Scanning / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 6065739 |

Cíntia Mirela Guimarães Nobre, Norbert Pütz, Matthias Hannig, "Adhesion of Hydroxyapatite Nanoparticles to Dental Materials under Oral Conditions", Scanning, vol. 2020, Article ID 6065739, 12 pages, 2020.

Adhesion of Hydroxyapatite Nanoparticles to Dental Materials under Oral Conditions

Academic Editor: Kislon Voïtchovsky
Received31 May 2019
Revised21 Feb 2020
Accepted22 Apr 2020
Published05 May 2020


Hydroxyapatite nanoparticles (nano-HAP) are receiving considerable attention for dental applications, and their adhesion to enamel is well established. However, there are no reports concerning the effects of HAP on other dental materials, and most of the studies in this field are based on in vitro designs, neglecting the salivary pellicle-apatite interactions. Thus, this in situ pilot study aims to evaluate the effects of three hydroxyapatite-based solutions and their interactions with different dental material surfaces under oral conditions. Hence, two volunteers carried intraoral splints with mounted samples from enamel and from three dental materials: titanium, ceramics, and polymethyl-methacrylate (PMMA). Three HAP watery solutions (5%) were prepared with different shapes and sizes of nano-HAP (HAP I, HAP II, HAP III). After 3 min of pellicle formation, 10 ml rinse was performed during 30 sec. Rinsing with water served as control. Samples were accessed immediately after rinsing, 30 min and 2 h after rinsing. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the particles, and SEM evaluated the pellicle-HAP interactions. SEM and TEM results showed a high variation in the size range of the particles applied. A heterogeneous HAP layer was present after 2 h on enamel, titanium, ceramics, and PMMA surfaces under oral conditions. Bridge-like structures were visible between the nano-HAP and the pellicle formed on enamel, titanium, and PMMA surfaces. In conclusion, nano-HAP can adhere not only to enamel but also to artificial dental surfaces under oral conditions. The experiment showed that the acquired pellicle act as a bridge between the nano-HAP and the materials’ surface.

1. Introduction

The application of hydroxyapatite nanoparticles (nano-HAP) in dentistry has received considerable attention in the past few years [14]. Hydroxyapatite (Ca10(PO4)6(OH)2) is a calcium-phosphate ceramic and the main mineral component of the dental enamel, the hard tissue on the exterior layer of a human tooth. This crystallite has a needle-like morphology and represents more than 90% of enamel mineral structure [57]. Synthetic nano-HAP are considered morphologically and structurally similar to the apatite crystals of enamel, revealing a high biocompatibility [1, 5, 6]. A recent literature review from Epple M. concluded that, when applied in adequate doses, HAP particles present no side effects to the human health, being a nontoxic and nonimmunogenic material [8]. Other characteristics that make it a desirable biomimetic material include high surface energy, high solubility, and optimal bioactivity [6, 8, 9].

Accordingly, nano-HAP has been increasingly employed for different dental applications. For instance, in restorative and preventive dentistry, HAP may be used to remineralize initial caries lesions on enamel, protecting teeth against caries and dental erosion [7, 1013]. Given its properties, hydroxyapatite was added in various toothpaste and mouthrinse as an additional compound, not only to serve as a reparative material for damaged enamel but also as a polishing, whitening, and desensitizing agent [5, 7, 1416]. Additionally, evidence on literature demonstrates that the size and shape of hydroxyapatite particles plays an important role, affecting the HAP properties and applications [17]. There are several kinds of raw synthetic HAP commercially available but, according to recent publications, those composed by smaller particles achieve better remineralizing effects [15, 16, 18, 19].

Although most of the literature confirmed these promising properties of hydroxyapatite nanoparticles, there are very divergent results [7]. While an increasing number of experiments revealed the potential of nano-HAP to repair enamel [1, 2, 1921], other studies present no difference between the nano-HAP treatment and the standard fluoride treatment regarding the remineralization effects, some even showing less effective results [3, 11, 22]. These varying conclusions might be related to the methodology applied. Most studies regarding hydroxyapatite nanoparticles as an oral care product comprise in vitro designs, which give limited results. This method does not reproduce the real intraoral conditions, due to various individual-related factors, such as salivary flow, nutrition, or bacteria existent in the oral cavity [23].

Furthermore, most of the in vitro results show the direct interaction between HAP and the enamel surface [1, 2, 4, 17]. However, under oral conditions, a proteinaceous layer called acquired pellicle is immediately formed on any surface after exposure to the intraoral environment. The acquired pellicle is defined as an acellular and bacteria-free film composed of many salivary molecules, such as proteins, glycoproteins, mucins, immunoglobulins, lipids, bacterial components, and other macromolecules [2325]. The pellicle acts as a protective barrier, has lubricant function, and also changes the free energy and charge of the material surface [25]. Thus, the pellicle-apatite interaction is the first step to understand the mechanisms behind the reported effects of the nano-HAP under oral conditions. Hence, an in situ design is the most appropriate method to evaluate such interaction, since it reproduces real-life oral condition, providing a more reliable result.

There are very few in situ studies concerning hydroxyapatite particles as an oral product, although they consistently show that HAP increases the protective effects of the pellicle against erosion [26], and that it can be used as remineralizing agent [2729]. Recent in situ publications also showed that nano-HAP containing rinsing solutions were capable of reducing the initial bacterial adhesion on enamel without killing the bacteria. This is caused by an antiadherent effect against biofilm formation on enamel surfaces, thus having the potential to act as a biomimetic biofilm managing agent [9, 30]. However, additional in situ/in vivo studies are needed to clarify the HAP-pellicle interactions and the hydroxyapatite’s mechanism of action.

As the pellicle is not restricted to enamel, another valuable question is whether the HAP particles would adhere to other dental materials, extending their benefits to artificial dental surfaces commonly used for oral rehabilitation. Thus, the aim of this in situ pilot study is to investigate if it is possible to adhere nano-HAP onto different dental materials’ surfaces under oral conditions and to evaluate the effects of three different HAP powders. Additionally, we also assessed if there is any difference in the pellicle-HAP interactions between enamel and other dental substrates, such as titanium, polymethyl methacrylate resin, and ceramics.

2. Materials and Methods

This in situ pilot experiment was conducted in two healthy volunteers, aged between 30 and 35 years old. The inclusion criteria were good oral health with no signs of gingivitis, caries, or unphysiologically salivary flow rate [31]; no systemic diseases; no use of antibiotics or any kind of periodontal treatment within the past 6 months; nonsmoker; not pregnant or breastfeeding and absence of orthodontic appliances. The study protocol was approved by the Medical Ethics Committee of the Medical Association of Saarland, Germany (no. 283/03–2016), and an informed written consent was obtained from the subjects.

2.1. Tested Solutions

Hydroxyapatite nanoparticles (nano-HAP) in different sizes were used for the test solution (Table 1). The particle size was verified by scanning electron microscopy (SEM) and by transmission electron microscope (TEM). The containing HAP test solution was prepared mixing 0.5 g in 10 ml bidistilled water. Water rinse (10 ml) served as negative control. The subjects used the different rinsing solutions in different weeks to avoid interferences between tests and control solutions, preventing a possible crossover effect. According to our established protocol, the first solution used by each volunteer was the water control. One week later, the HAP test solutions were introduced respecting the following order: HAP I, HAP II, and HAP III; and respecting also a two weeks clearance period between each of them.

CompanyCountryMedian sizeConfiguration

HAP IEpruiChina40 nmNeedle
HAP IIKalichemItaly100 nmNeedle
HAP IIISigma AldrichGermany< 200 nmSpherical

2.2. Samples

In addition to dental enamel, other common materials used for oral rehabilitation appliances were addressed: titanium (most used material on dental implants), feldspathic ceramics (used as dental restorative material), and polymethyl methacrylate resin (common material for the base of the prosthesis).

2.2.1. Enamel Samples

Square enamel slabs measuring approximately 5 mm long and 1 mm thick were prepared from bovine incisors teeth. Later, they followed a standardized grinding procedure with grid sandpapers (from 240 to 2500 grit for SEM and TEM), and the smear layer was removed according to the following standardized cleaning procedure [30]. First, samples were washed with 3% NaOCl for 3 min, followed by ultrasonication with distilled water for 5 minutes. Afterwards, a disinfection in 70% ethanol for 15 minutes took place. And, finally, samples were washed with sterile water and stored at 4°C in sterile water for 24 h.

2.2.2. Titanium Samples

Titanium (Ti) discs microstructured surface by sandblasting and acid etching (SLA) with , grade 2, were obtained from Dentsply Implant Systems Sirona, Mannheim, Germany (diameter 5 mm, height 1 mm). Ti discs were polished by wet grinding with abrasive paper (800 to 4000 grit). To remove the resulting smear layer and for disinfection purposes, Ti discs were immersed in isopropanol (70%) for 10 min, followed by washing in distilled water.

2.2.3. Ceramic Samples

Square/rectangular ceramic slabs measuring approximately 5 mm long and 1 mm thick were cut from feldspathic ceramic blocks (VITABLOCS Mark II from VITA Zahnfabrik, Germany). These slabs were polished with grit sandpapers (from 240 to 4000 grit). For cleaning and disinfection purposes, the ceramics samples were immersed in isopropanol (70%) for 15 min, followed by a wash in distilled water.

2.2.4. PMMA Samples

Polymethyl methacrylate (PMMA) resin with 5 mm diameter and 1 mm thick was prepared by a prosthetic technique from Universität des Saarlandes with an autopolymerizing prosthetic resin kit (powder and monomer) from Paladent® (Kulzer, Germany) in accordance with the manufacturer’s instructions. Polishing was performed with grid sandpapers (1200 to 4000 grit), and for cleaning purposes, the following protocol was applied. The samples were placed three times (10 min each) in the ultrasonicator, two times with isopropanol 70%, and one with sterile water. Finally, the samples were dried before attaching to the splints.

2.3. Oral Exposure

To evaluate the possible interaction between the hydroxyapatite particles and the acquired pellicle, the samples were mounted in customized maxillary splints (Figure 1). They were prepared from 1.5 mm thick methacrylate foils, extending from premolars to the first molar. Perforations in the buccal aspects of the splints were prepared to fix the polyvinyl siloxane impression material, in which each material was placed.

Before the use of the splints, the volunteers brushed the teeth without toothpaste and rinsed with tap water only to avoid possible interferences from the compounds of the toothpaste. After the splints were placed intraorally with 3 samples on each side (total of 6 samples of the selected material), a one-time rinse (30 s) of 10 ml of the selected solution (HAP I, HAP II, HAP III, or water) was performed after a 3 min of pellicle formation. One sample from each side was removed immediately after rinse, 30 min and 120 min after rinse. After each removal, the samples were rinsed with distilled running water to remove nonadsorbed particles. Then, samples were prepared for scanning electron microscopy (SEM). Each volunteer used the splint for two hours, from 10 h to 12 h. The use of the splint carrying 6 samples was repeated for each of the 4 materials and each of the 4 tested solutions, giving a total of 96 samples per volunteer.

2.4. Scanning Electron Microscopy

In order to characterize particle size and shape of the different powders, HAP I, HAP II, and HAP III solutions were directly applied to SEM sample holder (aluminium plate) and analyzed by SEM and energy-dispersive X-ray spectroscopy (EDX) evaluations in a XL30 ESEM FEG (FEI, Eindhoven, The Netherlands) at 5 kV and 10 kV at 20,000-fold magnification.

Intraorally exposed samples were prepared for SEM analysis to investigate the pellicle coverage at different times after rinsing and its relationship with hydroxyapatite particles. After oral exposure, samples were washed with sterile water followed by a fixation with 1 ml 2% glutaraldehyde in 0.1 M cacodylate buffer during 2 h at 4°C. Finally, the specimens were left to airdry overnight at room temperature in the air chamber. The next day, samples were sputter-coated with carbon and analyzed by SEM and energy-dispersive X-ray spectroscopy (EDX) evaluations in a XL30 ESEM FEG (FEI, Eindhoven, The Netherlands) at 5 kV and 10 kV, consecutively, at up to 20,000-fold magnification.

2.5. Transmission Electron Microscope

In order to evaluate the particle’s sizes, 5% nano-HAP solutions were prepared from each powder and directly applied on Pioloform-coated copper grids and analyzed on TEM Tecnai 12 Biotwin (FEI, Eindhoven, The Netherlands) under a magnification up to 100.000-fold.

Additionally, a supplementary experiment was performed to validate the presence of the pellicle layer. The volunteers carried the same splints with only 2 enamel specimens (one each side) and performed a one-time 30s-rinse with 10 ml of HAP II solution after 3 min of pellicle formation. The samples were removed from the oral cavity 30 min after rinsing. Immediately after volunteers took off their splints, the samples were washed with sterile water to remove not adhered bacteria. The specimens were placed in 1,5 ml tubes with 1 ml 1% Glutaraldehyde fixing solution at 4°C during 1 h. After primary fixation, samples were washed with cacodylate buffer 0.1 M 4 times, 10 min each, and stored at 4°C in cacodylate buffer. Samples were fixed in osmium tetroxide during 1 h in a dark chamber at room temperature, followed by 5 times of 10 min wash in distilled water and immersion in 30% ethanol overnight. Following the TEM preparation procedures, dehydration was performed at room temperature. The samples passed through series of 50% (2x 10 min), 70% (2x 20 min), 90% (2x 30 min), and 100% (2x 30 min) ethanol. Finally, they were further immersed in 100% acetone 2 times, 30 min each, and stored overnight in an acetone/Araldite (Agarscientific, Stansted, United Kingdom) mixture plus 3% accelerator (mixture A) at room temperature. On the following day, mixture A was poured out and a second mixture, mixture B was prepared (Araldite mixture with 2% accelerator). Samples were left again overnight in mixture B at room temperature in the air chamber. Next, a new mixture B was used to fill the embedding forms. Then, samples were incubated for polymerization for 48 h at 65°C.

Finally, ultrathin sections were cut in an ultramicrotome with a diamond knife (Leica EM UC7, Germany) and mounted on Pioloform-coated copper grids and contrasted with aqueous solutions of uranyl acetate and lead citrate at room temperature. After an intensive wash with distilled water, biofilms could be analyzed with a TEM Tecnai 12 Biotwin (FEI, Eindhoven, The Netherlands) under a magnification up to 100.000-fold.

3. Results and Discussion

This pilot study provided, for the first time, evidence that it is possible to accumulate round- and crystallite-shaped nano-HAP on the natural enamel surface, as well as on different artificial dental surfaces under oral conditions, and the pellicle may play an important role on the particles’ adhesion mechanism.

3.1. Enamel Samples

In this study, bovine enamel was applied. The use of human teeth for research has decreased over the last decades due to several factors, such as difficult standardization, difficulty to obtain sufficient amounts, and mostly due to ethical issues [32, 33]. Hence, the use of animal teeth came as an alternative. Bovine enamel has similarities with human enamel regarding mineral composition, density, and structure. Bovine teeth can be easily obtained on a large scale, and they have more uniform characteristics. Additionally, because of their bigger size and flatter surface, they are also easy to handle [4, 32, 34].

3.2. Hydroxyapatite Particles

Previously published studies demonstrate that the particles’ and aggregates’ size and shape affect the HAP properties and its applications, and the particle size is a key factor for adhesion on enamel [4, 15, 16, 18]. In an in vitro study, Li et al. proposed that crystallites of HAP with a 20 nm diameter would provide the best size for nano-HAP applications [17]. In the present study, three different hydroxyapatite powders, containing particles with a median size in the nanoscale were evaluated, hypothesizing that smaller nanoparticles (HAP I) would have better adhesion results. The particles’ size of each hydroxyapatite powder was analyzed with SEM and TEM. HAP I and HAP II had a small size range, presenting a certain uniformity in the size of its particles. HAP I had particles ranging from 30 to 70 nm (Figure 2), while HAP II particles ranged from 60 to 120 nm (Figure 3). HAP III had the largest size variation, ranging from approximately 50 nm to particles even bigger than 1 μm (Figure 4). These variations on the particles’ sizes of each hydroxyapatite powder applied in this study revealed a certain similarity between them. Therefore, the size influence of apatite particles on their adhesion behavior under oral conditions could not be evaluated in detail in this study. The present findings indicate that better methods for HAP synthetization should be performed to standardize the particle’ size.

Concerning the shape characteristics of HAP, the present SEM and TEM analysis confirmed the crystallite-like structures of the HAP I and HAP II particles (Figures 2 and 3). Figure 4 shows a majority of round-shaped particles for HAP III, but on the TEM picture, nonglobular structures are also present. Thus, HAP III is composed by rounded and a few needle-like particles. Interestingly, the round particles in this experiment adhered to each surface in a similar way as the needle-like particles. In vitro experiments revealed that HAP crystallites would have better adhesion to enamel because they have a morphology similar to natural enamel building units [4, 17]. But another in vitro study showed that spherical nano-HAP had a great potential to remineralize the enamel [1]. To our knowledge, this is the first in situ study comparing the effects between spherical and crystallite-like nano-HAP, and it showed that both can adhere to the pellicle formed in situ on different dental materials.

Additionally, regardless of their different sizes and shapes, all of the three tested hydroxyapatites had the tendency to agglomerate in aqueous solution (Figures 24), forming aggregates of different sizes and irregular shapes. Individual particles were more frequently seen in the HAP III solution, presenting a clear round-shaped conformation. HAP I and II rarely allowed observing individual crystallites when in watery solution. This propensity to aggregate might be related to the characteristic of hydroxyapatite being a dipole molecule and consequently to the Van der Waals and electrostatic forces in between the particles [30]. Another common result for all tested solutions was that the quantity of hydroxyapatite particles and the clusters’ size on each material surface decreased over time (Figures 58). This pattern can be explained by the continuous process of adsorption and desorption that takes place in the oral cavity [25]. After rinsing with the HAP solutions, the particles and clusters were deposited on the material surface. Over time, those particles are dissolved in the saliva. Thereby individual intraoral shearing forces help to disrupt them into small aggregates and single particles, where some of them are readsorbed to the pellicle and others are swallowed. The continuous dissolution of hydroxyapatite nanoparticles also takes place and intensifies these results. Additionally, bigger clusters are more susceptible to shearing forces, removal from the material surface, and later swallowing [4, 16].

3.3. Hydroxyapatite Adhesion Efficacy

SEM micrographs from the samples rinsed with water (control) (Figures 58) showed a thin and uneven film with globular structures on all surfaces after three minutes of intraoral exposure. In order to verify the existence of a pellicle layer on the specimens’ surface TEM-analysis of selected samples was performed. The TEM figure (Figure 9) verifies the presence of the acquired pellicle on the specimens. After 30 min, the pellicle coverage increased on all four tested materials, leading to an almost fully knotted surface after 2 h, composed by salivary protein aggregates with globular shape. Thus, the acquired pellicle formation in the control experiment progressed in accordance with the literature, which states that the adsorption of proteins and consequent formation of salivary pellicle starts within seconds after a material is exposed to oral cavity environment [25]. Protein-protein interactions continue, and a thicker and more homogeneous proteinaceous film is visible after 30 and 120 minutes. Thus, the amount of absorbed proteins increased over time in all tested samples. Literature indicates that the acquired pellicle growth reaches a plateau after 30-90 min, reaching its full thickness around one or two hours [25].

When the 5% nano-HAP solutions were applied, the nanoparticles were randomly distributed on all samples’ surfaces (Figures 58). Immediately after the mouthwash, most of the samples presented their surface heterogeneously covered with particles and clusters with large variations of size and shapes. HAP I and HAP II yielded large cluster structures with sizes up to 4 μm. HAP III had a better coverage distribution on all materials surfaces immediately after rinse. Thirty minutes after rinsing, the number of adhered particles decreased, and more disperse particles could be seen on SEM; however, smaller clusters were also visible. Surprisingly, almost all nanoparticles were washed out on titanium samples rinsed with HAP I. Finally, 2 h after rinsing, even smaller particles were visible on SEM figures (Figures 58) and small clusters could still be found, but particles and clusters larger than 1 μm were rarely seen. The amount and the size of the hydroxyapatite clusters on each material surface decreased over time. The influence of HAP particle sizes was also reported by Jin et al. in an in vitro experiment, showing that particles in a nanometer range (<1 μm) had better adhesion to enamel [16]. The in situ study from Kensche et al. also revealed only isolated microclusters 2 h after mouthrinsing [30]. Thus, due to the larger contact area, smaller particles and clusters would better adhere to the pellicle components.

In summary, after 2 h of intraoral exposure, all samples presented a scattered and heterogeneous layer of nano-HAP in contact with the pellicle outer layer. A homogeneous coverage could not be achieved, probably due to the complex interaction that occurs in the intraoral environment, or due to the shape and size of the selected particles. Until now, the scarce in situ literature on this topic reported only the presence of adhesion between the HAP particles and the enamel surface [9, 30]. But based on the present results, it is possible to conclude that the adhesion of hydroxyapatite nanoparticles also occurs on other dental surfaces as well, such as titanium, ceramics, and polymethyl methacrylate resin, opening a promising research field in preventive dentistry. This study, however, presented some limitations. The stability of these adhesion interactions of the apatite particles on the different tested surfaces was not evaluated over longer periods of time. Another clear limitation was the number of volunteers, which made it not possible to perform a quantitative analysis. The reasons behind this choice are related to the increased number of times that each volunteer had to use the intraoral appliance. Therefore, more in vivo/in situ experiments with a higher number of subjects need to be performed to elucidate the molecular mechanisms behind the pellicle-apatite interactions.

The physical and chemical characteristics of each material influence the pellicle and biofilm formation and might also have an influence on HAP deposition [35]. Comparisons between all materials showed that ceramic samples had the smallest quantity of HAP accumulated after 2 h (Figure 7), while the PMMA samples presented higher numbers of particles and clusters after the same time (Figure 8). The porosity and retention areas from PMMA explains its association with higher HAP deposition [36, 37]. Concerning the HAP solution used, HAP II and III were more effective in covering titanium samples, and hydroxyapatite particles from HAP I were almost absent. Similar coverage is visible between the three solutions on enamel and on PMMA surfaces. Figure 7 shows that particles from HAP III were also accumulated on surface irregularities of ceramics caused by the polishing process. Thus, regardless of the round or crystallite shape and size variations, all three tested HAP nanoparticles could adhere to pellicle-covered enamel, titanium, ceramics, and PMMA.

Higher SEM magnification was used to analyze the interactions between the accumulated nano-HAP and the pellicle that covered each substrate surface. Interestingly, when the hydroxyapatite containing solutions were applied, it was possible to observe connective structures between the particle and the pellicle formed on enamel, titanium, and PMMA surfaces after 2 h of oral exposure to the respective rinses (Figure 10). On ceramics, there was no possibility to find these connective structures due to reduced quantity of HAP on this surface after 2 h. According to Vukosavljevic et al., pellicle precursors proteins, such as histatins or statherins have a high affinity to hydroxyapatite crystals present on natural teeth, starting the acquired pellicle formation process [38]. Thus, the adhesion of the synthetic nano-HAP could be related to these pellicle components, which act as a bonding agent. More in vivo/in situ studies should be performed to clarify these relationships in detail.

4. Conclusions

It was presented for the first time that, regardless of the shape and size, all nano-HAP applied as oral rising solutions presented good, but heterogeneous coverage on enamel, titanium, ceramic, and PMMA surfaces under oral condition. Therefore, nano-HAP can adhere not only to enamel but also to artificial dental surfaces under oral conditions. The pilot experiment revealed that in the presence of the acquired pellicle, a bridge between the nano-HAP and the materials’ surface could be observed.

Given the increasing importance of HAP nanoparticles in dentistry, it is significant to understand the mechanism of interaction of these particles with the intraoral environment. Despite the interesting results obtained in this pilot study, its limitations imply the need for more experiments with a higher number of subjects to better elucidate the pellicle-apatite interactions.

Data Availability

All data supporting the results are in the manuscript.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.


The authors would like to acknowledge Belinda König, who prepared the samples for TEM and the German Research Foundation (DFG, SFB 1027) for supporting in part this study.


  1. S. R. Shaffiey and S. F. Shaffiey, “Surface enamel remineralization by biomimetic nano hydroxyapatite crystals and fluoride ions effects,” Journal of Ceramic Processing Research, vol. 17, no. 2, pp. 109–112, 2016. View at: Google Scholar
  2. M. Lombardini, M. Ceci, M. Colombo, S. Bianchi, and C. Poggio, “Preventive effect of different toothpastes on enamel erosion: AFM and SEM studies,” Scanning, vol. 36, no. 4, pp. 401–410, 2014. View at: Publisher Site | Google Scholar
  3. L. P. Comar, B. M. Souza, L. F. Gracindo, M. A. R. Buzalaf, and A. C. Magalhaes, “Impact of experimental nano-HAP pastes on bovine enamel and dentin submitted to a pH cycling model,” Brazilian Dental Journal, vol. 24, no. 3, pp. 273–278, 2013. View at: Publisher Site | Google Scholar
  4. K. Fabritius-Vilpoux, J. Enax, M. Herbig, D. Raabe, and H. O. Fabritius, “Quantitative Affinity Parameters of Synthetic Hydroxyapatite and Enamel Surfaces In Vitro,” Bioinspired, Biomimetic and Nanobiomaterials, vol. 8, no. 2, pp. 141–153, 2019. View at: Publisher Site | Google Scholar
  5. M. Hannig and C. Hannig, “Nanomaterials in preventive dentistry,” Nature Nanotechnology, vol. 5, no. 8, pp. 565–569, 2010. View at: Publisher Site | Google Scholar
  6. D. Elkassas and A. Arafa, “The innovative applications of therapeutic nanostructures in dentistry,” Nanomedicine, vol. 13, no. 4, pp. 1543–1562, 2017. View at: Publisher Site | Google Scholar
  7. J. Enax and M. Epple, “Synthetic hydroxyapatite as a biomimetic oral care agent,” Oral Health & Preventive Dentistry, vol. 16, no. 1, pp. 7–19, 2018. View at: Publisher Site | Google Scholar
  8. M. Epple, “Review of potential health risks associated with nanoscopic calcium phosphate,” Acta Biomaterialia, vol. 77, pp. 1–14, 2018. View at: Publisher Site | Google Scholar
  9. C. Hannig, S. Basche, T. Burghardt, A. Al-Ahmad, and M. Hannig, “Influence of a mouthwash containing hydroxyapatite microclusters on bacterial adherence in situ,” Clinical Oral Investigations, vol. 17, no. 3, pp. 805–814, 2013. View at: Publisher Site | Google Scholar
  10. E. Pepla, L. K. Besharat, G. Palaia, G. Tenore, and G. Migliau, “Nano-hydroxyapatite and its applications in preventive, restorative and regenerative dentistry: a review of literature,” Annali di Stomatologia, vol. 5, no. 3, pp. 108–114, 2014. View at: Google Scholar
  11. A. Nozari, S. Ajami, A. Rafiei, and E. Niazi, “Impact of nano hydroxyapatite, nano silver fluoride and sodium fluoride varnish on primary teeth enamel remineralization: an in vitro study,” Journal of Clinical and Diagnostic Research, vol. 11, no. 9, pp. Zc97–Zc100, 2017. View at: Publisher Site | Google Scholar
  12. F. G. De Carvalho, B. R. Vieira, R. L. Santos, H. L. Carlo, P. Q. Lopes, and B. A. de Lima, “In vitro effects of nano-hydroxyapatite paste on initial enamel carious lesions,” Pediatric Dentistry, vol. 36, no. 3, pp. 85–89, 2014. View at: Google Scholar
  13. M. Y. Kim, H. K. Kwon, C. H. Choi, and B. I. Kim, “Combined effects of nanohydroxyapatite and NaF on remineralization of early caries lesion,” Key Engineering Materials, vol. 1347, pp. 330–332, 2007. View at: Google Scholar
  14. M. Okada and T. Furuzono, “Hydroxylapatite nanoparticles: fabrication methods and medical applications,” Science and Technology of Advanced Materials, vol. 13, no. 6, p. 064103, 2012. View at: Publisher Site | Google Scholar
  15. N. Eliaz and N. Metoki, “Calcium phosphate bioceramics: a review of their history, structure, properties, Coating Technologies and Biomedical Applications,” Materials, vol. 10, no. 4, p. 334, 2017. View at: Publisher Site | Google Scholar
  16. J. Jin, X. Xu, G. Lai, and K. H. Kunzelmann, “Efficacy of tooth whitening with different calcium phosphate-based formulations,” European Journal of Oral Sciences, vol. 121, no. 4, pp. 382–388, 2013. View at: Publisher Site | Google Scholar
  17. L. Li, H. Pan, J. Tao et al., “Repair of enamel by using hydroxyapatite nanoparticles as the building blocks,” Journal of Materials Chemistry, vol. 18, no. 34, pp. 4079–4084, 2008. View at: Publisher Site | Google Scholar
  18. Q. Hu, Z. Tan, Y. Liu et al., “Effect of crystallinity of calcium phosphate nanoparticles on adhesion, proliferation, and differentiation of bone marrow mesenchymal stem cells,” Journal of Materials Chemistry, vol. 17, no. 44, pp. 4690–4698, 2007. View at: Publisher Site | Google Scholar
  19. S. Huang, S. Gao, L. Cheng, and H. Yu, “Remineralization potential of nano-hydroxyapatite on initial enamel lesions: an in vitro study,” Caries Research, vol. 45, no. 5, pp. 460–468, 2011. View at: Publisher Site | Google Scholar
  20. S. B. Huang, S. S. Gao, and H. Y. Yu, “Effect of nano-hydroxyapatite concentration on remineralization of initial enamel lesion in vitro,” Biomedical Materials, vol. 4, no. 3, article 034104, 2009. View at: Publisher Site | Google Scholar
  21. C. Poggio, M. Lombardini, P. Vigorelli, M. Colombo, and M. Chiesa, “The role of different toothpastes on preventing dentin erosion: an SEM and AFM study®,” Scanning, vol. 36, no. 3, pp. 301–310, 2014. View at: Publisher Site | Google Scholar
  22. M. Esteves-Oliveira, N. M. Santos, H. Meyer-Lueckel, R. J. Wierichs, and J. A. Rodrigues, “Caries-preventive effect of anti-erosive and nano-hydroxyapatite-containing toothpastes in vitro,” Clinical Oral Investigations, vol. 21, no. 1, pp. 291–300, 2017. View at: Publisher Site | Google Scholar
  23. C. Hannig and M. Hannig, “The oral cavity--a key system to understand substratum-dependent bioadhesion on solid surfaces in man,” Clinical Oral Investigations, vol. 13, no. 2, pp. 123–139, 2009. View at: Publisher Site | Google Scholar
  24. M. Hannig, “Ultrastructural investigation of pellicle morphogenesis at two different intraoral sites during a 24-h period,” Clinical Oral Investigations, vol. 3, no. 2, pp. 88–95, 1999. View at: Publisher Site | Google Scholar
  25. M. Hannig and A. Joiner, “The structure, function and properties of the acquired pellicle,” Monographs in Oral Science, vol. 19, pp. 29–64, 2006. View at: Publisher Site | Google Scholar
  26. A. Kensche, S. Pötschke, C. Hannig, G. Richter, W. Hoth-Hannig, and M. Hannig, “Influence of calcium phosphate and apatite containing products on enamel Erosion,” The Scientific World Journal, vol. 2016, Article ID 7959273, 12 pages, 2016. View at: Publisher Site | Google Scholar
  27. K. Kani, M. Kani, A. Isozaki, H. Shintani, T. Ohashi, and T. Tokumoto, “Effect to apatite-containing dentifrices on dental caries in school children,” Journal of Dental Health, vol. 39, no. 1, pp. 104–109, 1989. View at: Publisher Site | Google Scholar
  28. K. Najibfard, K. Ramalingam, I. Chedjieu, and B. T. Amaechi, “Remineralization of early caries by a nano-hydroxyapatite dentifrice,” The Journal of Clinical Dentistry, vol. 22, no. 5, pp. 139–143, 2011. View at: Google Scholar
  29. S. A. Hegazy and I. R. Salama, “Antiplaque and remineralizing effects of Biorepair mouthwash: a comparative clinical trial,” Pediatric Dental Journal, vol. 26, no. 3, pp. 89–94, 2016. View at: Publisher Site | Google Scholar
  30. A. Kensche, C. Holder, S. Basche, N. Tahan, C. Hannig, and M. Hannig, “Efficacy of a mouthrinse based on hydroxyapatite to reduce initial bacterial colonisation in situ,” Archives of Oral Biology, vol. 80, pp. 18–26, 2017. View at: Publisher Site | Google Scholar
  31. C. Dawes, “Physiological factors affecting salivary flow rate, oral sugar clearance, and the sensation of dry mouth in man,” Journal of Dental Research, vol. 66, 2_supplement, pp. 648–653, 1987. View at: Publisher Site | Google Scholar
  32. G. H. Yassen, J. A. Platt, and A. T. Hara, “Bovine teeth as substitute for human teeth in dental research: a review of literature,” Journal of Oral Science, vol. 53, no. 3, pp. 273–282, 2011. View at: Publisher Site | Google Scholar
  33. T. A. Melo, G. S. Grundling, F. Montagner, R. K. Scarparo, J. A. Figueiredo, and F. V. Vier-Pelisser, “Are bovine teeth a suitable substitute for human teeth in in vitro studies to assess endotoxin load in root canals?” Brazilian Oral Research, vol. 29, no. 1, pp. 1–6, 2015. View at: Publisher Site | Google Scholar
  34. A. Al-Ahmad, M. Wiedmann-Al-Ahmad, A. Fackler et al., “In vivo study of the initial bacterial adhesion on different implant materials,” Archives of Oral Biology, vol. 58, no. 9, pp. 1139–1147, 2013. View at: Publisher Site | Google Scholar
  35. Y. Hao, X. Huang, X. Zhou et al., “Influence of dental prosthesis and restorative materials interface on oral biofilms,” International Journal of Molecular Sciences, vol. 19, no. 10, p. 3157, 2018. View at: Publisher Site | Google Scholar
  36. R. Chen, Z. Han, Z. Huang et al., “Antibacterial activity, cytotoxicity and mechanical behavior of nano-enhanced denture base resin with different kinds of inorganic antibacterial agents,” Dental Materials Journal, vol. 36, no. 6, pp. 693–699, 2017. View at: Publisher Site | Google Scholar
  37. P. Spasojevic, M. Zrilic, V. Panic, D. Stamenkovic, S. Seslija, and S. Velickovic, “The Mechanical Properties of a Poly(methyl methacrylate) Denture Base Material Modified with Dimethyl Itaconate and Di-n-butyl Itaconate,” International Journal of Polymer Science, vol. 2015, 9 pages, 2015. View at: Publisher Site | Google Scholar
  38. D. Vukosavljevic, J. L. Hutter, E. J. Helmerhorst et al., “Nanoscale adhesion forces between enamel pellicle proteins and hydroxyapatite,” Journal of Dental Research, vol. 93, no. 5, pp. 514–519, 2014. View at: Publisher Site | Google Scholar

Copyright © 2020 Cíntia Mirela Guimarães Nobre et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles