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Crystallographic morphology of heterogeneous fluoridated carbonate apatites.

Carbonate-containing fluoridated apatites were synthesized with two different modes of fluoride incorporation: by supplying F-free solution initially, followed by a F-containing solution; and with the order of supply of these solutions reversed. Both of these heterogeneously synthesized fluoridated CO3 apatites showed typical apatitic x-ray diffraction patterns; and both had similar total fluoride contents (0.87 +/- 0.07 and 0.94 +/- 0.03 mmol/g, respectively), i.e., half of the maximum fluoride content of fluorapatite. However, they differed considerably in their crystallographic properties. The 300 reflection peaks of both apatites were split, and their patterns were slightly different. In the former, SEM observation revealed capsule-like crystals with a rounded hexagonal shape. However, the latter had many small crystals, similar to those of homogeneous CO3 apatite, adhering to the larger hexagonal crystals, which were also similar to homogeneous fluorCO3 apatite. Wavelength-dispersive spectroscopy attached to the SEM showed a higher fluoride intensity in the former spectrum than the latter. These results suggest that two different types of heterogeneous fluoridated CO3 apatites were formed, CO3 apatite covered with fluorCO3 apatite, and fluorCO3 apatite covered with CO3 apatite. The simple two-step supply system used in this study is helpful for the study of complicated heterogeneous formation of apatites.

Apatites↗

Microstructure and segregation behavior of palladium in silver-copper-palladium alloys.

It has been reported that the addition of palladium can modify the microstructure and improve the properties of Ag-Cu eutectic alloy as well as admixed Cu-rich amalgam. The purpose of this work was to study the microstructure and segregation behavior of palladium in a series of Ag-Cu-Pd alloys. All microstructural and microchemical results consistently indicated a strong tendency for palladium to form the ordered Cu3Pd superlattice in the copper-rich phase of the present ternary alloys. Transmission electron microscopic examination indicated that, in addition to the large Cu-rich particles, numerous small (typically tens of nanometers) Cu-rich particles were distributed in the Ag-rich phase. In the alloys containing 10 and 15 wt% Pd, the Cu3Pd superlattice had an L1(2)-type crystal structure. In the alloy containing 20 wt% Pd, the Cu3Pd had a periodic (regular) APB structure. The solubility of palladium in the Cu-rich phase was always much larger than that in the Ag-rich phase. The ratio of the palladium concentration in the copper-rich phase to that in the silver-rich phase decreased with the overall palladium content.

Chemical Phenomena↗

Abrasive particles in tobacco products: a possible factor in dental attrition.

Tobacco products are known to cause oral soft-tissue lesions, but they may also directly affect the teeth. Abrasive particles contained in tobacco products may contribute to dental attrition. We studied tobacco samples from 16 brands of cigars, eight brands of snuff, four brands of chewing tobacco and several unprocessed tobacco leaves used as cigar wrappers. Insoluble particulate matter made up about 0.5 percent of the weight of an average tobacco sample.

Electron Probe Microanalysis↗

Scanning electron microscopy and calcification in amelogenesis imperfecta in anterior and posterior human teeth.

Teeth fragments from members of a family clinically and genetically diagnosed as having amelogenesis imperfecta were studied by scanning electron microscopy and X-ray microprobe analysis to establish the morphological patterns and the quantitative concentration of calcium in the enamel of anterior (canine, incisor) and posterior (premolar and molar) teeth. The prism patterns in the enamel of teeth from both regions were parallel or irregularly decussate, with occasional filamentous prisms accompanied by small, irregularly rounded formations. Prismless enamel showed the R- and P-type patterns. Calcium levels in enamel of amelogenesis imperfecta and control teeth differed significantly between anterior and posterior teeth, indicating that the factors that influence normal mineralization in different regions of the dental arch are not altered in the process of amelogenesis imperfecta.

Amelogenesis Imperfecta↗

The inorganic content of pleromin in tooth plates of the living holocephalan, Chimaera phantasma, consists of a crystalline calcium phosphate known as beta-Ca3(PO4)2 (whitlockite).

The tooth plates in the living Holocephalan, Chimaera phantasma were studied by various techniques. They consisted of osteodentin and hypermineralized pleromin (kosmin). The degree of mineralization on the latter was as much as in the enameloid of Chondrichthyes and Osteichthyes. Scanning electron microscope observation indicated that the pleromin consisted of large and granular crystals. X-ray powder diffractometry, electron microprobe analysis and analytical electron microscopy revealed that the inorganic constituent of pleromin included, as an essential element, a beta-Ca3(PO4)2 (whitlockite) structure containing a small amount of Mg.

Animals↗

[A study on glass-ceramic for dental implant. Histopathological response in animal experiment].

The endosseous dental implants of glass-ceramic were implanted and holes were drilled as control in edentulous areas of adult dog mandibles. The implants were kept without function. After 2-84 days, the biological reaction of the tissue was examined by histological and ultrastructural methods, while the glass-ceramic surface was examined by EPMA analysis and X-ray diffraction. The results were as follows: 1. After 4 days the bone matrix formation started on the surface of the glass-ceramic. After 14 days, the area of bone formation on the implant surface was enlarged and about all surface was covered with this woven bone. 2. Being compared with the control, glass-ceramic didn't prevent the healing process of bone. 3. On the surface of glass-ceramic, apatite and beta-whitlockite crystal formation was observed by X-ray diffraction. And analysis by EPMA showed this areas combined bone. 4. TEM observation showed that there were many hemidesmosomes in interface between the implant and attached epithelium. In the subepithelial fibrous tissue collagen fibers and fibroblasts were arranged in parallel on the implant surface.

Animals↗

Tympanosclerosis of the ear drum in secretory otitis media.

Tympanosclerosis of the ear drum in children with SOM differs from normal ear drums in children with SOM. In tympanosclerosis the numbers of fibroblasts, fibrocytes and macrophages are increased in lamina propria and in the submucosa. The collagen microfibrils and procollagen filaments have increased in numbers with a partly disorganized pattern. Fibrolysis of microfibrils is conspicuous and hyaline degeneration appears in areas. Calcareous deposits are found scattered to a limited extent in lamina propria and in the submucosa. Profound calcification could only be found in children with tympanosclerosis coexisting with chronic perforation of the ear drum.

Adolescent↗

A classification of urinary calculi with respect to their composition and micromorphology.

Texture and micro-morphology of 1615 urinary calculi has been studied using scanning electron microscopy and X-ray micro analysis. Together with the results of X-ray diffractometry concerning their phase composition, a classification into five stone classes, 13 stone groups and 17 sub-groups could be evaluated. Especially the large and inhomogeneous class of the calcium-stones could be resolved into 13 stone types. Using this classification, the stone type is characterized by a three digit number containing the stone class, the stone group and in some cases the sub-group. Criteria for classification are typical texture patterns, the occurrence of special crystalline phases or both. These items are presented and clinical relationships discussed.

Calcium↗

Human root dentin: structural anisotropy and Vickers microhardness isotropy.

The demanding mechanical functions and the variable structure of dentin make it an invaluable material for studying the structure-mechanical function relations of a mineralized collagen-containing tissue. The mineralized collagen fibril axes in human root dentin are mainly located on the incremental plane. Within this plane there is a preferred orientation in the general root-crown direction. The apatite crystals are aligned in three dimensions within an individual collagen fibril, but this orientation does not necessarily extend to the neighboring fibrils. Crystals are also present as aggregates without any preferred orientation. The structure is therefore clearly anisotropic with respect to the collagen fibril orientation, but less so with respect to overall crystal orientation. Vickers microhardness measurements of the root dentin are essentially the same on the three orthogonal planes with respect to the incremental plane. Knoop microhardness measurements are also the same on all three orthogonal planes when the major diagonal is aligned perpendicular to the collagen fibril axis preferred orientation direction. In-plane variations of up to 20% are observed in the orthogonal direction. The material is thus isotropic in the three main directions with respect to Vickers microhardness, but anisotropic in structure. This paradoxical situation is attributed mainly to the variable modes of crystal organization.

Adolescent↗

WDX study of resin-dentin interface on wet vs. dry dentin.

The purpose of the present study was to determine the resin-dentin Interface conditions in Wet vs. Dry Dentin. Dentin disks were prepared from extracted human premolars. Sectioned dentin surfaces were used for SEM studies of wet vs. dried acid-etched dentin. These specimens were cut perpendicular to the surface into two equal halves. One-half of the sectioned specimen was observed by SEM in three treatment groups and the other half was observed for micromorphological differences in the resin-dentin interface using Wavelength Dispersive X-ray Spectrometer (WDX). SEM photomicrographs of the dentin surface showed the collapse of collagen fibrils in the demineralized layer and enlargement of the tubule orifices. A collagen rich layer approximately 8-10 microns thick (WDX) was observed at the resin-dentin interface when treated with the conventional dry-bonding technique. Dentin surfaces treated by the wet-bonding technique (SB), as observed by SEM, showed an uncollapsed collagen layer, while the collagen-rich layer was approximately 1-2 microns thick (WDX). The present findings suggest that moist bonding is required for optimum infiltration of adhesive resin into the demineralized layer.

Acid Etching, Dental↗

EPMA observation between dentin and resin interfaces. Part 1. Comparison of wet and dry technique after short-term stored in water.

The study was to evaluate the marginal leakage of wet or dry dentin condition after restoration on short-term. In the study we used Photobond adhesive system and Single Bond adhesive system. The specimens were prepared from premolars. A class V cavity was prepared at the CEJ with a high-speed hand piece and #010 round diamond point. The cavity's walls and floors were etched with phosphoric acids of the test materials by wet and dry bonding techniques. The specimens were cross-sectioned longitudinally through the center of the cavities with a low speed diamond micro-cutter and polished with carbide paper (#600-1200) after storage in distilled water for 1 day, and silver nitrate staining. Specimens were viewed with EPMA for elemental distribution of calcium, nitrogen and silver on the resin-dentin interface. The uptake of silver particles was less in samples treated with the wet-bonding technique when compared with dry-bonding technique. This in vitro study showed that bonding technique is important in establishing a seal along the restoration margins to control marginal leakage.

Acid Etching, Dental↗

[Initial corrosion of dental casting alloys in the oral environment].

In order to study the initial corrosive changes of dental casting alloys in the mouth, the condition and composition of the proximal surface of the class II inlay were analyzed by the scanning electron microscope (SEM) and the electron probe microanalyser (EPMA). These analyses on the same small areas of the proximal surface were carried out every week for four weeks. The results were compared with the condition and composition of the preplacement in the mouth, and also with the data from former studies. 1. Changes observed in the 70Au-3Pt-3Pd-10Ag-14Cu alloy (Au-alloy) were slight in comparison to the other alloys in this experiment, both on the surface condition and composition. 2. The 12Au-45Ag-20Pd-18Cu alloy (Pd-alloy) appeared to be stable in the mouth, but the changes were greater than that of the Au-alloy. 3. The Au- and the Pd-alloys appeared to be stabler after hardening heat treatment. 4. The greatest change was observed in the 65Ag-22Sn-13Zn alloy. 5. Little change was found in the 72Ni-19Cr-6Si alloy by visual inspection, but the dendritic structure was observed by SEM. 6. Almost all these changes of the alloys in this study showed somewhat greater changes than those observed in the conventional basic immersion tests of alloys.

Corrosion↗

The NiTi superelastic alloy application to the dentistry field.

The main properties of NiTi alloys are presented, discussed and compared with respect to those of stainless steels. Special regard is given to the use of NiTi alloy as orthodontic wires and endodontic instruments. The superelastic properties of orthodontic wires and endodontic files are measured as a function of the applied stress, of the strain and of the temperature. Both biomedical devices are submitted to surface analysis to control the interface with the biological environment in which they will be immersed.

Biocompatible Materials↗

Optimum surface properties of oxidized implants for reinforcement of osseointegration: surface chemistry, oxide thickness, porosity, roughness, and crystal structure.

PURPOSE: To investigate detailed surface characterization of oxidized implants in a newly invented electrolyte system and to determine optimal surface oxide properties to enhance the bone response in rabbits. MATERIALS AND METHODS: A total of 100 screw-type titanium implants were prepared and divided into 1 control group (machine-turned implants) and 4 test groups (magnesium ion-incorporated oxidized implants). Forty implants were used for surface analyses. A total of 60 implants, 12 implants from each group, were placed in the tibiae of 10 New Zealand white rabbits and measured with a removal torque test after a healing period of 6 weeks. RESULTS: For the test groups, the oxide thicknesses ranged from about 1,000 to 5,800 nm; for the control group, mean oxide thickness was about 17 nm. The surface morphology showed porous structures for test groups and nonporous barrier film for the control group. Pore diameter ranged from < or = 0.5 microm to < or = 3.0 microm. In regard to surface roughness, arithmetic average height deviation (Sa) values varied from 0.68 to 0.98 microm for test implants and 0.55 microm for control implants; developed surface ratio (Sdr) values ranged from 10.6% to 46% for the test groups and were about 10.6% for the control group. A mixture of anatase and rutile-type crystals were observed in the test groups; amorphous-type crystals were observed in the control group. After a healing period of 6 weeks, removal torque measurements in all 4 test groups demonstrated significantly greater implant integration as compared to machine-turned control implants (P < or = .033). DISCUSSION: Determinant oxide properties of oxidized implants are discussed in association with bone responses. Of all surface properties, RTVs were linearly increased as relative atomic concentrations of magnesium ion increase. CONCLUSIONS: Surface properties of the oxidized implants in the present study, especially surface chemistry, influenced bone responses. The surface chemistry of the optimal oxidized implant should be composed of approximately 9% magnesium at relative atomic concentration in titanium oxide matrix and have an oxide thickness of approximately 1,000 to 5,000 nm, a porosity of about 24%, and a surface roughness of about 0.8 microm in Sa and 27% to 46% in Sdr; its oxide crystal structure should be a mixture of anatase- and rutile-phase crystals.

Animals↗

[Biliary calculi resistant to dissolution with bile acids: their heterogeneous composition and diversity of treatment response].

We have studied thirteen biliary stones resistant to biliary acids, using technical methods of stereomicroscopy, scanning electronic microscopy and EDX analyses. We have investigated changes on surface. Three biliary stones did not change and were considered resistant. Seven biliary stones appear partially dissolved and we observed many irregularities on surface and/or concentric dips in relation with cholesterol dissolution. In six cases, biliary pigment alternates with cholesterol. In three cases we observed a calcium carbonate coat on surface. One case included organic fibers. One biliary stone showed cholesterol with spherical bodies of calcium carbonate and pigment. It was a relapsed case of combined treatment. Three stones are composed of small black portions of polymerized calcium bilirubinate, rich in copper and iron. Our results demonstrate that biliary stones previously selected for treatment are a heterogeneous group. Because of this fact we get variable and unpredictable results.

Bile Acids and Salts↗

[The composition and structure of cholesterol biliary calculi].

The order and composition of the various elements that are present in the cholesterol stones has been analyzed and a useful model that should help in the study of already formed stones is proposed and therefore a better understanding of the lithogenesis and the physiopathological conditions in which stones develop. The existing components are described from the core up to the crust, case emphasizing the heterogeneity of the core, the calcium palmitate around it and the cholesterol disposition. The various forms of presentation of calcium carbonate are defined as well as the different types of ooliths.

Cholelithiasis↗