fluorapatite and octacalcium-phosphate

Topics: Adsorption; Animals; Apatites; Bacterial Adhesion; Bone Matrix; Calcium Phosphates; Crystallization; Dental Enamel Proteins; Durapatite; Electrochemistry; Humans; Ion Exchange; Solubility; Static Electricity; Surface Properties

The present study investigated the effects of fluoride (F) concentration, lesion baseline severity (ΔZ(base)) and mineral distribution on lesion progression. Artificial caries lesions were created using three protocols [methylcellulose acid gel (MeC), hydroxyethylcellulose acid gel (HEC), carboxymethylcellulose acid solution (CMC)] and with low and high ΔZ(base) groups by varying demineralization times within protocols. Subsequently, lesions were immersed in a demineralizing solution for 24 h in the presence of 0, 1, 2 or 5 ppm F. Changes in mineral distribution characteristics of caries lesions were studied using transverse microradiography. At baseline, the protocols yielded lesions with three distinctly different mineral distributions. Secondary demineralization revealed differences in F response between and within lesion types. In general, lowΔZ lesions were more responsive to F than highΔZ lesions. LowΔZ MeC lesions showed the greatest range of response among all lesions, whereas highΔZ HEC lesions were almost unaffected by F. Laminations were observed in the presence of F in all but highΔZ HEC and CMC lesions. Changes in mineral distribution effected by F were most pronounced in MeC lesions, with remineralization/mineral redeposition in the original lesion body at the expense of sound enamel beyond the original lesion in a dose-response manner. Both ΔZ(base) and lesion mineral distribution directly impact the F response and the extent of secondary demineralization of caries lesions. Further studies - in situ and on natural white spot lesions - are required to better mimic in vivo caries under laboratory conditions.

Topics: Acetic Acid; Animals; Apatites; Calcium Fluoride; Calcium Phosphates; Carboxymethylcellulose Sodium; Cariostatic Agents; Cattle; Cellulose; Dental Enamel; Disease Progression; Dose-Response Relationship, Drug; Durapatite; Fluorides; Hydrogen-Ion Concentration; Lactic Acid; Methylcellulose; Microradiography; Minerals; Temperature; Time Factors; Tooth Demineralization; Tooth Remineralization

The present mechanistic in vitro study aimed to investigate dose-response effects of zinc and fluoride on caries lesion remineralization and subsequent protection from demineralization. Artificial caries lesions were created using a methylcellulose acid gel system. Lesions were remineralized for 2 weeks using citrate-containing artificial saliva which was supplemented with zinc (0-153 μmol/l) and fluoride (1.1 or 52.6 μmol/l) in a 7 × 2 factorial design. Lesions were also remineralized in the absence of zinc and citrate, but in the presence of fluoride. After remineralization, all lesions were demineralized for 1 day under identical conditions. Changes in mineral distribution characteristics of caries lesions after remineralization and secondary demineralization were studied using transverse microradiography. At 1.1 μmol/l fluoride, zinc exhibited detrimental effects on remineralization in a dose-response manner and mainly by preventing remineralization near the lesion surface. At 52.6 μmol/l fluoride, zinc retarded remineralization only at the highest concentration tested. Zinc enhanced overall remineralization at 3.8-15.3 μmol/l. At 76.5 and less so at 153 μmol/l, zinc showed extensive remineralization of deeper parts within the lesions at the expense of remineralization near the surface. Citrate did not interfere with remineralization at 1.1 μmol/l fluoride, but enhanced remineralization at 52.6 μmol/l fluoride. Lesions exhibiting preferential remineralization in deeper parts showed higher mineral loss after secondary demineralization, suggesting the formation of more soluble mineral phases during remineralization. In summary, zinc and fluoride showed synergistic effects in enhancing lesion remineralization, however only at elevated fluoride concentrations.

Topics: Animals; Apatites; Calcium Fluoride; Calcium Phosphates; Cariostatic Agents; Cattle; Citric Acid; Dental Caries; Dental Enamel; Dental Enamel Solubility; Dose-Response Relationship, Drug; Drug Synergism; Durapatite; Fluorides; Hydrogen-Ion Concentration; Lactic Acid; Methylcellulose; Microradiography; Minerals; Phosphates; Saliva, Artificial; Tooth Remineralization; Zinc; Zinc Compounds

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.. 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.. 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.. 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.

Topics: Amines; Animals; Apatites; Calcium Fluoride; Calcium Phosphates; Cariostatic Agents; Cattle; Dental Caries; Dentin; Diamines; Drug Combinations; Durapatite; Fluorides; Gels; Microradiography; Minerals; Mouthwashes; Random Allocation; Saliva, Artificial; Temperature; Time Factors; Tin Fluorides; Tooth Demineralization; Tooth Remineralization

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 (SH(1)) was measured. The specimens were longitudinally sectioned and transverse microradiography (TMR) and CSH measured at 10- to 220-microm depth from the surface. Overall, there was a medium correlation but non-linear and variable relationship between mineral content and radicalCSH. radicalSH(1) 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.

Topics: Acetates; Acrylic Resins; Anatomy, Cross-Sectional; Animals; Apatites; Buffers; Calcium Phosphates; Cariogenic Agents; Cariostatic Agents; Cattle; Dental Caries; Dental Enamel; Diphosphonates; Durapatite; Fluorides; Gels; Hardness; Hydrogen-Ion Concentration; Lactic Acid; Methylcellulose; Microradiography; Random Allocation; Solutions; Time Factors; Tooth Demineralization; Tooth Remineralization

To establish an in vitro model for the apatite crystal mineralization. To evaluate the influences of bovine serum albumin (BSA) and fluoride to the mineralization of apatite crystal.. The model was constructed using cation selective membrane (CMV) and dialysis membrane. Double distilled water (DDW), BSA, 5, 20, 100 mg x L(-1) fluoride were added into the reaction space of the model. Reaction was carried out at 37 degrees C for 3 days under gentle stirring. The crystals were identified by scanning electron microscope (SEM) and X-ray diffraction (XRD).. The model was established successfully. When DDW and BSA were added respectively, the main component of the deposit was octacalcium phosphate (OCP), but the shape and size of the crystals differs from each other. When fluoride with different concentration were added, the main component of the crystal turned to rod-like and prism-like fluoroapatite (FAP) crystal. The size and crystallinity of the FAP increased with the increase of the fluoride concentration.. It is an effective way to evaluate the influence factors of the apatite crystal mineralization by using the in vitro model.

Topics: Apatites; Calcium Phosphates; Crystallization; Fluorides; In Vitro Techniques; Phosphates; X-Ray Diffraction

Bidirectional diffusion of the Ca and PO4 solutions into the fibrin gel was performed at various pH conditions and fluoride concentrations to generate organic/inorganic composite materials mimicking biomineralization. The minerals produced in this system had a higher crystallinity than those generated by the solution mineralization system. The minerals generated in fibrin gel varied depending on the pH conditions as follows: Dicalcium phosphate dihydrate (DCPD) in the noncontrolled pH solution, the DCPD and octacalcium phosphate (OCP) mixture at pH 7.4, and the OCP and hydroxyapatite (HAp) mixture at pH 9.0. When fluoride ions were added in the range of 2-500 ppm, the minerals produced at pH 7.4 altered from OCP/HAp to HAp/fluorapatite (FAp). In addition, the crystallinity of the obtained minerals increased with an increase in fluoride ion concentration, and the solubility was inversely correlated to crystallinity. In conclusion, we established a novel fabrication method for synthesizing organic/inorganic composite materials composed of fibrin and calcium phosphate and revealed that the characteristics of the minerals in the synthesized material can be controlled by the fabrication condition.

Topics: Apatites; Biomimetic Materials; Calcium Phosphates; Crystallization; Durapatite; Fibrin; Fluorides; Gels; Hydrogen-Ion Concentration; Microscopy, Electron, Scanning; Solubility; X-Ray Diffraction

Subsurface lesions in bovine enamel slices were remineralized. The remineralization solutions contained either 0.03, 0.3, or 1.0 ppm fluoride at either pH 5.5 or 6.8. The amount of remineralization was determined after periods of up to 610 h, using quantitative microradiography. The results showed that after 126 h of remineralization in the presence of 0.03 ppm fluoride significantly (p less than 0.05) more remineralization occurred at pH 6.8 than at pH 5.5. At 0.3 and 1.0 ppm fluoride no significant differences between pH 5.5 and pH 6.8 were observed. An interaction between fluoride and pH was observed. The observed differences in the rates of remineralization are explained by the formation and subsequent transformation of the precursors octacalcium phosphate (pH 6.8) and brushite (pH 5.5) into (fluor)apatites.

Topics: Animals; Apatites; Calcium Phosphates; Cattle; Densitometry; Dental Enamel; Fluorides; Hydrogen-Ion Concentration; Microradiography; Time Factors; Tooth Demineralization; Tooth Remineralization