Synbiotic-fluoride synergism on enamel remineralization, cytotoxicity and genotoxicity

被引:4
作者
Bijle, Mohammed Nadeem [1 ,2 ]
Abdalla, Mohamed Mahmoud [3 ,4 ]
Chu, Chun Hung [5 ]
Yiu, Cynthia Kar Yung [6 ,7 ]
机构
[1] Ajman Univ, Coll Dent, Dept Clin Sci, Ajman, U Arab Emirates
[2] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, Ajman, U Arab Emirates
[3] Univ Hong Kong, Fac Dent, Paediat Dent, Hong Kong, Peoples R China
[4] Al Azhar Univ, Fac Dent Med, Dent Biomat, Cairo, Egypt
[5] Univ Hong Kong, Fac Dent, Restorat Dent Sci, Hong Kong, Peoples R China
[6] Univ Hong Kong, Fac Dent, Hong Kong, Peoples R China
[7] Univ Hong Kong, Prince Philips Dent Hosp, Fac Dent, Paediat Dent,Sai Ying Pun,Hong Kong Island, 2-F, 34 Hosp Rd, Hong Kong, Peoples R China
关键词
Arginine; Fluoride; Remineralization; Synbiotic; Toxicity; ALKALI PRODUCTION; ARGININE; PROBIOTICS; GROWTH; HEALTH;
D O I
10.1016/j.jdent.2022.104356
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective(s): The objectives of the present study were to examine the - a) enamel remineralization potential of synbiotic-fluoride (SF) therapy using a multi-species bacterial pH-cycling model; and b) cytotoxic and genotoxic effects of SF therapy extracts. Materials and methods: The SF therapy group comprised of 2% arginine (Arg), 0.2% NaF, and a probiotic Lactobacillus rhamnosus GG (LRG). The intervention groups studied were: 1) No treatment; 2) 2% Arg; 3) 0.2% NaF; 4) LRG; 5) 2% Arg+0.2% NaF; 6) 2% Arg+LRG; 7) 0.2% NaF+LRG; and 8) 2% Arg+0.2% NaF+LRG (SF therapy). The enamel remineralization potential of SF therapy was investigated under cariogenic biofilm challenge; while the cytotoxicity and genotoxicity of SF therapy extracts were examined on HGF-1 and Chinese hamster fibroblast V79, respectively. To determine the remineralization effect, the specimens were subjected to mineral density (MD) assessment using micro-CT, Ca/P molar ratio with SEM-EDX, and enamel fluoride uptake (EFU) estimates. The HGF-1 proliferation assessment was quantified using MTT/CCK-8 assays with qualitative analysis by nuclei staining Hoechst-based fluorescence imaging. The genotoxicity was determined by micronuclei formation test. Results: Mineral gain and %remineralization derived from MD assessment for the SF therapy were significantly higher than the other groups (p<0.05). The %Delta Ca/P for the SF and 2% Arg+0.2% NaF were significantly higher than the other groups (p<0.05). The SF and 2% Arg+0.2% NaF groups had the highest EFU compared to the other groups (p<0.05). No significant difference in the %viable HGF-1 cells were observed between the treatment interventions and no treatment group (p>0.05). Compared to the EMS-positive control, the micronuclei formation for all the intervention groups was significantly lower (p<0.05), with no significant difference among the treatment groups (p>0.05). Conclusion: The SF therapy enhanced enamel remineralization with no biocompatibility concerns. Clinical significance: With the enhanced enamel remineralization potential discerned in the present study, the SF therapy can be used as a promising caries-preventive agent targeted for high caries-risk individuals.
引用
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页数:9
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