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Mineralising and antibacterial effects of modified calcium phosphate treatment on human root cementum

Abstract

Background

Aging population will lead to the increase of incidence of root caries globally. The clinical management of root caries is challenging due to the difficulty in moisture isolation. The root caries is caused by the release of organic acids from cariogenic bacteria which results in the dissolution of cementum and dentin of the root. The purpose of this study is to study the efficacy of modified saturated calcium phosphate solution (CaP) supplement with zinc (Zn2+) and/or fluoride (F-) in providing root cementum surfaces less susceptible to acid dissolution and bacterial colonization.

Methods

Human root cementum sections from extracted premolars were treated with three modified calcium phosphate solutions (M/A-CaPs) respectively: (A) CaP-F/Zn, supplemented with F- and Zn2+; (B) CaP-F, supplemented with F- only; (C) CaP-Zn, supplemented with Zn2+ only. The surface characteristics of treated cementum sections were investigated using scanning electron microscopy (SEM) and fourier transform infrared spectroscopy (FT-IR). Following the acid attack and Streptococcus mutans challenge, M/A-CaPs treated cementum surfaces were analysed using inductive coupled plasma (ICP) and SEM respectively.

Results

Compared with the control group, M/A-CaPs treated cementum presented significant improvements in resistance to acid dissolution and bacterial colonization. Among M/A-CaPs, the CaP-F/Zn treated cementum surfaces released the lowest amount of Ca2+ ions (2.11 ± 0.51 ppm) upon acid challenge (n = 3, p < 0.01) and also presented the most significant inhibiting effect against the colonization of S. mutans (n = 180, p < 0.05).

Conclusions

Saturated calcium phosphate solution CaP supplemented with both F- and Zn2+ could be applied as an effective coating material providing acid resistance and antibacterial property on cementum surfaces. The modified calcium phosphate-based solution could be a new treatment strategy to prevent the development of root caries and arrest the further progression of root caries.

Peer Review reports

Background

Owing to the growing population of elderly people worldwide, root caries is becoming an urgent issue in geriatric dentistry [1, 2]. As one of the major causes of tooth loss in elderly, the prevalence of root caries has been revealed nearly half in the aging population by the recent studies [3, 4]. Du M et al. reported that the root surface caries prevalence rates were 13.1 % in the middle-aged group and 43.9 % in the elderly group. Prevalence increased with aging, such that by age 75 and over, over 50 % had one or more root surface lesions [5]. Compared with coronal caries, the clinical management of root caries is more challenging with respect to the limited accessibility and difficulty in tooth isolation.

Root caries differs from coronal caries primarily due to different tissue compositions forming the outer layer of the root. Coronal caries primarily begins in enamel, a highly mineralised tooth structure with 96 % mineral. Root caries, however, involves the less mineralised tissue, cementum, which contains only 50 % mineral. The natural root surface is covered by a cementum layer of varying thickness. Similar to enamel, the cementum could function as a barrier against the diffusion of the mineral ions out of the lesion and provide initial caries resistance for the root surface [6]. However, the cementum is a thinner layer of less mineralised tissue with considerably varied thickness, especially the cervical third with only 16–60 Î¼m thickness. It is susceptible to routine oral prophylaxis and periodontal treatments such as scaling and root planning where the cementum can be easily disintegrated or removed at the cementoenamel junction level even down to the coronal third of the root. Due to traumatic tooth brushing, periodontal diseases [7, 8], bleaching, and orthodontic movement of teeth [9], gingival recessions were found in more than 60 % of the younger population (<20 years) and more than 90 % of the older population (>50 years). It causes the early exposure of cementum on the root surface which increases susceptibility to root caries [10, 11].

The clinical features and locations of root caries cause technical difficulties in early diagnosis and treatment. Hence, more efforts should be made on the prevention and early management of this disease. Among the mineralised tissues, fluoride concentration of cementum is the greatest and it increases with age [12, 13] or with F- exposure [14, 15]. Intact cementum layer has intrinsic ability to protect the underlying dentin against acidic demineralisation via ions uptakes from the surroundings and accumulating fluoride [16]. However, fluoride is not generally bactericidal which cannot effectively inhibit the growth of many cariogenic pathogens such as lactobacilli, actinomyces spp, and streptococci [17]. Our previous results have shown the successful colonization of Streptococcus mutans on the dentin surfaces treated with experimental mineralising solution containing F- or F- bound dentin surfaces [18].

In our previous studies, modified calcium phosphate solution (M/A-CaPs) containing both F- and Zn2+ was found to be effective in the mineralisation of dentin surfaces, occluding dentin tubules [19], and providing antibacterial property especially at acidic pH condition [18]. The presence of F- alone increased the mineralising efficiency of CaP solution and inhibited dentin dissolution by the formation of fluoridated hydroxyapatite. Zinc salt has been demonstrated to provide antibacterial property, inhibit plaque formation, and prevent gingival inflammation [20–22]. To overcome the limited antimicrobial activity of fluoride, in addition to F-, Zn2+ element was also supplemented in our experimental CaP solution. Till now, there are limited options of dentifrices and agents can effectively bind to the cementum, to form a coating layer which is resistant to acidic dissolution and bacterial colonization [23]. In this study, we compared the coating efficacy of M/A-CaPs with or without F- and Zn2+ on the cementum remineralisation. This study would provide a new strategy to prevent the initiation of root caries especially in the susceptible population groups such as elderly people and patients suffering from gingival recession.

Methods

Preparation of cementum samples

The sound human premolars extracted for orthodontics reasons were collected from Guanghua School of Stomatology Sun Yan-sen University (age range, from 16 to 22), and patients suffering from periodontal diseases were not considered. After extraction, teeth were immediately stored in saline, followed by being sterilized by gamma radiation, and stored in saline (The study design, sampling method and written consent forms were approved by The Human Research Ethics Committee of Guanghua School of Stomatology, Sun Yat-sen University. All participants provided the consents before their participation in this project.). Periodontal ligament fibers were removed carefully from root surfaces under dissecting microscope with a sharp Gracey curette. Root surficial cementum was kept intact [24–26].

Following debridement and brushing with fluoride-free prophylactic paste, the crowns and lower half roots were removed using a water-cooled diamond-bladed saw (Series 15 HC Diamond, N 11-4244, Buehler, USA), to prepare upper root sections with dimensions of 6 mm × 6 mm × 2 mm. After sonication for 10 min to remove the polishing abrasive particles, the specimens were rinsed with double distilled water (DDW) and dried with compressed air.

Preparation of M/A-CaP solutions

Calcium deficient apatites (SH874) was prepared by mixing 10 mM calcium hydroxide (Ca(OH)2) and 6 mM anhydrous monobasic sodium phosphate (NaH2PO4) in 100 ml DDW at 90 Â°C, 2 h, according to the reaction below:

10 Ca(OH)2 + 6NaH2PO4 → (Ca,Na)10(PO4,HPO4)6(OH)2

The precipitate was filtered and collected, washed with DDW three times, dried in the oven at 70 Â°C and characterized using X-ray diffraction (Philips X’ pert X-ray diffractometer). The M/A-CaP solutions were prepared from mixtures of SH874, NaF, and/or ZnCl2 as detailed in Table 1 (patent application submitted).

Table 1 Ingredients of each 100 ml M/A-CaP solutions

Solutions A (CaP-F/Zn), B (CaP-F), and C (CaP-Zn) were adjusted to pH 5.5 using sodium hydroxide. The Ca2+, PO4 3-, and Zn2+ ion concentrations of the filtrates were determined by inductive coupled plasma (ICP, Thermo Jarrell Ash Model-Trace Scan Inductive Coupled Plasma, Waltham, MA) and the F- ion concentration was measured by fluoride tracer (Orion, 940900).

Treatment of the cementum samples

Sections were randomly distributed into treated groups and control group. The cementum sections were immersed with shaking (60/min) in CaP-F/Zn, CaP-F, CaP-Zn solutions or DDW for 4 min, then rinsed in DDW and dried with compressed air.

Determination of physiochemical properties

The coatings on cementum surfaces were characterized using scanning electron microscopy (SEM) (JEOL JSM-5400; JEOL USA, Inc., Peabody, MA; and Hitachi S-3500 N; Hitachi, Ltd., Tokyo, Japan) and fourier transform infrared spectroscopy (FT-IR) (Nicolet 550; France). For the SEM analysis, the cementum sections were mounted onto aluminium stubs and sputter coated with gold. SEM images were taken under the same magnification and working distance. Of six sections in each group, ten images were selected randomly on each section and six of these SEM images were captured. This experiment was independently repeated three times. For the FT-IR analysis, the apatite powder pellet was prepared by mixing 1 mg of the powdered material scraped from the treated cementum surfaces with 250 mg KBr (IR grade) and pressing at 10,000 psi using a hydraulic press (Carver laboratory press, mode C, Ser.No.33000-577, Fred S. Carver INC). The FT-IR scan covered the range from 4000 cm-1 to 400 cm-1. Assignment of absorption bands were determined according to earlier study on carbonate apatites and standard calcium phosphates [27].

Dissolution of the coating was determined by monitoring the release of calcium ions from M/A-CaPs pre-treated cementum surfaces in weak acidic buffer (0.1 M KAc, pH 6, 37 Â°C) over time using ICP. This experiment was carried out after applying nail varnish on all parts of cementum sections except a circular area (diameter, 5 mm).

Determination of anti-bacterial property

Streptococcus mutans strain ATCC 25175 was used to evaluate the effect of the coating on bacterial colonization on cementum surface. The bacteria from a brain heart infusion agar plate were inoculated into 200 ml brain heart infusion broth (OXOID) and incubated at 37 Â°C overnight. The M/A-CaPs pre-treated cementum sections were divided into 4 groups according to the treatment (18 sections/group) and put into 24-well plates. The bacterial cells were collected and adjusted to OD600 of 0.30 and 2 ml of bacterial culture for each well were applied to challenge the cementum. The specimens were then incubated at 37 Â°C in an anaerobic atmosphere. In order to ensure the specimens to be challenged by bacteria from the same growth phase, the culture was changed every 2 h. Every three cementum sections in each group were then taken out from wells at 6, 12, and 24 h and washed with phosphate-buffered saline (PBS) to remove the unbound bacterial cells.

Cementum samples were fixed in Trump’s fixative (VWR, Inc.) for 1 h and then rinsed with PBS, post-fixed for 1 h in 2 % Osmium Tetroxide (OsO4), rinsed with PBS then dehydrated in ethanol, and dried in vacuum desiccators. The specimens were viewed and six images of each sample were randomly captured by SEM under the 2000 × magnification. A Bioquant Nova Advanced Image Analysis apparatus (200 R&M Biometrics, Inc.) was used to count the number of bacteria on cementum surface.

Statistical analysis

All data were assessed by SPSS15.0 using one-way analysis of variance (ANOVA) followed by Student-Newman-Keuls or Dunnett’s T3 post hoc with α =0.01. If no significant difference was obtained, data were analysed again with α =0.05.

Results

Solution composition

Chemical analyses showed three solutions maintaining relatively constant calcium and phosphorus levels. The fluoride concentration is constant between CaP-F/Zn and CaP-F. Similarly, the zinc concentration is constant between CaP-F/Zn and CaP-Zn (Table 2).

Table 2 Chemical compositions (in ppm) of the 3 solutions with relatively constant Ca and P but varying F and Zn concentrations

Physicochemical properties of treated cementum surfaces

As shown in Fig. 1, the cementum sections treated with M/A-CaP solutions presented different amounts and various morphologies of crystal deposits on the surfaces. Cementum surfaces treated with CaP-F/Zn (Fig. 1a) and CaP-F (Fig. 1b) were shown to be coated by compact and homogenous fine crystal precipitates. In contrast, a loose crystal layer with heterogeneous precipitates was observed on the cementum surfaces treated with CaP-Zn (Fig. 1c). Notably, most of cementum cracks were filled effectively by crystal precipitates formed in CaP-F/Zn and CaP-F groups, although large cracks still could be visualised under low magnification (data not shown). The amount of crystals deposited on cementum surfaces appeared to be dependent on the composition of mineralising solutions. No crystal deposition was observed on cementum surfaces of negative control group treated with DDW (Fig. 1d).

Fig. 1
figure 1

Representative SEM images of cementum: (a) CaP-F/Zn; (b) CaP-F; (c) CaP-Zn; (d) DDW. Cementum treated with CaP-F/Zn showed the greatest amount of crystal deposition followed by groups treated with either CaP-F or CaP-Zn. No crystal deposition was observed on DDW treated cementum

In this study, FT- IR was applied to further explore the chemical features of treated cementum surfaces with coated layers. As shown in Fig. 2, F- and Zn2+ doped apatite (CaP-F/Zn) or F- alone doped apatite (CaP-F) treated cementum induced a slight rise in the resolution of the PO4 absorption band (ν3 P-O) at 1102, 1065, 1027 cm-1, which indicates an increase in crystal size and crystal perfection of the fluoride containing apatite on the treated cementum surfaces.

Fig. 2
figure 2

FT- IR absorption spectra of cementum: (A) CaP-F/Zn; (B) CaP-F; (C) CaP-Zn; (D) DDW. Note the spectra between 1300 cm-1 and 500 cm-1 showing greater resolution of PO4 absorption bands (at 1102 cm-1, 1065 cm-1, 1027 cm-1) in the spectra of materials scraped from cementum surface treated with CaP-F/Zn and CaP-F

To prevent or halt the pathophysiological process of caries, the coating layers on the cementum would be preferred to possess the acid resistance properties. Thus in this study, dissolution experiments were carried out by measuring the released calcium from coated cementum surfaces during the acid attack using inductively coupled plasma (ICP) mass spectrometry. As shown in Fig. 3, the amount of Ca2+ ions released from cementum sections treated by CaP-F/Zn was the least after 1 h immersion in the acidic buffer (0.1 M KAc, pH 6, 37 Â°C). Compared with the DDW treated group, cementum surfaces treated by CaP-F or CaP-Zn released significant less Ca2+ ions (p < 0.01). There was no statistical significant difference between CaP-F and CaP-Zn with regards to the released calcium level (p > 0.05). To be more specific, the total amount of Ca2+ ions liberated from treated cementum surfaces during the acidic attack was determined using ICP (Table 3). The CaP-F/Zn treated surfaces had the lowest amount of liberated Ca2+ ions (2.11 ± 0.51 ppm) which was almost half of the Ca2+ ions liberated from DDW control group (3.84 ± 0.17 ppm). The cementum surfaces treated by CaP-F and CaP-Zn liberated similar amount of Ca2+ ions responding to the acidic attack with 3.01 ± 0.35 ppm and 3.26 ± 0.31 ppm respectively. It indicated that CaP-F/Zn provided the most durable cementum coating surfaces regarding the dissolution and acidic resistance over time.

Fig. 3
figure 3

Comparative extent of Ca2+ ions released from cementum surfaces in acidic buffer: (A) CaP-F/Zn; (B) CaP-F; (C) CaP-Zn; (D) DDW. The amount of Ca2+ ions released in 60 min with acidic buffer challenge was the highest in the control group, and the lowest in CaP-F/Zn treated cementum group. *No significant difference was observed in the extent of Ca2+ ions released between cementum surfaces treated with CaP-F and CaP-Zn (p > 0.05, n = 3)

Table 3 The amount of Ca2+ ions released from cementum surfaces after 66.7 min in acidic buffer

Resistance against cariogenic bacterial colonization

Colonization of material surfaces by cariogenic bacteria is a causal event which produces acid, initiates the tooth structure demineralisation, and eventually leads to caries cavitation. Hence, bacterial adherence and growth on M/A-CaPs treated surfaces were investigated using SEM to evaluate the resistance against cariogenic S. mutans colonization. As shown in Fig. 4, there was no significant increase of S. mutans population on CaP-F/Zn treated cementum from 6 to 24 h. In contrast, a dramatic proliferation of the bacterial population was observed on the cementum surfaces treated by DDW. Similar findings were also noticed on the CaP-F and CaP-Zn treated cementum surfaces (data not shown). To further quantify the bacterial colonization on various treated surfaces, the bacterial cell numbers were counted in defined regions of interest (ROIs) under SEM. As illustrated in Fig. 5, there was no significant difference between CaP-F and DDW treated groups at the 6 h and between CaP-F and CaP-Zn treated groups at 12 h or 24 h time points regarding the mean number of bacteria colonizing the cementum surfaces. However, the number of the bacteria colonized on CaP-F/Zn, CaP-F or CaP-Zn treated cementum surfaces was significantly less than DDW control group at 3 different time points. This may be explained by the fact that M/A-CaPs coating layers on the treated cementum surfaces release bacteriostatic and/or bactericidal ions such as Zn2+ and F-, thus inhibiting S. mutans growing on the M/A-CaPs treated cumentum surfaces. Among the three M/A-CaPs, the CaP-F/Zn treated cementum surfaces showed the best inhibiting effect against the colonization of S. mutans which indicated that the Zn2+ and F- could have synergic effect.

Fig. 4
figure 4

Representative SEM images of bacterial colonization on CaP-F/Zn or DDW treated cementum surfaces after Streptococcus mutans culturing 6, 12 and 24 h

Fig. 5
figure 5

The mean number of Streptococcus mutans ATCC 25175 colonized on cementum surfaces were determined by average bacterial cells in ten randomly selected fields from each section (six sections in each group) and six SEM images for each section were captured. This experiment was independently repeated three times [41]. (A) CaP-F/Zn; (B) CaP-F; (C) CaP-Zn; (D) DDW (**p < 0.01; ## p < 0.01; △△ p < 0.01)

Discussion

Cementum is a calcified avascular mesenchymal tissue that covers the dentine and forms the outer layer of the anatomic root. There are two classes of cementum: Cellular cementum which contains cementocytes within the matrix and is mainly found in the apical area overlying the root; acellular cementum which is the one without any cells in its matrix and is located in the cervical and middle third of the root regions. Clinically, gingival recession and root surface exposure leads to the exposure of acellular cementum which predisposes the tooth to the development of root caries. In this study, only the mineralised ground acellular cementum was examined.

Treatment of cementum sections with three M/A-CaP solutions resulted in (a) deposition of a crystal precipitates coating layer on the cementum surface, (b) increasing resistance against acid dissolution, and (c) minimizing bacterial colonization. These effects were demonstrated to be dependent on the supplementation of F- and/or Zn2+ in M/A-CaP solutions. In the presence of both F- and Zn2+ in CaP-F/Zn, the treated cementum presented an improved performance in acid resistance and anti-bacterial property. Although the CaP-F coated the cementum with a similar smooth fine mineral precipitates layer to that of CaP-F/Zn, CaP-F performed poorly in acid resistance and bacterial inhibition. Notably, the CaP-Zn was not able to form a homogeneous fine layer of crystal precipitates whilst which could be seen on the cementum surfaces treated by CaP-F/Zn or CaP-F. It could be attributed to the larger crystalline formed in the presence of Zn2+leading to bulky crystal precipitates formation.

Under acidic condition with pH 5.5, the presence of F- and Zn2+ in the traditional CaP solutions significantly affected the mineralisation status of cementum surfaces [19]. The carbonate hydroxyapatite on the cementum surface was partially dissolved to release Ca2+, Mg2+, HPO4 2-, and CO3 2- ions. These irons subsequently combined with the Ca2+, Zn2+, HPO4 2-, and F- ions which were provided by the acid mineralising solutions, to form fluorapatite and/or Zn-doped apatite apatitic. Fluorapatite precipitates possessed lower solubility than the original cementum minerals which had a higher CO3 2- ion level and lower F- ion level [28–30]. Similarly, the formed Zn-doped apatite also presented a reduced mineral solubility in acidic environment [22, 31]. One limitation of the current study was that the durability of the CaP-F/Zn precipitates on root surface was not determined. Future studies will be carried out to further investigate the stability and wearability of CaP-F/Zn precipitates under strong acidic environment and mechanical challenge.

The decrease in the prevalence and severity of dental caries has been attributed to the widely application of fluoride-containing dentifrices [32]. Although fluoride could affect the cariogenic ability of Streptococcus mutans by reducing carbohydrate metabolism and inhibiting certain enzymes activities, it has been demonstrated that fluoride cannot effectively kill oral streptococci in the biofilms [33–35]. Hence, other antimicrobial chemicals such as Zn2+ has been drawn a great deal of attention. Liberated Zn2+ ions can bind to essential metabolic enzymes in bacteria to achieve the bactericidal or bacteriostatic effects [36, 37]. Recently, McDevitt et al found that zinc bound to the manganese transport protein in human pathogen Streptococcus pneumoniae and inhibited the uptake of essential nutrient manganese for this bacterium [38]. Previous studies also demonstrated that zinc phosphate mineralised membranes effectively inhibited the Actinobacillus actinomycetemcomitans ATCC 29522 to colonize on root surface of the tooth [21]. In this study, we showed that CaP-F/Zn coating layer was more effective in minimizing bacterial growth and colonization compared with CaP-F or CaP-Zn. Liberated ions from CaP-F/Zn solution promoted the formation of F- substitution and/or Zn2+ substitution apatite on the interface of coating layer and cementum underneath. Given the similarity of chemical components to human teeth hydroxyapatite, the M/A-CaP crystal precipitates coating layer processes promising biocompatibility. Furthermore, when bacteria attach on the cementum surface treated with CaP-F/Zn, acid produced by bacteria can dissolve the F- substitution and/or Zn2+ substitution apatite leading to the release of F- and Zn2+. The liberated F- and Zn2+ ions could act synergistically in inhibition of bacterial colonization on the treated cementum surfaces. These results are in agreement with previous reports which have demonstrated that the combination of Zn2+ and F- ions presented potential bactericidal effects [39, 40]. To further confirm the antimicrobial properties of CaP-F/Zn solution, the viable cell counts of adherent bacteria on cementum will be performed in future study.

Conclusions

Clinically, different types of fluoride-containing agents such as varnish, solution or dentifrices have been applied to prevent and manage the root caries. The modified CaP mineralising solution supplemented with Zn2+and F- has been demonstrated to be able to form an acid resistance shield with anti-cariogenic bacteria colonisation capacity in the current study. This new mineralisation solution could contribute to the development of a novel dentifrice to prevent and treat root cementum caries formation and progression.

References

  1. Nicolau B, Srisilapanan P, Marcenes W. Number of teeth and risk of root caries. Gerodontology. 2000;17:91–6.

    Article  PubMed  Google Scholar 

  2. Griffin SO, Griffin PM, Swann JL, Zlobin N. Estimating rates of new root caries in older adults. J Dent Res. 2004;83:634–8.

    Article  PubMed  Google Scholar 

  3. Marino RJ, Fu CS, Giacaman RA. Prevalence of root caries among ambulant older adults living in central Chile. Gerodontology. 2013;32:107–14.

    Article  PubMed  Google Scholar 

  4. Imazato S, Ikebe K, Nokubi T, Ebisu S, Walls AW. Prevalence of root caries in a selected population of older adults in Japan. J Oral Rehabil. 2006;33:137–43.

    Article  PubMed  Google Scholar 

  5. Du M, Jiang H, Tai B, Zhou Y, Wu B, et al. Root caries patterns and risk factors of middle-aged and elderly people in China. Community Dent Oral Epidemiol. 2009;37:260–6.

    Article  PubMed  Google Scholar 

  6. Phankosol P, Ettinger RL, Hicks MJ, Wefel JS. Depth of penetration of in vitro root surface lesions. J Dent Res. 1985;64:897–9.

    Article  PubMed  Google Scholar 

  7. Loe H, Anerud A, Boysen H. The natural history of periodontal disease in man: prevalence, severity, and extent of gingival recession. J Periodontol. 1992;63:489–95.

    Article  PubMed  Google Scholar 

  8. Serino G, Wennstrom JL, Lindhe J, Eneroth L. The prevalence and distribution of gingival recession in subjects with a high standard of oral hygiene. J Clin Periodontol. 1994;21:57–63.

    Article  PubMed  Google Scholar 

  9. Wennstrom JL, Lindhe J, Sinclair F, Thilander B. Some periodontal tissue reactions to orthodontic tooth movement in monkeys. J Clin Periodontol. 1987;14:121–9.

    Article  PubMed  Google Scholar 

  10. Kassab MM, Cohen RE. The etiology and prevalence of gingival recession. J Am Dent Assoc. 2003;134:220–5.

    Article  PubMed  Google Scholar 

  11. Slutzkey S, Levin L. Gingival recession in young adults: occurrence, severity, and relationship to past orthodontic treatment and oral piercing. Am J Orthod Dentofacial Orthop. 2008;134:652–6.

    Article  PubMed  Google Scholar 

  12. Gedalia I, Nathan H, Schapira J, Haas N, Feldmann J. Fluoride Concentration of Surface Enamel, Cementum, Lamina Dura, and Subperiosteal Bone from the Mandibular Angle of Hebrews. J Dent Res. 1965;44:452.

    Article  PubMed  Google Scholar 

  13. Sugihara N, Nakagaki H, Kunisaki H, Ito F, Noguchi T, et al. Distribution of fluoride in sound and periodontally diseased human cementum. Arch Oral Biol. 1991;36:383–7.

    Article  PubMed  Google Scholar 

  14. Nakata TM, Stepnick RJ, Zipkin I. Chemistry of human dental cementum: the effect of age and fluoride exposure on the concentration of ash, fluoride, calcium, phosphorus and magnesium. J Periodontol. 1972;43:115–24.

    Article  PubMed  Google Scholar 

  15. Kato S, Nakagaki H, Toyama Y, Kanayama T, Arai M, et al. Fluoride profiles in the cementum and root dentine of human permanent anterior teeth extracted from adult residents in a naturally fluoridated and a non-fluoridated area. Gerodontology. 1997;14:1–8.

    Article  PubMed  Google Scholar 

  16. McIntyre JM, Featherstone JD, Fu J. Studies of dental root surface caries. 2: The role of cementum in root surface caries. Aust Dent J. 2000;45:97–102.

    Article  PubMed  Google Scholar 

  17. Li YH, Bowden GH. The effect of environmental pH and fluoride from the substratum on the development of biofilms of selected oral bacteria. J Dent Res. 1994;73:1615–26.

    PubMed  Google Scholar 

  18. Gu H, Mijares D, Zhao Z, Boylan R, Ling J, et al. Experimental antibacterial and mineralising calcium phosphate-based treatment for dentin surfaces. J Biomater Appl. 2013;27:783–90.

    Article  PubMed  Google Scholar 

  19. Gu H, Ling J, LeGeros JP, LeGeros RZ. Calcium phosphate-based solutions promote dentin tubule occlusions less susceptible to acid dissolution. Am J Dent. 2011;24:169–75.

    PubMed  Google Scholar 

  20. Charles J, Sancey B, Morin-Crini N, Badot PM, Degiorgi F, et al. Evaluation of the phytotoxicity of polycontaminated industrial effluents using the lettuce plant (Lactuca sativa) as a bioindicator. Ecotoxicol Environ Saf. 2011;74:2057–64.

    Article  PubMed  Google Scholar 

  21. Chou AH, LeGeros RZ, Chen Z, Li Y. Antibacterial effect of zinc phosphate mineralised guided bone regeneration membranes. Implant Dent. 2007;16:89–100.

    Article  PubMed  Google Scholar 

  22. LeGeros RZ, Bleiwas CB, Retino M, Rohanizadeh R, LeGeros JP. Zinc effect on the in vitro formation of calcium phosphates: relevance to clinical inhibition of calculus formation. Am J Dent. 1999;12:65–71.

    PubMed  Google Scholar 

  23. Dietz W, Kraft U, Hoyer I, Klingberg G. Influence of cementum on the demineralisation and remineralisation processes of root surface caries in vitro. Acta Odontol Scand. 2002;60:241–7.

    Article  PubMed  Google Scholar 

  24. Polson AM, Hanes PJ. Cell and fiber responses to cementum from periodontitis-affected root surfaces after citric acid treatment. J Clin Periodontol. 1989;16:489–97.

    Article  PubMed  Google Scholar 

  25. Coldiron NB, Yukna RA, Weir J, Caudill RF. A quantitative study of cementum removal with hand curettes. J Periodontol. 1990;61:293–9.

    Article  PubMed  Google Scholar 

  26. Tsuboi S, Nakagaki H, Takami Y, Eba H, Kirkham J, et al. Magnesium and fluoride distribution in human cementum with age. Calcif Tissue Int. 2000;67:466–71.

    Article  PubMed  Google Scholar 

  27. LeGeros RZ. Calcium phosphates in oral biology and medicine. Monogr Oral Sci. 1991;15:1–201.

    Article  PubMed  Google Scholar 

  28. LeGeros RZ. Chemical and crystallographic events in the caries process. J Dent Res. 1990;69 Spec No:567–74. discussion 634-566.

    Article  PubMed  Google Scholar 

  29. Tang PF, Li G, Wang JF, Zheng QJ, Wang Y. Development, characterization, and validation of porous carbonated hydroxyapatite bone cement. J Biomed Mater Res B Appl Biomater. 2009;90:886–93.

    Article  PubMed  Google Scholar 

  30. Matsunaga K, Murata H, Mizoguchi T, Nakahira A. Mechanism of incorporation of zinc into hydroxyapatite. Acta Biomater. 2010;6:2289–93.

    Article  PubMed  Google Scholar 

  31. Ingram GS, Edgar WM. Interactions of fluoride and non-fluoride agents with the caries process. Adv Dent Res. 1994;8:158–65.

    PubMed  Google Scholar 

  32. Clarkson JJ, McLoughlin J. Role of fluoride in oral health promotion. Int Dent J. 2000;50:119–28.

    Article  PubMed  Google Scholar 

  33. Hamilton IR. Biochemical effects of fluoride on oral bacteria. J Dent Res. 1990;69 Spec No:660–7. discussion 682-663.

    Article  PubMed  Google Scholar 

  34. Marquis RE, Clock SA, Mota-Meira M. Fluoride and organic weak acids as modulators of microbial physiology. FEMS Microbiol Rev. 2003;26:493–510.

    Article  PubMed  Google Scholar 

  35. Giertsen E, Guggenheim B, Thurnheer T, Gmur R. Microbiological aspects of an in situ model to study effects of antimicrobial agents on dental plaque ecology. Eur J Oral Sci. 2000;108:403–11.

    Article  PubMed  Google Scholar 

  36. Scheie AA, Pearce EI. The effect of mineral-derived zinc ions on in vitro glucose metabolism of Streptococcus mutans NCTC 10449. Caries Res. 1994;28:329–34.

    Article  PubMed  Google Scholar 

  37. Moermann JE, Muehlemann HR. Synergistic inhibitory effect of zinc and hexetidine on in vitro growth and acid production of Streptococcus mutans. J Dent Res. 1983;62:135–7.

    Article  PubMed  Google Scholar 

  38. McDevitt CA, Ogunniyi AD, Valkov E, Lawrence MC, Kobe B, et al. A molecular mechanism for bacterial susceptibility to zinc. PLoS Pathog. 2011;7:e1002357.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Izaguirre-Fernandez EJ, Eisenberg AD, Curzon ME. Interactions of zinc with fluoride on growth, glycolysis and survival of Streptococcus mutans GS-5. Caries Res. 1989;23:18–25.

    Article  PubMed  Google Scholar 

  40. Santhosh K, Surbhi L, Harish T, Jyothi T, Arvind T, et al. Do active ingredients in non alcoholic chlorhexidine mouth wash provide added effectiveness? Observations from a randomized controlled trial. Odontostomatol Trop. 2010;33:26–34.

    PubMed  Google Scholar 

  41. Kenzaka T, Ishidoshiro A, Yamaguchi N, Tani K, Nasu M. rRNA sequence-based scanning electron microscopic detection of bacteria. Appl Environ Microbiol. 2005;71:5523–31.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

We would like to thank the professional collaboration of Drs. H. Bin, W. Zou, D. Holmes, and D. Harty. The authors also give special thanks to Prof Racquel LeGeros and Dr. John LeGeros for the indispensable collaboration and endless support. This investigation was supported by the National Natural Science Foundation of China (No. 81200777) and the Fundamental Research Funds for the Central Universities (No.12ykpy66).

Authors’ contributions

HG, LL, and JG conceived of and designed the experiments. HG, ZZ and JG analyse the data. HG, JG and XZ prepared the manuscript. JL contributed substantially to discussion. All authors have read and approved the final version for the manuscript.

Competing interests

The authors declare that they have no competing interests.

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Correspondence to Junqi Ling or Jin-Long Gao.

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Gu, H., Ling, J., Zhou, X. et al. Mineralising and antibacterial effects of modified calcium phosphate treatment on human root cementum. BMC Oral Health 17, 22 (2017). https://doi.org/10.1186/s12903-016-0246-4

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