OBJECTIVETo evaluate the efficacy of Tooth Mousse in reducing enamel demineralization lesions adjacent to bonded orthodontic brackets and promoting remineralization in vitro.

METHODS60 bovine teeth with bonded orthodontic brackets were randomly divided into three groups, negative control group, positive control group and experimental group, applied separately with distilled water, Duraphat fluoride varnish, Tooth Mousse. 3 groups were dipped into an artificial caries solution and an artificial saliva solution, cycling between them. All samples were detected by polarized light microscope, scanning electron microscope and electron probe micro-analysis.

RESULTSPolarized light microscope showed that the enamel surface of the experimental group were completed, the areas of positive birefringence were decreased obviously. Scanning electron microscope showed that a large number of deposits were found on the dental enamel surface of the experimental group, filled in the small local concave of enamel surface. Compared with the control group, electron probe micro-analysis showed that calcium and phosphate concentration of enamel surface was higher in experimental group than in negative control group (P<0.05), there was no significant differences between experimental group and positive control group (P>0.05).

CONCLUSIONTooth Mousse can reduce enamel demineralization and promoting remineralization in vitro.

Animals ; Cariostatic Agents ; Caseins ; Cattle ; Dental Caries ; Dental Enamel ; Fluorides ; Fluorides, Topical ; Orthodontic Brackets ; Phosphates ; Sodium Fluoride ; Tooth Demineralization

OBJECTIVETo evaluate the clinical effect of fluoride varnish in preventing caries of primary teeth, and to compare the caries prevention effects of fluoride varnish with two different concentrations.

METHODS150 children whose ages were three year-old were randomly chosen from one of nurseries of Chongqing, and were randomly divided into four groups with 37 children in 0.5% fluoride varnish group, 38 children in 0.1% fluoride varnish group, 39 children in 0.5% sodium fluoride group and 36 children in blank group. The groups included 71 'girls and 79 boys. Protective measure was applied every half an year and the research has lasted for two years. The research was designed by double-blinded methods, and was carried out with the dental caries standard suggested by World Health Organization. All the data were collected and the clinical effects of four groups were compared.

RESULTSThe average caries index and caries surface index of 0.1% fluoride varnish group and those of control groups were significantly higher than that of 0.5% fluoride varnish group. There were no significant difference between the average caries index and caries surface index of 0.1% fluoride varnish group and those of control groups.

CONCLUSION0.5% fluoride varnish was effective in preventing caries of primary teeth.

Cariostatic Agents ; Child ; Dental Caries ; Female ; Fluorides ; Fluorides, Topical ; Humans ; Male ; Paint ; Phosphates ; Sodium Fluoride ; Tooth, Deciduous

OBJECTIVETo determine the fluorine content in enamel before and after besmearing fluoride varnishes by neutron activation method.

METHODSA pair of mandibular deciduous central incisor teeth were chosen. One was removed, and the other was besmeared with fluoride varnishes and removed 24 hours later. The contents of fluorine were determined and analyzed statistically.

RESULTSThe fluorine content in the enamel of the tooth besmeared with fluoride varnishes was higher than that in the control tooth (P < 0.05).

CONCLUSIONSThe application of the fluoride varnishes can effectively increase the content of fluorine in the sclerous tissues.

Cariostatic Agents ; pharmacokinetics ; Child ; Dental Caries ; prevention & control ; Dental Enamel ; chemistry ; Female ; Fluorides ; analysis ; Fluorides, Topical ; pharmacokinetics ; Humans ; Male

Administration, Topical ; Cariostatic Agents ; administration & dosage ; therapeutic use ; Child ; China ; Dental Caries ; prevention & control ; Fluorides ; administration & dosage ; therapeutic use ; Humans

OBJECTIVE: To study and compare the effects of different demineralization-inhibition methods on the shear bond strength (SBS) and fracture mode of an adhesive used to bond orthodontic brackets to demineralized enamel surfaces. METHODS: Eighty freshly extracted, human maxillary premolars were divided into 4 equal groups and demineralized over the course of 21 days. Brackets were bonded to the demineralized enamel of teeth in Group 1. In Group 2, bonding was performed following resin infiltration (ICON(R), DMG, Hamburg, Germany). Before bonding, pre-treatment with acidulated phosphate fluoride (APF) or solutions containing casein phosphopeptide-amorphous calcium phosphate with 2% neutral sodium fluoride (CPP-ACP/wF) was performed in Groups 3 and 4, respectively. The SBS values of the brackets were measured and recorded following mechanical shearing of the bracket from the tooth surface. The adhesive remnant index (ARI) scores were determined after the brackets failed. Statistical comparisons were performed using one-way ANOVA, Tukey's post-tests, and G-tests. RESULTS: Significant differences were found in some of the intergroup comparisons of the SBS values (F = 39.287, p < 0.001). No significant differences were found between the values for the APF-gel and control groups, whereas significantly higher SBS values were recorded for the resin-infiltrated and CPP-ACP/wF-treated groups. The ARI scores were also significantly different among the 4 groups (p < 0.001). CONCLUSIONS: Tooth surfaces exposed to resin infiltration and CPP-ACP/wF application showed higher debonding forces than the untreated, demineralized surfaces.
Acidulated Phosphate Fluoride ; Adhesives ; Bicuspid ; Calcium ; Calcium Phosphates ; Caseins ; Dental Enamel ; Humans ; Oral Hygiene ; Orthodontic Brackets ; Sodium Fluoride ; Tooth

OBJECTIVETo compare the antibacterial effect between sodium fluoride and Galla Chinesis in bioflim model. To evaluate the feasibility of application of Gala Chinesis in the clinical practice of caries prevention.

METHODSStreptococcus mutans, Streptococcus sanguis, Streptococcus salivarius and Actinomyces naeslundii had been chosen as the experimental bacteria. In the experiment, biofilmn model was constructed, and two agents were added in the media. After a period of continuous culture, the number of bacteria adhering on the HA disc was examed, the planktonic pH in the flow cell was recorded continuously, and the morphology of the biofilmn formed on the HA disc was observed by SEM.

RESULTS(1) Galla Chinesis could inhibit the growth of the four oral bacteria in the biofilm just as sodium fluoride. (2) Galla Chinesis and sodium fluoride could prevent the descent of the planktonic pH in the flow cell, but Galla Chinesis was less efficient than sodium fluoride. (3) The biofilms formed after application of Galla Chinesis and fluoride, but the bacterial cells had less matrix than those applicated with sucrose.

CONCLUSIONGalla Chinesis is one kind of effective cariostatic natural agents.

Actinomyces ; Bacteria ; Biofilms ; Cariostatic Agents ; Dental Caries ; Fluorides ; Phosphates ; Sodium Fluoride ; Streptococcus mutans ; Streptococcus sanguis ; Sucrose

The aim of this study was to compare fluoride release and surface changes according to different orthodontic bracket adhesives the application of fluoride products. We used non-fluoridated composite resin Transbond fluoridated composite resins Blugloo and LightBond, resin-modified glass ionomer Rely XTM Luting 2, and conventional glass ionomer Fuji I®. Fluoride release of five orthodontic bracket adhesives and fluoride release ability after application of three fluoride products (1.23% acidulated phosphate fluoride gel, Tooth Mousse Plus®, Fluor Protector, and a toothbrush with sodium fluoride-containing toothpaste) were measured using a fluoride electrode that was connected to an ion analyzer. After 4 weeks of fluoride application, the surface roughness and surface morphology were examined using a surface roughness tester and field emission scanning electron microscopy. The amounts of fluoride release were observed not only on application of Tooth Mousse Plus® and Fluor Protector on resin-modified glass ionomer Rely XTM Luting 2 and Fuji I®, but also during tooth brushing using fluoride-containing toothpaste. After application of Tooth Mousse Plus®, except Transbond XT, the surface roughness increased, and all orthodontic adhesives showed a partial drop of micro-particle filler. On application of 1.23% acidulated phosphate fluoride gel on all orthodontic bracket adhesives, their surface roughness increased. To bond the orthodontic bracket, resin-modified glass ionomer Rely XTM Luting 2 and Fuji I® adhesives are highly recommended if the amount of fluoride release is considered to confer a preventative effect on dental caries, and among the fluoride products, Tooth Mousse Plus® and Fluor Protector are better than 1.23% acidulated phosphate fluoride gel, and these are expected to prevent dental caries even during tooth brushing with fluoride-containing toothpaste.
Acidulated Phosphate Fluoride ; Adhesives* ; Composite Resins ; Dental Caries ; Dental Cements ; Electrodes ; Fluorides* ; Glass ; Microscopy, Electron, Scanning ; Orthodontic Brackets* ; Sodium ; Surface Properties* ; Tooth ; Toothpastes

OBJECTIVETo investigate the effects of putative bacteriocin immunity proteins on the growth mode of Streptococcus mutans (Sm). To observe the differences of antimicrobial sensitivity in planktonic Sm wild-type strains and mutant strains caused by the inactivation of bacteriocin immunity proteins and their influence on the biofilm formation.

METHODSSm wild-type strains (WT) and its knockout mutants defective in immA and immB (ΔimmA(-) and ΔimmB(-) mutants) coding putative bacteriocin immunity proteins were cultured in brain heart infusion (BHI) and selected by erythromycin at the concentration of 10 mg/L. Optical density was detected by spectrophotometer every hour and growth curve was drawn. WT, ΔimmA(-) and ΔimmB(-) mutants were treated with ampicillin (0.04, 0.05, 0.06, 0.07, 0.08 mg/L), sodium fluoride (50, 100, 150, 200, 250 mg/L) and sodium hypochlorite (0.078%, 0.156%, 0.313%, 0.625%, 1.250%) for 24 hours. Optical density was detected by multifunctional micro plate reader. WT and the mutants were cultured in MBEC(TM) P&G Assay for 24 hours. The minimum biofilm eradication concentration (MBEC) of chlorhexidine against Sm was determined by serial dilution method. Confocal laser scanning microscopy (CLSM) was used to visualize the biofilm architecture, depth and ratio of live to dead bacteria.

RESULTSGrowth curve showed that it took about 3 hours to reach exponential phase and about 7 hours to stationary phase for WT, while 4 hours to exponential phase and 8 hours to stationary phase for mutants. Optical density of mutants were lower than WT in the presence of various antimicrobial agents (P < 0.01). In 0.06 mg/L ampicillin group, optical density value of WT, ΔimmA(-) and ΔimmB(-) mutants were 0.334 ± 0.016, 0.027 ± 0.016 and 0.047 ± 0.018. In 150 mg/L sodium fluoride group, optical density value of WT and mutants were 0.254 ± 0.018, 0.129 ± 0.011 and 0.167 ± 0.010. In 0.313% sodium hypochlorite group, optical density value of WT and mutants were 0.467 ± 0.008, 0.017 ± 0.006 and 0.050 ± 0.006. The MBEC of chlorhexidine against Sm WT, ΔimmA(-) and ΔimmB(-) mutants were 6.25, 1.57, and 3.13 mg/L. The results by CLSM showed a noticeable difference in biofilm architecture. The depth of WT biofilm was higher than the mutants biofilm (P < 0.01). The ratio of live to dead bacteria of WT biofilm was higher than ΔimmA(-) mutants in all layers (P < 0.05) and ΔimmB(-) mutants in the outer and intermedium layer (P < 0.01). There is no significant different between the inner layers of WT and ΔimmB(-) mutants (P = 0.191).

CONCLUSIONSPutative bacteriocin immunity proteins have influence on the growth mode of Sm. The antimicrobial sensitivity of planktonic Sm can be up-regulated by the inactivation of immA or immB. The MBEC of chlorhexidine against ΔimmA(-) and ΔimmB(-) mutants is lower than WT. The inactivation of immA or immB affects the biofilm formation.

Ampicillin ; pharmacology ; Anti-Bacterial Agents ; pharmacology ; Bacteriocins ; genetics ; immunology ; Biofilms ; drug effects ; growth & development ; Cariostatic Agents ; pharmacology ; Chlorhexidine ; pharmacology ; Disinfectants ; pharmacology ; Microbial Sensitivity Tests ; Mutation ; Plankton ; drug effects ; Sodium Fluoride ; pharmacology ; Sodium Hypochlorite ; pharmacology ; Streptococcus mutans ; drug effects ; genetics

The aim of this study is to compare the differences of the demineralization resistance of resin infiltration and 1.23% acidulated phosphate fluoride in bovine teeth with artificial caries. We applied 1.23% Acidulated phosphate fluoride (APF) gel and Icon® caries infiltrant on the artificial bovine enamel carious lesion and then demineralized all samples. The depth of demineralization was measured by using Confocal Laser Scanning Microscope (CLSM) and observed the roughness and irregularity of the enamel was observed by Scanning Electron Microscope (SEM).In this experiment with demineralization resistance on smooth artificial carious lesion, less depth of demineralization, roughness, and irregularity of enamel was observed in APF gel and Icon® group than in the control group. There was no significant difference between the depth of demineralization of 1.23% APF gel and Icon® caries infiltrant group. However, resin infiltration is beneficial as less roughness and irregularity was observed on the enamel surface than when 1.23% APF gel is applied.
Acidulated Phosphate Fluoride ; Dental Enamel ; Tooth

OBJECTIVETo investigate the effects of fluoride on Fas expression, caspase-3 and caspase-8 activity and apoptosis in rat incisor cells.

METHODSForty male SD rats were divided into 4 groups randomly and provided with distilled water containing NaF at the doses of 0, 10, 50 and 100 mg/L respectively. Each group had 10 animals. Five animals were sacrificed at 60 and 90 days respectively. Fas expression was measured with immunohistochemistry, and colorimetric assay was used to examine caspase-3 and caspase-8 activity with enzyme-labelled meter. The apoptosis was detected by flow cytometry in mandibular incisor cells.

RESULTSNaF at the doses of 10, 50 and 100 mg/L for 60 d and 90 d caused Fas overexpression, promoted activity of caspase-3 and caspase-8, increased apoptosis rate in mandibular incisor cells. At 60 days, the value of Fas expression was 0.1819 ± 0.0025 for control, 0.2120 ± 0.0084 for 10 mg/L NaF group, 0.2283 ± 0.0183 for 50 mg/L NaF group, 0.2818 ± 0.0233 for 100 mg/L NaF group. At 90 days, the value of Fas expression was 0.2077 ± 0.0289 for control, 0.2216 ± 0.0105 for 10 mg/L NaF group, 0.2377 ± 0.0059 for 50 mg/L NaF group, 0.2775 ± 0.0088 for 100 mg/L NaF group. Statistics analysis yielded close relationship between the dose of NaF in water and the Fas expression, and also between the dose of NaF in water and caspase-3 activities, and the relative coefficient was 0.9728 (60 d, P < 0.01) and 0.9889 (90 d, P < 0.01) for Fas expression, 0.9533 (60 d, P < 0.01) and 0.9849 (90 d, P < 0.01) for caspase-3 activity respectively. Apoptosis rate and caspase-8 activity also had close relationship with the NaF doses, and the relative coefficient was 0.9733 (90 d, P < 0.01) for apoptosis, 0.9928 (90 d, P < 0.01) for caspase-8. At the doses of 10, 50 and 100 mg/L NaF for 60 d and 90 d, obvious relationship was found between Fas expression and caspase-3 activity, and the relative coefficient was 0.9619 (60 d, P < 0.01) and 0.9912 (90 d, P < 0.01). Obvious relationship between Fas expression and apoptosis, between Fas expression and caspase-8 activity was found in groups for 90 d, and the relative coefficient was 0.9841 (P < 0.01) for apoptosis, 0.9767 (P < 0.01) for caspase-8.

CONCLUSIONSFluoride could induce Fas overexpression and mediate caspase activation and apoptosis at the doses of 10, 50 and 100 mg/L for 60 d and 90 d in rat mandibular incisor cells.

Animals ; Apoptosis ; drug effects ; Cariostatic Agents ; administration & dosage ; pharmacology ; Caspase 3 ; metabolism ; Caspase 8 ; metabolism ; Dose-Response Relationship, Drug ; Incisor ; cytology ; metabolism ; Male ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Signal Transduction ; Sodium Fluoride ; administration & dosage ; pharmacology ; fas Receptor ; metabolism