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Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR

Objective. To evaluate bacterial growth inhibition, mechanical properties, and compound release rate and stability of copolymers incorporated with anthocyanin (ACY; Vaccinium macrocarpon). Methods. Resin samples were prepared (Bis-GMA/TEGDMA at 70/30 mol%) and incorporated with 2 w/w% of either ACY...

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Autores principales: Hrynash, Halyna, Pilly, Vinay Kumar, Mankovskaia, Alexandra, Xiong, Yaoyang, Nogueira Filho, Getulio, Bresciani, Eduardo, Lévesque, Céline Marie, Prakki, Anuradha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947769/
https://www.ncbi.nlm.nih.gov/pubmed/24693287
http://dx.doi.org/10.1155/2014/289401
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author Hrynash, Halyna
Pilly, Vinay Kumar
Mankovskaia, Alexandra
Xiong, Yaoyang
Nogueira Filho, Getulio
Bresciani, Eduardo
Lévesque, Céline Marie
Prakki, Anuradha
author_facet Hrynash, Halyna
Pilly, Vinay Kumar
Mankovskaia, Alexandra
Xiong, Yaoyang
Nogueira Filho, Getulio
Bresciani, Eduardo
Lévesque, Céline Marie
Prakki, Anuradha
author_sort Hrynash, Halyna
collection PubMed
description Objective. To evaluate bacterial growth inhibition, mechanical properties, and compound release rate and stability of copolymers incorporated with anthocyanin (ACY; Vaccinium macrocarpon). Methods. Resin samples were prepared (Bis-GMA/TEGDMA at 70/30 mol%) and incorporated with 2 w/w% of either ACY or chlorhexidine (CHX), except for the control group. Samples were individually immersed in a bacterial culture (Streptococcus mutans) for 24 h. Cell viability (n = 3) was assessed by counting the number of colony forming units on replica agar plates. Flexural strength (FS) and elastic modulus (E) were tested on a universal testing machine (n = 8). Compound release and chemical stability were evaluated by UV spectrophotometry and (1)H NMR (n = 3). Data were analyzed by one-way ANOVA and Tukey's test (α = 0.05). Results. Both compounds inhibited S. mutans growth, with CHX being most effective (P < 0.05). Control resin had the lowest FS and E values, followed by ACY and CHX, with statistical difference between control and CHX groups for both mechanical properties (P < 0.05). The 24 h compound release rates were ACY: 1.33 μg/mL and CHX: 1.92 μg/mL. (1)H NMR spectra suggests that both compounds remained stable after being released in water. Conclusion. The present findings indicate that anthocyanins might be used as a natural antibacterial agent in resin based materials.
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spelling pubmed-39477692014-04-01 Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR Hrynash, Halyna Pilly, Vinay Kumar Mankovskaia, Alexandra Xiong, Yaoyang Nogueira Filho, Getulio Bresciani, Eduardo Lévesque, Céline Marie Prakki, Anuradha Int J Dent Research Article Objective. To evaluate bacterial growth inhibition, mechanical properties, and compound release rate and stability of copolymers incorporated with anthocyanin (ACY; Vaccinium macrocarpon). Methods. Resin samples were prepared (Bis-GMA/TEGDMA at 70/30 mol%) and incorporated with 2 w/w% of either ACY or chlorhexidine (CHX), except for the control group. Samples were individually immersed in a bacterial culture (Streptococcus mutans) for 24 h. Cell viability (n = 3) was assessed by counting the number of colony forming units on replica agar plates. Flexural strength (FS) and elastic modulus (E) were tested on a universal testing machine (n = 8). Compound release and chemical stability were evaluated by UV spectrophotometry and (1)H NMR (n = 3). Data were analyzed by one-way ANOVA and Tukey's test (α = 0.05). Results. Both compounds inhibited S. mutans growth, with CHX being most effective (P < 0.05). Control resin had the lowest FS and E values, followed by ACY and CHX, with statistical difference between control and CHX groups for both mechanical properties (P < 0.05). The 24 h compound release rates were ACY: 1.33 μg/mL and CHX: 1.92 μg/mL. (1)H NMR spectra suggests that both compounds remained stable after being released in water. Conclusion. The present findings indicate that anthocyanins might be used as a natural antibacterial agent in resin based materials. Hindawi Publishing Corporation 2014 2014-02-18 /pmc/articles/PMC3947769/ /pubmed/24693287 http://dx.doi.org/10.1155/2014/289401 Text en Copyright © 2014 Halyna Hrynash et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hrynash, Halyna
Pilly, Vinay Kumar
Mankovskaia, Alexandra
Xiong, Yaoyang
Nogueira Filho, Getulio
Bresciani, Eduardo
Lévesque, Céline Marie
Prakki, Anuradha
Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title_full Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title_fullStr Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title_full_unstemmed Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title_short Anthocyanin Incorporated Dental Copolymer: Bacterial Growth Inhibition, Mechanical Properties, and Compound Release Rates and Stability by (1)H NMR
title_sort anthocyanin incorporated dental copolymer: bacterial growth inhibition, mechanical properties, and compound release rates and stability by (1)h nmr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947769/
https://www.ncbi.nlm.nih.gov/pubmed/24693287
http://dx.doi.org/10.1155/2014/289401
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