Dental Restorative Materials Based on Thiol-Michael Photopolymerization

Step-growth thiol-Michael photopolymerizable resins, constituting an alternative chemistry to the current methacrylate-based chain-growth polymerizations, were developed and evaluated for use as dental restorative materials. The beneficial features inherent to anion-mediated thiol-Michael polymeriza...

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Veröffentlicht in:Journal of dental research 2018-05, Vol.97 (5), p.530-536
Hauptverfasser: Huang, S., Podgórski, M., Zhang, X., Sinha, J., Claudino, M., Stansbury, J.W., Bowman, C.N.
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container_end_page 536
container_issue 5
container_start_page 530
container_title Journal of dental research
container_volume 97
creator Huang, S.
Podgórski, M.
Zhang, X.
Sinha, J.
Claudino, M.
Stansbury, J.W.
Bowman, C.N.
description Step-growth thiol-Michael photopolymerizable resins, constituting an alternative chemistry to the current methacrylate-based chain-growth polymerizations, were developed and evaluated for use as dental restorative materials. The beneficial features inherent to anion-mediated thiol-Michael polymerizations were explored, such as rapid photocuring, low stress generation, ester content tunability, and improved mechanical performance in a moist environment. An ester-free tetrafunctional thiol and a ultraviolet-sensitive photobase generator were implemented to facilitate thiol-Michael photopolymerization. Thiol-Michael resins of varied ester content were fabricated under suitable light activation. Polymerization kinetics and shrinkage stress were determined with Fourier-transform infrared spectroscopy coupled with tensometery measurements. Thermomechanical properties of new materials were evaluated by dynamic mechanical analysis and in 3-point bending stress-strain experiments. Photopolymerization kinetics, polymerization shrinkage stress, glass transition temperature, flexural modulus, flexural toughness, and water sorption/solubility were compared between different thiol-Michael systems and the BisGMA/TEGDMA control. Furthermore, the mechanical performance of 2 thiol-Michael composites and a control composite were compared before and after extensive conditioning in water. All photobase-catalyzed thiol-Michael polymerization matrices achieved >90% conversion with a dramatic reduction in shrinkage stress as compared with the unfilled dimethacrylate control. One prototype of ester-free thiol-Michael formulations had significantly better water uptake properties than the BisGMA/TEGDMA control system. Although exhibiting relatively lower Young’s modulus and glass transition temperatures, highly uniform thiol-Michael materials achieved much higher toughness than the BisGMA/TEGDMA control. Moreover, low-ester thiol-Michael composite systems show stable mechanical performance even after extensive water treatment. Although further resin/curing methodology optimization is required, the photopolymerized thiol-Michael prototype resins can now be recognized as promising candidates for implementation in composite dental restorative materials.
doi_str_mv 10.1177/0022034518755718
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The beneficial features inherent to anion-mediated thiol-Michael polymerizations were explored, such as rapid photocuring, low stress generation, ester content tunability, and improved mechanical performance in a moist environment. An ester-free tetrafunctional thiol and a ultraviolet-sensitive photobase generator were implemented to facilitate thiol-Michael photopolymerization. Thiol-Michael resins of varied ester content were fabricated under suitable light activation. Polymerization kinetics and shrinkage stress were determined with Fourier-transform infrared spectroscopy coupled with tensometery measurements. Thermomechanical properties of new materials were evaluated by dynamic mechanical analysis and in 3-point bending stress-strain experiments. Photopolymerization kinetics, polymerization shrinkage stress, glass transition temperature, flexural modulus, flexural toughness, and water sorption/solubility were compared between different thiol-Michael systems and the BisGMA/TEGDMA control. Furthermore, the mechanical performance of 2 thiol-Michael composites and a control composite were compared before and after extensive conditioning in water. All photobase-catalyzed thiol-Michael polymerization matrices achieved &gt;90% conversion with a dramatic reduction in shrinkage stress as compared with the unfilled dimethacrylate control. One prototype of ester-free thiol-Michael formulations had significantly better water uptake properties than the BisGMA/TEGDMA control system. Although exhibiting relatively lower Young’s modulus and glass transition temperatures, highly uniform thiol-Michael materials achieved much higher toughness than the BisGMA/TEGDMA control. Moreover, low-ester thiol-Michael composite systems show stable mechanical performance even after extensive water treatment. 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Photopolymerization kinetics, polymerization shrinkage stress, glass transition temperature, flexural modulus, flexural toughness, and water sorption/solubility were compared between different thiol-Michael systems and the BisGMA/TEGDMA control. Furthermore, the mechanical performance of 2 thiol-Michael composites and a control composite were compared before and after extensive conditioning in water. All photobase-catalyzed thiol-Michael polymerization matrices achieved &gt;90% conversion with a dramatic reduction in shrinkage stress as compared with the unfilled dimethacrylate control. One prototype of ester-free thiol-Michael formulations had significantly better water uptake properties than the BisGMA/TEGDMA control system. Although exhibiting relatively lower Young’s modulus and glass transition temperatures, highly uniform thiol-Michael materials achieved much higher toughness than the BisGMA/TEGDMA control. 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Although further resin/curing methodology optimization is required, the photopolymerized thiol-Michael prototype resins can now be recognized as promising candidates for implementation in composite dental restorative materials.</description><subject>Composite materials</subject><subject>Crosslinking polymerization</subject><subject>Data analysis</subject><subject>Dental restorative materials</subject><subject>Fourier transforms</subject><subject>Infrared spectroscopy</subject><subject>Kinetics</subject><subject>Mechanical properties</subject><subject>Moisture absorption</subject><subject>Polymerization</subject><subject>Research Reports</subject><subject>Resins</subject><subject>Triethylene glycol dimethacrylate</subject><subject>Water treatment</subject><subject>Water uptake</subject><issn>0022-0345</issn><issn>1544-0591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1UUtL9DAUDfKJjo-9Kyl8GzfVmzRpk43gW0FRRNchk9w6lU4zJh1Bf70p4xtcZXEeOeceQrYo7FJaVXsAjEHBBZWVEBWVS2REBec5CEX_kdEA5wO-StZifASgislihawyxQtVcjYiZ8fY9abNbjH2Ppi-ecbsyvQYGtPG7NBEdJnvsrtJ49v8qrETg212M_G9n_n2ZZp4r0nkuw2yXCcFbr6_6-T-9OTu6Dy_vD67ODq4zK1gss8t1IIDyrIAW0peKkZx7DgKK12JruTcVU7VRoyhRgFW1m4sRe1Qla7ilBbrZH_hO5uPp-hsSh9Mq2ehmZrwor1p9E-kayb6wT9roYQsKpYMdt4Ngn-ap9Z62kSLbWs69POo2XA0qjgfqP9_UR_9PHSpnmYFgJBQqiERLFg2-BgD1p9hKOhhJf17pSTZ_l7iU_AxSyLkC0I0D_j165-Gb4V6mnw</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Huang, S.</creator><creator>Podgórski, M.</creator><creator>Zhang, X.</creator><creator>Sinha, J.</creator><creator>Claudino, M.</creator><creator>Stansbury, J.W.</creator><creator>Bowman, C.N.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180501</creationdate><title>Dental Restorative Materials Based on Thiol-Michael Photopolymerization</title><author>Huang, S. ; Podgórski, M. ; Zhang, X. ; Sinha, J. ; Claudino, M. ; Stansbury, J.W. ; Bowman, C.N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-c0f540e8630c6846921ebd4e5c8d6ed644d7d9fa5b0fe50c8fdb85fde96d74113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Composite materials</topic><topic>Crosslinking polymerization</topic><topic>Data analysis</topic><topic>Dental restorative materials</topic><topic>Fourier transforms</topic><topic>Infrared spectroscopy</topic><topic>Kinetics</topic><topic>Mechanical properties</topic><topic>Moisture absorption</topic><topic>Polymerization</topic><topic>Research Reports</topic><topic>Resins</topic><topic>Triethylene glycol dimethacrylate</topic><topic>Water treatment</topic><topic>Water uptake</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, S.</creatorcontrib><creatorcontrib>Podgórski, M.</creatorcontrib><creatorcontrib>Zhang, X.</creatorcontrib><creatorcontrib>Sinha, J.</creatorcontrib><creatorcontrib>Claudino, M.</creatorcontrib><creatorcontrib>Stansbury, J.W.</creatorcontrib><creatorcontrib>Bowman, C.N.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of dental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, S.</au><au>Podgórski, M.</au><au>Zhang, X.</au><au>Sinha, J.</au><au>Claudino, M.</au><au>Stansbury, J.W.</au><au>Bowman, C.N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dental Restorative Materials Based on Thiol-Michael Photopolymerization</atitle><jtitle>Journal of dental research</jtitle><addtitle>J Dent Res</addtitle><date>2018-05-01</date><risdate>2018</risdate><volume>97</volume><issue>5</issue><spage>530</spage><epage>536</epage><pages>530-536</pages><issn>0022-0345</issn><eissn>1544-0591</eissn><abstract>Step-growth thiol-Michael photopolymerizable resins, constituting an alternative chemistry to the current methacrylate-based chain-growth polymerizations, were developed and evaluated for use as dental restorative materials. 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subjects Composite materials
Crosslinking polymerization
Data analysis
Dental restorative materials
Fourier transforms
Infrared spectroscopy
Kinetics
Mechanical properties
Moisture absorption
Polymerization
Research Reports
Resins
Triethylene glycol dimethacrylate
Water treatment
Water uptake
title Dental Restorative Materials Based on Thiol-Michael Photopolymerization
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