Functionalized epigallocatechin gallate copolymer inhibit dentin matrices degradation: Mechanical, solubilized telopeptide and proteomic assays
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
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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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 |
|
_version_ |
1808129040385572864 |