Volume 113, Issue 1 pp. 53-59

Scanning microradiographic study on the influence of diffusion in the external liquid on the rate of demineralization in hydroxyapatite aggregates

Frédéric R. G. Bollet-Quivogne

Frédéric R. G. Bollet-Quivogne

Institute of Dentistry, Queen Mary, University of London, London, UK

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Paul Anderson

Paul Anderson

Institute of Dentistry, Queen Mary, University of London, London, UK

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Stephanie E. P. Dowker

Stephanie E. P. Dowker

Institute of Dentistry, Queen Mary, University of London, London, UK

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James C. Elliott

James C. Elliott

Institute of Dentistry, Queen Mary, University of London, London, UK

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First published: 04 February 2005
Citations: 10
Frédéric R. G. Bollet-Quivogne, Queen Mary, University of London, Dental Biophysics Group, Medical Sciences Building, Mile End Road, London E1 4NS, United Kingdom

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E-mail: [email protected]

Abstract

Subsurface demineralization in enamel caries is known to entail diffusion of reagents and products both within the lesion and within the plaque biofilm external to the lesion. However, development of a predictive mathematical model for subsurface demineralization is hindered by limited quantitative understanding of the effects of these diffusion processes. The purpose of this quantitative study was to investigate and understand the effect of external diffusion length on the rate of demineralization in a simple model system. Ten, 500-µm thick sections cut from a porous hydroxyapatite (HAP) pellet were inserted in scanning microradiography (SMR) cells. The exposed thin edges of the sections were initially separated by columns of water (diffusion lengths) of 0–0.9 cm from a 1-l reservoir of demineralizing buffer (pH 4). Buffer was found to diffuse from the reservoir through the increasing diffusion lengths to the exposed HAP surface, whilst dissolved product diffused along the reverse path. Rates of HAP loss (from SMR measurements) decreased as the diffusion length increased. Experimental data were fitted to a general diffusion-reaction model. This showed that the solution near the HAP surface was almost completely saturated with HAP, and that the diffusion of dissolution products, rather than of buffer species, was rate limiting.

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