Wolfgang Buchalla

In situ evaluation of different remineralization periods to decrease brushing abrasion of demineralized enamel.

The aim of the present in situ study was to evaluate the effect of different periods of intraoral remineralization to decrease the susceptibility of previously demineralized enamel against toothbrushing abrasion. Six human enamel specimens (A–F) were recessed in the buccal aspects of each of eight intraoral appliances which were worn for 21 days by 8 panelists. Demineralization of the samples was performed twice a day extraorally in the acidic beverage Sprite Light for 90 s. Subsequently, the enamel specimens were brushed at different times. Specimen A was brushed immediately after the demineralization. The remaining samples B–E were brushed after the intraoral appliances had been worn for various periods of remineralization: specimen B, 10 min; C, 20 min; D, 30 min and E, 60 min, respectively. Specimen F was only demineralized and remineralized, but not brushed. After 21 days, enamel wear was measured with a laser profilometer. The following values (mean ± standard deviation) were obtained: specimen A, 6.78±2.71 µm; B, 5.47±3.39 µm; C, 6.06±3.18 µm; D, 5.43±2.58 µm; E 4.78±2.57 µm, and F 0.66±1.11 µm. Analysis of variance revealed a significant influence of remineralization period on abrasive wear. However, even after a remineralization period of 60 min the wear was significantly increased as compared to the demineralized, but not brushed control. It is concluded that (1) abrasion resistance of softened enamel increases with remineralization period and (2) at least 60 min should elapse before toothbrushing after an erosive attack.

Curing shrinkage and volumetric changes of resin-modified glass ionomer restorative materials

OBJECTIVES The objective of the study was to evaluate initial curing shrinkage and volumetric change during water storage of six resin-modified glass ionomer cements (Dyract, DeTrey Dentsply; Fuji II LC, GC Dental Int.; Ionosit Fil, DMG; VariGlass VLC, DeTrey Dentsply; Vitremer, 3M Dental Products; Photac-Fil, ESPE), a hybrid composite (blend-a-lux, Blendax) and a chemical-cured glass ionomer cement (ChemFil Superior, DeTrey Dentsply). METHODS The curing shrinkage was determined 5 min and 24 h after polymerization and mixing, respectively. Volumetric changes were examined after 14 d and 28 d water storage. Curing shrinkage and volumetric changes were evaluated using the hydrostatic principle. In addition, the total water content of the materials was measured after 28 d water storage. RESULTS Curing shrinkage of most of the resin-modified glass ionomers was greater than the hybrid composite and the chemical-cured glass ionomer cement. After a 28 d water storage, the resin-modified glass ionomers showed volumetric expansion and the chemical-cured glass ionomer showed volumetric loss. All of the examined glass ionomer materials had a higher total water content than the composite. SIGNIFICANCE. The large curing shrinkage of the resin-modified glass ionomer materials measured in this in vitro study could affect the marginal integrity of glass ionomer restorations.

Effect of mineral supplements to citric acid on enamel erosion

The aim of this study was to evaluate the effect of mineral supplements to citric acid (1%; pH 2.21) on enamel erosion under controlled conditions in an artificial mouth. From each of 156 bovine incisors one polished enamel sample was prepared. The samples were divided among 13 experimental groups (n=12). In group 1 citric acid only was used (control). In groups 2-10 either calcium, phosphate or fluoride in various low concentrations was admixed to the citric acid. In groups 11-13 the citric acid was supplemented with a mixture of calcium, phosphate and fluoride. For demineralisation the specimens were rinsed with the respective solution for 1 min, immediately followed by a remineralisation period with artificial saliva (1 min). The specimens were cycled through this alternating procedure five times followed by rinsing for 8 h with artificial saliva. The de- and remineralisation cycle was repeated three times for each specimen interrupted by the 8 h-remineralisation periods. Before and after the experiments, the specimens were examined using microhardness testing (Knoop hardness) and laser profilometry. Hardness loss and enamel dissolution was significantly higher for the controls as compared to the remaining groups. Significantly lowest hardness loss for all groups was recorded for group 12 with admixture of calcium, phosphate and fluoride to citric acid. The significantly highest enamel loss was recorded for the controls compared to all other samples. Groups 3 and 4 revealed significantly lower and higher tissue loss compared to the remaining groups (2-13), respectively. The other groups did not differ significantly from each other. Modification of citric acid with calcium, phosphate and fluoride exerts a significant protective potential with respect to dental erosion. However, with the low concentrations applied enamel dissolution could not be completely prevented.

Brushing Abrasion of Softened and Remineralised Dentin: An in situ Study

The aim of the present in situ study was to evaluate the effect of different periods of intra-oral remineralisation on the susceptibility of softened dentin to toothbrushing abrasion. Groups of 6 human dentin specimens (A–F) were recessed in the buccal aspects of intra-oral appliances which were worn for 21 days by 11 volunteers. The samples were demineralised twice a day extra-orally in the acidic beverage Sprite Light (pH 2.9) for 90 s. Subsequently, the dentin specimens were brushed at different times. Specimen A was brushed immediately after demineralisation. Specimens B–E were brushed after the intra-oral appliances had been worn for various periods in the mouth: specimen B for 10 min, C for 20 min, D for 30 min and E for 60 min. Specimen F was not brushed (control). After 21 days, dentin wear was measured with a profilometer. The following values (means ± standard deviation) were recorded (µm): A, 23.6 ± 16.7; B, 37.9 ± 29.7; C, 31.8 ± 26.5; D, 18.5 ± 10.5; E, 15.3 ± 11.6; F, 12.6 ± 6.7. There was a statistically significantly increased dentin loss for groups A, B and C as compared to the controls (U test: p < 0.05). However, after intra-oral periods of 30 and 60 min, wear was not significantly higher than in unbrushed controls. It is concluded that for protection of dentin surfaces at least 30 min should elapse before toothbrushing after an erosive attack.

Prevention of Erosion and Abrasion by a High Fluoride Concentration Gel Applied at High Frequencies

The aim of this study was to determine maximum attainable protection of enamel from erosion and erosion abrasion using a highly fluoridated gel with and without additional fluoride from toothpaste. Thirty-six bovine enamel specimens were subjected to six erosive attacks per day (1% citric acid with pH 2.3 for 30 s), while the rest of the day the specimens were in artificial saliva. There were four treatment groups (9 specimens in each group): fluoride-free toothpaste/saliva slurry twice daily (group T0), fluoride-containing toothpaste/saliva slurry twice daily using 1,250 ppm F toothpaste (group TF), fluoride-containing toothpaste/saliva slurry twice per day plus application of a highly fluoridated gel (12,500 ppm F) twice a day for 120 s (group 2F) and a group with gel application 8 times a day (group 8F). Additionally, half of each specimen in all groups was subjected to brushing abrasion during application of the toothpaste/saliva slurry. Brushing abrasion alone led to no observable enamel loss measured with profilometry. After 14 days of cycling of erosion without toothbrushing abrasion, high-fluoride gel application 2 or 8 times daily showed significantly less enamel loss (median 24/19 µm) than with toothpaste with or without fluoride (41/45 µm). After 14 days of cycling of erosion and toothbrushing abrasion, gel application 2 or 8 times daily (33/29 µm) showed significantly less enamel loss than toothpaste with or without fluoride (57/62 µm). We conclude that a highly fluoridated acidic gel is able to protect enamel from erosion and toothbrushing abrasion while fluoridated tooth paste provides little protection.

Antimicrobial photodynamic therapy for inactivation of biofilms formed by oral key pathogens

With increasing numbers of antibiotic-resistant pathogens all over the world there is a pressing need for strategies that are capable of inactivating biofilm-state pathogens with less potential of developing resistances in pathogens. Antimicrobial strategies of that kind are especially needed in dentistry in order to avoid the usage of antibiotics for treatment of periodontal, endodontic or mucosal topical infections caused by bacterial or yeast biofilms. One possible option could be the antimicrobial photodynamic therapy (aPDT), whereby the lethal effect of aPDT is based on the principle that visible light activates a photosensitizer (PS), leading to the formation of reactive oxygen species, e.g., singlet oxygen, which induce phototoxicity immediately during illumination. Many compounds have been described as potential PS for aPDT against bacterial and yeast biofilms so far, but conflicting results have been reported. Therefore, the aim of the present review is to outline the actual state of the art regarding the potential of aPDT for inactivation of biofilms formed in vitro with a main focus on those formed by oral key pathogens and structured regarding the distinct types of PS.

Comparative fluorescence spectroscopy shows differences in noncavitated enamel lesions.

The aim of this study was to compare emission spectra from noncavitated enamel caries with different degrees of discoloration under a wide range of excitation wavelengths. Freshly extracted human molars with white spot, light discolored and dark discolored brown spot enamel caries were selected (n = 4 each). Rectangular blocks (3.5 × 3.5 mm) were cut from the carious area and a corresponding sound area of the same tooth. Emission spectra were recorded from carious and the corresponding sound areas using a fluorescence spectrophotometer at excitation wavelengths from 360 nm up to 580 nm in steps of 20 nm. The specimens were submerged in water during measurement. The spectra were corrected and normalized to peak intensity for comparisons between spectra from sound and carious areas of each tooth. Excitation spectra were recorded for selected emission wavelengths that showed maximum intensity. Emission spectra of all types of carious lesions were shifted towards longer wavelengths (red shift) when compared to the spectra of the corresponding sound enamel. The red shift was highest for dark brown spot lesions and lowest for white spot lesions (p ≤ 0.001). Distinct fluorescence bands within 600–700 nm typical for porphyrin compounds were strongest for excitation wavelengths from 400 to 420 nm and present in most of the lesions investigated.

Influence of Root Canal Disinfectants on Growth Factor Release from Dentin

INTRODUCTION During dentinogenesis, growth factors become entrapped in the dentin matrix that can later be released by demineralization. Their effect on pulpal stem cell migration, proliferation, and differentiation could be beneficial for regenerative endodontic therapies. However, precondition for success, as for conventional root canal treatment, will be sufficient disinfection of the root canal system. Various irrigation solutions and intracanal dressings are available for clinical use. The aim of this study was 2-fold: to identify a demineralizing solution suitable for growth factor release directly from dentin and to evaluate whether commonly used disinfectants for endodontic treatment will compromise this effect. METHODS Dentin disks were prepared from extracted human teeth and treated with EDTA or citric acid at different concentrations or pH for different exposure periods. The amount of transforming growth factor-β1 (TGF-β1), fibroblast growth factor 2, and vascular endothelial growth factor were quantified via enzyme-linked immunosorbent assay and visualized by gold labeling. Subsequently, different irrigation solutions (5.25% sodium hypochloride, 0.12% chlorhexidine digluconate) and intracanal dressings (corticoid-antibiotic paste, calcium hydroxide: water-based and oil-based, triple antibiotic paste, chlorhexidine gel) were tested, and the release of TGF-β1 was measured after a subsequent conditioning step with EDTA. RESULTS Conditioning with 10% EDTA at pH 7 rendered the highest amounts of TGF-β1 among all test solutions. Fibroblast growth factor 2 and vascular endothelial growth factor were detected after EDTA conditioning at minute concentrations. Irrigation with chlorhexidine before EDTA conditioning increased TGF-β1 release; sodium hypochloride had the opposite effect. All tested intracanal dressings interfered with TGF-β1 release except water-based calcium hydroxide. CONCLUSIONS Growth factors can be released directly from dentin via EDTA conditioning. The use of disinfecting solutions or medicaments can amplify or attenuate this effect.

Erosion and abrasion of tooth-colored restorative materials and human enamel

OBJECTIVES The aim of this study was to investigate the effects of erosion and toothbrush abrasion on different restorative materials and human enamel. METHODS Human enamel and 5 kinds of tooth-colored restorative materials were used. The restorative materials included three composite resins (Filtek Silorane, Tetric EvoCeram, and Tetric EvoFlow), a polyacid-modified composite (Dyract Extra), and a conventional glass-ionomer cement (Ketac Fil Plus). For each type of the material, 40 specimens were prepared and embedded in ceramic moulds and divided into four groups (n=10): control group (C), erosion group (E), abrasion group (A), and erosion-abrasion group (EA). The specimens were subjected to six daily erosive attacks (groups E and EA; citric acid, pH 2.3, 1 min) and/or six abrasive attacks (groups A and EA; toothbrush abrasion, 100 strokes, 1 min), while the control specimens (group C) were maintained in artificial saliva. After 10-day treatment, the substance loss and surface changes were determined by surface profilometry and scanning electron microscopy. RESULTS Human enamel presented higher substance loss when compared to restorative materials. Generally, combined erosion-abrasion (EA) caused the highest substance loss, followed by erosion, abrasion, and storage in artificial saliva. Composite resin presented highest durability under erosive and/or abrasive attacks. Enamel and restorative materials showed degradation in groups E and EA through SEM observation. CONCLUSIONS Toothbrush abrasion has a synergistic effect with erosion on substance loss of human enamel, polyacid-modified composite and glass-ionomer cement. The acid- and abrasive-resistance of human enamel was lower compared to restorative materials.

Comparison of Cross-Sectional Hardness and Transverse Microradiography of Artificial Carious Enamel Lesions Induced by Different Demineralising Solutions and Gels

The aims of this study were: (1) to correlate surface (SH) and cross-sectional hardness (CSH) with microradiographic parameters of artificial enamel lesions; (2) to compare lesions prepared by different protocols. Fifty bovine enamel specimens were allocated by stratified randomisation according to their initial SH values to five groups and lesions produced by different methods: MC gel (methylcellulose gel/lactic acid, pH 4.6, 14 days); PA gel (polyacrylic acid/lactic acid/hydroxyapatite, pH 4.8, 16 h); MHDP (undersaturated lactate buffer/methyl diphosphonate, pH 5.0, 6 days); buffer (undersaturated acetate buffer/fluoride, pH 5.0, 16 h), and pH cycling (7 days). SH of the lesions (SH1) was measured. The specimens were longitudinally sectioned and transverse microradiography (TMR) and CSH measured at 10- to 220-μm depth from the surface. Overall, there was a medium correlation but non-linear and variable relationship between mineral content and √CSH. √SH1 was weakly to moderately correlated with surface layer properties, weakly correlated with lesion depth but uncorrelated with integrated mineral loss. MHDP lesions showed the highest subsurface mineral loss, followed by pH cycling, buffer, PA gel and MC gel lesions. The conclusions were: (1) CSH, as an alternative to TMR, does not estimate mineral content very accurately, but gives information about mechanical properties of lesions; (2) SH should not be used to analyse lesions; (3) artificial caries lesions produced by the protocols differ, especially considering the method of analysis.