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 |
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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. |
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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 >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.</description><identifier>ISSN: 0022-0345</identifier><identifier>EISSN: 1544-0591</identifier><identifier>DOI: 10.1177/0022034518755718</identifier><identifier>PMID: 29439642</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>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</subject><ispartof>Journal of dental research, 2018-05, Vol.97 (5), p.530-536</ispartof><rights>International & American Associations for Dental Research 2018</rights><rights>International & American Associations for Dental Research 2018 2018 International & American Associations for Dental Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-c0f540e8630c6846921ebd4e5c8d6ed644d7d9fa5b0fe50c8fdb85fde96d74113</citedby><cites>FETCH-LOGICAL-c528t-c0f540e8630c6846921ebd4e5c8d6ed644d7d9fa5b0fe50c8fdb85fde96d74113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0022034518755718$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0022034518755718$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,776,780,881,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29439642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Dental Restorative Materials Based on Thiol-Michael Photopolymerization</title><title>Journal of dental research</title><addtitle>J Dent Res</addtitle><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.</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 & Medical Complete (Alumni)</collection><collection>Nursing & 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. 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.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>29439642</pmid><doi>10.1177/0022034518755718</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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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