IADR Abstract Archives

Factors Affecting Dietary Acid-based Erosion: A Nano-indentation Investigation

Objective:

Determining the effect of dietary-acid type, concentration and pH on the erosion of human enamel.

Method:

Solutions of citric (1% and 6% w/v) and phosphoric-acid (0.02 w/v%) were used as typical dietary-acids, either un-buffered or buffered to pH 3.8 with 3M NaOH. To simulate drinking a sequential model was developed involving immersing  third molar enamel specimens (n=18) in alternate solutions of either one of the candidate acid solution for 30 s and phosphate buffered saline (PBS) for 30 until four cycles of acid immersion had occurred. A control group (n=3) that was immersed only in PBS for four cycles was also analysed.

Erosion was monitored in terms of hardness and reduced modulus; measured using a nano-indenter (Hysitron, USA). Specimens were measured before and after acid exposure, with 16 measurements taken, in air, over a 30x30um area.

Result:

Both parameters proved to be useful measures of early erosion of enamel. In general, pH had the greatest effect (table 1). Un-buffered 6% citric acid produced with greatest reduction in both H and Er (P<0.01). Buffering the acids to the same pH reduced the overall reduction in either parameter but 6% citric-acid still produced the largest effect. Interestingly, acid type was also important, with un-buffered phosphoric acid only producing a significant reduction in H, while in buffered phosphoric-acid there was only a significant reduction in Er. No significant changes were found for the PBS specimens.

Conclusion:

We chose acids at dietary-relevant concentration and discovered that pH has the greatest effect on erosion. However, when acids are buffered to the same pH concentration becomes important. Importantly, by monitoring both Er and H differences in the behaviour elicited by individual acids could be identified.

Acid

pH 

Reduced Modulus [GPa]

Hardness [GPa]

t=0

t=120s

Change

[%]

t=0

t=120s

Change

[%]

Citric 6%

1.88

54(2)

19(7)

65 **

2.2(0.1)

0. (0.1)

91**

Citric 1%

2.28

59(3)

34(7)

42 **

2.4(0.2)

0.4(0.1)

83**

Phosphoric 0.02%

2.54

50(3)

50(4)

0

2.1(0.1)

1.3(0.2)

38*

Citric 6%

3.8

43(3)

28(3)

35 *

1.1(.2)

0.3(0.1)

73*

Citric 1%

3.8

45(3)

34(3)

24 *

1.2(0.2)

0.6(0.1)

50*

Phosphoric 0.02%

3.8

45(2)

39(2)

13 *

1.4(0.1)

1.4(0.1)

0

PBS

7.4

61(3)

63(3)

-3

2.3(0.2)

2.6(0.2)

-13

 Table 1 summarising results data: Data are mean(SD)
Significant differences shown in cells, where * P<0.05, ** P< 0.01 (two-way-ANOVA)

Division: British Division Meeting
Meeting: 2013 British Division Meeting (Bath, England)
Location: Bath England
Year: 2013
Final Presentation ID: 8
Abstract Category|Abstract Category(s): Scientific Groups
Authors
  • Pattem, Jacob  ( University of Newcastle-upon-Tyne, Newcastle upon Tyne, N/A, England )
  • SESSION INFORMATION
    Oral Session
    MINTIG Prizes and Orals
    09/09/2013