Degradation in the dentin–composite interface subjected to multi-species biofilm challenges
The mechanical integrity of composite restorations challenged with multi-species oral biofilms was studied. While most studies used single-species biofilms, we used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries....
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creator | Li, Y. Carrera, C. Chen, R. Li, J. Lenton, P. Rudney, J.D. Jones, R.S. Aparicio, C. Fok, A. |
description | The mechanical integrity of composite restorations challenged with multi-species oral biofilms was studied. While most studies used single-species biofilms, we used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Biofilm growth with sucrose pulsing caused preferential degradation of the composite–dentin interface, with significant differences in bond strength reduction and failure modes depending on the composite/adhesive system used.
Oral biofilms can degrade the components in dental resin-based composite restorations, thus compromising marginal integrity and leading to secondary caries. This study investigates the mechanical integrity of the dentin–composite interface challenged with multi-species oral biofilms. While most studies used single-species biofilms, the present study used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Dentin–composite disks were made using bovine incisor roots filled with Z100TM or FiltekTM LS (3M ESPE). The disks were incubated for 72h in paired CDC biofilm reactors, using a previously published protocol. One reactor was pulsed with sucrose, and the other was not. A sterile saliva-only control group was run with sucrose pulsing. The disks were fractured under diametral compression to evaluate their interfacial bond strength. The surface deformation of the disks was mapped using digital image correlation to ascertain the fracture origin. Fracture surfaces were examined using scanning electron microscopy/energy-dispersive X-ray spectroscopy to assess demineralization and interfacial degradation. Dentin demineralization was greater under sucrose-pulsed biofilms, as the pH dropped |
doi_str_mv | 10.1016/j.actbio.2013.08.034 |
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Oral biofilms can degrade the components in dental resin-based composite restorations, thus compromising marginal integrity and leading to secondary caries. This study investigates the mechanical integrity of the dentin–composite interface challenged with multi-species oral biofilms. While most studies used single-species biofilms, the present study used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Dentin–composite disks were made using bovine incisor roots filled with Z100TM or FiltekTM LS (3M ESPE). The disks were incubated for 72h in paired CDC biofilm reactors, using a previously published protocol. One reactor was pulsed with sucrose, and the other was not. A sterile saliva-only control group was run with sucrose pulsing. The disks were fractured under diametral compression to evaluate their interfacial bond strength. The surface deformation of the disks was mapped using digital image correlation to ascertain the fracture origin. Fracture surfaces were examined using scanning electron microscopy/energy-dispersive X-ray spectroscopy to assess demineralization and interfacial degradation. Dentin demineralization was greater under sucrose-pulsed biofilms, as the pH dropped <5.5 during pulsing, with LS and Z100 specimens suffering similar degrees of surface mineral loss. Biofilm growth with sucrose pulsing also caused preferential degradation of the composite–dentin interface, depending on the composite/adhesive system used. Specifically, Z100 specimens showed greater bond strength reduction and more frequent cohesive failure in the adhesive layer. This was attributed to the inferior dentin coverage by Z100 adhesive, which possibly led to a higher level of chemical and enzymatic degradation. The results suggested that factors other than dentin demineralization were also responsible for interfacial degradation. A clinically relevant in vitro biofilm model was therefore developed, which would effectively allow assessment of the degradation of the dentin–composite interface subjected to multi-species biofilm challenge.</description><identifier>ISSN: 1742-7061</identifier><identifier>EISSN: 1878-7568</identifier><identifier>DOI: 10.1016/j.actbio.2013.08.034</identifier><identifier>PMID: 24008178</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acrylic Resins - chemistry ; Adhesive bonding ; Animals ; Biofilms ; Biofilms - drug effects ; Bioreactors ; Bond strength ; Cattle ; Child, Preschool ; Composite Resins - chemistry ; Degradation ; Demineralizing ; Dental Bonding ; Dental restoration ; Dentin ; Dentin - microbiology ; Disks ; Humans ; Hydrogen-Ion Concentration - drug effects ; Interfacial Degradation ; Materials Testing ; Microscopy, Electron, Scanning ; Multi-species biofilm ; Polyurethanes - chemistry ; Reactors ; Resin composite ; Species Specificity ; Spectrometry, X-Ray Emission ; Sucrose ; Sucrose - pharmacology</subject><ispartof>Acta biomaterialia, 2014-01, Vol.10 (1), p.375-383</ispartof><rights>2013 Acta Materialia Inc.</rights><rights>Copyright © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.</rights><rights>2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-6b0e53f889f3e7c3dac563e705f6e0a7117d8d48a8df606d9e218854411bf1263</citedby><cites>FETCH-LOGICAL-c595t-6b0e53f889f3e7c3dac563e705f6e0a7117d8d48a8df606d9e218854411bf1263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1742706113004261$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24008178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Y.</creatorcontrib><creatorcontrib>Carrera, C.</creatorcontrib><creatorcontrib>Chen, R.</creatorcontrib><creatorcontrib>Li, J.</creatorcontrib><creatorcontrib>Lenton, P.</creatorcontrib><creatorcontrib>Rudney, J.D.</creatorcontrib><creatorcontrib>Jones, R.S.</creatorcontrib><creatorcontrib>Aparicio, C.</creatorcontrib><creatorcontrib>Fok, A.</creatorcontrib><title>Degradation in the dentin–composite interface subjected to multi-species biofilm challenges</title><title>Acta biomaterialia</title><addtitle>Acta Biomater</addtitle><description>The mechanical integrity of composite restorations challenged with multi-species oral biofilms was studied. While most studies used single-species biofilms, we used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Biofilm growth with sucrose pulsing caused preferential degradation of the composite–dentin interface, with significant differences in bond strength reduction and failure modes depending on the composite/adhesive system used.
Oral biofilms can degrade the components in dental resin-based composite restorations, thus compromising marginal integrity and leading to secondary caries. This study investigates the mechanical integrity of the dentin–composite interface challenged with multi-species oral biofilms. While most studies used single-species biofilms, the present study used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Dentin–composite disks were made using bovine incisor roots filled with Z100TM or FiltekTM LS (3M ESPE). The disks were incubated for 72h in paired CDC biofilm reactors, using a previously published protocol. One reactor was pulsed with sucrose, and the other was not. A sterile saliva-only control group was run with sucrose pulsing. The disks were fractured under diametral compression to evaluate their interfacial bond strength. The surface deformation of the disks was mapped using digital image correlation to ascertain the fracture origin. Fracture surfaces were examined using scanning electron microscopy/energy-dispersive X-ray spectroscopy to assess demineralization and interfacial degradation. Dentin demineralization was greater under sucrose-pulsed biofilms, as the pH dropped <5.5 during pulsing, with LS and Z100 specimens suffering similar degrees of surface mineral loss. Biofilm growth with sucrose pulsing also caused preferential degradation of the composite–dentin interface, depending on the composite/adhesive system used. Specifically, Z100 specimens showed greater bond strength reduction and more frequent cohesive failure in the adhesive layer. This was attributed to the inferior dentin coverage by Z100 adhesive, which possibly led to a higher level of chemical and enzymatic degradation. The results suggested that factors other than dentin demineralization were also responsible for interfacial degradation. A clinically relevant in vitro biofilm model was therefore developed, which would effectively allow assessment of the degradation of the dentin–composite interface subjected to multi-species biofilm challenge.</description><subject>Acrylic Resins - chemistry</subject><subject>Adhesive bonding</subject><subject>Animals</subject><subject>Biofilms</subject><subject>Biofilms - drug effects</subject><subject>Bioreactors</subject><subject>Bond strength</subject><subject>Cattle</subject><subject>Child, Preschool</subject><subject>Composite Resins - chemistry</subject><subject>Degradation</subject><subject>Demineralizing</subject><subject>Dental Bonding</subject><subject>Dental restoration</subject><subject>Dentin</subject><subject>Dentin - microbiology</subject><subject>Disks</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration - drug effects</subject><subject>Interfacial Degradation</subject><subject>Materials Testing</subject><subject>Microscopy, Electron, Scanning</subject><subject>Multi-species biofilm</subject><subject>Polyurethanes - chemistry</subject><subject>Reactors</subject><subject>Resin composite</subject><subject>Species Specificity</subject><subject>Spectrometry, X-Ray Emission</subject><subject>Sucrose</subject><subject>Sucrose - pharmacology</subject><issn>1742-7061</issn><issn>1878-7568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9u1DAQxiMEoqXwBgjlyCXBjh17ckFC5a9UiUt7RJZjj3e9SuLFdipx4x14Q54Er7YUeql6mpFm5puZ71dVLylpKaHiza7VJo8-tB2hrCXQEsYfVacUJDSyF_C45JJ3jSSCnlTPUtoRwoB28LQ66TghQCWcVt_e4yZqq7MPS-2XOm-xtrhkv_z--cuEeR-Sz1gqGaPTBuu0jjs0GW2dQz2vU_ZN2qPxmOpyjPPTXJutniZcNpieV0-cnhK-uIln1dXHD5fnn5uLr5--nL-7aEw_9LkRI8GeOYDBMZSGWW16UTLSO4FES0qlBctBg3WCCDtgRwF6zikdHe0EO6veHnX36zijNeWBqCe1j37W8YcK2qu7lcVv1SZcKwbFCTEUgdc3AjF8XzFlNftkcJr0gmFNqqwr7nEQ3QNa-4EPkj9ElYuCiw_s8AE_tpoYUorobo-nRB14q5068lYH3oqAKveUsVf_P3479BfwP2ew2H_tMapUWC0GrY8Fo7LB37_hD8j3wDQ</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Li, Y.</creator><creator>Carrera, C.</creator><creator>Chen, R.</creator><creator>Li, J.</creator><creator>Lenton, P.</creator><creator>Rudney, J.D.</creator><creator>Jones, R.S.</creator><creator>Aparicio, C.</creator><creator>Fok, A.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Degradation in the dentin–composite interface subjected to multi-species biofilm challenges</title><author>Li, Y. ; 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While most studies used single-species biofilms, we used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Biofilm growth with sucrose pulsing caused preferential degradation of the composite–dentin interface, with significant differences in bond strength reduction and failure modes depending on the composite/adhesive system used.
Oral biofilms can degrade the components in dental resin-based composite restorations, thus compromising marginal integrity and leading to secondary caries. This study investigates the mechanical integrity of the dentin–composite interface challenged with multi-species oral biofilms. While most studies used single-species biofilms, the present study used a more realistic, diverse biofilm model produced directly from plaques collected from donors with a history of early childhood caries. Dentin–composite disks were made using bovine incisor roots filled with Z100TM or FiltekTM LS (3M ESPE). The disks were incubated for 72h in paired CDC biofilm reactors, using a previously published protocol. One reactor was pulsed with sucrose, and the other was not. A sterile saliva-only control group was run with sucrose pulsing. The disks were fractured under diametral compression to evaluate their interfacial bond strength. The surface deformation of the disks was mapped using digital image correlation to ascertain the fracture origin. Fracture surfaces were examined using scanning electron microscopy/energy-dispersive X-ray spectroscopy to assess demineralization and interfacial degradation. Dentin demineralization was greater under sucrose-pulsed biofilms, as the pH dropped <5.5 during pulsing, with LS and Z100 specimens suffering similar degrees of surface mineral loss. Biofilm growth with sucrose pulsing also caused preferential degradation of the composite–dentin interface, depending on the composite/adhesive system used. Specifically, Z100 specimens showed greater bond strength reduction and more frequent cohesive failure in the adhesive layer. This was attributed to the inferior dentin coverage by Z100 adhesive, which possibly led to a higher level of chemical and enzymatic degradation. The results suggested that factors other than dentin demineralization were also responsible for interfacial degradation. A clinically relevant in vitro biofilm model was therefore developed, which would effectively allow assessment of the degradation of the dentin–composite interface subjected to multi-species biofilm challenge.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24008178</pmid><doi>10.1016/j.actbio.2013.08.034</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acrylic Resins - chemistry Adhesive bonding Animals Biofilms Biofilms - drug effects Bioreactors Bond strength Cattle Child, Preschool Composite Resins - chemistry Degradation Demineralizing Dental Bonding Dental restoration Dentin Dentin - microbiology Disks Humans Hydrogen-Ion Concentration - drug effects Interfacial Degradation Materials Testing Microscopy, Electron, Scanning Multi-species biofilm Polyurethanes - chemistry Reactors Resin composite Species Specificity Spectrometry, X-Ray Emission Sucrose Sucrose - pharmacology |
title | Degradation in the dentin–composite interface subjected to multi-species biofilm challenges |
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