Start Publications Influence of fluoride–detergent combinations on the ...
QSense

Influence of fluoride–detergent combinations on the visco-elasticity of adsorbed salivary protein films

Year: 2011

Journal: European Journal of Oral Sciences, Volume 119, Issue 1, pages 21–26, February 2011, 20110317

Authors: Veeregowda D.H., van der Mei H.C., Busscher H.J., Sharma P.K.

Last authors: Prashant K. Sharma

Organizations: Department of Biomedical Engineering, University Medical Center Groningen and University of Groningen, Groningen, the Netherlands

Country: The Netherlands

The visco-elasticity of salivary-protein films is related to mouthfeel, lubrication, biofilm formation, and protection against erosion and is influenced by the adsorption of toothpaste components. The thickness and the visco-elasticity of hydrated films (determined using a quartz crystal microbalance) of 2-h-old in vitro-adsorbed salivary-protein films were 43.5 nm and 9.4 MHz, respectively, whereas the dehydrated thickness, measured using X-ray photoelectron spectroscopy, was 2.4 nm. Treatment with toothpaste slurries decreased the thickness of the film, depending on the fluoride–detergent combination involved. Secondary exposure to saliva resulted in a regained thickness of the film to a level similar to its original thickness; however, no association was found between the thickness of hydrated and dehydrated films, indicating differences in film structure. Treatment with stannous fluoride/sodium lauryl sulphate (SnF2/SLS)-containing toothpaste slurries yielded a strong, immediate two-fold increase in characteristic film frequency (fc) with respect to untreated films, indicating cross-linking in adsorbed salivary-protein films by Sn2+ that was absent when SLS was replaced with sodium hexametaphosphate (NaHMP). Secondary exposure to saliva of films treated with SnF2 caused a strong, six-fold increase in fc compared with primary salivary-protein films, regardless of whether SLS or NaHMP was the detergent. This suggests that ionized stannous is not directly available for cross-linking in combination with highly negatively charged NaHMP, but becomes slowly available after initial treatment to cause cross-linking during secondary exposure to saliva.