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Effect of different adhesive application approaches on bond strength in over-etched dentin. 不同粘接方式对过度蚀刻牙本质粘接强度的影响。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-06-01
Phoebe Burrer, Shpresa Simoni, Paula Zwicky, Thomas Attin, Tobias T Tauböck

Purpose: To investigate the effect of over-etching and subsequent use of different adhesive application approaches including active, double, preheated, and ultrasonic application on dentin bond strength.

Methods: Dentin specimens from sound human third molars were prepared and allocated into six groups (n= 10 per group). In Group 1 (negative control), the dentin specimens were over-etched with phosphoric acid for 30 seconds, and a two-step etch-and-rinse adhesive (Prime & Bond XP; Dentsply Sirona) was applied for 20 seconds according to the manufacturer's instructions. In test Groups 2-5, the application of the adhesive varied: In Group 2, the adhesive was actively rubbed into the dentin surface, whereas in Group 3, a second adhesive layer was applied after light-curing of the first one. In Group 4, the adhesive was heated to 68°C prior to application, and in Group 5, the adhesive was ultrasonically activated. Acid-etching for 15 seconds and adhesive application for 20 seconds was performed in the positive control group (Group 6) according to the manufacturer's instructions. After light-curing and composite build-up [Ceram.x Spectra ST (HV); Dentsply Sirona], microtensile bond strength and fracture types were determined. Data were statistically analyzed by Kruskal-Wallis rank test, followed by post-hoc pairwise comparisons using Conover tests and P-value adjustment according to Holm (α= 0.05).

Results: Active, double, preheated, or ultrasonic adhesive application showed no significant effect on dentin bond strength when compared to the control groups. Predominantly adhesive failures were observed in all groups.

Clinical significance: A modification of adhesive application by using active, double, preheated, or ultrasonic application does not improve bonding to accidentally over-etched dentin.

目的:探讨过度蚀刻及后续使用不同的粘接方法,包括主动、双重、预热、超声等对牙本质粘接强度的影响。方法:制备健全人第三磨牙的牙本质标本,分为6组,每组10例。在第1组(阴性对照)中,牙本质标本用磷酸过度蚀刻30秒,并使用两步蚀刻-冲洗粘合剂(Prime & Bond XP;根据制造商的说明,应用Dentsply Sirona) 20秒。在测试组2-5中,胶粘剂的涂抹方式不同:第2组是主动将胶粘剂摩擦到牙本质表面,第3组是在第1层光固化后再涂抹第2层胶粘剂。第4组使用前将胶粘剂加热至68℃,第5组使用超声激活胶粘剂。阳性对照组(第6组)按照制造商的说明书进行酸蚀15秒,涂胶20秒。经过光固化和复合构筑[陶瓷]。x Spectra ST (HV);Dentsply Sirona],测定微拉伸粘结强度和断裂类型。数据采用Kruskal-Wallis秩检验进行统计学分析,采用Conover检验进行事后两两比较,并根据Holm进行p值调整(α= 0.05)。结果:与对照组相比,使用活性、双重、预热或超声黏合剂对牙本质黏结强度无显著影响。所有组中主要观察到粘附失败。临床意义:通过使用主动、双重、预热或超声等方法来改进粘接剂的应用,并不能改善意外过度蚀刻牙本质的粘接性。
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引用次数: 0
Secondary caries adjacent to bulk fill resin composite restorations lined with fluoride agents. 填充了氟化物剂的树脂复合修复体相邻的继发性龋齿。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-06-01
Tom Patterson, Hoda S Ismail, John Hicks, Franklin Garcia-Godoy

Purpose: To evaluate the potential secondary caries reduction of bulk-fill resin composite restorations treated with different fluoride (F)-based agents prior to restoration placement.

Methods: 25 upper extracted molars received Class V cavities on both buccal and lingual surfaces with an enamel margin and root surface margin. The teeth were randomly assigned into five groups with five teeth per group (n=10). The treatment groups were: control group, with no treatment; the other groups received treatment using different F-based agents prior to bonding. All teeth were restored using a selective etch bonding technique and bulk fill resin composite. All teeth received 10,000 thermal cycles followed by immersion in demineralizing solution to produce artificial caries-like lesions. Polarized light microscope evaluation was performed on longitudinal sections (30 enamel lesions and 30 root surface lesions per group). Lesion depth and wall lesions for both enamel and root surface adjacent to the restorations were evaluated.

Results: Both lesion depths and frequency of wall lesions in the enamel and root surfaces in all treatment groups were significantly reduced compared with the control group. Among the different F-based agents, no significant difference was seen on the enamel or root surface lesion depth, showing a similar presence of enamel and root cavosurface wall lesions.

Clinical significance: F-based agent treatment of adjacent enamel and root surfaces prior to placement of restorative materials provided resistance to the development of secondary caries during an in vitro caries model.

目的:评价在修复体放置前使用不同氟化物(F)基剂处理的块状填充树脂复合修复体的二次龋减少潜力。方法:25颗拔除的上颌磨牙在颊面和舌面均种植V类牙槽,牙釉质缘和牙根面缘。随机分为5组,每组5颗(n=10)。治疗组为:对照组,不进行治疗;其他组在粘接前使用不同的f基药物进行治疗。所有牙齿均采用选择性蚀刻粘接技术和大块填充树脂复合材料修复。所有牙齿接受10,000个热循环,然后浸泡在脱矿液中产生人工龋齿样病变。纵切面(每组牙釉质病变30个,牙根表面病变30个)进行偏光显微镜评价。评估修复体附近牙釉质和根表面的病变深度和管壁病变。结果:与对照组相比,各治疗组牙釉质和牙根表面管壁病变深度和频率均明显降低。不同f基药物对牙釉质和根表面病变深度的影响无显著差异,表明牙釉质和根茎表面病变的存在相似。临床意义:在体外龋齿模型中,在放置修复材料之前对相邻牙釉质和牙根表面进行含氟剂处理可以抵抗继发性龋齿的发展。
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引用次数: 0
Clinical evaluation of surface treatment on clinical performance of non-carious sclerotic cervical lesions: 18-month follow-up. 表面治疗对非龋齿硬化性宫颈病变临床表现的临床评价:随访18个月。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-06-01
Christiane de M Alencar, Gabriela C S Fernandes, Antonio Patrícia O Barros, Joissi F Zaniboni, Aryvelto M Silva, Fernanda F de A Jassé, Cecy M Silva, Edson A de Campos

Purpose: To evaluate the influence of different surface treatments on the clinical behavior of non-carious cervical sclerotic lesions (NCCLs) over an 18-month follow-up period.

Methods: 128 NCCLs from 32 volunteers were randomized into four groups (n=32): G1-control, without preoperative treatment of the dentin surface; G2, dentin conditioning with 17% ethylenediaminetetracetic acid (EDTA) for 2 minutes; G3, increase in dentin surface roughness with diamond bur and G4, increase in dentin surface roughness with diamond bur + dentin conditioning with 17% EDTA for 2 minutes.

Results: Differences between groups were tested using the Friedman test (α= 0.05). A questionnaire was administered to volunteers about risk factors related to NCCLs. The relationship between the questionnaire data and the clinical performance of the restorations was analyzed using the multiple logistic regression test (α= 0.05). The variables related to parafunctional habits, anxiety and/or depression were significantly related to the manifestation of postoperative sensitivity. Roughening the sclerotic dentin with a diamond bur increased postoperative sensitivity within 12 months. The presence of parafunctional habits and anxiety/depression may lead to postoperative sensitivity.

Clinical significance: Roughening the sclerotic dentin with a diamond bur increased postoperative sensitivity within 12 months.

目的:评价不同表面处理对非龋齿性宫颈硬化病变(ncls)临床行为的影响,随访18个月。方法:32名志愿者的128例ncls随机分为4组(n=32): g1组,术前不进行牙本质表面处理;G2,用17%乙二胺四乙酸(EDTA)调理牙本质2分钟;G3,金刚石钎剂增加牙本质表面粗糙度;G4,金刚石钎剂+ 17% EDTA处理2分钟牙本质表面粗糙度增加。结果:组间差异采用Friedman检验(α= 0.05)。对志愿者进行问卷调查,了解与ncls相关的危险因素。采用多元logistic回归检验分析问卷数据与修复体临床性能的关系(α= 0.05)。与功能习惯、焦虑和/或抑郁相关的变量与术后敏感性的表现显著相关。用金刚钻磨粗硬化的牙本质可在术后12个月内提高敏感性。功能不良习惯和焦虑/抑郁的存在可能导致术后敏感。临床意义:用金刚钻磨粗硬化牙本质可提高术后12个月内的敏感性。
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引用次数: 0
The potential of conventional and bulk-fill bioactive composites to inhibit the development of caries lesions around restorations. 传统和散装填充生物活性复合材料抑制修复体周围龋齿病变发展的潜力。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-06-01
Daylana P Silva, Matheus Kury, Camila S S Coelho, Mayara Dos S Noronha, Beatriz de O Medeiros, Carolina B André, Cinthia P M Tabchoury, Vanessa Cavalli

Purpose: To determine caries inhibition potential of conventional and bulk-fill bioactive composites around restorations.

Methods: Enamel and dentin blocks were prepared using a diamond saw under water irrigation, finished (SiC, 600- and 800-grit) and polished (SiC 1,200, final polish= 0.2 μm). Blocks were then selected through enamel surface microhardness, and enamel and dentin standard cavities were restored (n=10/group) with conventional bioactive composite (Beautifil II, BTF), bulk-fill bioactive composite (Activa BioACTIVE, ACT), glass-ionomer cement (Ionofil Plus, ION), conventional composite (GrandioSO, GSO), and bulk-fill composite (Admira Fusion X-TRA, ADM). Afterwards, the blocks were subjected to pH cycling: 4 hours in demineralization and 20 hours in remineralization solutions for 7 days, before being cut in the middle. One half was used to calculate the carious lesion area (ΔS) using values obtained by cross-sectional microhardness (CSMH) testing. The other half was submitted to polarized light microscopy (PLM) and scanning electron microscopy (SEM). The % of internal gap formation (GAP) of restorations' replicas were analyzed under SEM. Data were analyzed by ANOVA and Tukey test (α= 5%).

Results: In terms of CSMH, ION group exhibited the lowest ΔS values, with no significant difference to ADM. The composites BTF and ACT were similar to each other (P< 0.05) and to their negative controls (GSO and ADM), respectively. ION showed lower caries formation under PLM, whereas the GSO group presented a greater demineralized area. ION presented the highest % of internal GAP formation. Bioactive composites (BTF and ACT) were similar to their corresponding conventional ones (GSO and ADM) in terms of GAP formation.

Clinical significance: The glass-ionomer cement was more effective in inhibiting the formation of caries lesions around restorations. Because of the glass-ionomer cement's limited application in high load-bearing areas, the conventional bioactive composite would be a promising clinical choice.

目的:比较常规生物活性复合材料和填充型生物活性复合材料在修复体周围的龋抑制潜力。方法:用金刚石锯在水冲洗下制备牙釉质和牙本质块,抛光(SiC, 600和800),抛光(SiC 1200,最终抛光= 0.2 μm)。然后通过牙釉质表面显微硬度选择牙釉质块,用常规生物活性复合材料(Beautifil II, BTF)、填充型生物活性复合材料(Activa bioactive, ACT)、玻璃离子聚合物水泥(Ionofil Plus, ION)、常规复合材料(GrandioSO, GSO)和填充型复合材料(Admira Fusion X-TRA, ADM)修复牙釉质和牙本质标准腔(n=10/组)。然后进行pH循环:脱矿4小时,再矿化溶液20小时,持续7天,中间切割。其中一半用于计算龋病面积(ΔS),使用横截面显微硬度(CSMH)测试得到的值。另一半进行偏振光显微镜(PLM)和扫描电子显微镜(SEM)检查。在扫描电镜下分析修复体复制品的内部间隙形成率(gap)。数据采用方差分析和Tukey检验(α= 5%)。结果:在CSMH方面,离子组ΔS值最低,与ADM差异无统计学意义。复合材料BTF和ACT与阴性对照GSO和ADM相似(P< 0.05)。PLM组ION组龋形成较低,而GSO组脱矿面积较大。离子的内部GAP形成率最高。生物活性复合材料(BTF和ACT)在GAP形成方面与相应的常规复合材料(GSO和ADM)相似。临床意义:玻璃离子水门栓能更有效地抑制修复体周围龋齿的形成。由于玻璃离聚体水泥在高承载区域的应用有限,传统的生物活性复合材料将是一种有前途的临床选择。
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引用次数: 0
Candida albicans adhesion on 3D-printed and thermopolymerizable polymethyl methacrylate for removable prostheses. 白色念珠菌粘附在3d打印和热聚合的聚甲基丙烯酸甲酯上,用于可移动的假体。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-06-01
Michelle Cc Barros, Ricardo R Mazzon, Artur F Soto, Thais M Duque, Rangel Lidani, Cleonice S Teixeira, Gabriela P Sabatini, Maurício M Badaró

Purpose: To compare Candida albicans adhesion and quantify the biofilm formed on thermopolymerizable (T.PMMA) and 3D printing (3D.PMMA) polymethyl methacrylate through quantitative and qualitative analyses.

Methods: The specimens were made (n= 39/material) by conventional polymerization (T.PMMA) and designed in Autodesk Meshmixer software, followed by 3D printing (3D.PMMA) - CAD-CAM method. After the roughness standardization, the monospecies biofilm of C. albicans (ATCC 10231) was submitted to adhesion analysis, verifying the quantification and microbial load, in triplicate, by the methods of counting colony forming units (CFU/mL) and staining with crystal violet, followed by optical density reading, respectively. Qualitative analyses were performed by scanning electron microscopy to analyze the surface characteristics of the specimens and biofilm formed. The Mann-Whitney U test was used for comparisons between resins regarding the count of CFU/mL (log¹⁰+ 1) and optical density values (P≤ 0.05).

Results: T.PMMA (5.78 ± 0.43) had a CFU/mL count (P< 0.001) higher than 3D.PMMA (4.84 ± 0.39). There was a difference between C. albicans biofilm accumulation (P< 0.001), in which on T.PMMA (1.59 ± 0.31) was higher than 3D.PMMA (1.10 ± 0.14). The qualitative analyses corresponded to the quantitative ones and allowed the visualization of more porosities in T.PMMA.

Clinical significance: The adhesion (microbial load and biofilm accumulation) of C. albicans was lower in the 3D printed polymethyl methacrylate when compared to the thermopolymerizable model.

目的:比较白色念珠菌粘附性,定量分析热聚合(T.PMMA)和3D打印(3D. pmma)聚甲基丙烯酸甲酯上形成的生物膜。方法:采用常规聚合(T.PMMA)法制备标本(n= 39/材料),在Autodesk Meshmixer软件中进行设计,然后进行3D打印(3D. pmma) - CAD-CAM方法。粗糙度标准化后,将单种白色念珠菌(ATCC 10231)生物膜进行粘附分析,分别采用菌落形成单位计数(CFU/mL)、结晶紫染色、光密度读取等方法,对三份单种念珠菌生物膜进行定量和微生物负荷验证。通过扫描电镜进行定性分析,分析样品的表面特征和形成的生物膜。使用Mann-Whitney U检验比较树脂的CFU/mL计数(log¹⁰+ 1)和光密度值(P≤0.05)。结果:T.PMMA组CFU/mL计数(5.78±0.43)高于3D组(P< 0.001)。Pmma(4.84±0.39)。两组间白色念珠菌生物膜积累量差异(P< 0.001),其中T.PMMA(1.59±0.31)高于3D。Pmma(1.10±0.14)。临床意义:3D打印的聚甲基丙烯酸甲酯与热聚合模型相比,白色念珠菌的粘附力(微生物负荷和生物膜积累)更低。
{"title":"Candida albicans adhesion on 3D-printed and thermopolymerizable polymethyl methacrylate for removable prostheses.","authors":"Michelle Cc Barros,&nbsp;Ricardo R Mazzon,&nbsp;Artur F Soto,&nbsp;Thais M Duque,&nbsp;Rangel Lidani,&nbsp;Cleonice S Teixeira,&nbsp;Gabriela P Sabatini,&nbsp;Maurício M Badaró","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To compare Candida albicans adhesion and quantify the biofilm formed on thermopolymerizable (T.PMMA) and 3D printing (3D.PMMA) polymethyl methacrylate through quantitative and qualitative analyses.</p><p><strong>Methods: </strong>The specimens were made (n= 39/material) by conventional polymerization (T.PMMA) and designed in Autodesk Meshmixer software, followed by 3D printing (3D.PMMA) - CAD-CAM method. After the roughness standardization, the monospecies biofilm of C. albicans (ATCC 10231) was submitted to adhesion analysis, verifying the quantification and microbial load, in triplicate, by the methods of counting colony forming units (CFU/mL) and staining with crystal violet, followed by optical density reading, respectively. Qualitative analyses were performed by scanning electron microscopy to analyze the surface characteristics of the specimens and biofilm formed. The Mann-Whitney U test was used for comparisons between resins regarding the count of CFU/mL (log¹⁰+ 1) and optical density values (P≤ 0.05).</p><p><strong>Results: </strong>T.PMMA (5.78 ± 0.43) had a CFU/mL count (P< 0.001) higher than 3D.PMMA (4.84 ± 0.39). There was a difference between C. albicans biofilm accumulation (P< 0.001), in which on T.PMMA (1.59 ± 0.31) was higher than 3D.PMMA (1.10 ± 0.14). The qualitative analyses corresponded to the quantitative ones and allowed the visualization of more porosities in T.PMMA.</p><p><strong>Clinical significance: </strong>The adhesion (microbial load and biofilm accumulation) of C. albicans was lower in the 3D printed polymethyl methacrylate when compared to the thermopolymerizable model.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 3","pages":"130-135"},"PeriodicalIF":1.4,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10067061","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}
引用次数: 0
Multicenter study on visual color difference thresholds. A secondary analysis of light, medium, and dark tooth-colored specimens. 视觉色差阈值的多中心研究。对浅色、中色和深色牙齿标本进行二次分析。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-04-01
Eman H Ismail, Razvan I Ghinea, Luis J Herrera, Esam Tashkandi, Rade D Paravina

Purpose: This secondary analysis further analyzed variations in the 50:50% perceptibility and acceptability thresholds (PT and AT, respectively) pertaining to light, medium, and dark tooth-colored specimen sets.

Methods: Primary raw data from the original study was retrieved. Visual thresholds (Perceptibility - PT and Acceptability - AT) were analyzed among the three specimen sets - light, medium, and dark. The Wilcoxon signed-rank test was used for paired specimens, and the Wilcoxon rank-sum nonparametric test was used for independent specimens (α= 0.001).

Results: The 50:50% CIEDE2000 PT and AT values were significantly higher for the light-colored specimen set when compared with the medium and dark-colored specimens: 1.2, 0.7, 0.6, respectively (PT) and 2.2, 16, 14 (AT), respectively (P< 0.001). Independent of the observer group, the highest PT and AT values were always found for the light-colored specimen sets (P< 0.001). Dental laboratory technicians had the lowest visual thresholds, but not significantly different from the other observer groups studied (P> 0.001). Similarly, all research sites had statistically higher visual thresholds for the light-colored specimen set than for the medium- or dark-colored sets, except for two sites that showed statistically similar results for medium-colored specimens but were significantly different from the dark-colored set. Among the different research sites, sites 2 and 5 registered significantly higher PT thresholds for the light specimens (1.5 and 1.6, respectively), and site number 1 had a significantly higher AT threshold relative to the other sites. The 50:50% perceptibility and acceptability thresholds were significantly different among light-, medium-, and dark-colored specimens for different research sites and observer groups.

Clinical significance: The visual perception of color difference related to light-, medium-, and dark-colored specimens varied based on observer group and their geographic location. Therefore, a greater understanding of factors that affect visual thresholds, with the observers being "the most forgiving" for color differences among the light shades, will allow diverse clinicians to overcome some of the challenges of clinical color matching.

目的:这一二次分析进一步分析了50:50感知和接受阈值(分别为PT和AT)在浅色、中等色和深色牙色标本组中的变化。方法:从原始研究中检索主要原始数据。视觉阈值(感知性- PT和可接受性- AT)在三种标本组中进行分析-光,中,暗。配对样本采用Wilcoxon符号秩检验,独立样本采用Wilcoxon秩和非参数检验(α= 0.001)。结果:浅色标本组50:50%的CIEDE2000 PT和AT值显著高于中、深色标本组:分别为1.2、0.7、0.6 (PT)和2.2、16、14 (AT) (P< 0.001)。独立于观察组,浅色标本组的PT和AT值均最高(P< 0.001)。牙科实验室技师的视觉阈值最低,但与其他观察组无显著差异(P> 0.001)。同样,所有的研究地点对浅色标本集的视觉阈值在统计上都高于中、深色标本集,只有两个地点对中色标本集的视觉阈值在统计上相似,但与深色标本集的视觉阈值有显著差异。在不同的研究点中,站点2和站点5的光样PT阈值显著高于其他站点(分别为1.5和1.6),站点1的AT阈值显著高于其他站点。在不同的研究地点和观察组中,浅色、中色和深色标本的50:50可感知性和可接受性阈值存在显著差异。临床意义:浅、中、深色标本的色差视知觉因观察组及其地理位置的不同而不同。因此,对影响视觉阈值的因素有了更深入的了解,观察者对不同色调之间的颜色差异是“最宽容的”,这将使不同的临床医生能够克服临床配色的一些挑战。
{"title":"Multicenter study on visual color difference thresholds. A secondary analysis of light, medium, and dark tooth-colored specimens.","authors":"Eman H Ismail,&nbsp;Razvan I Ghinea,&nbsp;Luis J Herrera,&nbsp;Esam Tashkandi,&nbsp;Rade D Paravina","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>This secondary analysis further analyzed variations in the 50:50% perceptibility and acceptability thresholds (PT and AT, respectively) pertaining to light, medium, and dark tooth-colored specimen sets.</p><p><strong>Methods: </strong>Primary raw data from the original study was retrieved. Visual thresholds (Perceptibility - PT and Acceptability - AT) were analyzed among the three specimen sets - light, medium, and dark. The Wilcoxon signed-rank test was used for paired specimens, and the Wilcoxon rank-sum nonparametric test was used for independent specimens (α= 0.001).</p><p><strong>Results: </strong>The 50:50% CIEDE2000 PT and AT values were significantly higher for the light-colored specimen set when compared with the medium and dark-colored specimens: 1.2, 0.7, 0.6, respectively (PT) and 2.2, 16, 14 (AT), respectively (P< 0.001). Independent of the observer group, the highest PT and AT values were always found for the light-colored specimen sets (P< 0.001). Dental laboratory technicians had the lowest visual thresholds, but not significantly different from the other observer groups studied (P> 0.001). Similarly, all research sites had statistically higher visual thresholds for the light-colored specimen set than for the medium- or dark-colored sets, except for two sites that showed statistically similar results for medium-colored specimens but were significantly different from the dark-colored set. Among the different research sites, sites 2 and 5 registered significantly higher PT thresholds for the light specimens (1.5 and 1.6, respectively), and site number 1 had a significantly higher AT threshold relative to the other sites. The 50:50% perceptibility and acceptability thresholds were significantly different among light-, medium-, and dark-colored specimens for different research sites and observer groups.</p><p><strong>Clinical significance: </strong>The visual perception of color difference related to light-, medium-, and dark-colored specimens varied based on observer group and their geographic location. Therefore, a greater understanding of factors that affect visual thresholds, with the observers being \"the most forgiving\" for color differences among the light shades, will allow diverse clinicians to overcome some of the challenges of clinical color matching.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 2","pages":"86-90"},"PeriodicalIF":1.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9420365","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}
引用次数: 0
Evaluation of oral and perioral irritation and sensitization potential of a whitening gel and a whitening toothpaste containing potassium monopersulfate. 含过硫酸钾的美白凝胶和美白牙膏的口腔和口腔周围刺激和致敏潜力的评价。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-04-01
Yiming Li, Montry S Suprono, Connie Cheung, Daniella U Ross, Brian A Wall, Cajetan Dogo-Isonagie, Michele Arambula, Xing Xin

Purpose: Two clinical trials were conducted to investigate the oral and perioral irritation and sensitization potential of a tooth whitening leave-on-gel alone and in combination with a whitening toothpaste, each containing 1.0% of the active ingredient potassium monopersulfate (MPS).

Methods: Both clinical trials were Institutional Review Board (IRB) approved, double-blind, randomized, and parallel group designed studies. For the MPS leave-on gel study, 200 qualifying and consented subjects were randomly assigned to two groups: (1) 0.1% hydrogen peroxide (H₂O₂) gel pen (34 subjects); and (2) 0.1% H₂O₂ + 1.0% MPS gel pen (166 subjects). Subjects used the assigned products according to instructions provided and returned on Days 22 and 36 for oral and perioral tissue examination (pre-challenge). At the Day 36 visit, the subject applied the assigned gel on site (challenge) and received oral and perioral tissue examinations 1 and 24 hours following the application to detect any post-challenge tissue reactions. For the MPS toothpaste/MPS gel pen study, 200 qualifying and consented subjects were randomly assigned to three groups: (1) Placebo toothpaste + placebo gel pen (66 subjects); (2) 1.0% MPS toothpaste + 1.0% MPS gel pen (67 subjects); and (3) 1.0% MPS toothpaste + placebo gel pen (67 subjects). The study design and procedures were the same as those for the MPS gel pen study described above.

Results: For the MPS gel pen study, 192 subjects completed the study. None of the eight dropouts was related to the product use. The demographic data were comparable between the two groups. No evidence of tissue irritation and sensitization was detected in any subjects at any visit, and the findings were comparable between the groups. The detected and self-reported tissue issues were minimal and minor, and they were comparable between the two groups. For the MPS toothpaste/MPS gel pen study, 200 subjects were enrolled with 12 dropped from the study, resulting in an overall dropout rate of 6%. Of the 12 that did not complete the study, none were due to product-related use. The demographic data were comparable among the three groups. The detected and self-reported tissue issues were minimal and minor, and they were comparable among the three groups.

Clinical significance: Potassium monopersulfate (MPS) at the active concentration of 1.0% in the tooth whitening leave-on-gel and the toothpaste plus the gel did not cause oral/perioral irritation nor sensitization.

目的:进行了两项临床试验,研究了牙齿美白凝胶单独使用和与美白牙膏联合使用(每种牙膏含有1.0%的活性成分单过硫酸钾(MPS))对口腔和口腔周围的刺激和致敏潜力。方法:两项临床试验均为机构审查委员会(IRB)批准的双盲、随机、平行组设计的研究。对于MPS免洗凝胶研究,200名符合条件并同意的受试者被随机分为两组:(1)0.1%过氧化氢(H₂O₂)凝胶笔(34名受试者);(2) 0.1% h2o2 + 1.0% MPS凝胶笔(166例)。受试者根据提供的说明使用指定的产品,并于第22天和第36天返回进行口腔和口腔周围组织检查(预激药)。在第36天的访问中,受试者在现场涂抹指定的凝胶(攻毒),并在涂抹后1和24小时接受口腔和口周组织检查,以检测任何攻毒后组织反应。在MPS牙膏/MPS凝胶笔研究中,200名符合条件和同意的受试者被随机分为三组:(1)安慰剂牙膏+安慰剂凝胶笔(66名受试者);(2) 1.0% MPS牙膏+ 1.0% MPS凝胶笔(67例);(3) 1.0% MPS牙膏+安慰剂凝胶笔(67例)。研究设计和程序与上述MPS凝胶笔研究相同。结果:MPS凝胶笔研究有192名受试者完成了研究。8名退选患者都与产品使用无关。两组的人口统计数据具有可比性。在任何一次访问中,在任何受试者中都没有检测到组织刺激和致敏的证据,并且两组之间的发现具有可比性。检测到的和自我报告的组织问题是最小和轻微的,它们在两组之间具有可比性。在MPS牙膏/MPS凝胶笔研究中,200名受试者被纳入研究,其中12人退出研究,导致总退学率为6%。在12个没有完成研究的人中,没有一个是由于与产品相关的使用。三组人口统计数据具有可比性。检测到的和自我报告的组织问题是最小和轻微的,并且它们在三组之间具有可比性。临床意义:单过硫酸钾(MPS)在牙齿美白免洗凝胶和牙膏加凝胶中的活性浓度为1.0%时,没有引起口腔/口周刺激和致敏。
{"title":"Evaluation of oral and perioral irritation and sensitization potential of a whitening gel and a whitening toothpaste containing potassium monopersulfate.","authors":"Yiming Li,&nbsp;Montry S Suprono,&nbsp;Connie Cheung,&nbsp;Daniella U Ross,&nbsp;Brian A Wall,&nbsp;Cajetan Dogo-Isonagie,&nbsp;Michele Arambula,&nbsp;Xing Xin","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>Two clinical trials were conducted to investigate the oral and perioral irritation and sensitization potential of a tooth whitening leave-on-gel alone and in combination with a whitening toothpaste, each containing 1.0% of the active ingredient potassium monopersulfate (MPS).</p><p><strong>Methods: </strong>Both clinical trials were Institutional Review Board (IRB) approved, double-blind, randomized, and parallel group designed studies. For the MPS leave-on gel study, 200 qualifying and consented subjects were randomly assigned to two groups: (1) 0.1% hydrogen peroxide (H₂O₂) gel pen (34 subjects); and (2) 0.1% H₂O₂ + 1.0% MPS gel pen (166 subjects). Subjects used the assigned products according to instructions provided and returned on Days 22 and 36 for oral and perioral tissue examination (pre-challenge). At the Day 36 visit, the subject applied the assigned gel on site (challenge) and received oral and perioral tissue examinations 1 and 24 hours following the application to detect any post-challenge tissue reactions. For the MPS toothpaste/MPS gel pen study, 200 qualifying and consented subjects were randomly assigned to three groups: (1) Placebo toothpaste + placebo gel pen (66 subjects); (2) 1.0% MPS toothpaste + 1.0% MPS gel pen (67 subjects); and (3) 1.0% MPS toothpaste + placebo gel pen (67 subjects). The study design and procedures were the same as those for the MPS gel pen study described above.</p><p><strong>Results: </strong>For the MPS gel pen study, 192 subjects completed the study. None of the eight dropouts was related to the product use. The demographic data were comparable between the two groups. No evidence of tissue irritation and sensitization was detected in any subjects at any visit, and the findings were comparable between the groups. The detected and self-reported tissue issues were minimal and minor, and they were comparable between the two groups. For the MPS toothpaste/MPS gel pen study, 200 subjects were enrolled with 12 dropped from the study, resulting in an overall dropout rate of 6%. Of the 12 that did not complete the study, none were due to product-related use. The demographic data were comparable among the three groups. The detected and self-reported tissue issues were minimal and minor, and they were comparable among the three groups.</p><p><strong>Clinical significance: </strong>Potassium monopersulfate (MPS) at the active concentration of 1.0% in the tooth whitening leave-on-gel and the toothpaste plus the gel did not cause oral/perioral irritation nor sensitization.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 2","pages":"95-100"},"PeriodicalIF":1.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9413488","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}
引用次数: 0
Effect of effervescent tablets on removable partial denture hygiene. 泡腾片对可摘局部义齿卫生的影响。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-04-01
Victor G Morelli, Viviane C Oliveira, Glenda L L Vasconcelos, Patricia A Curylofo, Rachel M Monteiro, Ana P Macedo, Valéria de O Pagnano

Purpose: To evaluate the effectiveness of five alkaline peroxide-based effervescent tablets in reducing both biofilms and the food layer adhered on the cobalt-chromium surface.

Methods: Cobalt-chromium metal alloy specimens were contaminated with Candida albicans, Candida glabrata, Streptococcus mutans and Staphylococcus aureus. After biofilm maturation, the specimens were immersed in Polident 3 Minute, Polident for Partials, Efferdent, Steradent, Corega Tabs or distilled water (control). Residual biofilm rates were determined by colony forming units counts and biofilm biomass. In parallel, to investigate the denture cleaning capability of effervescent tablets, artificially contaminated removable partial dentures were treated with each cleanser. Data were analyzed by Kruskal-Wallis followed by Dunn post hoc test or ANOVA followed by Tukey post hoc test (α= 0.05).

Results: None of the hygiene solutions reduced C. albicans biofilm. Efferdent and Corega Tabs promoted reduction of C. glabrata biofilm, while Steradent was favorable against S. aureus biofilm. For S. mutans, lower biofilm rates were observed after immersion in Polident for Partials and Steradent. The effervescent tablets showed good cleaning performance, removing an artificial layer with carbohydrates, proteins, and fats, however, they were not effective in removing aggregated mature biofilm.

Clinical significance: The different effervescent tablets presented favorable antimicrobial activity against C. glabrata, S. mutans and S. aureus on cobalt-chromium surfaces and showed cleaning capability. However, for an appropriate biofilm control, a complementary method should be evaluated since none of the peroxide-based solutions reduced C. albicans biofilms or substantially removed aggregated biofilm.

目的:评价五种碱性过氧化物泡腾片对钴铬表面生物膜和食物层的降解效果。方法:对钴铬金属合金标本进行白色念珠菌、光面念珠菌、变形链球菌和金黄色葡萄球菌污染检测。生物膜成熟后,将标本浸泡在Polident 3 Minute、Polident for Partials、Efferdent、Steradent、Corega Tabs或蒸馏水(对照)中。剩余生物膜率由菌落形成单位数和生物膜生物量确定。同时,为了研究泡腾片对人工污染的可摘局部义齿的清洁能力,用每种清洁剂对人工污染的可摘局部义齿进行处理。数据分析采用Kruskal-Wallis + Dunn事后检验或ANOVA + Tukey事后检验(α= 0.05)。结果:所有卫生溶液均未降低白色念珠菌的生物膜。Efferdent和Corega tab对C. glabrata生物膜有抑制作用,Steradent对金黄色葡萄球菌生物膜有抑制作用。对于变形链球菌,浸泡在部分和固定的Polident后,观察到较低的生物膜率。泡腾片表现出良好的清洁性能,去除含有碳水化合物、蛋白质和脂肪的人工层,但对去除聚集的成熟生物膜没有效果。临床意义:不同泡腾片对钴铬表面的光秃葡萄球菌、变形葡萄球菌和金黄色葡萄球菌均有良好的抑菌活性,并表现出清洁能力。然而,对于适当的生物膜控制,应该评估一种补充方法,因为没有一种过氧化氢溶液减少白色念珠菌的生物膜或基本上去除聚集的生物膜。
{"title":"Effect of effervescent tablets on removable partial denture hygiene.","authors":"Victor G Morelli,&nbsp;Viviane C Oliveira,&nbsp;Glenda L L Vasconcelos,&nbsp;Patricia A Curylofo,&nbsp;Rachel M Monteiro,&nbsp;Ana P Macedo,&nbsp;Valéria de O Pagnano","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the effectiveness of five alkaline peroxide-based effervescent tablets in reducing both biofilms and the food layer adhered on the cobalt-chromium surface.</p><p><strong>Methods: </strong>Cobalt-chromium metal alloy specimens were contaminated with Candida albicans, Candida glabrata, Streptococcus mutans and Staphylococcus aureus. After biofilm maturation, the specimens were immersed in Polident 3 Minute, Polident for Partials, Efferdent, Steradent, Corega Tabs or distilled water (control). Residual biofilm rates were determined by colony forming units counts and biofilm biomass. In parallel, to investigate the denture cleaning capability of effervescent tablets, artificially contaminated removable partial dentures were treated with each cleanser. Data were analyzed by Kruskal-Wallis followed by Dunn post hoc test or ANOVA followed by Tukey post hoc test (α= 0.05).</p><p><strong>Results: </strong>None of the hygiene solutions reduced C. albicans biofilm. Efferdent and Corega Tabs promoted reduction of C. glabrata biofilm, while Steradent was favorable against S. aureus biofilm. For S. mutans, lower biofilm rates were observed after immersion in Polident for Partials and Steradent. The effervescent tablets showed good cleaning performance, removing an artificial layer with carbohydrates, proteins, and fats, however, they were not effective in removing aggregated mature biofilm.</p><p><strong>Clinical significance: </strong>The different effervescent tablets presented favorable antimicrobial activity against C. glabrata, S. mutans and S. aureus on cobalt-chromium surfaces and showed cleaning capability. However, for an appropriate biofilm control, a complementary method should be evaluated since none of the peroxide-based solutions reduced C. albicans biofilms or substantially removed aggregated biofilm.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 2","pages":"75-80"},"PeriodicalIF":1.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9420018","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}
引用次数: 0
Denture cleanser effect on resilient liners with distinct optical characteristics. 义齿清洁剂对具有独特光学特性的弹性衬垫的影响。
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-04-01
Isabella R P Coelho, Cláudia H Silva-Lovato, Carolina N F Arruda, Eliseu A Münchow, Gabriella R C Silveira, Rodrigo F Carvalho, Mauricio M Badaró

Purpose: To evaluate denture cleansing solutions regarding the surface roughness and color stability of two resilient liners with distinct optical characteristics used for the maximum recommended period of use.

Methods: The specimens of each resilient liner, transparent and white, were randomly distributed into groups (n= 15) of a daily 20-minute immersion simulation of 0.25%, 0.5% and 1% sodium hypochlorite (SH) and 4% acetic acid solutions. Surface roughness (Ra) and color stability (ΔE CIELab formula and NBS systems) were measured after 7, 14, 21, 30, 60, 90, 180, and 270 days. The factors of variations analyzed were material, solutions, and time of immersion. Statistical analysis used three-way ANOVA and Tukey tests (Ra), and repeated measure ANOVA (ΔE and NBS systems), P< 0.05.

Results: For Ra analysis, the variations occurred regardless of time and solution, as the white liner showed the greatest changes (P< 0.001). Regarding interactions between solution and time, in the period of 21 days until 270 days, Ra was equivalent for all solutions (P= 0.001). ΔE analysis showed a difference between solutions (P= 0.000) and interaction between time and solution (P= 0.000). For the transparent liner, the greatest changes were found for 1% SH after 60 days, however, at 270 days there was a color change equivalence with 0.5% SH, while 4% acetic acid solution showed intermediate values. For the white liner, 1% SH showed the highest color changes for all evaluated times, and the other evaluated solutions were similar after 270 days. For both resilient liners, 0.25% SH showed the smallest changes for the evaluated properties.

Clinical significance: The changes found were dependent on the concentration of the solution used, as well as the length of exposure to the solution. In addition, the white resilient liner showed to be less susceptible to color changes. For both resilient liners, 0.25% sodium hypochlorite showed the least changes for the evaluated properties.

目的:评估两种具有不同光学特性的弹性衬垫在建议的最长使用期限内的表面粗糙度和颜色稳定性:将透明和白色两种弹性衬垫的试样随机分配到各组(n= 15),每天用 0.25%、0.5% 和 1%次氯酸钠(SH)以及 4% 乙酸溶液进行 20 分钟的浸泡模拟。分别在 7、14、21、30、60、90、180 和 270 天后测量表面粗糙度(Ra)和颜色稳定性(ΔE CIELab 公式和 NBS 系统)。分析的变化因素包括材料、溶液和浸泡时间。统计分析采用三方方差分析和 Tukey 检验(Ra),以及重复测量方差分析(ΔE 和 NBS 系统),P< 0.05:在 Ra 分析中,无论时间和溶液如何变化,白色衬垫的变化都最大(P< 0.001)。关于溶液和时间之间的相互作用,在 21 天至 270 天期间,所有溶液的 Ra 值都相同(P= 0.001)。ΔE分析表明,不同溶液之间存在差异(P= 0.000),时间与溶液之间存在交互作用(P= 0.000)。对于透明衬垫,1% SH 在 60 天后的变化最大,但在 270 天后,0.5% SH 的颜色变化与透明衬垫相当,而 4% 乙酸溶液则显示出中间值。对于白色衬垫,在所有评估时间内,1% SH 的颜色变化最大,而其他评估溶液在 270 天后的颜色变化相近。对于两种弹性衬垫来说,0.25% 的 SH 在所有评估特性中显示出的变化最小:临床意义:所发现的变化取决于所用溶液的浓度以及接触溶液的时间长短。此外,白色弹性衬垫不易受颜色变化的影响。对于这两种弹性衬垫,0.25% 的次氯酸钠对所评估特性的影响最小。
{"title":"Denture cleanser effect on resilient liners with distinct optical characteristics.","authors":"Isabella R P Coelho, Cláudia H Silva-Lovato, Carolina N F Arruda, Eliseu A Münchow, Gabriella R C Silveira, Rodrigo F Carvalho, Mauricio M Badaró","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate denture cleansing solutions regarding the surface roughness and color stability of two resilient liners with distinct optical characteristics used for the maximum recommended period of use.</p><p><strong>Methods: </strong>The specimens of each resilient liner, transparent and white, were randomly distributed into groups (n= 15) of a daily 20-minute immersion simulation of 0.25%, 0.5% and 1% sodium hypochlorite (SH) and 4% acetic acid solutions. Surface roughness (Ra) and color stability (ΔE CIELab formula and NBS systems) were measured after 7, 14, 21, 30, 60, 90, 180, and 270 days. The factors of variations analyzed were material, solutions, and time of immersion. Statistical analysis used three-way ANOVA and Tukey tests (Ra), and repeated measure ANOVA (ΔE and NBS systems), P< 0.05.</p><p><strong>Results: </strong>For Ra analysis, the variations occurred regardless of time and solution, as the white liner showed the greatest changes (P< 0.001). Regarding interactions between solution and time, in the period of 21 days until 270 days, Ra was equivalent for all solutions (P= 0.001). ΔE analysis showed a difference between solutions (P= 0.000) and interaction between time and solution (P= 0.000). For the transparent liner, the greatest changes were found for 1% SH after 60 days, however, at 270 days there was a color change equivalence with 0.5% SH, while 4% acetic acid solution showed intermediate values. For the white liner, 1% SH showed the highest color changes for all evaluated times, and the other evaluated solutions were similar after 270 days. For both resilient liners, 0.25% SH showed the smallest changes for the evaluated properties.</p><p><strong>Clinical significance: </strong>The changes found were dependent on the concentration of the solution used, as well as the length of exposure to the solution. In addition, the white resilient liner showed to be less susceptible to color changes. For both resilient liners, 0.25% sodium hypochlorite showed the least changes for the evaluated properties.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 2","pages":"62-68"},"PeriodicalIF":1.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9420362","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}
引用次数: 0
Mechanical properties of bulk-fill resin composites with single increment up to 4 mm: A novel mechanical strength test. 单个增量达 4 毫米的块状填充树脂复合材料的机械性能:新型机械强度测试
IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pub Date : 2023-04-01
Jiaxue Yang, Ying Chen, Hongliang Meng, Jiadi Shen, Mengyuan Liao, Haifeng Xie

Purpose: To evaluate the mechanical properties of two brands of bulk-fill resin composites placed in a single increment up to 4 mm thickness via a novel mechanical strength test and provide related explanations.

Methods: Light transmission (LT), translucency parameter (TP), color difference (ΔE), Vickers hardness (HV) of two bulk-fill resin composites (Filtek Bulk Fill Posterior, Tetric N-Ceram Bulk Fill) and two conventional resin composites (Z100, Spectrum TPH) were evaluated. A novel flexural strength (FS) test method was applied for bulk-fill resin composite to determine the FS value of the bottom composites at depths of 1, 2, 3, and 4 mm after 24 hours of aging treatment (3 months water storage and 15,000 thermal cycles). The conventional resin composites were also tested for FS and all the FS results were subjected to Weibull analysis. Degree of conversion (DC) in the bulk-fill resin composites, light-cured at depths of 1, 2, 3, and 4 mm and conventional resin composites at depths of 2 and 4 mm, were assessed by FTIR.

Results: Both bulk-fill resin composites showed higher light transmission and translucency than that of conventional ones at each of the same thicknesses (1, 2, 3, 4 mm), wherein their flexural strength was not affected by depth. The Weibull analysis suggested both bulk-fill resin composites achieved good reliability and structural integrity under each curing thickness. Vickers hardness was affected by the material type and thickness. Bulk-fill resin composites showed a decrease in degree of conversion between 1 mm and 4 mm, but both were over 55%.

Clinical significance: Filtek Bulk Fill Posterior, Tetric N-Ceram Bulk Fill achieved acceptable mechanical properties when cured at depths of up to 4 mm, which was beneficial from their optical and polymerized properties.

目的:通过新颖的机械强度测试,评估两种品牌的散装填充树脂复合材料的机械性能,最大厚度为 4 毫米,并提供相关解释:方法: 评估两种团状填充树脂复合材料(Filtek Bulill Posterior、Tetric N-Ceram Bulk Fill)和两种传统树脂复合材料(Z100、Spectrum TPH)的透光率(LT)、半透明参数(TP)、色差(ΔE)和维氏硬度(HV)。在经过 24 小时的老化处理(3 个月的水贮存和 15,000 次热循环)后,采用一种新型的挠曲强度(FS)测试方法来测定底部填充树脂复合材料在 1、2、3 和 4 毫米深度处的挠曲强度值。还对传统树脂复合材料进行了 FS 测试,并对所有 FS 结果进行了 Weibull 分析。傅立叶变换红外光谱(FTIR)对光固化深度为 1、2、3 和 4 毫米的填充树脂复合材料和深度为 2 和 4 毫米的传统树脂复合材料的转化率(DC)进行了评估:结果:在厚度相同的情况下(1、2、3、4 毫米),两种块状填充树脂复合材料的透光率和半透明度均高于传统复合材料,而它们的抗弯强度不受深度的影响。Weibull 分析表明,在每种固化厚度下,两种填充树脂复合材料都具有良好的可靠性和结构完整性。维氏硬度受材料类型和厚度的影响。团状填充树脂复合材料的转化率在 1 毫米和 4 毫米之间有所下降,但都超过了 55%:临床意义:Filtek Bulk Fill Posterior 和 Tetric N-Ceram Bulk Fill 在固化深度达 4 毫米时达到了可接受的机械性能,这有利于它们的光学和聚合性能。
{"title":"Mechanical properties of bulk-fill resin composites with single increment up to 4 mm: A novel mechanical strength test.","authors":"Jiaxue Yang, Ying Chen, Hongliang Meng, Jiadi Shen, Mengyuan Liao, Haifeng Xie","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the mechanical properties of two brands of bulk-fill resin composites placed in a single increment up to 4 mm thickness via a novel mechanical strength test and provide related explanations.</p><p><strong>Methods: </strong>Light transmission (LT), translucency parameter (TP), color difference (ΔE), Vickers hardness (HV) of two bulk-fill resin composites (Filtek Bulk Fill Posterior, Tetric N-Ceram Bulk Fill) and two conventional resin composites (Z100, Spectrum TPH) were evaluated. A novel flexural strength (FS) test method was applied for bulk-fill resin composite to determine the FS value of the bottom composites at depths of 1, 2, 3, and 4 mm after 24 hours of aging treatment (3 months water storage and 15,000 thermal cycles). The conventional resin composites were also tested for FS and all the FS results were subjected to Weibull analysis. Degree of conversion (DC) in the bulk-fill resin composites, light-cured at depths of 1, 2, 3, and 4 mm and conventional resin composites at depths of 2 and 4 mm, were assessed by FTIR.</p><p><strong>Results: </strong>Both bulk-fill resin composites showed higher light transmission and translucency than that of conventional ones at each of the same thicknesses (1, 2, 3, 4 mm), wherein their flexural strength was not affected by depth. The Weibull analysis suggested both bulk-fill resin composites achieved good reliability and structural integrity under each curing thickness. Vickers hardness was affected by the material type and thickness. Bulk-fill resin composites showed a decrease in degree of conversion between 1 mm and 4 mm, but both were over 55%.</p><p><strong>Clinical significance: </strong>Filtek Bulk Fill Posterior, Tetric N-Ceram Bulk Fill achieved acceptable mechanical properties when cured at depths of up to 4 mm, which was beneficial from their optical and polymerized properties.</p>","PeriodicalId":7538,"journal":{"name":"American journal of dentistry","volume":"36 2","pages":"101-108"},"PeriodicalIF":1.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9413490","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}
引用次数: 0
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American journal of dentistry
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