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The morphology of dentinal cavity walls, wetting by poly (methyl methacrylate), and resistance to tensile forces was studied with a scanning electron microscope, before and after etching or fixation, or both, with glutaraldehyde. Results indicated that the surface layer of dentinal cavity walls after etching is of an aqueous-organic nature, that glutaraldehyde fixation improves the mechanical properties of the surface layer of the cavity wall, and that wetting by poly (methyl methacrylate) is effective.

Tritiated proline was administered to domestic cats during the development of their permanent dentition. The amount of residual radioactivity was determined autoradiographically at various times after cavity preparation in mature molars and premolars. Two wk after cavity preparation, the amount of radiolabel beneath the axial cavity wall decreased to about 50% of that present in corresponding contralateral cavity-free teeth. The observed decreases are ascribed to an enhancement of the protein metabolism in dentin. At 45 wk, 80-90% of the radiolabel has disappeared. This paper discusses the role of an eventual effect of microleakage on the latter results.

To investigate the permeability of the dental enamel of erupted and unerupted human pre-molars and its variation with depth, we determined the resistivity of successive 100-μm-thick layers. The electrical resistance of halved tooth crowns at zero Hertz, which according to Scholberg et al. (1982, 1984) is inversely related to the permeability, was measured before and after removal of successive enamel layers from the outer surface toward the dentino-enamel junction (D.E.J.). The resistivity of the successive enamel layers increased from the D.E.J. toward the outer surface in approximately the same way in erupted as well as in unerupted pre-molars, except within the outermost layer of 100 to 200 μm thickness. The resistivity of this layer in erupted pre-molars was considerably higher than that in unerupted pre-molars, which may be due to post-eruptive mineralization.

Intact roots of human molars, which had not been exposed to the oral environment, were exposed to buffer solutions of pH 5.5, which contained, besides calcium and phosphate, various concentrations offluoride. Densitometric measurements on contact-microradiograms of transverse sections of these roots produced data which were used to calculate the rate of demineralization ( Vdem). Vdem appeared to be reduced with increasing fluoride concentration and with decreasing pIOHA (i.e., the negative logarithm of the ionic product of hydroxyapatite) of the buffer solution. In addition, it was observed that, after some days of exposure, remineralization started to occur within the surface layer at some μm from the outer surface and that the region within which remineralization took place was extended inward with increasing time of exposure. These data suggest that fluoride is effective in the prevention of root surface caries. The mechanism of the interaction of fluoride with the root mineral is discussed.

Tritiated proline was administered as protein marker to domestic cats during the development of their permanent dentition (age 11-18 wk). At 30, 43, 56, and 75 wk, the amount of tritium in the mature dentin was determined by quantitative autoradiography. At 43, 56, and 75 wk the residual amount of label was 92, 92, and 77%, respectively, of that at 30 wk. The metabolism of dentinal collagen (with possibly a recycling of proline) and the metabolism of non-collagenous proline-containing proteins are suggested as factors that may contribute to the decrease of tritium label.

Crowns and roots of human molars, the roots from which had not been exposed to the oral environment, were exposed for 0, 3.5, 7, and 14 days to buffer solutions which were undersaturated or supersaturated with respect to hydroxyapatite. Densitometric measurements on contact-microradiograms of transverse sections of the crowns and of the cervical parts of the roots yielded plots of the mineral content as a function of the distance to the outer surface. From these plots, the rate of demineralization was calculated. It was found that the mineral of the roots dissolved even in buffer solutions which were supersaturated with respect to hydroxyapatite. Comparison of the results obtained from the crowns with those from the roots showed that the root hard tissues were more vulnerable to demineralization than was the dental enamel.

Roots of extracted human molars were treated for both 10 and 30 min with a saturated solution of dicalcium phosphate dihydrate (DCPD) of pH 2.4 and subsequently with a 5.3 mmol.L -1 solution of sodium fluoride of pH 7.0. The objective of these combined treatments was to convert the highly-soluble root mineral into the less-soluble fluoridated hydroxylapatite, with DCPD as an intermediate, to improve caries resistance. The mineral content of the surface layer was not affected in a significant way. Roots treated in this way were subjected to 50 mmol.L-1 acetate buffer solutions of pH 5.5 and with pIOHA-values of 112, 116, and 122. The proportional reduction of the rate of demineralization (Vdem) of similarly treated roots subjected to buffer solutions of pIOHA 112 and 116 appeared to be equal initially. Since fluoridated hydroxylapatite is insoluble under these conditions, these findings are in agreement with expectations. The reduction of Vdem amounted to about 45 and 70% for roots treated for 10 and 30 min, respectively. When roots were treated for 10 and 30 min and then exposed to buffer solutions with a pIOHA 122, reductions of Vdem of about 30 and 55%, respectively, were found. Conversion of the root mineral into fluoridated hydroxylapatite can eliminate, in principle, the existing difference in caries susceptibility of the root and of the dental enamel.

Tritiated proline was administered to domestic cats during the development of their permanent premolars. The metabolic activity of collagen in the mature premolar dentin was determined by quantitating the amount of tritiated hydroxyproline in the dentin as a function of time. It has been demonstrated that the metabolic activity of the dentinal collagen was extremely low and remained within the experimental error for a period of 45 weeks.