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Biomedical subjects

J C Elliott

Publications and source records attributed to J C Elliott.

At least 55 records · Page 3Linked to original sources

Preparation of an experimental low-fluoride diet from single-cell organisms for rats and mice.

1. A method for producing a standard low-fluoride diet from a green alga and yeast is described. Chlorella pyrenoidosa was grown in a culture medium prepared with distilled water and analytical grade chemical salts. The spent culture medium from the alga culture was reclaimed and replenished with salts and sucrose for the production of yeast, Saccharomyces cerevisiae. 2. The single-cell organisms were separated by centrifugation from their culture media and the dried cells were blended with sucrose, maize oil, cellulose and a salt mix to produce diet pellets for rats and mice. 3. The diet was readily accepted as food by rats and mice and it was found to contain 100-300 micrograms fluoride/kg dry weight. Two generations of rats and four generations of mice were bred on this diet. 4. The use of hydroxyapatite to reduce the fluoride content of the chemical used in the production of the alga and yeast biomass was investigated. Diet pellets prepared with this biomass contained 45-60 micrograms fluoride/kg dry weight.

Amino Acids↗

Rates of mineral loss in human enamel during in vitro demineralization perpendicular and parallel to the natural surface.

Human enamel is a structurally anisotropic material. The aim of this study was to investigate whether this structural anisotropy is reflected in the demineralization behaviour of enamel. Kinetics of demineralization of in vitro caries lesions with the direction of acid attack perpendicular to the natural surface of dental enamel from human premolar teeth were compared with kinetics when demineralized parallel to this surface. Pairs of enamel samples from the same tooth were demineralized under identical conditions. Loss of mineral with time was very nearly linear for both directions (consistent with the rate-controlling step being reaction at the advancing front rather than transport processes), but the perpendicular rate was, on average, about 14% higher than the parallel rate. The rate of demineralization parallel to the surface increased from the natural surface to the enamel-dentine junction by 10-25%, depending on sample. The origin of fine structure and slight departures from linearity in the loss of mineral with time plots are discussed. Mineral masses per unit area were determined from absorption of a 15-microm diameter X-ray beam using photon (AgKalpha) counting methods.

Anisotropy↗

Optical profilometric study of changes in surface roughness of enamel during in vitro demineralization.

The application of non-contact optical profilometry for non-destructive study of changes in the surface roughness of natural enamel surfaces during in vitro demineralization was investigated. Repeated measurement of profiles of the same enamel surfaces after successive demineralization episodes was achieved by a kinematic specimen mount that could be removed, then accurately repositioned. Surface roughness parameters and reflectivity of natural enamel surfaces exposed to either a demineralizing solution (test) or deionized water (control) for up to 6 days were measured at 6- to 24-hour intervals. The results prior to demineralization showed that surface roughness varies with position on the enamel surface. During demineralization there was an approximately linear increase in surface roughness for the first 70 h followed by somewhat erratic behaviour, and a saturating exponential with time increase in reflectivity for the first 70 h which subsequently remained constant. Changes in enamel surface during in vitro demineralization were also observed using scanning electron microscopy.

Dental Enamel↗

Longitudinal study of the three-dimensional development of subsurface enamel lesions during in vitro demineralisation.

A longitudinal study was made of the 3D development of subsurface enamel lesions in whole human molars. X-ray microtomography (XMT) was used to measure the 3D distribution of linear attenuation coefficients in the tissue at 8-15 stages during cumulative times of 36-107 days demineralisation through approximately 1-mm-wide windows. Although lesion morphology was consistent with preferential anisotropic dissolution parallel to enamel prisms at the advancing front, detail (at a scale of approximately 100 microm) varied in relation to exposed surface sites separated by <1 mm. The distribution of mineral in the most superficial region varied across the exposed face of each lesion. Within lesions, localised foci of low mineral concentration (at a scale of approximately 200 microm) retained their general form through successive stages of demineralisation before coalescing. The most advanced regions within a lesion seemed to correspond with surface regions with lowest mineral concentration. These findings indicate that local variations in fractional pore volume of partially demineralised enamel influence the subsequent spatial development of lesions.

Dental Enamel↗

Synchrotron x-ray microtomographic investigation of mineral concentrations at micrometre scale in sound and carious enamel.

Synchrotron X-ray microtomography (XMT) was used to measure the linear attenuation coefficient (LAC) for 1.9-microm sidelength voxels within approximal brown spot lesions and sound human enamel. XMT demonstrated three-dimensional features, notably sheets with approximately 30 microm periodicity having low LAC, identified as regions of demineralization corresponding to Retzius lines. Quantitative three-dimensional measurements of mineral concentration, derived from LAC with assumption of a single model composition, were consistent with previous measurements of sound and carious enamel from microradiographic projections. The uncertainty in measurements of mineral concentration and mineral fraction volume was investigated by modelling enamel with a range of composition and component densities. This analysis showed that, although mineral concentration can be determined from LAC with an error of <0.2 g cm(-3), the variation in pore fraction volume within caries lesions cannot be reliably determined from X-ray attenuation measurements alone.

Apatites↗