Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line

Bibliographic Details
Main Author: Freitas da Silva, Emily Vivianne [UNESP]
Publication Date: 2016
Other Authors: Goiato, Marcelo Coelho [UNESP], Santos, Daniela Micheline dos [UNESP], Bonatto, Liliane da Rocha [UNESP], Balera Brito, Victor Gustavo [UNESP], Penha de Oliveira, Sandra Helena [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.prosdent.2016.06.001
http://hdl.handle.net/11449/162135
Summary: Statement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group.
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spelling Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell lineStatement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group.National Council for Scientific and Technological DevelopmentCoordination for the Improvement of Higher Education PersonnelFoundation for Support to Research of the State of Sao Paulo scholarshipSao Paulo State Univ, Aracatuba Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Basic Sci, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Dent Mat & Prosthodont, Sao Paulo, BrazilSao Paulo State Univ, Aracatuba Dent Sch, Dept Basic Sci, Sao Paulo, BrazilFoundation for Support to Research of the State of Sao Paulo scholarship: 2013/11830-4Elsevier B.V.Universidade Estadual Paulista (Unesp)Freitas da Silva, Emily Vivianne [UNESP]Goiato, Marcelo Coelho [UNESP]Santos, Daniela Micheline dos [UNESP]Bonatto, Liliane da Rocha [UNESP]Balera Brito, Victor Gustavo [UNESP]Penha de Oliveira, Sandra Helena [UNESP]2018-11-26T17:10:32Z2018-11-26T17:10:32Z2016-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article818-823application/pdfhttp://dx.doi.org/10.1016/j.prosdent.2016.06.001Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016.0022-3913http://hdl.handle.net/11449/16213510.1016/j.prosdent.2016.06.001WOS:000387302400018WOS000387302400018.pdf9719883814872582Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Prosthetic Dentistry1,087info:eu-repo/semantics/openAccess2024-01-07T06:31:33Zoai:repositorio.unesp.br:11449/162135Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-07T06:31:33Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
title Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
spellingShingle Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
Freitas da Silva, Emily Vivianne [UNESP]
title_short Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
title_full Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
title_fullStr Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
title_full_unstemmed Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
title_sort Effect of different methods of polymerizing ocular prosthesis acrylic resin on a human conjunctival cell line
author Freitas da Silva, Emily Vivianne [UNESP]
author_facet Freitas da Silva, Emily Vivianne [UNESP]
Goiato, Marcelo Coelho [UNESP]
Santos, Daniela Micheline dos [UNESP]
Bonatto, Liliane da Rocha [UNESP]
Balera Brito, Victor Gustavo [UNESP]
Penha de Oliveira, Sandra Helena [UNESP]
author_role author
author2 Goiato, Marcelo Coelho [UNESP]
Santos, Daniela Micheline dos [UNESP]
Bonatto, Liliane da Rocha [UNESP]
Balera Brito, Victor Gustavo [UNESP]
Penha de Oliveira, Sandra Helena [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Freitas da Silva, Emily Vivianne [UNESP]
Goiato, Marcelo Coelho [UNESP]
Santos, Daniela Micheline dos [UNESP]
Bonatto, Liliane da Rocha [UNESP]
Balera Brito, Victor Gustavo [UNESP]
Penha de Oliveira, Sandra Helena [UNESP]
description Statement of problem. Ocular prosthesis acrylic resins should be biocompatible regardless of the polymerization method. The authors are unaware of a study that evaluated the biocompatibility of ocular prostheses. Purpose. The purpose of this in vitro study was to evaluate the cytotoxicity of different methods of polymerizing ocular prosthesis acrylic resin. This was accomplished by analyzing the cell proliferation, production of proinflammatory cytokines, and expression of extracellular matrix proteins related to tissue remodeling and repair of a human conjunctival cell line. Material and methods. Nine acrylic resin specimens were divided into 3 groups: polymerization in a water bath, by microwave, or by autopolymerization. Eluates (prepared for 72 hours) were exposed to cells for 72 hours. A medium without specimens served as negative control (non stimulated group). The tetrazolium dye MTT (3[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay was performed to evaluate the cytotoxic effect, and an enzyme-linked immunosorbent assay was executed for analysis of interleukin 1 beta (IL1 beta), IL6, tumor necrosis factor alpha (TNF alpha), and CCL3/MIP1 alpha production. Also, real-time reverse transcriptase (RT)-PCR was performed for analysis of mRNA expression of type IV collagen (COL IV), TGF beta, and MMP9, and data were tested using ANOVA with Bonferroni post hoc test (alpha=.05). Results. Microwave-processed resin showed slight cytotoxicity due to a significant reduction in cell proliferation and an increase in IL6 quantity. Higher levels of mRNA expression of COL IV, MMP9, and TGF beta were verified in water bath-processed resin, which were similar to those in the nonstimulated group. Conclusions. Microwave-processed resin showed a significant reduction in cell proliferation and an increase in IL6 quantity. Heat-polymerized resin exhibited a higher mRNA expression of COL IV, MMP9, and TGF beta; this result was similar to that in the nonstimulated group.
publishDate 2016
dc.date.none.fl_str_mv 2016-11-01
2018-11-26T17:10:32Z
2018-11-26T17:10:32Z
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.prosdent.2016.06.001
Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016.
0022-3913
http://hdl.handle.net/11449/162135
10.1016/j.prosdent.2016.06.001
WOS:000387302400018
WOS000387302400018.pdf
9719883814872582
url http://dx.doi.org/10.1016/j.prosdent.2016.06.001
http://hdl.handle.net/11449/162135
identifier_str_mv Journal Of Prosthetic Dentistry. New York: Mosby-elsevier, v. 116, n. 5, p. 818-823, 2016.
0022-3913
10.1016/j.prosdent.2016.06.001
WOS:000387302400018
WOS000387302400018.pdf
9719883814872582
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Prosthetic Dentistry
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dc.format.none.fl_str_mv 818-823
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
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