Effect of CPP-ACP paste on mechanical properties of bovine enamel as determined by an ultrasonic device

OBJECTIVE: The purpose of this study was to determine the effect of Casein Phosphopeptide-Amorphous Calcium Phosphate (CPP-ACP) paste on demineralization of bovine enamel by measuring changes in the ultrasound transmission velocity. METHODS: The enamel specimens were prepared by cutting bovine teeth into blocks. The specimens were stored in 0.1 M lactic acid buffer solution (pH 4.75, Ca 0.75 mM, P 0.45 mM) for 10 min twice a day, and then stored in the artificial saliva (pH 7.0). Other specimens were stored in a 10-times diluted solution of CPP-ACP paste and a placebo paste without CPP-ACP for 10 min, followed by 10 min immersion into a demineralization solution twice a day before storage in the artificial saliva. The propagation time of longitudinal ultrasonic waves was measured by a Pulser-Receiver (Model 5900, Panametrics) with a transducer (V112, Panametrics). Six specimens were used for each condition, and one-way ANOVAs followed by the Tukey HSD tests (alpha = 0.05) were done. RESULTS: The sonic velocity was found to decrease with time for specimens stored in the demineralization solution. On the other hand, a significant increase in sonic velocity was found for specimens stored in the CPP-ACP solution. CONCLUSIONS: From the result of this study, it was suggested that the conditions of de- and remineralization of the enamel structure could be measured non-destructively by using an ultrasonic pulse method. It could be concluded that the inorganic components contained in high concentrations in CPP-ACP acted to enhance remineralization of the enamel structure.     

Enamel remineralization effect of a dentifrice containing calcium sodium phosphosilicate: an optical coherence tomography observation

Objective: The purpose of this study was to examine the effects of a dentifrice containing 5% calcium sodium phosphosilicate (CSP) on the remineralization of the enamel using optical coherence tomography (OCT).

Materials and methods: Bovine incisors were sliced and shaped in a rectangular form. One group of five specimens was treated with undersaturated 0.1 M lactic acid buffer solution (pH 4.75) for 10?min and then placed in artificial saliva (pH 7.0) (De group). Other specimens were stored in solutions of toothpaste containing CSP for 10?min, followed by 10-min immersion in the lactic acid buffer solution twice a day before storage in artificial saliva (CSP group). An additional group was stored in only artificial saliva (control group). OCT imaging on the selected location of the enamel surface was performed. The peak intensity and width at 1/e² were recorded in each of the six areas on the sample and averaged, and the sample size of each group was six. The integrated value in units (dB?×?μm) was calculated in the area of peak intensity. The data for each group was subjected to one-way repeated-measures ANOVA and Tukey HSD tests (α?=?0.05).

Results: The changes in integrated values of each group were different. A slight but significant increase in the integrated value was observed in the control group, whereas a slight but significant decrease in the value was observed the De group. Integrated values increased in the CSP group.

Conclusions: Remineralization occurred upon immersion in the toothpaste containing CSP.     

Effect of CPP-ACP paste on tooth mineralization: an FE-SEM study

Milk and milk products, such as cheese, have been shown to exhibit anticariogenic properties in human and animal models. CPP-ACP shows an anti-caries effect by suppressing demineralization, enhancing remineralization, or possibly a combination of both. The purpose of this study was to evaluate the effect of CPP-ACP paste on demineralization by observing the treated tooth surface using an FE-SEM. The specimens were prepared by cutting enamel and dentin of bovine teeth into blocks. A few specimens were stored in 0.1 M lactic acid buffer solution for 10 min and then in artificial saliva (negative control). The remaining specimens were stored in a 10 times-diluted solution of CPP-ACP paste or a placebo paste containing no CPP-ACP for 10 min, followed by 10 min immersion in a demineralizing solution (pH = 4.75, Ca) twice a day before storage in artificial saliva. After treatment of the specimens for 3, 7, 21 and 28 days, they were fixed in 2.5% glutaraldehyde in cacodylate buffer solution, dehydrated in ascending grades of tert-butyl alcohol, and then transferred to a critical-point dryer. The surfaces were coated with a thin film of Au in a vacuum evaporator, and were observed under field emission-scanning electron microscopy (FE-SEM). The SEM observations revealed different morphological features brought about by the various storage conditions. Demineralization of the enamel and dentin surfaces was more pronounced with the longer test period in the control and negative control specimens. On the other hand, enamel and dentin specimens treated with CPP-ACP paste revealed slight changes in their morphological features. From the morphological observations of the enamel and dentin surfaces, it could be considered that the CPP-ACP paste might prevent demineralization of the tooth structure.     

Effect of mucin alone and in combination with various dentifrices on in vitro Remineralization

The aim of this in vitro study was to evaluate the effect of combining various fluoridated dentifrices with mucin on remineralization of bovine enamel. Enamel specimens were embedded in epoxy resin, partly covered with nail varnish, and demineralized in a lactic acid solution (pH 5.0, 14 days). Parts of the demineralized areas of the specimens were then covered with nail varnish. Half of the samples were exposed to a mucin-containing (2.7 g/l) remineralizing solution, the other half to a mucin-free remineralizing solution for 30 days. In each group, the specimens were divided into four subgroups, which were brushed twice a day with a toothpaste containing sodium, stannous/amine, or amine fluoride. The specimens of the fourth subgroup were not brushed, but stored in one of the two solutions. Mineral loss and lesion depth were evaluated from microradiographs. After the remineralization period, specimens that were brushed with one of the dentifrices and stored in the mucin-containing remineralizing solution reacquired more mineral than those brushed and stored in the mucin-free solution (p < 0.05; Bonferroni post hoc test). The results indicate that mucin in combination with various fluorides seems to affect enamel remineralization significantly. Thus, mucin could be considered as an additive to saliva substitutes or mouthwashes in patients with hyposalivation.     

Anti‐erosive effects of fluoride and phytosphingosine: an in vitro study

A selection of commercially available products containing stannous fluoride (SnF₂)/sodium fluoride (NaF), SnF₂/amorphous calcium phosphate (ACP), SnF₂/NaF/ACP, tin (Sn)/fluorine (F)/chitosan were compared with phytosphingosine (PHS) with respect to their anti‐erosive properties in vitro. One‐hundred and twenty bovine enamel specimens were immersed in the respective product slurries for 2 min, twice daily. The formulations were diluted with either remineralization solution or artificial saliva. After each treatment, an erosive challenge was performed for 10 min, twice daily, using citric acid, pH 3.4. The specimens were stored in remineralization solution or artificial saliva until the next treatment‐erosion challenge. After 10 d, tissue loss was determined using profilometry. Enamel softening was determined through surface microhardness measurements. Tissue‐loss values (measured in μm and expressed as mean ± SD) for PHS, SnF₂/NaF, SnF₂/ACP, SnF₂/ACP/NaF, and Sn/F/chitosan treatment groups and for the negative‐control group, were, respectively, 35.6 ± 2.8, 15.8 ± 1.8, 22.1 ± 2.0, 22.9 ± 1.8, 16.2 ± 1.2, and 51.2 ± 4.4 in the presence of remineralization solution and 31.7 ± 3.3, 15.6 ± 2.9, 16.5 ± 2.7, 16.8 ± 2.1, 13.1 ± 3.0, and 50.7 ± 2.8 in the presence of artificial saliva. There were no significant differences in surface microhardness measurements between the treatment groups. In conclusion, PHS resulted in a significant reduction of tissue loss compared with the negative control, but in comparison, the toothpastes containing Sn²⁺ and F^? ions were significantly more effective compared with PHS.     

Effect of fluoride treatment on remineralization of bleached enamel

summary The objective of the study was to evaluate the remineralizing capacity of different fluoride treatments on dental enamel bleached with carbamide peroxide (Opalescence®). Sixty bovine enamel slabs were subjected to four cycles comprising bleaching (12 h) and remineralization in artificial saliva (8 h). The samples were evenly distributed among four groups (A-D). During the first hour of the remineralization period the specimens in group A were covered with a fluoride varnish (Duraphat®; 2.23% F⁻). In group B the enamel slabs were stored in a fluoride solution (0.2% F⁻ as NaF) for 1 min prior to remineralization. Group C did not receive a fluoride treatment, and group D (control) was stored in distilled water instead of bleaching. Microhardness (VHN) was evaluated before the experimerits and after the second and fourth cycle, respectively. Final hardness was calculated as percentage of the initial hardness. Analysis of variance was applied to the data followed by pairwise comparisons with corrected level of significance ( P < 0.01). Hardness decreased significantly in groups A-C compared to the control group (D). The bleached and unfluoridated specimens (group C) showed a significantly higher hardness loss compared to the fluoridated specimens, whereas no significant difference was observed between the two fluoridated groups. It is concluded that remineralization of bleached enamel is improved by application of highly concentrated fluorides.     

Effect of olive oil and an olive-oil-containing fluoridated mouthrinse on enamel and dentin erosion in vitro

Objective. The study aimed to analyse the impact of olive oil and an olive-oil-containing fluoridated mouthrinse on enamel and dentin erosion. Material and Methods. Bovine enamel and dentin specimens were submitted to 10 alternating demineralization and remineralization cycles each consisting of 5 min pretreatment with the test solutions, i.e. distilled water as negative control, 100% olive oil, 2% olive oil emulsion, 2% olive-oil-containing mouthrinse (Xerostom®), acidic 13.2 mmol·l^?1 (250 ppm) fluoride solution as positive control, storage in artificial saliva (30 min), demineralization in citric acid (3 min, pH 2.3) and again storage in artificial saliva (60 min). Each group contained 10 enamel and dentin samples. Enamel and dentin loss was analyzed by profilometry after 10 cycles. Results. Treatment with 100% olive oil was not effective in reducing enamel and dentin loss. Application of 2% olive oil or the olive-oil-containing mouthrinse also showed protection against erosion, but to a lesser degree compared to the positive control. Conclusion. Olive oil offered protection against enamel and dentin erosion when applied as 2% emulsion or 2% olive-oil-containing mouthrinse, but is not effective when applied as pure oil (100%). However, 2% olive oil emulsion is less effective in reducing erosion compared to the acidic 13.2 mol·l^?1 fluoride solution.     

In vitro assessment of artificial saliva formulations on initial enamel erosion remineralization

Objectives

Various formulations of artificial saliva are present in the literature and little guidance is available on the standardization of type of saliva for use in in vitro protocols for erosive studies. The aim of this study was to evaluate the remineralizing capacity of different formulations of artificial saliva on initial enamel erosive lesion.

Methods

Bovine enamel blocks were subjected to short-term acidic exposure by immersion in citric acid 0.05 M (pH 2.5) for 15 s, resulting in surface softening without tissue loss. Then 90 selected eroded enamel blocks were randomly and equally divided into 6 groups according to saliva formulation (n = 15): Saliva 1 (contain mucin); Saliva 2 (Saliva 1 without mucin); Saliva 3; Saliva 4; Saliva 5 (contain sodium carboxymethyl cellulose) and control (C) (deionized water). After demineralization enamel blocks were subjected to remineralization by immersion in the saliva's formulations for 2 h. Enamel remineralization was measured by superficial hardness test (% superficial hardness change). The data were tested using ANOVA and Tukey's test (p < 0.05).

Results

All the tested formulations of artificial saliva resulted in significantly higher enamel remineralization compared to control (p < 0.001). Saliva 3 showed higher percentage of enamel remineralization than Saliva 5 (p < 0.05).

Conclusions

Besides the variety of artificial saliva for erosion in vitro protocols, all the formulations tested were able to partially remineralize initial erosive lesions.     

The potential of deciduous and permanent bovine enamel as substitute for deciduous and permanent human enamel: Erosion-abrasion experiments

Aim of the present study was to compare toothbrushing abrasion of eroded human and bovine enamel utilizing a toothpaste slurry. The surfaces of each 36 teeth from cattle and calves and from each 36 human wisdom teeth and deciduous teeth were polished. Each 12 specimens from the respective tooth type were used for assessing toothbrushing abrasion only (A), erosion only (E) and the combination of erosion and toothbrushing abrasion (EA). The EA samples were subjected to 20 cycles comprising a demineralization/remineralization procedure directly followed by toothbrushing abrasion (100 strokes, 300 g load, toothpaste slurry: 3 ml artificial saliva mixed with 1g dentifrice). Demineralization in form of erosion was performed with 1% citric acid (1 min), remineralization with artificial saliva (15 min). Between the cycles, the samples were stored in artificial saliva. Wear of the treated surfaces with reference to untreated areas was determined profilometrically. The samples subjected to abrasion only (A) did not show a significantly different wear between the different kinds of teeth. The comparisons of substance loss between teeth of different species revealed that hard tissue loss of the human deciduous teeth was significantly lower as compared to calves' teeth after both erosion and erosion-abrasion. Also, both erosion only and erosion-abrasion caused higher enamel loss in cattle's teeth than in human wisdom teeth. It is concluded that human eroded enamel offers better resistance against brushing than bovine enamel.     

Dual-functional adhesive containing amorphous calcium phosphate nanoparticles and dimethylaminohexadecyl methacrylate promoted enamel remineralization in a biofilm-challenged environment

ObjectiveThe cariogenic biofilm on enamel, restoration, and bonding interface is closely related to dental caries and composite restoration failure. Enamel remineralization at adhesive interface is conducive to protecting bonding interface and inhibiting secondary caries. This study intended to assess the remineralization efficiency of adhesive with dimethylaminohexadecyl methacrylate (DMAHDM) and nanoparticles of amorphous calcium phosphate (NACP) on initial caries lesion of biofilm-coated enamel.MethodsArtificial initial carious lesion was created via 72-hour immersion in demineralization solution and cariogenic biofilm was formed after 24-hour culture of Streptococcus mutans (S. mutans). Specimens were then divided into 4 groups: enamel control, enamel treated with NACP, DMAHDM and NACP+DMAHDM respectively. Samples next underwent 7-day cycling, 4 h in BHIS (brain heart infusion broth containing 1 % sucrose) and 20 h in AS (artificial saliva) per day. The pH of BHIS was tested daily. So did the concentration of calcium and phosphate in BHIS and AS. Live/dead staining, colony-forming unit (CFU) count, and lactic acid production of biofilms were measured 7 days later. The enamel remineralization efficiency was evaluated by microhardness testing and transverse microradiography (TMR) quantitatively.ResultsEnamel of NACP+DMAHDM group demonstrated excellent remineralization effectiveness. And the NACP+DMAHDM adhesive released a great number of Ca²⁺ and PO₄^3- ions, increased pH to 5.81 via acid neutralization, decreased production of lactic acid, and reduced CFU count of S. mutans (P < 0.05).SignificanceThe NACP+DMAHDM adhesive would be applicable to preventing secondary caries, strengthening enamel-adhesive interface, and extending the lifespan of composite restoration.     

Preventive effect of iron gel with or without fluoride on bovine enamel erosion in vitro

Background: The aim of this study was to evaluate the preventive effect in vitro of experimental gel containing iron and/or fluoride on the erosion of bovine enamel. Methods: To standardize the blocks (n = 80), specimens (4 × 4 mm) were previously selected to measure the initial microhardness. The blocks were randomly allocated into four groups of 20 samples each: C (control, placebo gel); F (fluoride gel, 1.23% NaF); Fe (iron gel, 10 mmol/L FeSO₄) and F + Fe (fluoride + iron gel). The gels were applied and removed after 1 minute. The blocks were then submitted to six alternating remineralization and demineralization cycles. The beverage Coca‐Cola^® (10 minutes, 30 mL) was used for demineralization, and artificial saliva (1 hour) for remineralization. The effect of erosion was measured by wear analysis (profilometry). Data were analysed by ANOVA and the Tukey test for individual comparisons (p <0.05). Results: The mean wear (± SD, μm) was C: 0.94 ± 0.22; F: 0.55 ± 0.12; Fe: 0.49 ± 0.11 and F + Fe: 0.55 ± 0.13. When the experimental gels were used, there was statistically significant reduction in enamel wear in comparison with the control (p <0.001). However, the experimental gels did not differ significantly among them. Conclusions: The gels containing iron with or without fluoride are capable of interfering with the dissolution dental enamel in the presence of erosive challenge.     

Influence of coffee and red wine on tooth color during and after bleaching

Abstract

Objective. The aim of this study was to evaluate the influence of coffee and red wine staining on tooth color during and after bleaching. Materials and methods. Blocks obtained from human molars were divided into 11 groups (n = 5) in accordance with the bleaching treatment—peroxide carbamide 10%, 15% or 20%—and in accordance with the stain therapy—coffee, wine or without staining (control). Color change analysis was performed by photo-reflectance using a spectrophotometer, during (3-times/week) and after (7, 15 and 30 days) the bleaching treatment. During the experiment, the samples were stored in artificial saliva. The results were submitted to statistical analysis with the Dunnet and Tukey tests (p < 0.05). Results. The concentrations of carbamide peroxide (10%, 15% and 20%) did not differ significantly from the control group during bleaching (up to the 22nd day), with (Tukey, p > 0.05) or without storage in pigment solution. After the bleaching, there were statistically significant differences between the groups treated with coffee (30th day) and wine (7th and 30th days) relative to the control, which was treated with whitening agents. Conclusion. During bleaching, remineralization of the enamel with artificial saliva and the subsequent bleaching session were effective in preventing enamel staining. After the whitening procedures, both stain therapies—coffee and wine—caused enamel color changes; however, the wine led to greater staining than did coffee.     

Mineral distribution of artificial dentinal caries lesions after treatment with fluoride agents in combination with saliva substitutes

Objective: Some saliva substitutes have been shown to demineralize dentine in vitro. This effect is counteracted by the application of various fluorides. In contrast, remineralizing saliva substitutes might be supported by these treatments, depending on the dynamics during remineralization. The aim of this in vitro study was to evaluate the effects of fluoride mouthrinses or gels in combination with de-/remineralizing saliva substitutes on dentinal subsurface lesions. Design: Demineralized bovine dentine specimens were stored either in mineral water [saturation with respect to octacalcium phosphate (S_OCP): 0.7], Glandosane (G, S_OCP: 0.3) or in a modified saliva substitute Saliva natura (SN, S_OCP: 1.9) for five weeks (37 °C). Fluoride agents were applied twice daily for 10 min (n = 15/group): no treatment, Meridol mouthrinse, Elmex sensitive solution, ProSchmelz fluoride gel, Elmex gelée. After storage thin sections were prepared and mineral losses before and after storage were evaluated from microradiographs. Results: Specimens stored in G alone showed significantly higher mineral loss compared to those stored in water, SN or G in combination with any additional treatment (p < 0.05). Storage in SN and treatment with ProSchmelz fluoride gel led to significantly higher remineralization compared to all other groups (p < 0.05) and resulted in distinct mineral gain within the lesion body. Conclusions: Under the in vitro conditions chosen, use of fluoride agents in combination with a demineralizing saliva substitute resulted in reduced mineral loss. Storage in modified Saliva natura in combination with the application of ProSchmelz fluoride gel induced the most pronounced remineralization also of deeper lesion areas.     

酪蛋白磷酸多肽牙膏抑制牙釉质脱矿和促进牙釉质再矿化的实验研究

目的　评价含酪蛋白磷酸多肽 (CPP)的牙膏抑制牙釉质脱矿和促进再矿化的作用。方法　牙釉质片分为实验组 (A组 :含 0 1%CPP、B组 :含 0 5 %CPP)和对照组 (C组 :不含CPP)。①抑制脱矿实验 :釉质片每天用脱矿液处理 2次 ,再分别用 3种牙膏处理 15min ,于实验第 1、3、5、10、15天取每组 3例送检表面钙、磷含量。②再矿化实验 :脱矿的釉质片置于再矿化液 ,每天分别用 3种牙膏处理 2次 ,于实验第 5、10、15天取每组 3例送检。结果　①抑制脱矿实验 :实验组与对照组钙、磷含量差异无显著性。②再矿化实验 :10d时两实验组钙含量高于对照组 ;15d时仅B组钙高于对照组。结论　未能证明实验牙膏有抑制釉质脱矿的作用 ,但提示有促进再矿化的功能 ,B牙膏的作用较A牙膏稳定和持久。     

In vitro effect of a resin infiltrant on different artificial caries-like enamel lesions

ObjectivesA resin infiltrant was employed for the treatment of active white spot lesions due to its ability to penetrate into the enamel pores and prevent the progression of the lesion. However, limited information is available about its mechanical effect on different artificial enamel lesions as well as on its resistance to further demineralization. Therefore, this study aimed to evaluate the effects of the Icon® infiltrant on different artificial caries-like enamel lesions and its resistance to new acid challenges.DesignArtificial lesions were produced in bovine enamel using three different protocols (demineralization/remineralization cycling, DE-RE; 8% methylcellulose gel, MC; and methyl ethyl diphosphonate solution, MHDP; n = 13). The specimens were treated with Icon® and subjected to a new acid challenge using DE-RE cycling. The surface and cross-sectional hardness were evaluated in sound, demineralized, treated and further demineralized enamel areas. Data were statistically analyzed using ANOVA and Tukey’s test (p < 0.05).ResultsAll of the demineralizing protocols produced subsurface artificial caries lesions. The infiltrant was able to partially recover the surface hardness and prevent further surface hardness loss in enamel previously demineralized using the DE-RE and MHDP protocols. In regard to cross-sectional hardness, no positive effect was found.ConclusionsThe effect of the infiltrant depends on the type of lesion created in vitro, and its action is limited to the lesion surface.     

Resistance to demineralization of remineralizing agents on dentin – An Atomic Absorbtion spectrophotometric study

ObjectivesTo evaluate the effect of various Remineralizing agents on Intact Human dentin surface exposed to a demineralizing agent quantitatively using Atomic Absorption Spectrophotometer (AAS).Materials and methods10 Freshly extracted intact human premolars from patients of age group 14–18 yrs extracted for orthodontic purposes were used for the study. 40 dentinal sections of size measuring 4 × 4 × 2 mm were prepared from the surfaces of teeth. All the specimens were then divided into 4 groups of 10 specimens. Group I (Control Group) – No Surface treatment, stored in artificial saliva only. Group II (Control Group) – Demineralization only, No surface treatment with remineralizing agent. Group III – Demineralization followed by CPP-ACFP [4 mins twice daily for 14 days]. Group IV – Demineralization followed by β-TCP [4 mins twice daily for 14 days]. Specimens were stored in artificial saliva throughout the study. Artificial saliva was then evaluated for calcium dissolution using Atomic Absorption Spectrometer (AAS). Data obtained were compared and statistically analysed using one way ANOVA and Tukey's HSD test.ResultsBoth the Remineralizing agents showed resistance to release of calcium and phosphate from dentin. Group 3 (CPP-ACPF) Showed lesser release of calcium and phosphate when compared to group 4 (β-TCP) which was not statistically significant.ConclusionBoth the remineralizing agents tested showed resistance to release of calcium and phosphate from dentin on simulation of oral conditions. Among the Remineralizing agents tested, Fluoride Enriched Casein Phosphopeptide-Amorphous calcium Phosphate (CPP-ACPF) showed marginally better remineralization potential on dentin than Beta tricalcium phosphate (β-TCP).     

Ultrasonic determination of the effect of casein phosphopeptide-amorphous calcium phosphate paste on the demineralization of bovine dentin

The purpose of this study was to investigate the demineralization of dentin by measuring changes in the velocity of the sonic longitudinal waves transmitted through this substrate. One group of samples was immersed in demineralization solution for 10 min twice a day and then stored in artificial saliva. Two additional groups of samples were treated with a solution of casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) paste or a placebo paste without CPP-ACP before demineralization and a control group was stored in artificial saliva. The sonic velocity of the demineralized specimens was found to decrease significantly over time. No significant increase in sonic velocity was observed in specimens treated with CPP-ACP, suggesting that CPP-ACP acted to prevent demineralization.     

酪蛋白磷酸肽-磷酸钙溶液体外再矿化作用的化学分析及显微硬度测试

目的研究酪蛋白磷酸肽-磷酸钙溶液在体外对牛牙釉质早期人工龋的再矿化作用。方法用不同浓度的酪蛋白磷酸肽-磷酸钙（CPP—CP）溶液对牛牙釉质早期人工龋进行再矿化处理后，首先采用化学分析法测量处理液中的残余矿物质，得出沉积在龋损区内的矿物质含量；然后采用显微硬度法测量处理前后牙釉质剖面硬度变化。结果CPP—CP溶液可以在体外使龋损牙釉质发生再矿化，再矿化作用与CPP—CP浓度呈剂量-效应关系。再矿化后龋损区矿物沉积量与再矿化液的CPP—CP浓度成正比。结论酪蛋白磷酸肽-磷酸钙溶液能凭借高钙磷浓度梯度促进牛牙釉质早期人工龋的再矿化。     

Tooth Mousse护牙素抑制牙釉质脱矿和促进牙釉质再矿化的实验研究

目的评价Tooth Mousse护牙素抑制离体牛牙牙釉质脱矿及促进牙釉质再矿化的作用。方法60颗带托槽的离体牛牙随机分成3组,每组20颗。实验组涂擦Tooth Mousse护牙素,阴性对照组涂擦蒸馏水,阳性对照组涂擦氟化物。3组标本在人工致龋液和人工唾液中循环浸泡60d,用扫描电镜与偏光显微镜检查牙釉质脱矿及再矿化情况,用显微硬度计检查牙釉质显微硬度并进行统计学分析。结果扫描电镜观察结果显示实验组牙釉质表面有不规则的矿化物沉积;偏光显微镜下实验组牙釉质表面完整,以矿化为主的负性双折射区变宽;实验组牙釉质显微硬度高于阴性对照组(P<0.05),与阳性对照组间差异无统计学意义(P>0.05)。结论Tooth Mousse护牙素在体外实验中能抑制酸性环境中牛牙釉质脱矿,促进釉质再矿化。     

Remineralization effectiveness of the PAMAM dendrimer with different terminal groups on artificial initial enamel caries in vitro

ObjectiveDisruption of the demineralization–remineralization balance could trigger the development of dental caries, making it challenging for enamel to “self-heal”. Thus, extrinsic assistance is needed to restore enamel lesions and stop undermining progression. The aim of this study was to investigate enamel remineralization in a simulated oral environment via poly (amino amine) (PAMAM) dendrimers quantitatively.MethodsBovine enamel specimens were shaken in demineralization solution (pH 4.5, 37 °C, 50 rpm/min) for 72 h to create initial enamel carious lesions. The subsurface-demineralized specimens were then divided into four groups: enamel treated with PAMAM-NH₂, enamel treated with PAMAM−COOH, enamel treated with PAMAM−OH, and enamel treated with deionized water. The treated specimens underwent subsequent 12-day pH cycling. Enamel blocks were analyzed by transverse microradiography (TMR), surface microhardness testing and scanning electron microscopy (SEM) before and after demineralization and pH cycling.ResultsGroups treated with PAMAM dendrimers showed lower lesion depth and less mineral loss, attained more vertical-section surface microhardness recovery, and adsorbed more mineral deposits (p < 0.05). The enamel lesion remineralization values of PAMAM-NH₂, PAMAM-COOH, and PAMAM-OH groups were 76.42 ± 3.32%, 60.07 ± 5.92% and 54.52 ± 7.81%, respectively.SignificanceIn conclusion, PAMAM with different terminal groups could induce enamel remineralization, among which PAMAM-NH₂ showed the most prominent competence, followed by PAMAM-COOH and PAMAM-OH, in that order.