Conversion of a new monomer for dental resin application

Objective: The aim of this study was to investigate the degree of conversion and cross-linking of polyurethane dimethacrylate (PUDMA), derived from palm oil polyol, for dental resin application. Methods: Polyurethane dimethacrylate was synthesized by reacting excess amount of Methylene diphenyl diis...

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Main Authors: Al-Sanabani, F., Abu Kasim, N.H., Gan, S.N.
Format: Article
Language:English
Published: 2008
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Online Access:http://eprints.um.edu.my/2569/1/Conversion_of_a_NEW_Monomer_for_Dental_Resin_Application.pdf
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spelling my.um.eprints.25692014-12-18T04:32:10Z http://eprints.um.edu.my/2569/ Conversion of a new monomer for dental resin application Al-Sanabani, F. Abu Kasim, N.H. Gan, S.N. R Medicine R Medicine (General) RK Dentistry Objective: The aim of this study was to investigate the degree of conversion and cross-linking of polyurethane dimethacrylate (PUDMA), derived from palm oil polyol, for dental resin application. Methods: Polyurethane dimethacrylate was synthesized by reacting excess amount of Methylene diphenyl diisocyanate (MDI) with palm oil polyol. The resulting isocyanate polyurethane prepolymer was then acrylated using hydroxymethacrylate (HEMA). Fourier transform infrared spectroscopy was used to ascertain the formation of PUDMA, and to determine the degree of conversion (DC) of: I) PUDMA, II) Bis-GMA, III)Bis-EMA,IV) Bis-GMA/TEGDMA (3:1), V) Bis-GMA/TEGDMA(3:1)/Bis-EMA (3:1), VI) PUDMA/Bis-EMA (3:1), VII) Bis-GMA/TEGDMA(3:1)/PUDMA (1:1), and VIII) Bis-GMA/TEGDMA(3:1)/PUDMA/Bis-EMA (1-1-1). The photo initiator system Camphorquinone (CQ) and Ethyl-4-N,N-dimethylaminobenzoate (EDMAB) was used with ratio 0.25 and 0.75 by weight, respectively, for all monomers. The results were analyzed using one way ANOVA and Post Hoc Dunnett T3 for multiple comparisons. Results: The FTIR spectrum of PUDMA showed that the isocyanate peaks was absent and appearance of urethane peak. The results of degree of conversion showed that, the unreacted C=C in Bis-GMA is more than 50 , however, the DC of PUDMA is 63 with cross linking 0.4. The resin systems which contain PUDMA showed higher DC and cross-linking than that of other resin system. Conclusions: The degree of conversion of PUDMA monomer is highly significant than Bis-GMA, with more cross-linking. The PUDMA could improve the DC and cross-linking of resin system. Therefore, PUDMA may have promising mechanical properties and biocompatibility. 2008 Article PeerReviewed application/pdf en http://eprints.um.edu.my/2569/1/Conversion_of_a_NEW_Monomer_for_Dental_Resin_Application.pdf Al-Sanabani, F. and Abu Kasim, N.H. and Gan, S.N. (2008) Conversion of a new monomer for dental resin application. Journal of Dental Research. http://iadr.confex.com/iadr/sea08/techprogramforcd/A112964.htm
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
language English
topic R Medicine
R Medicine (General)
RK Dentistry
spellingShingle R Medicine
R Medicine (General)
RK Dentistry
Al-Sanabani, F.
Abu Kasim, N.H.
Gan, S.N.
Conversion of a new monomer for dental resin application
description Objective: The aim of this study was to investigate the degree of conversion and cross-linking of polyurethane dimethacrylate (PUDMA), derived from palm oil polyol, for dental resin application. Methods: Polyurethane dimethacrylate was synthesized by reacting excess amount of Methylene diphenyl diisocyanate (MDI) with palm oil polyol. The resulting isocyanate polyurethane prepolymer was then acrylated using hydroxymethacrylate (HEMA). Fourier transform infrared spectroscopy was used to ascertain the formation of PUDMA, and to determine the degree of conversion (DC) of: I) PUDMA, II) Bis-GMA, III)Bis-EMA,IV) Bis-GMA/TEGDMA (3:1), V) Bis-GMA/TEGDMA(3:1)/Bis-EMA (3:1), VI) PUDMA/Bis-EMA (3:1), VII) Bis-GMA/TEGDMA(3:1)/PUDMA (1:1), and VIII) Bis-GMA/TEGDMA(3:1)/PUDMA/Bis-EMA (1-1-1). The photo initiator system Camphorquinone (CQ) and Ethyl-4-N,N-dimethylaminobenzoate (EDMAB) was used with ratio 0.25 and 0.75 by weight, respectively, for all monomers. The results were analyzed using one way ANOVA and Post Hoc Dunnett T3 for multiple comparisons. Results: The FTIR spectrum of PUDMA showed that the isocyanate peaks was absent and appearance of urethane peak. The results of degree of conversion showed that, the unreacted C=C in Bis-GMA is more than 50 , however, the DC of PUDMA is 63 with cross linking 0.4. The resin systems which contain PUDMA showed higher DC and cross-linking than that of other resin system. Conclusions: The degree of conversion of PUDMA monomer is highly significant than Bis-GMA, with more cross-linking. The PUDMA could improve the DC and cross-linking of resin system. Therefore, PUDMA may have promising mechanical properties and biocompatibility.
format Article
author Al-Sanabani, F.
Abu Kasim, N.H.
Gan, S.N.
author_facet Al-Sanabani, F.
Abu Kasim, N.H.
Gan, S.N.
author_sort Al-Sanabani, F.
title Conversion of a new monomer for dental resin application
title_short Conversion of a new monomer for dental resin application
title_full Conversion of a new monomer for dental resin application
title_fullStr Conversion of a new monomer for dental resin application
title_full_unstemmed Conversion of a new monomer for dental resin application
title_sort conversion of a new monomer for dental resin application
publishDate 2008
url http://eprints.um.edu.my/2569/1/Conversion_of_a_NEW_Monomer_for_Dental_Resin_Application.pdf
http://eprints.um.edu.my/2569/
http://iadr.confex.com/iadr/sea08/techprogramforcd/A112964.htm
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score 13.214268