Does dentifrice provide the necessary saturation of ions in oral fluids to favour remineralisation?

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Authors: 
Pavel V. Seredin, Dmitry L. Goloshchapov, Yuri A. Ippolitov, Edvard S. Kalivradzhiyan
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Article type: 
CID: 
e0106
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Abstract: 
Background ― Changes in the molecular composition of mixed human saliva using endogenous and exogenous methods of caries prevention were studied and the duration of these changes in relation to the initial state of the oral fluid was determined. Material and Methods ― In total, 200 European healthy, addiction-free, university-educated males and females, aged 22–30 were recruited for the study. Participants collected their mixed saliva samples after the use of a multi-mineral toothpaste (exogenous prevention) and after three days of taking a calcium glycerophosphate tablet (endogenous prevention). In the first stage of the study, samples of mixed saliva were analysed by infrared (IR) lab spectrometer and equipment of infrared microspectroscopy beamline at the Australian Synchrotron (Victoria, Australia) was used in the second stage of study. Results ― Based on the experimental data obtained by IR-spectroscopy technique, the mineral/organic and carbon/phosphate ratios were calculated. The changes in the organic mineral balance of the oral cavity induced by these two preventive methods were analysed. The statistical significance of the results for the confidence level of p is indicated. The data shows that changes in the molecular composition of mixed saliva when using an exogenous method of caries prevention only provides a short-term effect, continuing for the first 30 minutes after the preceding prevention. Moreover, calcium glycerophosphate tablets can change the organic-mineral balance in mixed saliva, increasing the content of mineral groups and complexes. The content of endogenous, biologically accessible phosphate groups and complexes in the mixed saliva exceeds by approximately 12% that of the mixed saliva before the use of the prevention agents. Conclusion ― Use of calcium glycerophosphate tablets in combination with brushing (a combination of endogenous and exogenous prevention methods) leads to the long-term presence of high concentrations of ions, mineral complexes and groups (phosphates) in the oral fluid.
Cite as: 
Seredin PV, Goloshchapov DL, Ippolitov YuA, Kalivradzhiyan ES. Does dentifrice provide the necessary saturation of ions in oral fluids to favour remineralisation? Russian Open Medical Journal 2018; 7: e0106.

Introduction

It is well-known that hygienic methods for oral cavity care and caries prevention induce changes in the molecular composition of fluids within the oral cavity, thereby affecting teeth health [1-3]. The significance of the changes in the molecular composition of mixed saliva has been previously shown in diabetes, oncology and pathologies of the oral cavity [4-9]. Considerable deviation of the molecular composition in the oral fluid can have an influence on the content of mineral complexes in plaque fluid and thus, impact on the process of enamel remineralisation [1, 10–13]. Remineralisation is the recognised process of dental enamel recovery promoted by the plaque fluid and mixed saliva being oversaturated with ions (Са2+, HPO42-, Na+, Mg2+, Cl-, F-, OH-, etc.) relative to the composition of dental enamel [12, 14]. Therefore, the change of concentration for both organic and inorganic substances in the oral fluid results in a decrease in the gradient relative to dental biofilm, impacting on the state of the dental enamel health [15-18]. Consequently, studies of the impact of exogenous and endogenous preventive drugs on the change in the molecular composition of the oral fluid are relevant.

The investigation and comparison of different prevention methods, including fluoridation, will determine which phosphorus- and calcium-containing agents promote the recovery of dental enamel [11, 15, 19-23]. The prophylactic efficiency of exogenous methods, namely tooth brushing, gel application and laser irradiation, has been demonstrated [20, 21, 24-28]. However, such exogenous methods do not promote the balance between the natural processes of mineral loss and their replacement in the plaque fluid and mixed saliva [29]. The development of some tooth lesions is a long-term process and in cases where the concentration of the necessary mineral and organic sources is reduced, the factors resulting in demineralisation will dominate. These processes prove to be a consequence of the changes in mineral-organic of the plaque fluid and mixed saliva. However, the molecular composition of these substances can be altered due to the intake of special preventive drugs (endogenous prophylaxis) on the basis of calcium phosphates [16, 17, 20, 30, 31], in particular, the endogenous prophylactic calcium glycerophosphate [32-35]. The use of such preventive drugs can achieve optimal concentrations of calcium and phosphate in mixed human saliva, however, possible changes in composition have not been considered. Moreover, there is no information in literature regarding the comparative analysis of changes in the mixed saliva molecular composition when using different caries preventive drugs since this issue requires an interdisciplinary approach. The significance of this information for explaining the processes proceeding at the tentative boundary between plaque fluid and mixed saliva is indisputable, as confirmed by a number of investigations [6, 8, 29, 30]. Therefore, the aim of this study is to investigate the changes in the molecular composition of human mixed saliva with the use of endogenous and exogenous methods for caries prevention and to determine the duration of these changes in relation to the initial state of the oral fluid.

 

Material and Methods

Study population

Two hundred healthy, addiction-free, university-educated participants (100 men and 100 women) aged 22–30 were recruited via the website of Voronezh State Medical University n.a. N.N. Burdenko (Voronezh, Russia). Informed consent was obtained from all participants and they all provided their own mixed saliva for the investigations. All participants collected their samples at the dental lab.

 

Mixed saliva sampling

It should be noted that this study investigated mixed saliva with the composition being different from that of a mix of salivary glands. For exogenous and endogenous prevention, there will be derivatives of the prevention substances in the mixed saliva which will enter through the oral cavity (a toothpaste) or salivary glands (use of a mineral complex based on calcium glycerophosphate). All procedures concerning the collection of mixed saliva samples were performed in laboratory conditions, with participants invited to the laboratory in groups of 20 for salvia collection.

Mixed saliva sampling was implemented as follows: in the week prior to, and during sampling, the participants mainly ate vegetables, followed a standard water consumption pattern (recommended daily water consumption was 1.0-1.5 l, without the use of mineralized or preconditioned water) and they not take any remedies or alcohol. The collection of mixed saliva was repeated twice, without any stimulation and all samples were collected into sterile 15 ml tube. In the first stage of the study, mixed saliva was sampled on the eighth day after the beginning of the observations (without any changes in conditions of the oral cavity hygiene in the morning just before eating), after preliminary oral rinsing. This mixed saliva was used as a reference sample.

In order to explore the changes in the molecular composition of human mixed saliva when using an exogenous method of prevention, a pea-sized amount of toothpaste with a multi-mineral complex was used in combination with a calcium glycerophosphate tablet. On the same day, the participants applied toothpaste for brushing after collection of the reference sample and collected the mixed saliva sample 5 minutes after that. A third sample was collected 30 minutes later. The next day, the participants began to take the tablets (a pelleted mineral complex of calcium glycerophosphate), one tablet three times a day after food intake. Three days after that, when the first pellet was taken in the morning, food intake, and after oral rinsing, mixed saliva was sampled once again.

During the second stage of experiment the following regulations were specified for mixed saliva sampling. Similar to the first stage of the experiment, seven days later (after the beginning of this second stage without the changes of conditions for hygienic measures of the oral cavity), in the morning before eating, participants of the experiment sampled their own mixed saliva for the first time after oral rinsing. On the same day, after sampling the mixed saliva, the participants used the same toothpaste for teeth brushing. Five minutes later, after proceeding with the hygienic measures for the oral cavity with the use of toothpaste and a thorough oral rinsing, mixed saliva was sampled once again. Thirty minutes later after a thorough oral rinsing, the mixed saliva was sampled for the third time. The next day, participants began to take the calcium glycerophosphate tablets, one tablet three times a day. Three days after that in the morning, on an empty stomach, the patients thoroughly carried out oral rinsing and they were again subjected to mixed saliva sampling.

 

Sample preparation

The mixed saliva was collected into a sterile container, immediately centrifuged at the dental lab and dried at 36°C in a desiccator to remove excess water. Sample biospecimen description data, in accordance with the Biospecimen Reporting for Improved Study Quality (BRISQ) recommendations, are presented in Table 1.

 

Table 1. Biospecimen description in accordance with the Biospecimen Reporting for Improved Study Quality (BRISQ) recommendations

Data elements

Objects and properties

Biospecimen type

Mixed saliva

Anatomical site

Mixed saliva

Disease status of patients

Healthy

Clinical characteristics of patients

Patients who regularly maintain oral hygiene, without pernicious habits

Vital state of patients

Alive

Collection mechanism

Direct collection of the saliva

Type of stabilisation

Air-tight container

Type of long-term preservation

Drying in the air (36.6°C)

Constitution of preservative

Air-tight container

Storage temperature

20 to 25°C

Storage duration

4 and 7 days (for the first and second experiment, respectively)

Shipping temperature

20°C to 25°C

 

 

Infrared microspectroscopy analysis

Mixed saliva samples were analysed by infrared (IR) spectroscopy, a highly selective and sensitive method allowing extensive information on the structure of substances, the effect of atomic groups comprising compounds, as well as the detection of neogenic organic and mineral phases [5, 9, 36-38]. It can also be used to analyse multi-component compounds. For the first stage of the study, Vertex-70 (Bruker, Germany) was applied to a survey of IR spectra and an attachment for the attenuated total reflection (ATR) spectroscopy (PLATINUM ATR, Bruker, Germany) with a diamond prism. IR spectra were surveyed in the range of 4000–500 cm-1.

For the second stage of the study, an IR microspectroscopy technique utilising the equipment of the infrared microspectroscopy (IRM) beamline at Australian Synchrotron (Victoria, Australia) was used. A Bruker V80v Fourier Transform Infrared (FTIR) spectrometer and a Hyperion 3000 IR microscope (Bruker, Germany) were used to perform the analysis of a microprobe of the specimens as well as a diamond high-pressure cell. Transmission IR spectra were measured within the range of 4000–500 cm-1.

Figure 1 shows a diagram detailing the experimental design, i.e. how the use of the IR spectroscopy method allows the study of samples of mixed saliva. As noted in [36], the use of any medications is revealed in the molecular spectra of mixed saliva as also confirmed in [39, 40]. Hence, the application of IR-spectroscopy for the analysis of the changes in the molecular composition of the oral fluid is a logical and tested approach demonstrating high-precision results [4, 5, 41, 36]. All the vibration mods of the samples were signed in accordance of the reference sources of IR spectroscopy [5, 38, 41-45] and tabulated in Table 2.

Spectra collection, plotting, manipulation with spectra, their normalisation and averaging, and evaluation and integration of spectra and all data calculations were performed using the professional Bruker Optics software OPUS (versions 7.2 and 7.5). Final conversion from OPUS figure pdf format to figure (600 dpi) jpg format and inscriptions in figures were made using CorelDRAW Graphics Suite X7.

 


Figure 1. Design of experiment to study of mixed saliva samples with use of IR-spectroscopy.

 

Table 2. Active vibrations bands in the IR-spectra at the first and second stages of the experiments and reference data

Substance

Vibration modes

Wavenumbers, cm-1

Experiment

Refs

 

 

 

Exp.1

Exp.2

Proteins

Amide VI Out-of-plane C=O bending of proteins

537−606

 

+

40, 44

Amide V Out-of-plane NH bending of proteins

Amide IV OCN bending of proteins

625−767

 

+

40, 44

Phosphates

Р-О band of Р2О7

730-770

+

+

45

 

Oligo-& polysaccharides, glycosilated proteins and phosphorus derivatives

1025-1078

+

+

41

 

Mono and oligosaccharides

1029

+

+

41

 

Derivative of phosphate, glycerophosphate and phosphatase. Phospholipids, C–O–P–O–C vibrations

1054

+

+

41

- Proteins (α-Amylase, Albumin, Cystatins, Mucins, Proline-rich proteins, sIgA)

- Hormones (Cortisol, Testosterone)

P=O stretching (asymmetric) of >PO2– phosphodiesters stretching vibrations of C=O groups (Amide I)

1240-1244

+

+

5, 38, 41

Amide III (CN stretching, NH bending) band components of proteins

1272

 

+

5

Amide III (CN stretching, NH bending) band components of proteins

1316

+

 

5

Stretch - carboxyl group vCOO

1330-1345

 

+

5, 41

Amide II (CN stretching, NH bending)

1378

+

 

5

C=O stretching (symmetric) of COO-

1401

+

+

5

CH2/CH3

1397-1410, 1452

+

+

5, 38, 41

- Proteins (α-Amylase, Albumin, Cystatins, Mucins, Proline-rich proteins; sIgA)

Tyrosineb and N-H (amide II), α-helix: proteins, amino acids

1516

 

 

5

Amide II (CN stretching, NH bending)

1548 -1553

+

+

5, 38, 41

(HNH)(NH2) Amide II (CN stretching, NH bending vibrations) (aminoacids, peptides, protein)

1570

+

+

5, 41

N-H (amide II), α-helix: proteins, amino acids

1594

 

 

5

Amide I (C=O stretching) of β-pleated sheet structures

1621

 

 

5

Amide I (C=O stretching) of β-pleated sheet structures

1634

 

 

5

Amide I (C=O stretching) of β-pleated sheet structures

Amide I (C=O stretching) and (COO-) stretching vibration

1645-1650

+

+

5, 38, 41

Amide I of α-helical structures

1658

 

 

5

Amide I (C=O stretching)  of α-helical structures

1659

 

 

5

Amide I (C=O stretching) band components resulting from antiparallel pleated sheets and  β-turns of proteins

1675

 

 

5

C-H stretching (symmetric)  of > CH2 in fatty acids

2852

+

 

5, 38

 

Stretching vibrations of SCN, unique to saliva, converted by salivary peroxidases to hypothiocyanate, a local antibacterial age

2137-2140

+

+

41

 

Stretching vibrations of CH- links of lipid molecules

2280-2380

 

+

41

 -Lipids (cholesterol and mono/diglycerides of fatty acids)

C-H stretching (symmetric)  of – CH3

2875

 

+

5

C-H stretching of C-H in methine groups

2899

 

 

5

C-H stretching of C-H

2916

 

 

5

C-H stretching (symmetric)  of > CH2 in fatty acids

2925

+

+

5, 38

C-H stretching (symmetric)  of > CH2 in fatty acids

2964

+

+

5

- Proteins (α-Amylase, Albumin, Cystatins, Mucins, Proline-rich proteins, sIgA)

- Hormones (Cortisol, Testosterone)

Primary and secondary amines (H2 and NHR)

3067

+

+

5

N-H stretching (Amide A) of proteins

3130

 

 

5

N-H stretching (amide A) of proteins

3204

+

+

5

N-H stretching (amide A) of proteins

3290-3293

+

+

38, 41

N-H stretching (amide A) of proteins

3349

 

 

5

(ΝΗ)(ΝΗ2) asymmetric vibrations

3411

 

 

5

O-H stretching of hydroxyl groups

3437

 

 

5

O-H stretching of hydroxyl groups

3461

 

 

5

 

Statistical analysis

Statistical analysis of the changes in mineral-organic and carbon-phosphate ratios in the dry residues of mixed saliva for the groups of patients was performed with the use of the professional software for the statistical analysis SPSS v.19 for Windows (SPSS Inc., Chicago, Illinois, USA). Statistical analysis was conducted at the statistical significance level of p<0.05, n=200. To find statistical significant differences in experimental data t-tests have been used after Shapiro-Wilk test to check normal distribution in sampling. The results in Table 3 and in Figures 5–6 are presented as a mean with standard deviation (M±SD), and the p-level of statistical significance of the results is also indicated.

 

Results

The IR transmission spectra of mixed saliva collected at the different stages of the study (according to the described regulations) were obtained for all the participants and are presented in Figures 2-5. As seen from these figures, the application of synchrotron radiation in the second stage of the study for the analysis of samples (together with the IR microscope) compared with the technique used in the first stage made it possible to obtain IR transmission spectra of the samples, providing a better signal-to-noise ratio and better resolution. 

The primary analysis of the experimental data demonstrated that all of the obtained spectra included the same set of vibration modes and were only slightly different in the intensities of certain vibration modes. It should be noted that IR spectra obtained in the second stage revealed more information on the qualitative composition of the samples due to the specific features of their excitation. Taking this in account, only normalised IR transmission spectra of the mixed saliva were averaged over the group of patients participating in the experiment (as presented in Figures 2-5).

IR transmission spectra obtained with the use of synchrotron radiation and a high-pressure attachment with a diamond prism to an IR microscope are given in Figures 4-5.

 


Figure 2. IR transmission spectra, obtained with the use of ATR attachment with a diamond prism, of the mixed saliva taken before and after the use of multi-mineral toothpaste at the first stage of the study. 1 – IR spectrum of the reference mixed saliva sample, 2 – spectrum of mixed saliva taken five minutes after use of multi-mineral complex toothpaste, 3 – spectrum of the mixed saliva taken 30 minutes after the use of toothpaste, 4 – spectrum of the multi-mineral complex toothpaste.

 


Figure 3. IR transmission spectra obtained with the use of ATR attachment with a diamond prism, of the mixed saliva sampled before and after intake of calcium glycerophosphate tablets in the first stage of the study. 1 – IR-spectrum of the mixed saliva reference sample, 2 – IR-spectrum of the mixed saliva taken on the fourth day after taking the calcium glycerophosphate for three days, 3 – spectrum of a calcium glycerophosphate tablet.

 


Figure 4. IR transmission spectra obtained with the use of synchrotron radiation and high-pressure attachment with a diamond prism to IR microscope of the mixed saliva taken before and after the use of multi-mineral complex toothpaste in the second stage of the study. 1– IR-spectrum of the mixed saliva reference sample, 2 – spectrum of the mixed saliva taken five minutes after the use of toothpaste and a thorough oral rinsing, 3 – spectrum of the mixed saliva taken 30 minutes after the use of toothpaste and a thorough oral rinsing, 4 – spectrum of the multi-mineral complex toothpaste.

 


Figure 5. IR transmission spectra obtained with the use of synchrotron radiation and high-pressure attachment with a diamond prism to IR microscope of the mixed saliva taken before and after intake of calcium glycerophosphate tablets in the second stage of the study. 1 – IR-spectrum of the mixed saliva reference sample, 2 – IR-spectrum of the mixed saliva taken on the fourth day after three days tablet taking and a thorough oral rinsing, 3 – spectrum of the calcium glycerophosphate tablet.

 

The analysis of the obtained IR spectra was performed based on a number of data taken from a set of reference sources, where human mixed saliva and hard dental tissues, as well as phosphates related to the formation of dentin and enamel were investigated by means of IR spectroscopy [5, 38, 41-45]. A list of the active vibrations in the spectra of the first and second stages of the study, the ranges, and the frequencies with the peaks of vibration bands are presented in Table 1 along with their assignments to the groups of vibrations.

From the obtained experimental data (Figures 2-5, Table 2), it follows that the main vibration bands in the IR transmission spectra of all the mixed saliva samples from the first and second stages of the study can be assigned to the following groups and complexes. The first and most interesting group of high-intensity vibrations arranged in all spectra within 900–1200 cm-1 is related to the modes, and their appearance is connected with the presence of phosphorus derivatives in the samples, such as phosphates, glycerophosphates and phospholipids [38, 40]. The observed similarity of blood and saliva spectra concerning the modes arranged at the value of 1050 cm-1 indicates that these vibrations are due to the organic derivatives of phosphates, glycerophosphates and phosphatase, namely to the C–O–P–O–C complex (Table 2).

The subsequent large group of vibration bands localised in the range of 1240–1700 cm-1 can be related to the secondary amides: Amide I (80% C=O stretch in the range of 1615–1675 cm-1), Amide II (60% N–H bend and 40% C–N stretch in the range of 1520–1575 cm-1) and Amide III (40% C–N stretch and 30% N–H bend in the range of 1270–1315 cm-1). Modes arranged in the experimental spectra in the range of 1400–1430 cm-1 belong to C=O stretch (symmetric) vibrations of COO and CH2/CH3 groups (Table 2).

A group of bands in the IR spectra, localised in the range of 2750–2950 cm-1, correspond to vibrations of C-H bonds. A broad vibration band within the range of 3250–3450 cm-1 is related to N‑H bonds of proteins and hormones. It can also be connected with the presence of O-H hydroxyl groups (i.e. water) in the samples.

Moreover, in the IR absorption spectra of the mixed saliva, obtained with the use of synchrotron radiation (Figures 3 and 4), certain vibration bands were observed that can be associated with the appearance of OCN (Amide IV), NH (Amide V) and C=O (Amide VI) vibrations of proteins  arranged at 500–700 cm-1.

One should note that in the IR spectra of the mixed saliva collected on the fourth day, after three days of taking tablets and the spectrum of the calcium glycerophosphate, there is one more additional group of vibrations with a peak in the range of 730–770 cm-1. In the spectra obtained with the use of synchrotron radiation, two vibrations can be well resolved within the indicated spectral range, while in the spectra obtained with the use of an ATR attachment with the diamond prism, only one mode is observed for the samples from the first stage. This is the result of the better resolution for low-intensity vibration bands provided by the use of synchrotron radiation and methods of IR spectromicroscopy. It is necessary to emphasise that the appearance of these vibrations, their intensity and spectral position are identical for IR spectra from the first and second stages of the study. This fact is indicative of the complete correlation of IR spectroscopy data, independent of the method of excitation of IR radiation, as well as of the reproducibility of the experimental data.

There are no vibrations in the above mentioned range of IR-spectrum before proceeding with the endogenous prophylaxis or exogenous prophylaxis. Based on the principles previously described [43], it seems impossible to correlate a group of vibrations characterised by the maxima at 730–770 cm-1 with the vibrations of C-H bonds. However, this vibration mode can be related to the vibrations of the P-O bond in the Р2О7 group as a result of decomposition of the inorganic phosphate complexes. Indeed, these vibration modes have been observed under thermal decomposition of inorganic compounds [45].

Figures 2-5 represent IR spectra of the mixed saliva samples (together with the transmission spectra of multi-mineral complex toothpaste) on the basis of calcium glycerophosphate and IR spectra of the tablet on the basis of the mineral complex and a calcium glycerophosphate. The analysis of the experimental data and their comparison with the spectra of the mixed saliva demonstrated that in the IR spectra of the preventive agents, one can see the groups of vibrations identical to those observed in the spectra of mixed salivas. It is due to the presence of similar organic-mineral groups and complexes in the composition of these preventive agents. Thus, application of the chosen preventive agents must be revealed in the changes of an organic-mineral balance of the mixed saliva and it can be observed in the IR spectra of the investigated samples.

Based on the proposed assumptions and using IR spectroscopy data, the above-named changes in the organic-mineral balance can be explored by the calculations and analysis of mineral-organic and carbon-phosphate ratios between the mineral and organic components in the mixed saliva. To calculate the first ratio it is sufficient to consider the ratio of the integral area (S3, Sˊ3) in the IR spectra (spectral regions at 900–1200 cm-1 and 730–770 cm-1) to the integral area (S1, Sˊ1) of vibration band 1615–1775 cm-1, related to Amide I (Figures 2-5, δ(S3/S1), δ(Sˊ3/Sˊ1)). The carbon-phosphate ratio can be calculated from the ratio of integral area (S2, Sˊ2) of vibration bands for C=O and CH2/CH3 bonds, localised in the range of 1430–1400 cm-1, to the integral area (S3, Sˊ3)  of phosphate bands in the IR spectrum (900–1200 cm-1 and 730–770 cm-1) (Figures 2–5, δ(S2/S3), δ(Sˊ2/Sˊ3)). Calculations of these ratios were performed with the use of the software OPUS (Bruker), including a wide set of functional facilities for different types of measurements, data treatment and evaluation obtained by IR spectroscopy. The results of quantitative calculations of relative changes in mineral-organic and carbon-phosphate ratios between the mineral and organic components in the mixed saliva in comparison of the reference sample at the different stages of the experiment are presented in Table 3 and in the Figures 6 and 7. It should be noted these ratios are averaged over the groups of participants taking part in the investigations for the different stages of the study and are presented as a mean ± standard deviation.

 


Figure 6. Relative changes in mineral-organic ratios at the first and the second stages of the study. δ1(S3/S1) – 5 min after the use of multi-mineral complex toothpaste; δ2(S3/S1) – 30 min after the use of multi-mineral complex toothpaste; δ3(Sˊ3/Sˊ1) – use of calcium glycerophosphate tablets. S3,S’3 – the integral area of phosphates in the IR spectra (spectral regions at 900–1200 cm-1 and 730–770 cm-1); S1,S’1 – the integral area of vibration band 1615–1775 cm-1, related to Amide I.

 


Figure 7. Relative changes in carbon-phosphate ratios at the first and the second stages of the study. δ1(S2/S3) – 5 min after the use of multi-mineral complex toothpaste; δ2(S2/S3) – 30 min after the use of multi-mineral complex toothpaste; δ3(Sˊ2/Sˊ3) – use of calcium glycerophosphate tablets. S2,Sˊ2 – the integral area of vibration bands for C=O and CH2/CH3 bonds, localised in the range of 1430–1400 cm-1, S3,S’3 – the integral area of phosphates in the IR spectra (spectral regions at 900–1200 cm-1 and 730–770 cm-1).

 

Table 3. Calculations of sampling-averaged relative changes in mineral-organic and carbon-phosphate ratios between the mineral and organic components in the mixed saliva in comparison to the reference sample at the different stages of the study

The stages of the study/types of preventive measures

AvRC in M/O ratio, %

AvRC in C/Ph ratio, %

Experiment №1

5 min after the use of m-m complex toothpaste (ex. preventive measure)

+69.8±2.1, p=0.032

-47.8±1.9, p=0.025

30 min after the use of m-m complex toothpaste (ex. preventive measure)

-3.1±1.4, p>0.05

+1.1±1.6, p>0.05

use of CaGP tablets (end. preventive measure)

+9.7±2.0, p=0.015

–50.6±1.9, p=0.011

Experiment № 2

5 min after the use of m-m complex toothpaste + thorough oral rinsing (ex. preventive measure )

+7.1±2.2, p=0.029

–9.3±2.7, p=0.033

30 min after the use of m-m complex toothpaste + thorough oral rinsing (ex. preventive measure )

-1.7±1.9, p>0.05

–2.0±1.7, p>0.05

 

On the fourth day after taking the CaGP tablets + thorough oral rinsing (end. preventive measure)

+11.7±1.8, p=0.017

–53.7±1.4, p=0.009

The data are presented as mean with standard deviation - M±SD.
AvRC, averaged relative change; M/O ratio, mineral-organic ratio; C/Ph ratio, carbon-phosphate ratio; m-m, multi-mineral; ex., exogenous; end., endogenous; CaGP, calcium glycerophosphate.

 

Discussion

Our approach is based on the mathematical estimation of the changes in mineral-organic and carbon-phosphate ratios for human mixed saliva before and after the use of exo- and endogenous drug prevention based on the experimental data obtained by IR-spectroscopy. The use of IR-spectroscopy is appropriate due to its high precision, non-invasive character, clarity and selectivity, especially in dental research [38, 41–46].

The qualitative evaluation of changes in the mineral-organic δ1(S3/S1), δ2(S3/S1), δ3(Sˊ3/Sˊ1) (Figure 6) and carbon-phosphate δ1(S2/S3), δ2(S2/S3), δ3(Sˊ2/Sˊ3) (Figure 7) ratios  were deduced from mixed saliva composition (Table 3). It is well known that the oral cavity contains mixed saliva with a composition different from that of a mix of gland fluids [1, 8, 47]. For exogenous and endogenous prevention, there will also be derivatives of the preventive measures which enter the mixed saliva, either through the oral cavity (toothpaste) or through the gland fluids (use of a mineral complex of calcium glycerophosphate). Hence, based on changes occurring in the composition of the mixed saliva at different stages of prevention, one can evaluate their efficiency for long-term maintenance of the mineral and organic composition of the mixed saliva to compensate for mineral loss. Obvious changes in carbon/phosphate and mineral/organic ratios can be observed at the different experimental stages as shown in Figures 6-7. 

As indicated by the results from the first stage of the study (see Figures 6 and 7), the use of multi-mineral complex toothpaste results in a considerable increase in the mineral-organic ratio and a decrease in the carbon-phosphate ratio, suggesting that the exogenous source can considerably increase the mixed saliva phosphate content δ1(S3/S1) and δ1(S2/S3). However, this effect is short-term as the values returned to those observed before toothpaste use 30 minutes after brushing δ2(S3/S1) and δ2(S2/S3) (analysis demonstrated almost total absence of statistically valuable difference for the level of p<0.05).  

Furthermore, thorough oral rinsing directly after brushing and 30 minutes later completely nullified the positive effect of the multi-mineral toothpaste directed at changing the organic-mineral balance of the mixed saliva δ2(S3/S1) and δ2(S2/S3) (Figures 6, 7 – columns marked oral rinsing). In both cases, a negative relative change of the organic-mineral ratio as compared with the reference sample was observed, with no statistical significant difference, thus, there was a washing-out of the mineral groups and complexes remaining in the oral cavity after the application of the toothpaste (Table 3). Nonetheless, the main purpose of these complexes and mineral groups is to promote remineralisation. 

Analysis of the changes in the mineral-organic and carbon-phosphate ratios after the participants had taken the calcium glycerophosphate tablets for three days showed statistically significant differences (p<0.05) and 9% increase in the mineral-organic ratio compared to the reference sample δ3(Sˊ3/Sˊ1) and δ3(Sˊ2/Sˊ3). Similarly, an average increase of ~12% was observed in the mineral-organic ratio compared to the reference sample in the second stage of the study. This increase is statistically significant (p<0.05). The relative change in mineral-organic value in the second stage as compared with the first stage is due to the use of synchrotron radiation and an IR microscope, which allows a more precise determination of the corresponding values (Figures 6).

The data shows that calcium glycerophosphate tablets can change the organic-mineral balance in mixed saliva, increasing the content of mineral groups and complexes. Note that the content of endogenous, biologically accessible phosphate groups and complexes in the mixed saliva, according to our data, exceeds by approximately 12% that of the mixed saliva before the use of the prevention agents (in the reference (check) sample). It is also important to point out that just in this case a long-term effect of the mineral groups obtained by an endogenous way can be achieved.

Due to the multi-stage character of the ion exchange, the mineral groups and complexes (phosphates) should be retained for a long time within the oral cavity and should be in contact with the dental enamel [1, 6, 48-50]. As shown, this could be realised only under an endogenous supply of the ions [34, 35, 51]. The concentration of the ions in the mixed saliva ought to exceed the concentration in the hydrate layer of enamel in order to provide an efficient process of diffusion from the surface of enamel [1, 14].

It is well known that excessive levels of calcium and phosphates in mixed saliva result in a rapid deposition of calcium phosphates in the form of mineral phases on the surface of enamel, which hinders normal remineralisation [6]. A short-term increase in the concentration over the standard values stipulates the deposition and formation of foreign calcium phosphates resulting in the limited permeability of substances through the biofilm, the origin of dental deposit, and enhanced enamel solubility. Therefore, we believe that the identified effect of the long-term presence of the necessary groups and complexes during the use of both endo- and exogenous prevention methods creates the necessary conditions for the standard organic and mineral exchange in the oral cavity.

The use of endogenous and exogenous methods of caries prevention induces changes in the mineral-organic and carbon-phosphate ratios within human mixed saliva. However, the exogenous method only provides a short-term effect. Moreover, a thorough oral rinsing after brushing eliminates the beneficial effects directed at saturating the mixed saliva with ions, mineral complexes and groups (phosphates). On the contrary, the use of calcium glycerophosphate tablets in combination with exogenous prevention allows long-term saturation of the mixed saliva with mineral groups and complexes of phosphates, i.e. an average increase of 12% in their content in the mixed saliva.

 

Conclusion

Changes in the molecular composition of mixed saliva when using an exogenous method of caries prevention only provides a short-term effect, continuing for the first 30 minutes after the preceding prevention. Nonetheless, the use of calcium glycerophosphate tablets in combination with brushing (a combination of endogenous and exogenous prevention methods) leads to the long-term presence of high concentrations of ions, mineral complexes and groups (phosphates) in the oral fluid.

 

Acknowledgements

The part of this research was undertaken with The Infrared Microspectroscopy (IRM) beamline at the Australian Synchrotron (Victoria, Australia).

 

Funding

This work was supported by the grant of Russian Science Foundation, grant number 16-15-00003.

 

Availability of data and materials

All data collected is available by request.

 

Conflict of interests

The authors declare no conflict of interests.

 

Ethics approval and consent to participate

All patients whose data were used within the created survey had signed institutional consent for the participation research. All persons who participated in the survey signed written consent. Voronezh State University Ethics Committee approved this study (approval number 001.066-2015). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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About the Authors: 

Pavel V. Seredin – PhD, Associate Professor, Department of Solid State Physics and Nanostructures, Voronezh State University, Voronezh, Russia. http://orcid.org/0000-0002-6724-0063.
Dmitry L. Goloshchapov – PhD, Researcher, Department of Solid State Physics and Nanostructures, Voronezh State University, Voronezh, Russia. http://orcid.org/0000-0002-1400-2870.
Yuri A. Ippolitov – MD, PhD, Head of Pediatric Dentistry with Orthodontia, Voronezh State Medical University n.a. N.N. Burdenko, Voronezh, Russia. http://orcid.org/0000-0001-9922-137X.
Edvard S. Kalivradzhiyan – MD, DSc, Professor, Department of Orthopaedic Dentistry, Voronezh State Medical University n.a. N.N. Burdenko, Voronezh, Russia. http://orcid.org/0000-0001-5874-8327.

 

Received 3 October 2017, Revised 15 December 2017, Accepted 24 December 2017

© 2017, Seredin P.V., Goloshchapov D.L., Ippolitov Yu.A., Kalivradzhiyan E.S.
© 2017, Russian Open Medical Journal

Correspondence to Pavel V. Seredin. Address: Department of Solid State Physics and Nanostructures, Voronezh State University, University sq. 1, Voronezh, 394006, Russia. E-mail: paul@phys.vsu.ru. Phone: +7 4732 208363.

DOI: 
10.15275/rusomj.2018.0106