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Crystal growth on enamel in relation to acid etching.

Crystal formation may occur during etching of enamel surfaces with phosphoric acid. In this in vitro study we observed, from a morphological standpoint, some crystals left after etching, on the surfaces, using the scanning electron microscope. More often, after water-spraying, a thin generalized precipitate remains on the surface. This precipitate may be harmful for the retention of composite resins. On few specimens we obtained needle-shaped or petal-like crystals. Crystal deposits were spread evenly, on the surface, or nucleated from different points. We tempted to identify these crystal formations by X-ray diffraction and microprobe analysis. Chemical identification seems very important because calcium phosphates solubility varies. Crystal dissolution in saliva can lead to marginal leakage and impairs the quality of esthetic restorations. On the contrary insoluble crystals may ensure microscopic retentions and crystal growth is now considered as an alternative for enamel pretreatment in bracket bonding. Crystal formation, in these first experiments, is too scarce to be used for crystal bonding. But it appears that two factors may enhance the crystal number: a preliminary topical application of fluoride and adsorption of an acidic protein, on the surface, before etching. However, further investigations are still necessary.

Acid Etching, Dental↗

An analysis of nodular deposits on soft contact lenses.

Approximately 6.8 percent of soft contact lens wearers develop multiple nodular deposits on the front surface of their soft contact lenses. It was the purpose of this investigation to evaluate the role of calcium in the newly formed and mature deposits. Nodular deposits were examined using scanning electron microscopy and Energy Dispersive X-ray (EDX) analysis for calcium content. Any deposit which did not demonstrate the presence of calcium was sectioned, and the individual section re-examined by EDX analysis. Our results indicate that calcium was present in all but three of 72 nodular deposits investigated. The calcium was finely distributed throughout the deposits in a non-crystalline pattern, especially in the basal layers. Sections of the deposits also were examined at the light microscope level for the presence of lipids, calcium, and polysaccharides (mucin). All deposits stained positively for lipids, but polysaccharides were more evident in newer deposits. These results may indicate that both calcium and polysaccharides are involved in the genesis of nodular deposits.

Calcium↗

Zinc sulfide in intestinal cell granules of Ancylostoma caninum adults.

A source of confusion has existed since the turn of the century about the reddish brown, weakly birefringent "sphaerocrystals" located in the intestines of strongyle nematodes, Strongylus and Ancylostoma. X-ray diffraction and energy dispersive spectrometric analyses were used for accurate determination of the crystalline order and elemental composition of the granules in the canine hookworm Ancylostoma caninum. The composition of the intestinal pigmented granules was identified unequivocally as zinc sulfide. It seems most probable that the granules serve to detoxify high levels of metallic ions (specifically zinc) present due to the large intake of host blood.

Ancylostoma↗

Structural analysis of phleboliths and salivary calculi.

Three phleboliths and ten salivary calculi in the submandibular duct were studied with scanning electron microscopy (SEM) and computer aided microanalyser (CMA). The surface of the phleboliths was rather even with some irregularity. According to their surface structure the salivary calculi were divided into three types: the rock-like type, the granular type, and the globular type. The phleboliths were classified into two types according to their cut surface: the calcified-core type, and the uncalcified-core type. The core structure was similar to the surface structure in the calcified-core type of phleboliths, but in the salivary calculi the core structure was different from the surface structure in that the cut surface of the core was an accumulation of circular or polygonal structures forming a honey-comb pattern which was surrounded by small projections distributed radially. On the basis of these results some etiological factors of phleboliths and salivary calculi are discussed.

Electron Probe Microanalysis↗

Scanning electron microscopy and electron probe microanalyses of the crystalline components of human and animal dental calculi.

A review of the use of scanning electron microscopy (SEM) and electron probe microanalyses in the study of dental calculus showed that such studies provided confirmatory and supplementary data on the morphological features of human dental calculi but gave only limited information on the identity of the crystalline or inorganic components. This study aimed to explore the potential of combined SEM and microanalyses in the identification of the crystalline components of the human and animal dental calculi. Human and animal calculi were analyzed. Identification of the crystalline components were made based on the combined information of the morphology (SEM) and Ca/P molar ratios of the crystals with the morphology and Ca/P molar ratio of synthetic calcium phosphates (brushite or DCPD; octacalcium phosphate, OCP; Mg-substituted whitlockite, beta-TCMP; CO3-substituted apatite, (CHA); and calcite. SEM showed similarities in morphological features of human and animal dental calculi but differences in the forms of crystals present. Microanalyses and crystal morphology data suggested the presence of CaCO3 (calcite) and CHA in the animal (cat, dog, tiger) and of OCP, beta-TCMP and CHA in human dental calculi. X-ray diffraction and infrared (IR) absorption analyses confirmed these results. This exploratory study demonstrated that by taking into consideration what is known about the crystalline components of human and animal dental calculi, combined SEM and microanalyses can provide qualitative identification.

Adult↗

Secretory ameloblasts and calcium distribution during normal and experimentally altered mineralization.

The distribution of calcium in relation to secretory ameloblasts of the rat incisor was studied. An experimental model system in which enamel mineralization was temporarily inhibited by injecting sodium fluoride and cobalt chloride was used. Potassium pyroantimonate (PPA) cytochemistry, electron energy loss spectroscopy (EELS), and energy dispersive X-ray spectrometry (EDS) were used to clarify the role of the ameloblast in controlling calcium distribution during normal and experimentally altered enamel mineralization. Secretory ameloblasts chemically-preserved in glutaraldehyde either with or without PPA were analyzed for calcium; those preserved with PPA showed higher concentrations of calcium than did those preserved with glutaraldehyde only. Freeze-dried control and experimental tissues showed an increasing gradient of calcium from stratum intermedium cells to the distal ends of the ameloblasts. Calcium levels were reduced near the distal ends of the cells following fluoride and cobalt injections, while magnesium levels were increased markedly in the same region. This multi-method approach showed correlated calcium localization in specific regions of this cell in relation to changes in function. The study thus provides additional evidence for active involvement of the ameloblasts in enamel mineralization.

Ameloblasts↗