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Biomedical subjects

W L Jongebloed

Publications and source records attributed to W L Jongebloed.

8 recordsLinked to original sources

Ultrastructural studies of synthetic apatite crystals.

In this paper a survey is given of some ultrastructural properties of synthetic hydroxyapatite. The preparation method by which single crystals with a length in the range of 0.1-3.0mm and a defined purity and stoïchiometry can be produced is given. Two groups of materials are considered in detail: carbonate-rich (greater than 0.1% CO3) and low-carbonate hydroxyapatites. The experiments on carbonate-rich material, being the most interesting from a biological point of view, show that acids attack at an active site in the hexagonal basal-plane of the crystals. Later on the crystals dissolve in the center of the crystal parallel to the c-axis forming tube-like structures. The active site can be protected from dissolution if the crystals are pretreated by EHDP or MFP. A comparison with lattice defect theory shows that most likely dislocations of the "hollow-core" type are responsible for the preferential dissolution.

Acids

Crystallites dimensions of enamel.

In this paper the average diameter of enamel crystallites in mature, deciduous and fluorosed human enamel as well as in bovine enamel (in vivo and in vitro remineralized) is discussed. The investigation was carried out on broken surfaces of the various kinds of enamel with a scanning electron microscope. Corrections have been applied for the thickness of the gold-layer deposited. The average crystallite diameters for sound, deciduous and fluorosed human enamel were : 36 nm; 46 nm and 81 nm, respectively. The values for sound, remineralized in vitro and remineralized in vivo bovine enamel were 57 nm; 97 nm and 63 nm, respectively. The results indicate furthermore that if a correction for the sputtered goldlayer is applied, the results for SEM and TEM microscopy are in good agreement with each other. The difference between in vivo and in vitro remineralized bovine enamel is most likely due to differences in speed of remineralization and/or the presence of saliva.

Animals

Mechanism of enamel dissolution and its prevention.

In this paper the mechanism of dental enamel dissolution is discussed. Special attention is given to the anisotropic solubility behaviour (hollow tube formation) of demineralized enamel crystallites. The combined evidence strongly indicates that this peculiar dissolution behaviour is caused by dislocations. The dislocations--linear lattice defects--are present in the crystallite center and are the cause of two active dissolution sites in each crystallite. Initial as well as later stages in the caries process are discussed. Experimental evidence is presented which indicates that the active sites can be inactivated by agents like EHDP and MFP. After inactivation, acid penetration is either prevented or strongly retarded.

Apatites

The enamel substrate-characteristics of the enamel surface.

The outer enamel surface is of considerable interest in dentistry as it is the substrate for the acquired pellicle; the pellicle itself is the plaque carrier. In this paper the interface between outer enamel and pellicle is discussed with special emphasis on the outer enamel from a structural and chemical point of view. The outer enamel layer (less than 1 micron from the anatomical surface) is most likely a non-stoĭchiometric apatite. The chemical composition is obviously strongly different from the composition of bulk enamel. A model for the structure and atomic composition of surface enamel is presented. The available experimental evidence indicates that at an atomic scale, enamel crystallites have mainly phosphate groups (HPO42-groups) on the solid surface; the liquid adhering Stern layer contains most likely large amounts of calcium ions.

Dental Enamel