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Novel methodology for determining the effect of adsorbates on human enamel acid dissolution

OBJECTIVE: The effect of various interventions on enamel demineralisation can be determined by chemically measuring mineral ions dissolved by the attacking acid. Results are usually expressed as mineral loss per surface area of enamel exposed. Acid resistant varnish or adhesive tape are typically us...

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Autores principales: Pechlivani, N., Devine, D.A., Marsh, P.D., Mighell, A., Brookes, S.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713683/
https://www.ncbi.nlm.nih.gov/pubmed/29031237
http://dx.doi.org/10.1016/j.archoralbio.2017.09.035
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author Pechlivani, N.
Devine, D.A.
Marsh, P.D.
Mighell, A.
Brookes, S.J.
author_facet Pechlivani, N.
Devine, D.A.
Marsh, P.D.
Mighell, A.
Brookes, S.J.
author_sort Pechlivani, N.
collection PubMed
description OBJECTIVE: The effect of various interventions on enamel demineralisation can be determined by chemically measuring mineral ions dissolved by the attacking acid. Results are usually expressed as mineral loss per surface area of enamel exposed. Acid resistant varnish or adhesive tape are typically used to delineate an area of enamel. However, enamel surface curvature, rugosity and porosity reduce the reliability of simple area measurements made at the macro scale. Our aim was to develop a simple method for investigating the effect of adsorbates on enamel demineralisation that does not rely on knowing the area of enamel exposed. As an exemplar we have used salivary proteins as a model adsorbate. DESIGN: Natural human tooth enamel surfaces were subjected to five sequential acid challenges and then incubated in adsorbate (whole clarified saliva) followed by a further 15 acid challenges. Demineralisation was determined by measuring the phosphate released into the acid during each exposure by a spectrophotometric assay. The initial five challenges established a mean baseline mineral loss for each tooth against which the effect of subsequently adsorbed proteins could be compared. RESULTS: Salivary proteins significantly reduced the acid demineralisation of human enamel by 43% (p < 0.01). Loss of proteins during each challenge corresponded to a gradual reduction in the degree of protection afforded. CONCLUSIONS: The methodology provides a simple and flexible means to investigate the effect of any adsorbate on enamel acid dissolution. Knowledge of the area of exposed enamel is irrelevant as each tooth acts as its own negative control.
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spelling pubmed-57136832018-01-01 Novel methodology for determining the effect of adsorbates on human enamel acid dissolution Pechlivani, N. Devine, D.A. Marsh, P.D. Mighell, A. Brookes, S.J. Arch Oral Biol Article OBJECTIVE: The effect of various interventions on enamel demineralisation can be determined by chemically measuring mineral ions dissolved by the attacking acid. Results are usually expressed as mineral loss per surface area of enamel exposed. Acid resistant varnish or adhesive tape are typically used to delineate an area of enamel. However, enamel surface curvature, rugosity and porosity reduce the reliability of simple area measurements made at the macro scale. Our aim was to develop a simple method for investigating the effect of adsorbates on enamel demineralisation that does not rely on knowing the area of enamel exposed. As an exemplar we have used salivary proteins as a model adsorbate. DESIGN: Natural human tooth enamel surfaces were subjected to five sequential acid challenges and then incubated in adsorbate (whole clarified saliva) followed by a further 15 acid challenges. Demineralisation was determined by measuring the phosphate released into the acid during each exposure by a spectrophotometric assay. The initial five challenges established a mean baseline mineral loss for each tooth against which the effect of subsequently adsorbed proteins could be compared. RESULTS: Salivary proteins significantly reduced the acid demineralisation of human enamel by 43% (p < 0.01). Loss of proteins during each challenge corresponded to a gradual reduction in the degree of protection afforded. CONCLUSIONS: The methodology provides a simple and flexible means to investigate the effect of any adsorbate on enamel acid dissolution. Knowledge of the area of exposed enamel is irrelevant as each tooth acts as its own negative control. Pergamon Press 2018-01 /pmc/articles/PMC5713683/ /pubmed/29031237 http://dx.doi.org/10.1016/j.archoralbio.2017.09.035 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pechlivani, N.
Devine, D.A.
Marsh, P.D.
Mighell, A.
Brookes, S.J.
Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title_full Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title_fullStr Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title_full_unstemmed Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title_short Novel methodology for determining the effect of adsorbates on human enamel acid dissolution
title_sort novel methodology for determining the effect of adsorbates on human enamel acid dissolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713683/
https://www.ncbi.nlm.nih.gov/pubmed/29031237
http://dx.doi.org/10.1016/j.archoralbio.2017.09.035
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