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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Veröffentlicht in:Acta biomaterialia 2014-01, Vol.10 (1), p.375-383
Hauptverfasser: Li, Y., Carrera, C., Chen, R., Li, J., Lenton, P., Rudney, J.D., Jones, R.S., Aparicio, C., Fok, A.
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container_issue 1
container_start_page 375
container_title Acta biomaterialia
container_volume 10
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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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 &lt;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. 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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 &lt;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. 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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 &lt;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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source MEDLINE; Elsevier ScienceDirect Journals
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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