP- and CTX-ELISA) assays. The treatment media were also submitted to proteomic analysis. Results: HPLC identified released unreacted copolymer species and showed higher release of CHX compared to EGCG from respective copolymer extracts. EGCG extract inhibited activity of dentin proteolytic enzymes and promoted collagen biomodification observed by the telopeptide assays and in the changes to dentin matrix properties. The proteomic results showed less collagenous peptide hits in the EGCG extract media compared to CHX, and suggest compound-specific dentin protein binding interactions. Significance: This study demonstrates specific antiproteolytic effect and protein interactions of EGCG copolymer extract directly on dentin. This represents an advancement in dental materials which can impact the clinical procedures.
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spelling Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assaysBis-GMADentinEGCGHPLCProteomicsTEGDMAObjectives: We investigated the biostability of dentin organic matrices treated with epigallocatechin gallate (EGCG) in comparison to chlorhexidine (CHX), both extracted from functionalized copolymers. Methods: Copolymers were prepared with bis-GMA:TEGDMA and incorporated with 1% of EGCG or CHX (w/w). Blank copolymers were used as control. Copolymer samples were individually stored in 1 mL deionized water to produce copolymer extracts. Dentin matrices were obtained by demineralization of dentin disks in 10% phosphoric acid solution. Matrices were individually treated with 1 mL of the copolymer extracts or distilled water for 48 h. Collected extracts were analyzed by high-performance liquid chromatography (HPLC) for the presence and quantification of EGCG, CHX, and copolymer by-products. Treated dentin matrices were tested for ultimate tensile strength, gravimetric changes, and swelling ratio. The treatment media were tested for total protein concentration, and dentin protease activity through solubilized telopeptide (ICTP- and CTX-ELISA) assays. The treatment media were also submitted to proteomic analysis. Results: HPLC identified released unreacted copolymer species and showed higher release of CHX compared to EGCG from respective copolymer extracts. EGCG extract inhibited activity of dentin proteolytic enzymes and promoted collagen biomodification observed by the telopeptide assays and in the changes to dentin matrix properties. The proteomic results showed less collagenous peptide hits in the EGCG extract media compared to CHX, and suggest compound-specific dentin protein binding interactions. Significance: This study demonstrates specific antiproteolytic effect and protein interactions of EGCG copolymer extract directly on dentin. This represents an advancement in dental materials which can impact the clinical procedures.Natural Sciences and Engineering Research Council of CanadaDepartment of Clinical Sciences — Restorative Faculty of Dentistry University of TorontoDepartment of Prosthodontics School of Medicine Shanghai Jiaotong UniversityDepartment of Restorative Dentistry Institute of Science and Technology of São José dos Campos Sao Paulo State UniversityDepartment of Restorative Dental Sciences College of Dentistry Taibah UniversityDepartment of Restorative Dentistry Institute of Science and Technology of São José dos Campos Sao Paulo State UniversityUniversity of TorontoShanghai Jiaotong UniversityUniversidade Estadual Paulista (UNESP)Taibah UniversityPrakki, AnuradhaXiong, YaoyangBortolatto, JanaínaGonçalves, Lucélia Lemes [UNESP]Bafail, ArwaAnderson, GregStavroullakis, Alexander Terry2022-04-29T08:27:32Z2022-04-29T08:27:32Z2018-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1625-1633http://dx.doi.org/10.1016/j.dental.2018.08.297Dental Materials, v. 34, n. 11, p. 1625-1633, 2018.0109-5641http://hdl.handle.net/11449/22859010.1016/j.dental.2018.08.2972-s2.0-85052920530Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDental Materialsinfo:eu-repo/semantics/openAccess2022-04-29T08:27:32Zoai:repositorio.unesp.br:11449/228590Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:14:42.683952Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
title Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
spellingShingle Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
Prakki, Anuradha
Bis-GMA
Dentin
EGCG
HPLC
Proteomics
TEGDMA
title_short Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
title_full Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
title_fullStr Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
title_full_unstemmed Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
title_sort Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
author Prakki, Anuradha
author_facet Prakki, Anuradha
Xiong, Yaoyang
Bortolatto, Janaína
Gonçalves, Lucélia Lemes [UNESP]
Bafail, Arwa
Anderson, Greg
Stavroullakis, Alexander Terry
author_role author
author2 Xiong, Yaoyang
Bortolatto, Janaína
Gonçalves, Lucélia Lemes [UNESP]
Bafail, Arwa
Anderson, Greg
Stavroullakis, Alexander Terry
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv University of Toronto
Shanghai Jiaotong University
Universidade Estadual Paulista (UNESP)
Taibah University
dc.contributor.author.fl_str_mv Prakki, Anuradha
Xiong, Yaoyang
Bortolatto, Janaína
Gonçalves, Lucélia Lemes [UNESP]
Bafail, Arwa
Anderson, Greg
Stavroullakis, Alexander Terry
dc.subject.por.fl_str_mv Bis-GMA
Dentin
EGCG
HPLC
Proteomics
TEGDMA
topic Bis-GMA
Dentin
EGCG
HPLC
Proteomics
TEGDMA
description Objectives: We investigated the biostability of dentin organic matrices treated with epigallocatechin gallate (EGCG) in comparison to chlorhexidine (CHX), both extracted from functionalized copolymers. Methods: Copolymers were prepared with bis-GMA:TEGDMA and incorporated with 1% of EGCG or CHX (w/w). Blank copolymers were used as control. Copolymer samples were individually stored in 1 mL deionized water to produce copolymer extracts. Dentin matrices were obtained by demineralization of dentin disks in 10% phosphoric acid solution. Matrices were individually treated with 1 mL of the copolymer extracts or distilled water for 48 h. Collected extracts were analyzed by high-performance liquid chromatography (HPLC) for the presence and quantification of EGCG, CHX, and copolymer by-products. Treated dentin matrices were tested for ultimate tensile strength, gravimetric changes, and swelling ratio. The treatment media were tested for total protein concentration, and dentin protease activity through solubilized telopeptide (ICTP- and CTX-ELISA) assays. The treatment media were also submitted to proteomic analysis. Results: HPLC identified released unreacted copolymer species and showed higher release of CHX compared to EGCG from respective copolymer extracts. EGCG extract inhibited activity of dentin proteolytic enzymes and promoted collagen biomodification observed by the telopeptide assays and in the changes to dentin matrix properties. The proteomic results showed less collagenous peptide hits in the EGCG extract media compared to CHX, and suggest compound-specific dentin protein binding interactions. Significance: This study demonstrates specific antiproteolytic effect and protein interactions of EGCG copolymer extract directly on dentin. This represents an advancement in dental materials which can impact the clinical procedures.
publishDate 2018
dc.date.none.fl_str_mv 2018-11-01
2022-04-29T08:27:32Z
2022-04-29T08:27:32Z
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.dental.2018.08.297
Dental Materials, v. 34, n. 11, p. 1625-1633, 2018.
0109-5641
http://hdl.handle.net/11449/228590
10.1016/j.dental.2018.08.297
2-s2.0-85052920530
url http://dx.doi.org/10.1016/j.dental.2018.08.297
http://hdl.handle.net/11449/228590
identifier_str_mv Dental Materials, v. 34, n. 11, p. 1625-1633, 2018.
0109-5641
10.1016/j.dental.2018.08.297
2-s2.0-85052920530
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dental Materials
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1625-1633
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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