Mechanisms of Bioactive Glass on Caries Management: A Review
Abstract
:1. Introduction
2. Materials and Methods
2.1. Searching Strategy
2.2. Study Inclusion and Exclusion
2.2.1. Inclusion Criteria:
- Laboratory studies
- Studies related to the antimicrobial effect of bioactive glass
- Studies on the remineralization effect of bioactive glass on dental hard tissues (enamel and dentine)
2.2.2. Exclusion Criteria:
- Studies on root canal therapy and pulp regeneration
- Studies on periodontal disease
- Studies on orthodontic treatment
- Studies on tissue engineering
- Studies on bioactive composites or other bioactive materials
3. Results
3.1. Effect of Bioactive Glass on Cariogenic Bacteria
3.2. Effect of Bioactive Glass on the Mineral Content of Enamel and Dentine
3.3. Effect of Bioactive Glass on the Organic Content of Dentine
4. Discussion
5. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
- Kutsch, V.K. Dental caries: An updated medical model of risk assessment. J. Prosthet. Dent. 2014, 111, 280–285. [Google Scholar] [CrossRef] [PubMed]
- Pitts, N.B.; Zero, D.T.; Marsh, P.D.; Ekstrand, K.; Weintraub, J.A.; Ramos-Gomez, F.; Tagami, J.; Twetman, S.; Tsakos, G.; Ismail, A. Dental caries. Nat. Rev. Dis. Primers 2017, 3, 17030. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wong, A.; Subar, P.E.; Young, D.A. Dental Caries: An Update on Dental Trends and Therapy. Adv. Pediatr. 2017, 64, 307–330. [Google Scholar] [CrossRef] [PubMed]
- Schwendicke, F.; Frencken, J.E.; Bjorndal, L.; Maltz, M.; Manton, D.J.; Ricketts, D.; Van Landuyt, K.; Banerjee, A.; Campus, G.; Domejean, S.; et al. Managing Carious Lesions: Consensus Recommendations on Carious Tissue Removal. Adv. Dent. Res. 2016, 28, 58–67. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gonzalez-Cabezas, C.; Fernandez, C.E. Recent Advances in Remineralization Therapies for Caries Lesions. Adv. Dent. Res. 2018, 29, 55–59. [Google Scholar] [CrossRef] [PubMed]
- Walsh, T.; Oliveira-Neto, J.M.; Moore, D. Chlorhexidine treatment for the prevention of dental caries in children and adolescents. Cochrane Database Syst. Rev. 2015, CD008457. [Google Scholar] [CrossRef]
- Jefferies, S.R. Bioactive and biomimetic restorative materials: A comprehensive review. Part I. J. Esthet. Restor. Dent. Off. Publ. Am. Acad. Esthet. Dent. 2014, 26, 14–26. [Google Scholar] [CrossRef]
- Jones, J.R. Review of bioactive glass: From Hench to hybrids. Acta Biomater. 2013, 9, 4457–4486. [Google Scholar] [CrossRef]
- Ali, S.; Farooq, I.; Iqbal, K. A review of the effect of various ions on the properties and the clinical applications of novel bioactive glasses in medicine and dentistry. Saudi Dent. J. 2014, 26, 1–5. [Google Scholar] [CrossRef] [Green Version]
- Hench, L.L. The story of Bioglass. J. Mater. Sci. Mater. Med. 2006, 17, 967–978. [Google Scholar] [CrossRef]
- Izquierdo-Barba, I.; Salinas, A.J.; Vallet-Regi, M. Bioactive Glasses: From Macro to Nano. Int. J. Appl. Glass Sci. 2013, 4, 149–161. [Google Scholar] [CrossRef]
- Shivaprasad, B.M.; Padmavati, P.; Nehal, N.S. Chair Side Application of NovaMin for the Treatment of Dentinal Hypersensitivity—A Novel Technique. J. Clin. Diagn. Res. JCDR 2014, 8, Zc05-8. [Google Scholar]
- Burwell, A.; Jennings, D.; Muscle, D.; Greenspan, D.C. NovaMin and dentin hypersensitivity—In vitro evidence of efficacy. J. Clin. Dent. 2010, 21, 66–71. [Google Scholar] [PubMed]
- Fiume, E.; Barberi, J.; Verne, E.; Baino, F. Bioactive Glasses: From Parent 45S5 Composition to Scaffold-Assisted Tissue-Healing Therapies. J. Funct. Biomater. 2018, 9, 24. [Google Scholar] [CrossRef] [Green Version]
- Xu, Y.T.; Wu, Q.; Chen, Y.M.; Smales, R.J.; Shi, S.Y.; Wang, M.T. Antimicrobial effects of a bioactive glass combined with fluoride or triclosan on Streptococcus mutans biofilm. Arch. Oral Biol. 2015, 60, 1059–1065. [Google Scholar] [CrossRef]
- Martins, C.H.G.; Carvalho, T.C.; Souza, M.G.M.; Ravagnani, C.; Peitl, O.; Zanotto, E.D.; Panzeri, H.; Casemiro, L.A. Assessment of antimicrobial effect of Biosilicate against anaerobic, microaerophilic and facultative anaerobic microorganisms. J. Mater. Sci. Mater. Med. 2011, 22, 1439–1446. [Google Scholar] [CrossRef]
- Jung, J.H.; Kim, D.H.; Yoo, K.H.; Yoon, S.Y.; Kim, Y.; Bae, M.K.; Chung, J.; Ko, C.C.; Kwon, Y.H.; Kim, Y.I. Dentin sealing and antibacterial effects of silver-doped bioactive glass/mesoporous silica nanocomposite: An in vitro study. Clin. Oral Investig. 2018, 23, 253–266. [Google Scholar] [CrossRef]
- Siqueira, R.L.; Alves, P.F.S.; Moraes, T.D.; Casemiro, L.A.; da Silva, S.N.; Peitl, O.; Martins, C.H.G.; Zanotto, E.D. Cation-doped bioactive ceramics: In vitro bioactivity and effect against bacteria of the oral cavity. Ceram. Int. 2019, 45, 9231–9244. [Google Scholar] [CrossRef]
- Palaniswamy, U.K.; Prashar, N.; Kaushik, M.; Lakkam, S.R.; Arya, S.; Pebbeti, S. A comparative evaluation of remineralizing ability of bioactive glass and amorphous calcium phosphate casein phosphopeptide on early enamel lesion. Dent. Res. J. 2016, 13, 297–302. [Google Scholar] [CrossRef]
- Rajan, R.; Krishnan, R.; Bhaskaran, B.; Kumar, S.V. A Polarized Light Microscopic Study to Comparatively evaluate Four Remineralizing Agents on Enamel viz CPP-ACPF, ReminPro, SHY-NM and Colgate Strong Teeth. Int. J. Clin. Pediatr. Dent. 2015, 8, 42–47. [Google Scholar] [CrossRef]
- Soares, R.; De Ataide, I.N.; Fernandes, M.; Lambor, R. Assessment of Enamel Remineralisation After Treatment with Four Different Remineralising Agents: A Scanning Electron Microscopy (SEM) Study. J. Clin. Diagn. Res. JCDR 2017, 11, Zc136–zc141. [Google Scholar] [CrossRef] [PubMed]
- Ramashetty Prabhakar, A.; Arali, V. Comparison of the remineralizing effects of sodium fluoride and bioactive glass using bioerodible gel systems. J. Dent. Res. Dent. Clin. Dent. Prospects 2009, 3, 117–121. [Google Scholar] [PubMed]
- Chinelatti, M.A.; Tirapelli, C.; Corona, S.A.M.; Jasinevicius, R.G.; Peitl, O.; Zanotto, E.D.; Pires-de-Souza, F.C.P. Effect of a Bioactive Glass Ceramic on the Control of Enamel and Dentin Erosion Lesions. Braz. Dent. J. 2017, 28, 489–497. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Milly, H.; Festy, F.; Watson, T.F.; Thompson, I.; Banerjee, A. Enamel white spot lesions can remineralise using bio-active glass and polyacrylic acid-modified bio-active glass powders. J. Dent. 2014, 42, 158–166. [Google Scholar] [CrossRef] [PubMed]
- Bakry, A.S.; Takahashi, H.; Otsuki, M.; Tagami, J. Evaluation of new treatment for incipient enamel demineralization using 45S5 bioglass. Dent. Mater. 2014, 30, 314–320. [Google Scholar] [CrossRef]
- Zhang, J.; Boyes, V.; Festy, F.; Lynch, R.J.M.; Watson, T.F.; Banerjee, A. In-vitro subsurface remineralisation of artificial enamel white spot lesions pre-treated with chitosan. Dent. Mater. Off. Publ. Acad. Dent. Mater. 2018, 34, 1154–1167. [Google Scholar] [CrossRef] [Green Version]
- Narayana, S.S.; Deepa, V.K.; Ahamed, S.; Sathish, E.S.; Meyappan, R.; Satheesh Kumar, K.S. Remineralization efficiency of bioactive glass on artificially induced carious lesion an in-vitro study. J. Ind. Soc. Pedodon. Prevent. Dent. 2014, 32, 19–25. [Google Scholar]
- Mehta, A.B.; Kumari, V.; Jose, R.; Izadikhah, V. Remineralization potential of bioactive glass and casein phosphopeptide-amorphous calcium phosphate on initial carious lesion: An in-vitro pH-cycling study. J. Conserv. Dent. JCD 2014, 17, 3–7. [Google Scholar] [CrossRef]
- El-Wassefy, N.A. Remineralizing effect of cold plasma and/or bioglass on demineralized enamel. Dent. Mater. J. 2017, 36, 157–167. [Google Scholar] [CrossRef] [Green Version]
- Zhang, J.; Lynch, R.J.M.; Watson, T.F.; Banerjee, A. Chitosan-bioglass complexes promote subsurface remineralisation of incipient human carious enamel lesions. J. Dent. 2019, 84, 67–75. [Google Scholar] [CrossRef] [Green Version]
- Sleibi, A.; Tappuni, A.R.; Davis, G.R.; Anderson, P.; Baysan, A. Comparison of efficacy of dental varnish containing fluoride either with CPP-ACP or bioglass on root caries: Ex vivo study. J. Dent. 2018, 73, 91–96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sauro, S.; Thompson, I.; Watson, T.F. Effects of common dental materials used in preventive or operative dentistry on dentin permeability and remineralization. Oper. Dent. 2011, 36, 222–230. [Google Scholar] [CrossRef] [PubMed]
- Saffarpour, M.; Mohammadi, M.; Tahriri, M.; Zakerzadeh, A. Efficacy of Modified Bioactive Glass for Dentin Remineralization and Obstruction of Dentinal Tubules. J. Dent. 2017, 14, 212–222. [Google Scholar]
- Forsback, A.P.; Areva, S.; Salonen, J.I. Mineralization of dentin induced by treatment with bioactive glass S53P4 in vitro. Acta Odontol. Scand. 2004, 62, 14–20. [Google Scholar] [CrossRef]
- Vollenweider, M.; Brunner, T.J.; Knecht, S.; Grass, R.N.; Zehnder, M.; Imfeld, T.; Stark, W.J. Remineralization of human dentin using ultrafine bioactive glass particles. Acta Biomater. 2007, 3, 936–943. [Google Scholar] [CrossRef]
- Santos Cardoso, O.; Coelho Ferreira, M.; Moreno Carvalho, E.; Campos Ferreira, P.V.; Bauer, J.; Carvalho, C.N. Effect of Root Repair Materials and Bioactive Glasses on Microhardness of Dentin. Iran. Endod. J. 2018, 13, 337–341. [Google Scholar]
- Zhang, Y.; Wang, Z.; Jiang, T.; Wang, Y. Biomimetic regulation of dentine remineralization by amino acid in vitro. Dent. Mater. Off. Publ. Acad. Dent. Mater. 2019, 35, 298–309. [Google Scholar] [CrossRef]
- De Morais, R.C.; Silveira, R.E.; Chinelatti, M.; Geraldeli, S.; Pires-de-Souza, F.D.P. Bond strength of adhesive systems to sound and demineralized dentin treated with bioactive glass ceramic suspension. Clin. Oral Investig. 2018, 22, 1923–1931. [Google Scholar] [CrossRef]
- Ma, Q.; Wang, T.D.; Meng, Q.F.; Xu, X.; Wu, H.Y.; Xu, D.J.; Chen, Y.M. Comparison of in vitro dentinal tubule occluding efficacy of two different methods using a nano-scaled bioactive glass-containing desensitising agent. J. Dent. 2017, 60, 63–69. [Google Scholar] [CrossRef]
- Zhao, I.S.; Gao, S.S.; Hiraishi, N.; Burrow, M.F.; Duangthip, D.; Mei, M.L.; Lo, E.C.; Chu, C.H. Mechanisms of silver diamine fluoride on arresting caries: A literature review. Int. Dent. J. 2018, 68, 67–76. [Google Scholar] [CrossRef] [Green Version]
- Peng, J.J.; Botelho, M.G.; Matinlinna, J.P. Silver compounds used in dentistry for caries management: A review. J. Dent. 2012, 40, 531–541. [Google Scholar] [CrossRef] [PubMed]
- Buzalaf, M.A.R.; Pessan, J.P.; Honorio, H.M.; Ten Cate, J.M. Mechanisms of action of fluoride for caries control. Monogr. Oral. Sci. 2011, 22, 97–114. [Google Scholar] [PubMed]
- De Caluwe, T.; Vercruysse, C.W.J.; Declercq, H.A.; Schaubroeck, D.; Verbeeck, R.M.H.; Martens, L.C. Bioactivity and biocompatibility of two fluoride containing bioactive glasses for dental applications. Dent. Mater. 2016, 32, 1414–1428. [Google Scholar] [CrossRef] [PubMed]
- Daguano, J.; Milesi, M.T.B.; Rodas, A.C.D.; Weber, A.F.; Sarkis, J.E.S.; Hortellani, M.A.; Zanotto, E.D. In vitro biocompatibility of new bioactive lithia-silica glass-ceramics. Mater. Sci. Eng. C Mater. Biol. Appl. 2019, 94, 117–125. [Google Scholar] [CrossRef] [PubMed]
- Polini, A.; Bai, H.; Tomsia, A.P. Dental applications of nanostructured bioactive glass and its composites. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2013, 5, 399–410. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Author (Year) | Methods | Main Findings |
---|---|---|
Xu et al. (2015) [15] | MIC and MBC were determined to test the antibacterial effect of a bioactive glass against Streptococcus mutans. | The MBC and MIC of bioactive glass was 37.5 and 18.75 mg/mL, respectively. |
Martins et al. (2011) [16] | Three methods (agar diffusion, direct contact, and MIC) were used to determine the antibacterial effect of a bioactive glass-ceramic (Biosilicate) against a wide spectrum of bacteria. The assessed cariogenic species were Streptococcus mutans, Lactobacillus casei, Actinomyces naeslundii). | The MIC of Biosilicate ranged from ≤ 2.5 mg/mL to 20 mg/mL in different bacterial species. The best antibacterial effect of Biosilicate was against S. mutans (inhibition halo: 19.0 ± 2.0 mm) and S. mutans clinical isolate (MIC ≤ 2.5 mg/mL). |
Jung et al. (2018) [17] | Light absorbance was used to evaluate the antibacterial effect of silver-doped bioglass MSN against Lactobacillus casei. | The increasing density of silver-doped bioglass MSN induced reduction of light absorbance. It illustrated that bacterial growth was inhibited. |
Siqueira et al. (2019) [18] | Agar dilution method was used to determine the MIC values. The assessed cariogenic species were Streptococcus mutans and Lactobacillus casei. | Both the MIC of Bioglass and Biosilicate against S. mutans were 4mg/mL, which was the same as the MIC against L. casei. Bio-FP doped with different cations had different MIC against S. mutans and L. casei: Ag (8 and 4 mg/mL), Mg (2 and 4 mg/mL), Sr (2 and 4 mg/mL), Zn (2 and 4 mg/mL), Ga (2 and 4 mg/mL). |
Author (Year) | Methods | Main Findings |
---|---|---|
Palaniswamy et al. (2015) [19] | Demineralized enamel was treated with ACP-CPP and BAG, followed by microhardness test. BAG and ACP-CPP were applied on samples for 10 days in the first remineralization cycle and applied for another 5 days in the second remineralizing cycle. | Microhardness of dentine treated with ACP-CPP and BAG both increased but showed no significant difference between the 1st and 2nd remineralization cycles (BAG after 10 days: 346 ± 45; BAG after 15 days: 363 ± 65). |
Rajan et al. (2015) [20] | Demineralized teeth were allocated into five groups as follows: fluoridated toothpaste, CPP-ACPF, ReminPro, SHY-NM and control group. Micro-CT was used to measure lesion depth. | Lesion depth after remineralization in SHY-NM group showed the least mean score of 987 µm compared to other groups. |
Soares et al. (2017) [21] | Enamel samples with artificial lesions were treated with CPP-ACP, BAG, ReminPro, and self-assembling peptide. The recovery rate of microhardness was assessed. | Microhardness recovery rate of enamel treated with peptide was the highest (62.1%), followed by CPP-ACPF (48.4%) and BAG group (28.8%). |
Prabhakar et al. (2009) [22] | Teeth with artificial carious lesions were divided into 2 experimental groups (sodium fluoride films, bioactive glass films) and 2 control groups (control films placed interproximally and no treatment group). | Percentages of regain of lesion depth after remineralization in BAG were more in the experimental groups (NaF films: 67.7% ± 3.8%; and BAG films: 73.0% ± 3.0%) than those in the control groups (control film: 21.1% ± 3.3%; and no treatment: 30.7% ± 2.5%). |
Chinelatti et al. (2017) [23] | Artificial caries lesions were formed on enamel fragments and either treated with Biosilicate or acidulated phosphate fluoride (APF), or had no treatment (control), followed by microhardness test. | Biosilicate group had higher microhardness on enamel surface (265 ± 10 KHN) than APF and control group. CLSM also displayed shallower lesions in Biosilicate group when compared to APF and control group. |
Milly et al. (2013) [24] | Enamel samples with artificial WSLs were assigned to 4 groups: BAG slurry, PAA-BAG slurry, remin solution, and deionized water; the surface and cross-sectional microhardness of enamel was assessed. | BAG group illustrated the highest surface microhardness (138 ± 5 KHN), but there were no significant differences among the other groups. |
Bakry et al. (2014) [25] | Demineralized enamel specimens were divided into 4 groups: (1) no intervention, (2) only bioglass, (3) only brushing abrasion challenge, and (4) bioglass + brushing abrasion. After demineralizing and application of bioglass, all specimens were stored in remineralizing medium for 24 h, followed by removing the thin layer of bonding agent on bioglass in Groups 2 and 4, and then Groups 3 and 4 were sent to brushing abrasion challenge. | Hydroxyapatite was detected using XRD on the surface of enamel in Group 2 and Group 4 and these two groups also exhibited 100% coverage of crystalline structures on enamel surface. |
Zhang et al. (2018) [26] | Artificial enamel WSLs were assigned to BG slurry, BG+PAA, CS-BG, CS-BG+PAA, remin solution, and deionized water groups. Microhardness was assessed and the intensity of surface mineral content was measured by Raman intensity mapping. | Intensity increase in BG group was significantly greater when compared to those without BG. CS-BG+PAA group showed the highest microhardness (222 ± 38 KHN) of enamel surface. Other groups with BG also exhibited higher microhardness than the control group. |
Narayana et al. (2014) [27] | Enamels with artificial carious lesions were treated with bioactive glass, fluoride toothpaste, CPP-ACP, or CPP-ACPF and the control had no treatment. EDS was used to test the weight change of different elements. | BAG group showed significant difference when compared with control group for elements Ca and P. The mean weight percentage of Ca was 40.0% (BAG) and 31.1% (control), while the percentage of P was 14.0% (BAG) and 13.2% (control). |
Mehta et al. (2014) [28] | Enamel specimens were randomly distributed into two groups: BAG and CPP-ACP dentifrice. Vickers microhardness test was used. | Mean microhardness values were 372 VHN in BAG group and 357 VHN in CPP-ACP group afterremineralization, but the difference was not significant. |
EI-Wassefy et al. (2016) [29] | Demineralized enamels were treated with no treatment, fluoride varnish, cold plasma, bioglass paste, cold plasma + bioglass paste. Microhardness was assessed by Vickers hardness tester. | Microhardness of enamel surface become higher in PB groups (175 VHN and 221 VHN) when compared with bioglass groups (153 VHN and 201 VHN) at 30 and 50 µm depth, but with no significant difference between the two groups at 70–200 µm depth. |
Zhang et al. (2019) [30] | Enamel slabs with artificial WSL were assigned into 4 groups: bioglass (chitosan pre-treated lesions), chitosan-bioglass slurry, remin solution (PC), and deionized water (NC). Subsurface microhardness was assessed. | Mean hardness of bioglass group and chitosan–bioglass group were 56.7 ± 8.7 and 65.1 ± 8.9 KHN, which were significantly higher than those of NC group (12.7 ± 1.3 KHN) and PC group (18.6 ± 5.8 KHN). |
Author (Year) | Methods | Main Findings |
---|---|---|
Sleibi et al. (2018) [31] | Teeth with root caries were divided into 4 groups and treated with different agents (CPP-ACP+fluoride, bioglass+fluoride, fluoride only, no treatment). Severity index of root caries was evaluated through visual–tactile examinations. X-ray microtomography was used to measure mineral change. | The bioglass and fluoride group had the maximum reduction (100%) in severity index of root caries and it also had the highest percentage (60%) increase in mineral deposition. |
Rajan et al. (2015) [20] | Demineralized teeth were treated with fluoridated toothpaste, CPP-ACPF, ReminPro, SHY-NM (bioglass), and no treatment (negative control). Lesion depth was measured after application. | SHY-NM (bioglass) group showed the lowest mean lesion depth after remineralization procedure. |
Sauro et al. (2011) [32] | Dentine segments were treated with bioactive glass (Sylc), NaH C2O4 H2O, Cavitron Prophy Powder, EMS Perio, CPP-ACP, Colgate Sensitive Pro-Relief, NUPRO Solution Prophy Paste. Microhardness and EDX were evaluated. | The dentine surface hardness increased after treated with bioactive glass (Sylc). There was no significant change in Ca and P/O ratios. |
Saffarpour et al. (2017) [33] | Demineralized dentine discs were treated with 3 agents: bioactive glass (BG), BG modified with 5% strontium, BG modified with 10% strontium and followed by evaluation of morphology. | BG with 10% strontium showed highest rate of remineralization and completely occluded dentinal tubules. |
Forsback et al. (2004) [34] | Dentine discs were treated with bioactive glass S53P4 and control glass (CG). Weight loss of dentine discs was measured by weighing before and after remineralization. | Weight loss was less when discs were pretreated with BAG (21.0 ± 7.4 µg/mm2) than without BAG (49.1 ± 6.5 µg/mm2). |
Vollenweider et al. (2007) [35] | Demineralizing dentine bars were applied by nanometric bioactive glass (NBG) and PeriGlas (PG) suspension. SEM was used to observe the dentine surface. | Dentine specimens treated with NBG showed apatite depositions on the surface after 10 or 30 days. |
Jung et al. (2018) [17] | Demineralized dentine discs were divided into four groups: bioglass, MSN, silver-doped bioglass MSN, and no treatment, followed by acid resistance test. | Silver-doped bioglass MSN group had dentinal tubules completely occluded to a depth of 2–3 µm and the highest proportion (83.4% ± 7.5%) of occluded area after acid challenge. |
Cardoso et al. (2018) [36] | Root dentine slices were allocated into four groups: MTA, ERRM, Bioglass 45S5, and NbG. Microhardness was assessed. | Bioglass 45S5 group showed an increase in microhardness. |
Zhang et al. (2019) [37] | Dentine discs treated with EDTA were allocated to 4 groups: AS (artificial saliva), Asp, BAG, Asp-BAG, and followed by 6% citric acid challenge. The mineral matrix ratio was measured. | Compared to AS and Asp group, BAG group (17.8 ± 2.3) and Asp-BAG group (12.5 ± 2.3) had significantly higher mineral matrix area ratio. |
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Dai, L.L.; Mei, M.L.; Chu, C.H.; Lo, E.C.M. Mechanisms of Bioactive Glass on Caries Management: A Review. Materials 2019, 12, 4183. https://doi.org/10.3390/ma12244183
Dai LL, Mei ML, Chu CH, Lo ECM. Mechanisms of Bioactive Glass on Caries Management: A Review. Materials. 2019; 12(24):4183. https://doi.org/10.3390/ma12244183
Chicago/Turabian StyleDai, Lin Lu, May Lei Mei, Chun Hung Chu, and Edward Chin Man Lo. 2019. "Mechanisms of Bioactive Glass on Caries Management: A Review" Materials 12, no. 24: 4183. https://doi.org/10.3390/ma12244183
APA StyleDai, L. L., Mei, M. L., Chu, C. H., & Lo, E. C. M. (2019). Mechanisms of Bioactive Glass on Caries Management: A Review. Materials, 12(24), 4183. https://doi.org/10.3390/ma12244183