# Dental Erosion Management: From Remineralization to Emerging Regenerative Approaches—A Narrative Review

**Authors:** Ruvienath Daham Weerasinghe Rajapaksa, Yu-Ching Wang, Yong Chen Chin, Kevin Jang, Abdala Abdal-hay, Sašo Ivanovski, Sandleen Feroz

PMC · DOI: 10.3390/biomimetics11020107 · Biomimetics · 2026-02-03

## TL;DR

This review discusses the causes and modern treatments for dental erosion, from mineral restoration to regenerative techniques like stem cells and 3D bioprinting.

## Contribution

The paper highlights emerging regenerative approaches for dental erosion, moving beyond traditional remineralization methods.

## Key findings

- Fluoride and calcium phosphate-based agents like CPP-ACP and HAP are effective for remineralization.
- Laser-assisted and electrically enhanced methods show promise in accelerating mineral restoration.
- Regenerative strategies such as 3D bioprinting and CRISPR are being explored to biologically restore tooth structure.

## Abstract

Dental erosion has emerged as a significant modern oral health problem, characterized by the chemical dissolution of tooth structure resulting from frequent exposure to intrinsic or extrinsic acids. With a high global prevalence ranging from 30% to 50% in children and 20% to 40% in adults, its management is a clinical priority to prevent long-term complications like dentine hypersensitivity and functional impairment. This review outlines the multifactorial etiology of erosion, encompassing dietary acids, gastroesophageal reflux, and reduced salivary flow. The historical context of oral care is explored, leading to a discussion on contemporary management strategies centered on remineralization. Fluoride ions play a crucial role by inhibiting demineralization, facilitating the formation of acid-resistant fluorapatite, and exerting antibacterial effects. A major focus is placed on advanced biomimetic, calcium phosphate-based topical agents such as Casein Phosphopeptide–Amorphous Calcium Phosphate (CPP-ACP), functionalized Tricalcium Phosphate (fTCP), and Hydroxyapatite (HAP), which effectively replenish lost minerals. The review further explores innovative methods, such as laser-assisted and electrically enhanced remineralization. Finally, it outlines next-generation regenerative strategies, including self-assembling peptides (P11-4), stem cell therapies, 3D bioprinting, and gene-editing (CRISPR) technologies, which aim to biologically regenerate lost enamel and dentine. The field is rapidly evolving from a preventive to a restorative paradigm, with future directions focusing on biologically based, minimally invasive therapies to fully restore tooth structure and function.

## Linked entities

- **Chemicals:** fluoride (PubChem CID 28179), Tricalcium Phosphate (PubChem CID 24456), Hydroxyapatite (PubChem CID 14781)

## Full-text entities

- **Genes:** BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, NTF3 (neurotrophin 3) [NCBI Gene 4908] {aka HDNF, NGF-2, NGF2, NT-3, NT3}, BMP7 (bone morphogenetic protein 7) [NCBI Gene 655] {aka OP-1}, SCGB1A1 (secretoglobin family 1A member 1) [NCBI Gene 7356] {aka CC10, CC16, CCPBP, CCSP, UGB, UP-1}, BMP2 (bone morphogenetic protein 2) [NCBI Gene 650] {aka BDA2, BMP2A, SSFSC, SSFSC1}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}
- **Diseases:** abrasion (MESH:D065306), functional impairment (MESH:D003072), eating disorders (MESH:D001068), dental disease (MESH:D009057), Dental Erosion (MESH:D014077), dehydration (MESH:D003681), caries (MESH:D003731), dentine hypersensitivity (MESH:D003807), tumorigenic (MESH:D002471), tooth discoloration (MESH:D014075), Tooth Wear (MESH:D057085), vomiting (MESH:D014839), cavitated lesions (MESH:D009059), fluorosis (MESH:D009050), calculus (MESH:D002137), SDF (MESH:D005458), injury to (MESH:D014947), GERD (MESH:D005764), inflammation (MESH:D007249), tooth surface loss (MESH:D016388), enamel loss (MESH:D003744)
- **Chemicals:** Pyrophosphates (MESH:D011756), CPP (MESH:C014896), hydrogen (MESH:D006859), SHMP (MESH:C009285), xylitol (MESH:D014993), Calcium (MESH:D002118), APF (MESH:D000149), carbon dioxide (MESH:D002245), lipids (MESH:D008055), Pyrophosphate (MESH:C107241), tetrasodium pyrophosphate (MESH:C003319), HF (MESH:D006195), OH- (MESH:C031356), titanium (MESH:D014025), Calcium Lactate (MESH:C110051), Cl (MESH:D002713), HA (MESH:D017886), arginine (MESH:D001120), TiF4 (MESH:C032240), CPP-ACP (-), ACP (MESH:C519480), Sodium Phosphate (MESH:C018279), STMP (MESH:C009293), iron oxide (MESH:C000499), Calcium Phosphate (MESH:C020243), silver (MESH:D012834), Stannous fluoride (MESH:D014002), AgCl (MESH:C037548), vitamin C (MESH:D001205), tin (MESH:D014001), polyphosphate (MESH:D011122), hydroxyl (MESH:D017665), aspirin (MESH:D001241), TCP (MESH:C018392), water (MESH:D014867), apatite (MESH:D001031), gluconate (MESH:C030691), F , (MESH:D005461), beta-tricalcium phosphate (MESH:C485817), CaF2 (MESH:D002124), SDF (MESH:C024633), NaF (MESH:D012969), Fluoride (MESH:D005459), fumaric acid (MESH:C032005), Calcium silicate (MESH:C031293), metal (MESH:D008670), carbonate (MESH:D002254), silicate (MESH:D017640), Fluoroapatite (MESH:C025105), acid (MESH:D000143), phosphorus (MESH:D010758), inorganic phosphate (MESH:D010710), oxygen (MESH:D010100)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937671/full.md

## References

157 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937671/full.md

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Source: https://tomesphere.com/paper/PMC12937671