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An investigation of some food-approved polymers as agents to inhibit hydroxyapatite dissolution.

Authors :
Barbour, Michele E.
Shellis, R. Peter
Parker, David M.
Allen, Geoff C.
Addy, Martin
Source :
European Journal of Oral Sciences; Dec2005, Vol. 113 Issue 6, p457-461, 5p
Publication Year :
2005

Abstract

Dental erosion involves dissolution of the hydroxyapatite fraction of enamel and dentine, so agents that reduce the dissolution rate of hydroxyapatite could find application in food products aimed at reducing erosion. This study was performed to test some common food ingredients and additives for their effect on the dissolution rate of hydroxyapatite in a citric acid solution representative of soft drinks. Pyrophosphate, tripolyphosphate and a linear chain polyphosphate (average 25 phosphate units) significantly reduced the hydroxyapatite dissolution rate by 35, 46 and 64%, respectively. Xanthan gum and carboxymethylcellulose significantly reduced the hydroxyapatite dissolution rate by 29 and 16%, respectively. The protective effect may be ascribed to the binding of condensed phosphate or to the formation of an adsorbed layer of gum at the hydroxyapatite surface. Several other common food additives had no statistically significant effect on the hydroxyapatite dissolution rate. Polyphosphate exhibited a considerable persistence of action, causing a reduction in the dissolution rate for 3 h after treatment. Tripolyphosphate was slightly persistent, and pyrophosphate and xanthan gum did not exhibit a substantial persistence of action. A solution containing polyphosphate and xanthan gum reduced the hydroxyapatite dissolution rate by 70% and exhibited a similar persistence of action to the solution containing only polyphosphate. These compounds are suggested to have potential as erosion-reducing agents in soft drinks. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09098836
Volume :
113
Issue :
6
Database :
Complementary Index
Journal :
European Journal of Oral Sciences
Publication Type :
Academic Journal
Accession number :
18942854
Full Text :
https://doi.org/10.1111/j.1600-0722.2005.00248.x