
Remineralization is a natural process and does not have to involve fluoride.
Tooth remineralization is the natural repair process for non-cavitated tooth lesions,[1][2] in which calcium, phosphate and sometimes fluoride ions are deposited into crystal voids in demineralized enamel. Remineralization can contribute towards restoring strength and function within tooth structure.[3]
Demineralization is the removal of minerals (mainly calcium) from any of the hard tissues: enamel, dentine, and cementum.[4] It begins at the surface, and may progress into either cavitation (tooth decay) or erosion (tooth wear). Tooth decay demineralization is caused by acids from bacteria in the dental plaque biofilm whilst tooth wear is caused by acids from non-bacterial sources. These can be extrinsic in source, such as carbonated drinks, or intrinsic acids, usually from stomach acid coming into the mouth. Both types of demineralization will progress if the acid attacks continue unless arrested or reversed by remineralization.[5][6]
Tooth decay process
When food or drinks containing fermentable sugars enter the mouth, the bacteria in dental plaque rapidly feed on the sugars and produce organic acids as by-products.[1] The glucose produced from starch by salivary amylase is also digested by the bacteria. When enough acid is produced so that the pH goes below 5.5, the acid dissolves carbonated hydroxyapatite, the main component of tooth enamel.[7][8] However, the pH threshold for dissolving dentin ranges from 6.2 to 6.4.[9][10][11] The plaque can hold the acids in contact with the tooth for up to two hours, before it is neutralized by saliva. Once the plaque acid has been neutralized, the minerals can return from the plaque and saliva to the enamel surface.
However, the capacity for remineralization is limited, and if sugars enter the mouth too frequently then a net loss of minerals from enamel produces a cavity, through which bacteria can infect the inner tooth and destroy the latticework. This process requires many months or years.[12][4]
Natural tooth remineralization
Role of saliva
Remineralization occurs on a daily basis after attack by acids from food, through the presence of calcium, phosphate and fluoride found in saliva.[13][14] Saliva, a bodily fluid important in the maintenance of tooth integrity, acts as a natural buffer to neutralize acid, preventing demineralization in the first place.[4] If there is reduced saliva flow or reduced saliva quality, this will increase the risk of demineralization and create the need for treatment in order to prevent demineralization progression.[4]
As the demineralization process continues, the pH of the mouth becomes more acidic, which promotes the development of cavities. Dissolved minerals then diffuse out of the tooth structure and into the saliva surrounding the tooth. The buffering capacity of saliva greatly impacts the pH of plaque surrounding the enamel, thereby inhibiting tooth decay progression. Plaque thickness and the number of bacteria present determine the effectiveness of salivary buffers.[4] The high salivary concentrations of calcium and phosphate which are maintained by salivary proteins may account for the development and remineralization of enamel. The presence of fluoride in saliva speeds up crystal precipitation forming a fluorapatite-like coating which will be more resistant to decay.[4]
Treatment and prevention

Besides professional dental care, there are other ways for promoting tooth remineralization.
Fluoride
Fluoride therapy
Fluoride is a mineral found naturally in rock, air, soil, plants and water. It promotes remineralization through reparing white spot lesions (caused by acid) on the surface of enamel that may develop into cavities.[15] Fluoride therapy is often used to promote remineralization. This produces the stronger and more acid-resistant fluorapatite, rather than the natural hydroxyapatite. Both materials are made of calcium. In fluorapatite, fluoride takes the place of a hydroxide.[16] There are multiple methods of administering fluoride, including fluoridated toothpaste, fluoridated water, and fluoride varnishes. Regular use of a fluoridated toothpaste has been shown to provide a significant source of fluoride to the mouth by the means of direct fluoride contact to tooth structure.[4][17] The types of fluoride added to toothpaste include sodium fluoride, sodium monofluorophosphate (MFP), and stannous fluoride.[18][19] Similarly, community water fluoridation is the addition of fluoride in the drinking water with the aim of reducing tooth decay by adjusting the natural fluoride concentration of water to that recommended for improving oral health. Fluoride varnishes were developed late 1960s and early 1970s and since then they have been used both as a preventative agent in public health programs and as a specific treatment for patients at risk of tooth decay by the 1980s, mostly in European countries.[17] Fluoride varnishes are a concentrated topical fluoride containing 5% sodium fluoride (NaF) except the Fluor protector which contains difluorosilane.[17] Fluoride varnishes were developed primarily to overcome their shortcoming which is to prolong the contact time between fluoride and tooth surfaces.[17]
A reduction in cavities may result in the following downstream benefits:
- Protects children and adults against tooth decay and cavities[20][21][22][23]
- Helps prevent premature tooth loss of baby teeth due to decay and overall assists in guiding the adult teeth to correct tooth eruption
- Aids in the prevention of invasive dental treatment therefore reducing the amount of money spent on dental treatment
- Provides an overall community advantage, especially individuals from low socioeconomic communities, who have less access to other forms of fluoride treatments
Nano-Hydroxyapatite
Another remineralizing agent used widely in toothpastes and other oral care products is synthetic nano-hydroxyapatite, a calcium phosphate mineral almost identical to the natural hydroxyapatite that forms the substance of teeth. Roughly 97% of tooth enamel and 70% of dentin consists of hydroxyapatite at a nanoparticle scale.[24][25] At the nanoparticle scale, it supports the role of saliva by supplying mineral to fill and repair microfissures on the enamel surface and to remineralize incipient lesions, i.e. areas below the surface that have become demineralized by the action of acids from sources such as dental plaque, carbonated beverages and food.[26]
Nano-hydroxyapatite was first developed for use in toothpastes in Japan in the 1980s. It was approved as an anti-decay agent by the Japanese government in 1993 on the basis of laboratory testing and field trials in Japanese schools.[27] The first nano-hydroxyapatite toothpastes began appearing in Europe in the early 2000s,[28] and its use in oral care products has now spread worldwide both as an anti-decay and anti-hypersensitivity agent.[29][30][31]
Plaque control
Oral hygiene practices involve the mechanical removal of plaque from hard tissue surfaces.[32] Cariogenic bacteria levels in the plaque greatly affect the development of tooth decay, therefore, effective removal of plaque is paramount to inhibit the demineralization of teeth.[33]
Diet
Demineralization is, in part, caused by bacteria excreting acids as a product of their metabolism of carbohydrates. Thus, by reducing the intake frequency of carbohydrates (most notably sugar) in an individual's diet, remineralization is increased. This disturbance of demineralization caused by the presence of fermentable carbohydrates continues until the saliva has returned to a normal pH and had sufficient time to penetrate and neutralize the acids within any cariogenic biofilm present.[34]
Recent studies on diet and tooth decay have been confounded by the widespread use of fluoride toothpastes. While some studies have argued that with greater exposure to fluoride, the relationship between sugar consumption and decay relationship may be weaker, as fluoride raises the threshold of sugar intake at which decay progresses to cavitation. However, other studies have found that despite the widespread use of fluorides, that a significant relationship between sugars and decay.[35][36]
Sugar alcohols
Xylitol is a naturally-occurring sugar alcohol that is commonly used as a sweetener in various products, including chewing gums and lozenges.[14] Xylitol inhibits acid production by oral bacteria and promotes remineralization of the teeth.[14] Xylitol has been found to reduce the amount of Streptococcus mutans in plaque and saliva and their binding to the acquired enamel pellicle, leading to a decrease in bacteria acid production.[14] In addition, chewing gum with xylitol will stimulate increased salivary flow which in turn increases the amount of calcium in the saliva and enhances the oral clearance. Furthermore, there is some evidence that erythritol may have greater protective action against demineralization compared to other sugar alcohols.[37]
Biomimetic glass and ceramics
Biomimetic glass and ceramic particles, including amorphous calcium sodium phosphosilicate (Bioglass 45S5; known commercially as NovaMin) and amorphous calcium phosphate (ACP; known commercially as Recaldent), are used in some toothpastes and topical preparations to promote remineralization of teeth.[38] These particles have a structure mimicking hydroxyapatite, providing new sites for mineralization to occur.[39] Their binding to the teeth also occludes open dentin tubules, helping to reduce dentin hypersensitivity. There is insufficient evidence for their efficiency but the evidence for Bioglass 45S5 is stronger than that for ACP.[38][40]
Oligopeptide P11-4
P11-4 (known commercially as Curolox) is a synthetic, pH controlled self-assembling β-peptide used for biomimetic mineralization.[41] It builds a 3-D bio-matrix with binding sites for calcium ions serving as nucleation point for hydroxyapatite formation. It has a high affinity to tooth mineral[42] and binds directly as matrix to the tooth mineral and forms a stable layer on the teeth.[43] However, the remineralization activity is significantly reduced in comparison with a fluoride treatment alone.[44]
See also
References
- Featherstone, J. D. B. (2008). "Dental caries: A dynamic disease process". Australian Dental Journal. 53 (3): 286–291. doi:10.1111/j.1834-7819.2008.00064.x. PMID 18782377.
- Fejerskov, O., Nyvad, Bente, & Kidd, Edwina A. M. (2015). Dental caries: The disease and its clinical management (Third ed.),
- Cochrane NJ, Cai F, Huq NL, Burrow MF, Reynolds EC. New approaches to enhanced remineralization of tooth enamel. Journal of Dental Research. 2010 Nov 1;89(11):1187-97.
- Li, Xiaoke; Wang, Jinfang; Joiner, Andrew; Chang, Jiang (2014). "The remineralization of enamel: a review of the literature". Journal of Dentistry. 42: S12–S20. doi:10.1016/s0300-5712(14)50003-6. PMID 24993850.
- Garcia- Godoy, F. & Hicks, J. (2008). Maintaining the integrity of the enamel surface. American Dental Association, 139(3).
- Hicks J, Garcia-Godoy F, Flaitz C. Biological factors in dental caries: role of saliva and dental plaque in the dynamic process of demineralization and remineralization (part 1). Journal of Clinical Pediatric Dentistry. 2004 Sep 1;28(1):47-52.
- Fejerskov O, Nyvad B, Kidd EA: Pathology of dental caries; in Fejerskov O, Kidd EAM (eds): Dental caries: The disease and its clinical management. Oxford, Blackwell Munksgaard, 2008, vol 2, pp 20-48.
- Nunn, June H.; Ng, Salina K.F.; Sharkey, Ian; Coulthard, Malcolm (2001). "The dental implications of chronic use of acidic medicines in medically compromised children". Pharmacy World and Science. 23 (3): 118–119. doi:10.1023/A:1011202409386. PMID 11468877. Retrieved 2025-06-11.
the critical pH of 5.5 at which enamel demineralisation takes place.
- Xu, Grace Yuchan; Zhao, Irene Shuping; Lung, Christie Ying Kei; Yin, Iris Xiaoxue; Lo, Edward Chin Man; Chu, Chun Hung (2024). "Frontiers of Global Research Trend on Root Caries: A Bibliometric Analysis". International Dental Journal. 74 (6): 1197–1204. doi:10.1016/j.identj.2024.06.007. PMC 11551568. PMID 39003120.
Dentine and cementum have lower mineral contents than enamel. The demineralization threshold pH value for dentin (6.2-6.4) is higher compared to enamel (5.5).
- Sung, Young-Hye; Son, Ho-Hyun; Yi, Keewook; Chang, Juhea (2016). "Elemental analysis of caries-affected root dentin and artificially demineralized dentin" (PDF). Restorative Dentistry & Endodontics. 41 (4): 255–261. doi:10.5395/rde.2016.41.4.255. ISSN 2234-7658. PMC 5107426. PMID 27847746. Retrieved 2025-06-11.
- Bachand, William R. (2022-09-26). "The Delicate Balance of Remineralization and Demineralization". Decisions in Dentistry. Retrieved 2025-06-11.
- Soi S, Roy AS, Vinayak V. Fluorides and Their Role in Demineralization and Remineralization. Principal's Message.:19.
- Nanci, A., & Ten Cate, A. (2008). Ten Cate's oral histology. St. Louis, Mo.: Mosby Elsevier.
- García-Godoy, Franklin; Hicks, M. John (2008-05-01). "Maintaining the integrity of the enamel surface: The role of dental biofilm, saliva and preventive agents in enamel demineralization and remineralization". The Journal of the American Dental Association. 139, Supplement 2: 25S–34S. doi:10.14219/jada.archive.2008.0352. PMID 18460677.
- "Ask the Expert: Why is fluoride good for dental health? | National Institute of Dental and Craniofacial Research". www.nidcr.nih.gov. Retrieved 2026-05-21.
- Better health channel. "Dental care - fluoride", April 2012. retrieved on 2016-04-15.
- Beltrán-Aguilar; Goldstein; Lockwood (2000). "Fluoride Varnishes: A Review of Their Clinical Use, Cariostatic Mechanism, Efficacy and Safety: A Review of Their Clinical Use, Cariostatic Mechanism, Efficacy and Safety". The Journal of the American Dental Association. 131 (5): 589–596. doi:10.14219/jada.archive.2000.0232. PMID 10832252.
- Wiegand, A; Bichsel, D; Magalhães, AC; Becker, K; Attin, T (Aug 2009). "Effect of sodium, amine and stannous fluoride at the same concentration and different pH on in vitro erosion" (PDF). Journal of Dentistry. 37 (8): 591–5. doi:10.1016/j.jdent.2009.03.020. PMID 19403228.
- Talwar M, Borzabadi-Farahani A, Lynch E, Borsboom P, Ruben J (2019). "Remineralization of Demineralized Enamel and Dentine Using 3 Dentifrices-An InVitro Study". Dent J. 7(3):91 (3): 91. doi:10.3390/dj7030091. PMC 6784461. PMID 31480726.
- Ten Cate, J. M. (2013). "Contemporary perspective on the use of fluoride products in caries prevention". British Dental Journal. 214 (4): 161–167. doi:10.1038/sj.bdj.2013.162. PMID 23429124.
- Hellwig, E.; Lennon, Á. M. (2004). "Systemic versus Topical Fluoride". Caries Research. 38 (3): 258–262. doi:10.1159/000077764. PMID 15153698.
- Aoba, T.; Fejerskov, O. (2002). "Dental Fluorosis: Chemistry and Biology". Critical Reviews in Oral Biology & Medicine. 13 (2): 155–70. doi:10.1177/154411130201300206. PMID 12097358.
- Dr RS Levine. "The British Fluoridation Society", A guide to the action of fluoride in the prevention of dental decay, 2016. retrieved on 2016-05-3.
- Dorozhkin SV, Epple M. Biological and medical significance of calcium phosphates. Angewandte Chemie International Edition 2002, 41:3030-46
- Cui FZ, Ge J. New observations of the hierarchical structure of human enamel, from nanoscale to microscale. Journal of Tissue Engineering and Regenerative Medicine 2007, 1:185-91
- Najibfard K, et al. Remineralization of Early Caries by a Nano-Hydroxyapatite Dentifrice. Journal of Clinical Dentistry, 2011. Vol22(5): 139-143
- Kani T, Kani M. Isozaki A, Shintani A, Ohashi T, Tokumoto T. Effect of apatite-containing dentifrices on dental caries in school children. Journal of Dental Health 1989, 39(1):104-9
- Pepla E, et al. Nano-hydroxyapatite and its application in preventative, restorative and regenerative dentistry: a review of the literature. Annali di Stomatologie 2014, (V)3:10,8-14
- Pawinska M, et al. Clinical evidence of caries prevention by hydroxyapatite; An updated systematic review and meta-analysis. Journal of Dentistry, 2024. doi.org/10.1016/j.dent.2024.105429
- Limeback H, et al. Clinical Evidence of Biomimetic Hydroxyapatite in Oral Care Products for Reducing Dentin Hypersensitivity: An Updated Systematic Review and Meta-Analysis. Biomimetics 2023. doi.org/10.3390/biomimetics8010023
- Meyer F, Enax J. Hydroxyapatite in Oral Biofilm Management. European Journal of Dentistry, 2019. 13:287-290
- Darby ML, Walsh M. Dental hygiene: theory and practice. Elsevier Health Sciences; 2014 Apr 15.
- Hicks, John; Garcia-Godoy, Franklin; Flaitz, Catherine (2003-01-01). "Biological factors in dental caries: role of saliva and dental plaque in the dynamic process of demineralization and remineralization (part 1)". The Journal of Clinical Pediatric Dentistry. 28 (1): 47–52. doi:10.17796/jcpd.28.1.yg6m443046k50u20 (inactive 8 August 2025). ISSN 1053-4628. PMID 14604142.
{{cite journal}}: CS1 maint: DOI inactive as of August 2025 (link) - Arathi Rao, Neeraj Malhotra. "The Role of Remineralizing Agents in dentistry: A Review". Volume 32, Number 6. 2011. retrieved on 2016-05-22.
- Cury, J; Tenuta, L (24 Jan 2014). "Evidence-based recommendation on toothpaste use". Brazilian Oral Research. 28: 1–7. doi:10.1590/S1806-83242014.50000001. PMID 24554097.
- "Eating habits for a healthy smile and body" (PDF). The Journal of the American Dental Association. 141 (12): 1544. Jan–Feb 2011. doi:10.14219/jada.archive.2010.0115. PMID 21119136. Retrieved 22 May 2016.
- de Cock, Peter (21 August 2016). "Erythritol Is More Effective Than Xylitol and Sorbitol in Managing Oral Health Endpoints". International Journal of Dentistry. 2016 9868421. doi:10.1155/2016/9868421. PMC 5011233. PMID 27635141.
- Zhu, M; Li, J; Chen, B; Mei, L; Yao, L; Tian, J; Li, H (2015). "The Effect of Calcium Sodium Phosphosilicate on Dentin Hypersensitivity: A Systematic Review and Meta-Analysis". PLOS ONE. 10 (11) e0140176. Bibcode:2015PLoSO..1040176Z. doi:10.1371/journal.pone.0140176. PMC 4636152. PMID 26544035.
- Van Haywood, B (2002). "Dentine hypersensitivity: bleaching and restorative considerations for successful management". International Dental Journal. 52 (5): 376–384. doi:10.1002/j.1875-595x.2002.tb00937.x. S2CID 72558772.
- Hani, Thikrayat Bani; O'Connell, Anne C.; Duane, Brett (24 June 2016). "Casein phosphopeptide-amorphous calcium phosphate products in caries prevention". Evidence-Based Dentistry. 17 (2): 46–47. doi:10.1038/sj.ebd.6401168. PMID 27339237. S2CID 10479902.
- Brunton, P.A.; Davies, R.P.W. (2 July 2013). "Treatment of early caries lesions using biomimetic self-assembling-peptides – a clinical safety trial". Br Dent J. 215 (E6): E6. doi:10.1038/sj.bdj.2013.741. PMC 3813405. PMID 23969679.
- Kirkham, J; et al. (May 2007). "Self-assembling Peptide Scaffolds Promote Enamel Remineralization". J Dent Res. 86 (5): 426–430. doi:10.1177/154405910708600507. PMID 17452562. S2CID 21582771.
- Chen, X; et al. (Sep 2014). "Dentine Tubule Occlusion of a Novel Self-n Vitro Evaluation of Dentine Remineralization by a Self-Assembling Peptide Using Scanning Electron Microscopy". Caries Res. 48: 402. doi:10.1159/000360836. Retrieved 1 July 2015.
- Alkilzy, M; et al. (May 15, 2015). "Efficacy, Clinical Applicability and Safety, of CurodontTM Repair in Children with Early Occlusal Caries". Caries Res. 49: 311. doi:10.1159/000381323. S2CID 79016534.
Further reading
- Chow, L. (2010). "Diffusion of Ions Between Two Solutions Saturated With Respect to Hydroxyapatite: A Possible Mechanism for Subsurface Demineralization of Teeth" (PDF). Journal of Research of the National Institute of Standards and Technology. 115 (4). National Institute of Science and Technology: 217–224. doi:10.6028/jres.115.015. PMC 2966276. PMID 21037801.