J Korean Acad Oral Health.  2017 Mar;41(1):50-55. 10.11149/jkaoh.2017.41.1.50.

Comparative remineralization effects of human and artificial saliva compositions on incipient dental caries

Affiliations
  • 1Department of Preventive & Public Health Dentistry, Chonnam National University School of Dentistry, Gwangju, Korea.
  • 2Dental Science Research Institute, Chonnam National University School of Dentistry, Gwangju, Korea.
  • 3Department of Preventive Dentistry and Public Oral Health, Yonsei University College of Dentistry, Seoul, Korea. yspd8050@naver.com

Abstract


OBJECTIVES
The purpose of this study was to compare enamel remineralization effects of human whole saliva and currently available artificial saliva compositions, using teeth exposed to chemical pH cycling conditions, and to obtain data that can inform future design and manufacturing of additional artificial saliva compositions.
METHODS
Seventy-two specimens of bovine tooth enamel were embedded in resin, then polished and exposed to a lactate/carbopol buffer system for 48-52 hours. Specimens were allocated into six experimental groups (n=12 specimens per group) by randomized blocks, such that each group contained an equivalent proportion of specimens at each Vickers hardness number (VHN) stratum: deionized water as a negative control, human whole saliva and artificial saliva compositions A, B, C and D. Surface hardness was measured before and after 15 days of chemical pH cycling. Surface microhardness was measured (Fm-7, Future-tech Corp, Japan) before and after treatment with test saliva compositions. One-way ANOVA, with post hoc Tukey test, was used to evaluate statistical differences with a significance threshold of P<0.05.
RESULTS
The intragroup changes in microhardness (ΔVHN) for treatment with each saliva composition were (in ascending order of ΔVHN): "•0.39±16.08 (deionized water control), 7.32±11.52 (artificial saliva B), 39.18±11.94 (artificial saliva C), 3.83±13.81 (artificial saliva D), 62.44±29.23 (artificial saliva A) and 102.90±25.89 (human whole saliva). Enamel treated with human saliva, or with artificial saliva compositions A, C, or D, demonstrated comparatively greater microhardness than enamel treated with deionized water or artificial saliva B. There was no difference in surface hardness between enamel treated with artificial saliva B and enamel treated with deionized water.
CONCLUSIONS
Our study suggests that human saliva and artificial saliva compositions A, C, and D are effective remineralization solutions for use in pH cycling.

Keyword

Artificial saliva; Dental caries; Remineralization

MeSH Terms

Dental Caries*
Dental Enamel
Hardness
Humans*
Hydrogen-Ion Concentration
Saliva
Saliva, Artificial*
Tooth
Water
Saliva, Artificial
Water

Reference

1. Edgar WM, O'Mullane DM. Saliva and oral health. 2nd ed. London: British Dental Asso;1996. p. 1–25.
2. Tenovuo J. Salivary parameters of relevance for assessing caries activity in individuals and populations. Community Dent Oral Epidemiol. 1997; 25:82–86.
Article
3. Heintze U, Birkhed D, Björn H. Secretion rate and buffer effect of resting and stimulated whole saliva as a function of age and sex. Swed Dent J. 1983; 7:227–238.
4. Lagerof F, Oliveby A. Caries protestive factors in saliva. Adv Dent Res. 1994; 8:229–238.
5. Edgar WM, Higham SM, Manning RH. Saliva stimulation and caries prevention. Adv Dent Res. 1994; 8:239–245.
Article
6. Head JA. A study of saliva and its action on tooth enamel in reference to its hardening and softening. J Am Med Assoc. 1912; 19:333–385.
Article
7. ten Cate JM, Arends J. Remineralization of artificial enamel lesion in vitro III. A study of the deposition mechanism. Caries Res. 1980; 14:351–358.
8. Koulourides T, Housch T. Hardness testing and microradiography of enamel in relation to intra-oral de- and remineralization; in Leach, Edgar, Demineralization and remineralization of the teeth. Oxford: IRL Press;1983. p. 255–272.
9. Koulourides T, Phantumvanit P, Munkgaard EC, Housch T. An intraoral model used for studies of fluoride incorporation in enamel. J Oral pathol. 1974; 3:185–195.
Article
10. Souder W, Sweeney WT. Is mercury poisonous in dental amalgam restoration. Dental Cosmos. 1931; 73:1145–1152.
11. Muhler JC, Swenson HM. Preparation of synthetic saliva from direct analysis of human saliva. J Dent Res. 1947; 26:474.
12. Swartz ML, Phillips RW, Tannir MD. Tarnish of certain dental alloys. J Dent Res. 1958; 37:837–847.
Article
13. Fusayama T, Katayori T, Nomoto S. Corrosion of gold and amalgam placed in contact with each other. J Dent Res. 1963; 42:1183–1197.
Article
14. Matzker J, Schreiber J. Synthetic saliva for treatment of hypoptyalism especially in radiation induced sialadenitis. Quintessence Int. 1973; 4:87–88.
15. ten Cate JM, Duijsters PP. Alternating demineralization and remineralization of artificial enamel lesions. Caries Res. 1982; 16:201–210.
Article
16. Stookey GK, Stahlman DB. Enhanced fluoride uptake in enamel with a fluoride-impregnated prophylactic cup. J Dent Res. 1976; 55:333–341.
Article
17. Leung VW, Darvell BW. Artificial salivas for in vitro studies of dental materials. J Dent. 1997; 25:475–484.
18. Featherstone JD, Shariati M, Brugler S, Fu J, White DJ. Effect of an anticalculus dentifrice on lesion progression under pH cycling conditions in vitro. Caries Res. 1988; 22:337–341.
Article
19. ten Cate JM, Timmer K, Shariati M, Featherstone JDB. Effect of timing of fluoride treatment on enamel de- and remineralization in vitro:A pH cycling. Caries Res. 1988; 22:20–26.
Article
20. Hong SJ, Park KC, Stookey GK. Effect of fluoride dentifrices on subsurface enamel caries. J Korean Acad Dent Health. 1996; 20:1–10.
21. KIMS Medicine Information Center. [internet]. cited 2006. Feb. 02. Available from: http://kimsonline.co.kr/drugsearch/result_form_print.asp?bi=2536&mpi=7192.
22. Oh KT, Choo SU, Kim KM, Kim KN. A stainless steel bracket for orthodontic application. Eur J Orthod. 2005; 27:237–244.
Article
23. Van Eygen I, Bart VV, Henrich W. Influence of a soft drink with low pH on enamel surfaces: An in vitro study. Am J Orthod Dentofacial Orthop. 2005; 128:372–327.
24. White DJ. Reactivity of fluoride dentifrices with artificial caries. II. Effects on subsurface lesions: F uptake, F distribution, surface hardening and remineralization. Caries Res. 1988; 22:27–36.
Article
25. Christoffersen J, Arends J. Progress of artificial carious lesions in enamel. Caries Res. 1982; 16:433–439.
Article
26. Bakaletz LO. Developing animal models for polymicrobial diseases. Nat Rev Microbiol. 2004; 2:552–568.
Article
27. Edgar WM, O'Mullane DM. Saliva and oral health. 2nd Ed. British Dental J London;1996. p. 27–41. p. 43–66.
28. Park KC. Prospective preventive dentistry. Seoul: Jungmunkag;1997. p. 161–166.
29. Margolis HC, Moreno EC, Murphy BJ. Effects of low levels of fluoride in solution on enamel demineralization in vitro. J Dent Res. 1986; 65:23–29.
Article
30. Featherstone JDB, Duncan JF, Cutress TW. A mechanism for dental caries based on chemical processes and diffusion phenomena during in vitro caries simulation on human tooth enamel. Arch oral Biol. 1979; 24:101–112.
Article
31. Moreno EC, Zahradnik RT. Chemistry of enamel subsurface demineralization in vitro. J Dent Res. 1974; 53:226–235. sup. 2.
Article
32. Theuns HM, van Dijk JWE, Driessens FCM, Groeneveld A. Effect of time, degree of saturation, pH and acid, concentration of buffer solutions on the rate of in vitro demineralization of human enamel. Arch oral Biol. 1985; 30:37–42.
Article
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