D L Falcione, C E Pena, C P Turssi, Fmg França, Flb do Amaral, J Tagami, R T Basting
The present study aimed to evaluate the influence of application mode on the short-term microshear bond strength longevity of self-etching and universal adhesive systems to enamel, the failure mode, and the resulting enamel surface micromorphology. Ninety enamel surfaces were obtained from sound third molars, planed, and randomly assigned to nine groups, according to the application mode and the adhesive system (n=10). There were three primer application modes: according to the manufacturer's recommended application time (control), using double the application time recommended for the primer and selective enamel etching. The adhesive systems used were: Clearfil SE Bond (Kuraray), FL-Bond II (SHOFU), and Futurabond U (Voco). At least two resin-bonded composite cylinders (Grandioso Light Flow, Voco) were placed on each enamel surface, and then evaluated for microshear bond strength at 24 hours and 180 days of storage in solution body fluid (SBF) at pH 7.4. Failure modes were evaluated with a stereoscopic microscope at 20× magnification. A micromorphological analysis of the enamel surface was performed under a scanning electron microscope at 5000× magnification before and after the treatments. Mixed models for repeated measures over time showed significant interaction among application modes, adhesive systems, and time periods (p=0.0331). The bond strength of FL-Bond II adhesive to enamel observed after performing selective enamel etching was significantly higher than that observed after applying the control treatment (p=0.0010) at both 24 hours and 180 days. However, no significant difference was observed between the application of this same adhesive at double the time recommended by the manufacturer and the other two application modes (p>0.05). There was also no significant difference in the microshear bond strength for the enamel treatments applied using Clearfil SE Bond and Futurabond U (p>0.05). A significant reduction in bond strength to enamel was observed at the 180-day storage time for all the adhesive systems when selective enamel etching was performed (p<0.0001). No significant association was observed between the adhesive system failure mode and the enamel treatments (p=0.1402 and p=0.7590 for 24 hours and 180 days, respectively). The most prevalent failure was the adhesive type.
本研究旨在评估应用模式对自蚀刻和通用粘接系统与牙釉质短期微剪切粘接强度寿命的影响、失效模式以及由此产生的牙釉质表面微形貌。从健全的第三磨牙中获得90个牙釉质表面,刨平,根据应用方式和粘接剂系统随机分为9组(n=10)。底漆有三种使用方式:根据厂家推荐的使用时间(控制),使用两倍的推荐使用时间进行底漆和选择性珐琅蚀刻。使用的粘合剂系统有:Clearfil SE Bond (Kuraray)、FL-Bond II (SHOFU)和Futurabond U (Voco)。在每个牙釉质表面放置至少两个树脂结合的复合圆柱体(Grandioso Light Flow, Voco),然后在pH 7.4的溶液体液(SBF)中储存24小时和180天,评估微剪切结合强度。在20倍放大的立体显微镜下评估失效模式。在5000x扫描电镜下观察治疗前后牙釉质表面的微观形态变化。随时间重复测量的混合模型显示,应用模式、粘合剂系统和时间段之间存在显著的相互作用(p=0.0331)。选择性牙釉质蚀刻处理后24小时和180天FL-Bond II胶粘剂与牙釉质的结合强度均显著高于对照组(p=0.0010)。然而,在制造商推荐的两倍时间内使用同一胶粘剂与其他两种应用模式之间没有显著差异(p>0.05)。使用Clearfil SE bond和Futurabond U处理牙釉质的微剪切粘接强度也无显著差异(p>0.05)。当进行选择性牙釉质蚀刻时,在180天的储存时间内观察到所有胶粘剂系统与牙釉质的结合强度显著降低(p
{"title":"Influence of Application Modes on Increasing Bond Strength Longevity of Self-etching and Universal Adhesive Systems to Enamel.","authors":"D L Falcione, C E Pena, C P Turssi, Fmg França, Flb do Amaral, J Tagami, R T Basting","doi":"10.2341/22-133-L","DOIUrl":"10.2341/22-133-L","url":null,"abstract":"<p><p>The present study aimed to evaluate the influence of application mode on the short-term microshear bond strength longevity of self-etching and universal adhesive systems to enamel, the failure mode, and the resulting enamel surface micromorphology. Ninety enamel surfaces were obtained from sound third molars, planed, and randomly assigned to nine groups, according to the application mode and the adhesive system (n=10). There were three primer application modes: according to the manufacturer's recommended application time (control), using double the application time recommended for the primer and selective enamel etching. The adhesive systems used were: Clearfil SE Bond (Kuraray), FL-Bond II (SHOFU), and Futurabond U (Voco). At least two resin-bonded composite cylinders (Grandioso Light Flow, Voco) were placed on each enamel surface, and then evaluated for microshear bond strength at 24 hours and 180 days of storage in solution body fluid (SBF) at pH 7.4. Failure modes were evaluated with a stereoscopic microscope at 20× magnification. A micromorphological analysis of the enamel surface was performed under a scanning electron microscope at 5000× magnification before and after the treatments. Mixed models for repeated measures over time showed significant interaction among application modes, adhesive systems, and time periods (p=0.0331). The bond strength of FL-Bond II adhesive to enamel observed after performing selective enamel etching was significantly higher than that observed after applying the control treatment (p=0.0010) at both 24 hours and 180 days. However, no significant difference was observed between the application of this same adhesive at double the time recommended by the manufacturer and the other two application modes (p>0.05). There was also no significant difference in the microshear bond strength for the enamel treatments applied using Clearfil SE Bond and Futurabond U (p>0.05). A significant reduction in bond strength to enamel was observed at the 180-day storage time for all the adhesive systems when selective enamel etching was performed (p<0.0001). No significant association was observed between the adhesive system failure mode and the enamel treatments (p=0.1402 and p=0.7590 for 24 hours and 180 days, respectively). The most prevalent failure was the adhesive type.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"52-64"},"PeriodicalIF":2.2,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138451996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M A Américo, F F Portella, R Zimmer, F R Garcia, D J Porto, V L Barbosa, Hjr Oballe, E G Reston
<p><strong>Objectives: </strong>The present study aimed to evaluate the desensitizing effect of toothpaste for sensitive teeth on patient tooth sensitivity and on bleaching efficacy of the 38% hydrogen peroxide bleaching agent used for in-office bleaching compared to a regular toothpaste in a randomized clinical trial.</p><p><strong>Methods and materials: </strong>Forty-eight patients having maxillary right central incisors with darkness greater than A1 were selected for the present double-blind randomized clinical trial. Patients were randomly allocated into two groups: the placebo group, which used regular toothpaste, and the experimental group, which used sensitivity toothpaste. The intervention consisted of applying toothpaste with the aid of an individual tray for a period of 4 minutes daily, starting one week before the first bleaching session and interrupting use immediately after the second session. After allocation to one of the groups, individuals received in-office dental bleaching with a 40-minute application of 38% hydrogen peroxide for two sessions with an interval of one week. The incidence and intensity of sensitivity were assessed using a visual analogue scale and a numeric analogue scale. Sensitivity was measured immediately before each session, 1 hour, 24 hours, and 48 hours after each bleaching session and four weeks after the second bleaching session. Tooth shade was evaluated using a spectrophotometer and by comparison with the VITA Classical Shade Guide (Vita Zahnfabrik, Bad Säckingen, Germany). Tooth shade was evaluated before the first bleaching session, one week after the first bleaching session, one week after the second bleaching session and four weeks after the second bleaching session. Participants and professionals who performed the bleaching, shade, and sensitivity assessments were blinded to the group of patients they were treating or assessing. For the incidence of hypersensitivity, the results were evaluated by comparing the groups at different evaluation times with the Mann-Whitney test for comparison between groups, the Friedman test for repeated measures, and the Tukey test for comparison of times. Shade change on the guide was analyzed using the Mann-Whitney test for comparison between groups and the Wilcoxon test for comparison between times. Shade change by the spectrophotometer was analyzed using the t-test for comparison between groups and the paired t-test for comparison between times. All analyses were performed with a significance level of 5%.</p><p><strong>Results: </strong>There was no difference in the pattern of dental hypersensitivity between groups. For all shade measures, there was no difference between the bleaching results, and no statistically significant difference was observed between the study groups.</p><p><strong>Conclusion: </strong>The use of arginine-based desensitizing toothpaste did not interfere with the bleaching ability of hydrogen peroxide and was not effective in reducing the
{"title":"Effect of a Toothpaste for Sensitive Teeth on the Sensitivity and Effectiveness of In-office Dental Bleaching: A Randomized Clinical Trial.","authors":"M A Américo, F F Portella, R Zimmer, F R Garcia, D J Porto, V L Barbosa, Hjr Oballe, E G Reston","doi":"10.2341/23-009-C","DOIUrl":"10.2341/23-009-C","url":null,"abstract":"<p><strong>Objectives: </strong>The present study aimed to evaluate the desensitizing effect of toothpaste for sensitive teeth on patient tooth sensitivity and on bleaching efficacy of the 38% hydrogen peroxide bleaching agent used for in-office bleaching compared to a regular toothpaste in a randomized clinical trial.</p><p><strong>Methods and materials: </strong>Forty-eight patients having maxillary right central incisors with darkness greater than A1 were selected for the present double-blind randomized clinical trial. Patients were randomly allocated into two groups: the placebo group, which used regular toothpaste, and the experimental group, which used sensitivity toothpaste. The intervention consisted of applying toothpaste with the aid of an individual tray for a period of 4 minutes daily, starting one week before the first bleaching session and interrupting use immediately after the second session. After allocation to one of the groups, individuals received in-office dental bleaching with a 40-minute application of 38% hydrogen peroxide for two sessions with an interval of one week. The incidence and intensity of sensitivity were assessed using a visual analogue scale and a numeric analogue scale. Sensitivity was measured immediately before each session, 1 hour, 24 hours, and 48 hours after each bleaching session and four weeks after the second bleaching session. Tooth shade was evaluated using a spectrophotometer and by comparison with the VITA Classical Shade Guide (Vita Zahnfabrik, Bad Säckingen, Germany). Tooth shade was evaluated before the first bleaching session, one week after the first bleaching session, one week after the second bleaching session and four weeks after the second bleaching session. Participants and professionals who performed the bleaching, shade, and sensitivity assessments were blinded to the group of patients they were treating or assessing. For the incidence of hypersensitivity, the results were evaluated by comparing the groups at different evaluation times with the Mann-Whitney test for comparison between groups, the Friedman test for repeated measures, and the Tukey test for comparison of times. Shade change on the guide was analyzed using the Mann-Whitney test for comparison between groups and the Wilcoxon test for comparison between times. Shade change by the spectrophotometer was analyzed using the t-test for comparison between groups and the paired t-test for comparison between times. All analyses were performed with a significance level of 5%.</p><p><strong>Results: </strong>There was no difference in the pattern of dental hypersensitivity between groups. For all shade measures, there was no difference between the bleaching results, and no statistically significant difference was observed between the study groups.</p><p><strong>Conclusion: </strong>The use of arginine-based desensitizing toothpaste did not interfere with the bleaching ability of hydrogen peroxide and was not effective in reducing the ","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"627-637"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A V Foscarini, L S Barros, C P Turssi, Fmg França, R T Basting, W F Vieira
Objective: To evaluate the flexural strength of two types of high-viscosity resin composites (conventional or bulk-fill) that were repaired with either high-viscosity composites (conventional or bulk-fill) or low-viscosity composites (conventional or bulk-fill) of the same manufacturer (3M Oral Care, St Paul, MN, USA).
Methods and materials: Specimens (25 mm × 2 mm × 2 mm) of both conventional nanofilled resin (Filtek Z350XT), and bulk-fill nanofilled resin (Filtek One Bulk Fill) were prepared. After fracture of the specimens in the 3-point bending test (initial), half of the specimens were repaired immediately afterwards (24 hours), and the other half were repaired after 6 months of storage in distilled water. Repairs were performed with (n=15) high-viscosity resin composites (Filtek Z350XT, Filtek One Bulk Fill), or their low-viscosity versions (Filtek Supreme XT Flow, Filtek Bulk Fill Flowable Restorative). The repair was performed by roughening the surface and applying phosphoric acid, silane, and adhesive. The bending test (results reported in MPa) was performed in a universal testing machine, and the fracture pattern was determined. Data were evaluated by generalized linear models, chi-square test and the Fisher exact test (α=0.05).
Results: There was no significant difference between the former pair of high-viscosity resins in terms of initial flexural strength (p=0.42). The repairs performed with low-viscosity resin composites after 24 hours or 6 months obtained higher MPa values compared with those using high-viscosity composites (p=0.0006). There was a significant decrease in MPa values when the repair was performed after 24 hours and an increase after 6 months, regardless of the material (p<0.0001). After 6 months, fractures involving the old (conventional) resin were more frequent in the repair performed with bulk-fill resin composites compared with the conventional composites (p=0.02).
Conclusions: Considering the tested products, the material to be repaired did not influence the flexural strength of the repair composite; however, the use of the low-viscosity resin composites resulted in greater flexural strength of the repaired material. The repair of the aged composite resulted in an increase in its flexural strength, regardless of the material repaired or used to perform the repair.
目的:评估用同一制造商(3M口腔护理公司,美国明尼苏达州圣保罗市)的高粘度复合材料(常规或散装填充物)或低粘度复合物(常规或大块填充物)修复的两种类型的高粘度树脂复合物(传统或散装填充)的弯曲强度。方法和材料:两种常规树脂的样品(25mm×2mm×2mm)制备了纳米填充树脂(Filtek Z350XT)和本体填充纳米填充树脂。在三点弯曲试验(初始)中试样断裂后,立即修复一半试样(24小时),另一半试样在蒸馏水中储存6个月后进行修复。使用(n=15)高粘度树脂复合材料(Filtek Z350XT,Filtek One Bulk Fill)或其低粘度版本(FiltekSupreme XT Flow,FiltekBulk Fill Flowable Restorative)进行修复。通过使表面粗糙化并施加磷酸、硅烷和粘合剂来进行修复。在万能试验机中进行弯曲试验(以MPa为单位报告的结果),并确定断裂模式。数据通过广义线性模型进行评估,卡方检验和Fisher精确检验(α=0.05)。结果:前一对高粘度树脂在初始弯曲强度方面没有显著差异(p=0.42)。低粘度树脂复合材料在24小时或6个月后进行的修复获得了比使用高粘度复合材料更高的MPa值(p=0.0006)当在24小时后进行修复时,MPa值降低,不管材料如何(p结论:考虑到测试产品,待修复的材料不会影响修复复合材料的弯曲强度;然而,使用低粘度树脂复合材料会使修复材料的抗弯强度更高。无论修复或用于执行测试的材料是什么,对老化复合材料的修复都会使其抗弯强度增加。)他修理。
{"title":"Flexural Strength of Conventional or Bulk-fill Resin Composite Repaired with High- or Low-viscosity Restorative Materials.","authors":"A V Foscarini, L S Barros, C P Turssi, Fmg França, R T Basting, W F Vieira","doi":"10.2341/22-125-L","DOIUrl":"10.2341/22-125-L","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the flexural strength of two types of high-viscosity resin composites (conventional or bulk-fill) that were repaired with either high-viscosity composites (conventional or bulk-fill) or low-viscosity composites (conventional or bulk-fill) of the same manufacturer (3M Oral Care, St Paul, MN, USA).</p><p><strong>Methods and materials: </strong>Specimens (25 mm × 2 mm × 2 mm) of both conventional nanofilled resin (Filtek Z350XT), and bulk-fill nanofilled resin (Filtek One Bulk Fill) were prepared. After fracture of the specimens in the 3-point bending test (initial), half of the specimens were repaired immediately afterwards (24 hours), and the other half were repaired after 6 months of storage in distilled water. Repairs were performed with (n=15) high-viscosity resin composites (Filtek Z350XT, Filtek One Bulk Fill), or their low-viscosity versions (Filtek Supreme XT Flow, Filtek Bulk Fill Flowable Restorative). The repair was performed by roughening the surface and applying phosphoric acid, silane, and adhesive. The bending test (results reported in MPa) was performed in a universal testing machine, and the fracture pattern was determined. Data were evaluated by generalized linear models, chi-square test and the Fisher exact test (α=0.05).</p><p><strong>Results: </strong>There was no significant difference between the former pair of high-viscosity resins in terms of initial flexural strength (p=0.42). The repairs performed with low-viscosity resin composites after 24 hours or 6 months obtained higher MPa values compared with those using high-viscosity composites (p=0.0006). There was a significant decrease in MPa values when the repair was performed after 24 hours and an increase after 6 months, regardless of the material (p<0.0001). After 6 months, fractures involving the old (conventional) resin were more frequent in the repair performed with bulk-fill resin composites compared with the conventional composites (p=0.02).</p><p><strong>Conclusions: </strong>Considering the tested products, the material to be repaired did not influence the flexural strength of the repair composite; however, the use of the low-viscosity resin composites resulted in greater flexural strength of the repaired material. The repair of the aged composite resulted in an increase in its flexural strength, regardless of the material repaired or used to perform the repair.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"677-688"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Negative effects of bleaching on dentin have previously been reported in vitro.
Objective: The purpose of this study was to determine the effect of carbamide peroxide bleaching on dentin fatigue resistance using a clinically relevant in situ model.
Methods and materials: Following research ethics board approval, 60 human teeth requiring extraction were collected. Sterilized human dentin specimens were cut (1.2x1.2x10 mm) and secured into customized bleaching trays to be used by study participants. Participants were randomly assigned to either bleach (10% carbamide peroxide, n=23) or control (gel without bleach, n=26) treatment groups. Treatment was applied to the bleaching trays and worn overnight by participants for 14 days. After treatment completion, dentin specimens were removed from the bleaching trays and subjected to fatigue testing (10 N, 3 mm/s, 2x105 cycles) while submerged in artificial saliva. Kaplan-Meier survival analysis was conducted to compare the number of cycles to failure during fatigue testing in both groups. A log rank test was run to determine if there were differences in the survival distribution between the two groups (α<0.05).
Results: The median number of cycles to failure was 352 ± 202 and 760 ± 644 for the bleach and control groups, respectively. The survival distributions for the two groups were significantly different (p=0.020). Dentin fatigue resistance was significantly lower in the bleach group compared to the control.
Conclusions: Direct bleaching of human dentin using an at-home tray bleaching protocol in situ reduced dentin fatigue resistance. This has implications for tooth fracture risk and longevity.
{"title":"Effect of Tooth Bleach on Dentin Fatigue Resistance in Situ.","authors":"J M Fitzgerald, G De Souza, L Tam","doi":"10.2341/22-093-C","DOIUrl":"10.2341/22-093-C","url":null,"abstract":"<p><strong>Background: </strong>Negative effects of bleaching on dentin have previously been reported in vitro.</p><p><strong>Objective: </strong>The purpose of this study was to determine the effect of carbamide peroxide bleaching on dentin fatigue resistance using a clinically relevant in situ model.</p><p><strong>Methods and materials: </strong>Following research ethics board approval, 60 human teeth requiring extraction were collected. Sterilized human dentin specimens were cut (1.2x1.2x10 mm) and secured into customized bleaching trays to be used by study participants. Participants were randomly assigned to either bleach (10% carbamide peroxide, n=23) or control (gel without bleach, n=26) treatment groups. Treatment was applied to the bleaching trays and worn overnight by participants for 14 days. After treatment completion, dentin specimens were removed from the bleaching trays and subjected to fatigue testing (10 N, 3 mm/s, 2x105 cycles) while submerged in artificial saliva. Kaplan-Meier survival analysis was conducted to compare the number of cycles to failure during fatigue testing in both groups. A log rank test was run to determine if there were differences in the survival distribution between the two groups (α<0.05).</p><p><strong>Results: </strong>The median number of cycles to failure was 352 ± 202 and 760 ± 644 for the bleach and control groups, respectively. The survival distributions for the two groups were significantly different (p=0.020). Dentin fatigue resistance was significantly lower in the bleach group compared to the control.</p><p><strong>Conclusions: </strong>Direct bleaching of human dentin using an at-home tray bleaching protocol in situ reduced dentin fatigue resistance. This has implications for tooth fracture risk and longevity.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"638-647"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C A Jurado, K Arndt, F X Azpiazu-Flores, F Faddoul, R França, N G Fischer, H Watanabe
Objective: The purpose of this study was to evaluate the effectiveness of glazing, two zirconia, and two lithium disilicate polishing systems on surface roughness of a CAD/CAM lithium disilicate and virgilite ceramic with atomic force microscopy (AFM) and visual assessment performed by dental students and faculty.
Methods and materials: Sixty maxillary right central incisor crowns made of a novel chairside CAD/CAM lithium disilicate and virgilite (CEREC Tessera) were milled for glazing and polishing. The crowns were divided into six groups: no polishing/glazing provided (NoP/G); glazed (GZ); glazed and polished with Brasseler Dialite LD Lithium Disilicate (DiLD); glazed and polished with Meisinger Luster Lithium Disilicate (LuLD); glazed and polished with Brasseler Dialite ZR Zirconia (DiZR); and glazed and polished with Meisinger Luster Zirconia (LuZR). Surfaces were scanned with AFM to measure roughness (Ra) and root mean square roughness (Rq) and generate micrographs. Crowns were visually assessed by 10 dental students and 10 dental school faculty members to determine clinical acceptableness.
Results: Glazing and all polishing kits significantly reduced Ra and Rq compared to no polishing/glazing. No significant Ra differences were found between glazing and all polishing kits (p>0.05). DiZR significantly reduced Rq compared to other groups (p<0.05). Visual assessment showed that GZ, LuLD, and DiZR were the most clinically acceptable crowns.
Conclusion: Polishing and glazing considerably improve the surface smoothness of maxillary central incisor crowns fabricated out of a chairside CAD/CAM lithium disilicate and virgilite ceramic. Altogether, zirconia polishing systems provided smoother and more clinically acceptable surfaces than the lithium disilicate kits.
{"title":"Evaluation of Glazing and Polishing Systems for Novel Chairside CAD/CAM Lithium Disilicate and Virgilite Crowns.","authors":"C A Jurado, K Arndt, F X Azpiazu-Flores, F Faddoul, R França, N G Fischer, H Watanabe","doi":"10.2341/23-017-L","DOIUrl":"10.2341/23-017-L","url":null,"abstract":"<p><strong>Objective: </strong>The purpose of this study was to evaluate the effectiveness of glazing, two zirconia, and two lithium disilicate polishing systems on surface roughness of a CAD/CAM lithium disilicate and virgilite ceramic with atomic force microscopy (AFM) and visual assessment performed by dental students and faculty.</p><p><strong>Methods and materials: </strong>Sixty maxillary right central incisor crowns made of a novel chairside CAD/CAM lithium disilicate and virgilite (CEREC Tessera) were milled for glazing and polishing. The crowns were divided into six groups: no polishing/glazing provided (NoP/G); glazed (GZ); glazed and polished with Brasseler Dialite LD Lithium Disilicate (DiLD); glazed and polished with Meisinger Luster Lithium Disilicate (LuLD); glazed and polished with Brasseler Dialite ZR Zirconia (DiZR); and glazed and polished with Meisinger Luster Zirconia (LuZR). Surfaces were scanned with AFM to measure roughness (Ra) and root mean square roughness (Rq) and generate micrographs. Crowns were visually assessed by 10 dental students and 10 dental school faculty members to determine clinical acceptableness.</p><p><strong>Results: </strong>Glazing and all polishing kits significantly reduced Ra and Rq compared to no polishing/glazing. No significant Ra differences were found between glazing and all polishing kits (p>0.05). DiZR significantly reduced Rq compared to other groups (p<0.05). Visual assessment showed that GZ, LuLD, and DiZR were the most clinically acceptable crowns.</p><p><strong>Conclusion: </strong>Polishing and glazing considerably improve the surface smoothness of maxillary central incisor crowns fabricated out of a chairside CAD/CAM lithium disilicate and virgilite ceramic. Altogether, zirconia polishing systems provided smoother and more clinically acceptable surfaces than the lithium disilicate kits.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"689-699"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
K Zancopé, Gcs Borges, Mth Ribeiro, R R Miranda, T S Peres, C J Soares
Objectives: This study evaluated the Knoop hardness (KH, N/mm2) and degree of conversion (DC, %) on the margins of light-cured resin cements with different photoinitiators using a single light-curing unit (LCU) with two heads (mono- and multiwave).
Methods and materials: Three types of resin cements were used with different photoinitiators: Megalink Esthetic (Odontomega, São Paulo, Brazil) with a camphorquinone photoinitiator; Allcem Veneer (FGM, Joinville, Brazil) with the Advanced Polymerization system (APS), and Variolink Esthetic LC (Ivoclar Vivadent, Schaan, Liechtenstein). Thirty samples were collected and divided into six groups (n=5 each). The resin cement samples were made into the shape of a maxillary right central incisor and photoactivated under a 0.5-mm-thick ceramic sheet. A single LCU (Radii Xpert, SDI) with two heads (mono- and multiwave) was used. The tip of the LCU was positioned at the center of the sample in a standardized manner. Raman spectroscopy was performed to evaluate the DC, and KH was evaluated through the Knoop microhardness test. Five regions were evaluated: cervical, mesial, buccal (center), distal, and incisal.
Results: There was a significant difference in the DC only for the type of cement (p<0.001), indicating that the cement with the APS photoinitiator presented excellent results. There were significant differences in the type of cement (p<0.001), type of light (p<0.001), region (p<0.001), and the interaction between the type of cement and type of light (p<0.001). The resin cement with the APS photoinitiator cured with monowave light showed the highest KH values. The beam profiles of all groups, with and without the interposition of ceramic and resin cement, were examined by light transmission.
Conclusions: The cement with the APS photoinitiator presented the best results with respect to the DC and KH. In comparison with mono- and multiwaves, the LCU may not be a determining factor for the properties of light-cured resin cements. The buccal region showed the best results for DC and KH, indicating the need for a greater amount of light-curing at the cementation margins.
{"title":"Influence of Mono- and Multiwave Light-curing Units on the Microhardness and Degree of Conversion of Light-cured Resin Cements.","authors":"K Zancopé, Gcs Borges, Mth Ribeiro, R R Miranda, T S Peres, C J Soares","doi":"10.2341/23-039-L","DOIUrl":"10.2341/23-039-L","url":null,"abstract":"<p><strong>Objectives: </strong>This study evaluated the Knoop hardness (KH, N/mm2) and degree of conversion (DC, %) on the margins of light-cured resin cements with different photoinitiators using a single light-curing unit (LCU) with two heads (mono- and multiwave).</p><p><strong>Methods and materials: </strong>Three types of resin cements were used with different photoinitiators: Megalink Esthetic (Odontomega, São Paulo, Brazil) with a camphorquinone photoinitiator; Allcem Veneer (FGM, Joinville, Brazil) with the Advanced Polymerization system (APS), and Variolink Esthetic LC (Ivoclar Vivadent, Schaan, Liechtenstein). Thirty samples were collected and divided into six groups (n=5 each). The resin cement samples were made into the shape of a maxillary right central incisor and photoactivated under a 0.5-mm-thick ceramic sheet. A single LCU (Radii Xpert, SDI) with two heads (mono- and multiwave) was used. The tip of the LCU was positioned at the center of the sample in a standardized manner. Raman spectroscopy was performed to evaluate the DC, and KH was evaluated through the Knoop microhardness test. Five regions were evaluated: cervical, mesial, buccal (center), distal, and incisal.</p><p><strong>Results: </strong>There was a significant difference in the DC only for the type of cement (p<0.001), indicating that the cement with the APS photoinitiator presented excellent results. There were significant differences in the type of cement (p<0.001), type of light (p<0.001), region (p<0.001), and the interaction between the type of cement and type of light (p<0.001). The resin cement with the APS photoinitiator cured with monowave light showed the highest KH values. The beam profiles of all groups, with and without the interposition of ceramic and resin cement, were examined by light transmission.</p><p><strong>Conclusions: </strong>The cement with the APS photoinitiator presented the best results with respect to the DC and KH. In comparison with mono- and multiwaves, the LCU may not be a determining factor for the properties of light-cured resin cements. The buccal region showed the best results for DC and KH, indicating the need for a greater amount of light-curing at the cementation margins.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"711-719"},"PeriodicalIF":1.4,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
N R Silva, Gm de Araújo, Dmd Moura, Lnm de Araújo, Bc de Vasconcelos Gurgel, R M Melo, M A Bottino, M Özcan, Y Zhang, Roa Souza
There is a lack of reports in the literature on the long-term clinical performance of ultratranslucent zirconia, especially considering its use in manufacturing monolithic veneers. The purpose of this case series is to describe the aesthetic treatment steps of three patients with minimally invasive ultratranslucent zirconia veneers and to report the clinical findings up to five years. Three patients (woman: 2, man: 1; mean age: 30 years) unsatisfied with their dental aesthetics sought dental treatment. The treatment plan involved cementing ultratranslucent zirconia veneers. Air-abrasion was performed on the internal surface of zirconia with alumina particles coated by silica (silicatization), followed by silane and adhesive applications for the adhesive cementation. All veneers were adhesively cemented to enamel with resin cement (Variolink Esthetic, Ivoclar). The patients were clinically evaluated annually considering the Ryge modified/ California Dental Association criteria. After a mean follow-up of 4.33 years (4-5 years), a survival rate of 100% was detected for the 28 minimally invasive ultratranslucent zirconia veneers cemented in the 3 patients. There were no absolute failures such as debonding, veneer fracture, or secondary caries. Superficial marginal discoloration was observed in one element (maxillary left lateral incisor) of one patient. Ultratranslucent zirconia is a viable option for manufacturing veneers due to its excellent clinical performance and longevity. However, further long-term clinical studies are essential to consolidate this material as an option for esthetic restorations.
{"title":"Clinical Performance of Minimally Invasive Monolithic Ultratranslucent Zirconia Veneers: A Case Series up to Five Years of Follow-up.","authors":"N R Silva, Gm de Araújo, Dmd Moura, Lnm de Araújo, Bc de Vasconcelos Gurgel, R M Melo, M A Bottino, M Özcan, Y Zhang, Roa Souza","doi":"10.2341/22-118-T","DOIUrl":"10.2341/22-118-T","url":null,"abstract":"<p><p>There is a lack of reports in the literature on the long-term clinical performance of ultratranslucent zirconia, especially considering its use in manufacturing monolithic veneers. The purpose of this case series is to describe the aesthetic treatment steps of three patients with minimally invasive ultratranslucent zirconia veneers and to report the clinical findings up to five years. Three patients (woman: 2, man: 1; mean age: 30 years) unsatisfied with their dental aesthetics sought dental treatment. The treatment plan involved cementing ultratranslucent zirconia veneers. Air-abrasion was performed on the internal surface of zirconia with alumina particles coated by silica (silicatization), followed by silane and adhesive applications for the adhesive cementation. All veneers were adhesively cemented to enamel with resin cement (Variolink Esthetic, Ivoclar). The patients were clinically evaluated annually considering the Ryge modified/ California Dental Association criteria. After a mean follow-up of 4.33 years (4-5 years), a survival rate of 100% was detected for the 28 minimally invasive ultratranslucent zirconia veneers cemented in the 3 patients. There were no absolute failures such as debonding, veneer fracture, or secondary caries. Superficial marginal discoloration was observed in one element (maxillary left lateral incisor) of one patient. Ultratranslucent zirconia is a viable option for manufacturing veneers due to its excellent clinical performance and longevity. However, further long-term clinical studies are essential to consolidate this material as an option for esthetic restorations.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":"48 6","pages":"606-617"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"92155937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
L P Derigi, L S Barros, M M Sugii, C P Turssi, Fmg França, R T Basting, W F Vieira
Objective: To evaluate the effects of commercial mouth rinses on color, roughness, sorption (SR), and solubility (SL) of resin composites.
Methods and materials: Disc-shaped specimens (stage I: 6 mm × 2 mm; stage II: 10 mm × 1.5 mm) were made from the following resin composites (n=10): conventional nanofilled (Filtek Z350XT, 3M Oral Care), conventional nanohybrid (Luna, SDI), bulk-fill nanofilled (Filtek One Bulk-Fill, 3M Oral Care), and bulk-fill nanohybrid (Aura Bulk-Fill, SDI) exposed to distilled water (control), blue mouth rinse without alcohol (Colgate Total 12 Clean Mint, Colgate-Palmolive), or blue mouth rinse with alcohol and essential oil (Listerine Tartar Control, Johnson & Johnson). In stage I, tests were performed at the baseline, and after the immersion in solution time points to evaluate coordinates of the CIEL*a*b* system (ΔL*, Δa*, Δb*), general color change (ΔEab, ΔE00, and ΔSGU), and surface roughness (Ra). In stage II, SR and SL were evaluated (ISO 4049:2019) after immersion in the solutions for 7 days. The results were evaluated by generalized linear models (Ra, SR), Kruskal-Wallis, and Dunn tests (color, SL), with α = 0.05.
Results: There were no significative differences for Ra between the solutions. Both mouth rinses promoted significantly negative ΔL* (Luna), Δa* (Filtek One Bulk-fill), and Δb* (all materials except conventional nanofilled resin composite). Mouth rinse without alcohol promoted significantly negative Δa* on all resin composites tested. Both mouth rinses promoted higher ΔEab and ΔE00 for bulk-fill resin composites compared to control. Mouth rinse with alcohol caused higher ΔSGU for bulk-fill nanofilled resin composite. It also promoted greater SR in all the resin composites compared with mouth rinse without alcohol and higher SR in nanohybrid resin composites compared with control. Both mouth rinses promoted higher SL values in Luna and differed significantly from control.
Conclusions: The physical properties were manufacturer dependent and mediated by mouth rinses. The mouth rinses promoted color changes in the resin composites, pointing out that bulk-fill resin composites were more affected by these effects, especially when the mouth rinse contained essential oil and alcohol.
目的:评价市售漱口液对树脂复合材料的颜色、粗糙度、吸附性(SR)和溶解性(SL)的影响。方法和材料:圆盘状试样(阶段I:6mm×2mm;阶段II:10mm×1.5mm)由以下树脂复合材料(n=10)制成:暴露于蒸馏水的常规纳米填充物(Filtek Z350XT,3M口腔护理)、常规纳米杂化物(Luna,SDI)、大块填充物纳米填充物,不含酒精的蓝色漱口液(高露洁棕榄公司的高露洁Total 12 Clean Mint),或含酒精和精油的蓝色漱口剂(强生公司的Listerine Tartar Control)。在第一阶段,在基线和浸入溶液后的时间点进行测试,以评估CIEL*a*b*系统的坐标(ΔL*、Δa*、Δb*)、一般颜色变化(ΔEab、ΔE00和ΔSGU)和表面粗糙度(Ra)。在第二阶段,SR和SL在溶液中浸泡7天后进行评估(ISO 4049:2019)。通过广义线性模型(Ra,SR)、Kruskal-Wallis和Dunn检验(color,SL)评估结果,α=0.05。结果:两种溶液之间的Ra没有显著差异。两种漱口液都显著促进了ΔL*(Luna)、Δa*(Filtek One Bulk填充物)和Δb*(除传统纳米填充树脂复合物外的所有材料)的负增长。在所有测试的树脂复合材料上,不含酒精的漱口液显著促进了Δa*的阴性。与对照组相比,两种漱口液都能提高散装填充树脂复合材料的ΔEab和ΔE00。用酒精漱口会导致散装填充纳米填充树脂复合材料的ΔSGU更高。与不含酒精的漱口液相比,它还促进了所有树脂复合材料中更高的SR,并且与对照相比,纳米杂化树脂复合材料的SR更高。两种漱口液都能提高Luna的SL值,并且与对照组有显著差异。结论:其物理性质依赖于制造商,并由漱口液介导。漱口液促进了树脂复合材料的颜色变化,指出散装填充树脂复合材料更容易受到这些影响,尤其是当漱口液含有精油和酒精时。
{"title":"Effect of Commercial Mouth Rinses on Physical Properties of Conventional and Bulk-fill Resin Composites.","authors":"L P Derigi, L S Barros, M M Sugii, C P Turssi, Fmg França, R T Basting, W F Vieira","doi":"10.2341/23-041-L","DOIUrl":"10.2341/23-041-L","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the effects of commercial mouth rinses on color, roughness, sorption (SR), and solubility (SL) of resin composites.</p><p><strong>Methods and materials: </strong>Disc-shaped specimens (stage I: 6 mm × 2 mm; stage II: 10 mm × 1.5 mm) were made from the following resin composites (n=10): conventional nanofilled (Filtek Z350XT, 3M Oral Care), conventional nanohybrid (Luna, SDI), bulk-fill nanofilled (Filtek One Bulk-Fill, 3M Oral Care), and bulk-fill nanohybrid (Aura Bulk-Fill, SDI) exposed to distilled water (control), blue mouth rinse without alcohol (Colgate Total 12 Clean Mint, Colgate-Palmolive), or blue mouth rinse with alcohol and essential oil (Listerine Tartar Control, Johnson & Johnson). In stage I, tests were performed at the baseline, and after the immersion in solution time points to evaluate coordinates of the CIEL*a*b* system (ΔL*, Δa*, Δb*), general color change (ΔEab, ΔE00, and ΔSGU), and surface roughness (Ra). In stage II, SR and SL were evaluated (ISO 4049:2019) after immersion in the solutions for 7 days. The results were evaluated by generalized linear models (Ra, SR), Kruskal-Wallis, and Dunn tests (color, SL), with α = 0.05.</p><p><strong>Results: </strong>There were no significative differences for Ra between the solutions. Both mouth rinses promoted significantly negative ΔL* (Luna), Δa* (Filtek One Bulk-fill), and Δb* (all materials except conventional nanofilled resin composite). Mouth rinse without alcohol promoted significantly negative Δa* on all resin composites tested. Both mouth rinses promoted higher ΔEab and ΔE00 for bulk-fill resin composites compared to control. Mouth rinse with alcohol caused higher ΔSGU for bulk-fill nanofilled resin composite. It also promoted greater SR in all the resin composites compared with mouth rinse without alcohol and higher SR in nanohybrid resin composites compared with control. Both mouth rinses promoted higher SL values in Luna and differed significantly from control.</p><p><strong>Conclusions: </strong>The physical properties were manufacturer dependent and mediated by mouth rinses. The mouth rinses promoted color changes in the resin composites, pointing out that bulk-fill resin composites were more affected by these effects, especially when the mouth rinse contained essential oil and alcohol.</p>","PeriodicalId":19502,"journal":{"name":"Operative dentistry","volume":" ","pages":"720-731"},"PeriodicalIF":2.2,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50162395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}