Microcosm Biofilm Formation on Titanium Surfaces

Abstract

Risk factors associated with peri-implantitis are related to the biofilm composition around the implant and the ability of bacterial adhesion. This study evaluated the biofilm formation on different surfaces of commercially pure titanium (CP Ti) grade 4 after 12, 24, 48 and 168 hours using the microcosm technique and scanning electron microscopy (SEM). The following surface conditions were examined: S (control)- smooth and plain; B- sand-blasted with aluminum oxide; E- etched using nitric acid; and BE- the combination of J and A treatments. Statistical differences on biofilm formation (CFU/ mg) were found between the control (S) and B surfaces at the first 12 hours, which are related to the lowest (R_a = 0.21 µm) and highest (R_a = 0.62 µm) mean roughness values. At 168-hour all surfaces showed similar biofilm formation. Yet, microbial growth occurred on all surfaces, regardless of the surface treatment.

Keywords:
titanium; microcosm; biofilms; peri-implantitis

1 Introduction

In Dentistry, titanium implants are used as the material of choice for a wide variety of cases, from the replacement of a single dental element to complete restorations^1-5. Titanium is indicated because of its excellent mechanical, physicochemical and biochemical properties, tissue tolerance, biocompatibility^6-8, hardness, corrosion resistance and bone-like modulus of elasticity².

The technological evolution of implants has enabled the development of models with different surface topographies⁹, increasing the available area and allowing for osseointegration^10,11. Changes in the topography and in the surface free energy of titanium are possible through surface treatment using, for example, abrasive particles (sand-blasting) and acid etching¹². Although surface roughness benefits osseointegration, it may facilitate the accumulation of microbial species and lead to peri-implant infection, resulting in bone destruction and failure of restorations with this type of biomaterial^13,14.

Human dental plaque is a complex biofilm with different concentrations of bacterial species in different environments and in vivo study is hindered due to its heterogeneity, available amount and limited access, in addition to ethical problems. Considering these limitations, Wong & Sissons¹⁵ developed an “artificial mouth” plaque culture system in order to investigate microcosm and to minimize the limitations of biofilm studies. Microcosm is defined as a microbiological entity that represents the natural in vitro dental plaque. This way, microcosm maintains the natural complexity of the oral biofilm, its biodiversity and its heterogeneous structure¹⁶. The aim of this study was to evaluate the biofilm formation in different time periods on titanium surfaces submitted to different surface treatments using the microcosm technique.

2 Material and Methods

The study protocol (no. 141/2012) was approved by the local Ethics in Research Committee. A randomized in vitro study was performed, in which biofilms were allowed to form in microplates on titanium discs and saliva (microcosm) was used as inoculum. The saliva was collected from a nonsmoking donor with periodontal disease that did not take antibiotics for 30 days and abstained from oral hygiene for 24 hours before saliva collection. The selection parameters were periodontal pockets deeper than 4 mm with bleeding and/or suppuration at periodontal probing and with clinical insertion levels of approximately 7 mm. Titanium specimens (164) were fabricated, 40 specimens were assigned for each surface treatment and biofilm experiment, and four were randomly selected for SEM analysis without biofilm formation. Biofilms were grown up to 12, 24, 48 and 168 hours (n=10). At each time-point, 9 specimens were used for microbiological analysis and 1 specimen was randomly selected for SEM analysis.

2.1 Specimens

Titanium specimens were donated by Titanium Fix® - AS Technology Ltda (São José dos Campos, SP, Brazil) measuring 5 mm in diameter and 3mm in thickness with surface treatments as follows:

• S (control)- smooth, plain surface;

• B- sand-blasted with aluminum oxide;

• E- etched with nitric acid; and

• BE- sand-blasted with aluminum oxide and etched with nitric acid.

The initial roughness of a disc in each condition was measured by an optical profilometer (Surr-Corder SE1200 – Koxaka Lab, Tokyo, Japan), calibrated with V 200, H 25 mm/λc and λc 0.25 mm, and the mean roughness (R_a) was used for comparison of the surfaces. For each specimen, three measurements were performed on each side and in different directions to obtain the mean roughness (ABNT NBR ISO 4288).

2.2 Artificial saliva (DMM) preparation

The artificial saliva or defined medium mucin (DMM) was obtained as proposed by Wong & Sissons¹⁵: porcine gastric mucin (2.5 g/L), urea (1.0 mmol/L), salts (in mmol/L (CaCl₂, 1.0; MgCl₂, 0.2; KH₂PO₄, 3.5; K₂HPO₄, 1.5; NaCl, 10.0; KCl, 15.0; NH₄Cl, 2.0), 21 free amino acids, 17 vitamins, and growth factors. The medium contained amino acids for the protein/peptide equivalent (in mmol/L), whose concentrations are based on human saliva. The amino acids included alanine (1.95), arginine (1.30), asparagine (1.73), aspartic acid (1.52), cysteine (0.05), glutamic acid (5.41), glutamine (3.03), glycine (1.95), histidine (1.08), isoleucine (2.38), leucine (3.68), serine (3.46), threonine (1.08), tryptophan (0.43), tyrosine (2.17), valine (2.38), and casein (5.0).

2.3 Saliva collection and processing

Saliva was collected from a donor with periodontal disease. It was stimulated with parafilm (Parafilm “M”®, American National Can TM, Chicago, IL, USA) and collected 70 mL of saliva that was placed in a sterile graded collector and transported in a foam ice chest to the local Laboratory of Microbiology. The saliva was filtered in sterile glass wool and homogenized in a vortex mixer^17,18. An aliquot of such saliva was used for bacterial quantification (CFU/mL).

2.4 Biofilm growth

The titanium specimens was inoculated on microplates with 400 µL of the prepared saliva. After 60 minutes, the saliva was gently aspirated and 1.8 mL of artificial saliva was added to each microplate. The plates were incubated under anaerobic conditions (80% N₂, 10% CO₂ and 10% H₂) at 37 °C for up to 168 hours and the plates were stirred on a daily basis and the supernatant was removed, the pH was measured (pH meter – Analion PM608 Plus, São Paulo, SP) and the DMM was replaced. After 12, 24, 48 and 168 hours of incubation^19,20, the discs were removed from the wells with sterile tweezers and the non-adherent cells were gently removed by washing with sterile saline (2 mL). After that, the discs were placed in tubes containing 1 mL of reduced transport fluid (RTF) and sonicated (Sonicador Vibra Cell – Sonics and Materials, Danbury, CT, USA) at 40 W and at a range of 5%, using six pulses of 9.9 s each. Thereafter, the suspensions were serially diluted to 10⁷, inoculated in duplicate on blood agar and incubated under anaerobic conditions (80% N₂, 10% CO₂, 10% H₂) at 37 °C for 96 h. The colony forming units were counted and the results were expressed in CFU/mg of biofilm specimen (dry weight)²¹.

2.5 Preparation of samples for scanning electron microscopy (SEM)

The specimens were placed in 24-well microplates and immersed in 2.5% glutaraldehyde solution in phosphate buffer to transport to the local Center for Electron Microscopy to exam under SEM (JSM 6060), with a voltage from 0.1 to 30 Kv.

2.6 Statistical analysis

The results were statistically analyzed using two-way ANOVA and Tukey tests (α=0.05), based on the normal distribution model and equal variance (IBM SPSS Statistics Software version 2.0).

3 Results and Discussion

The roughness and biofilm formation values are summarized in Tables 1 and 2. Representative SEM images of the biofilm formation on different titanium treated surfaces are shown in Figure 1. At first 12 hours the biofilm formation was greater on the sand-blasted (B) surface than on S or E surfaces. At 24 hours the B surface showed greater biofilm formation than E surface, which was not different from S and BE surfaces. At 48 hours, biofilm formation was greater on BE surface than on S surface. At 168 hours, there was no statistical difference in biofilm formation between all examined surfaces (p>0.05).

Table 1
Values for the three roughness measurements and the average roughness value (in µm) of titanium discs with different surface treatments.

Surface treatments	Roughness measurements 1st 2nd 3rd			Mean roughness (Ra)
Smooth	0.196	0.256	0.191	0.214
Sand-blasted	0.632	0.583	0.658	0.624
Acid-etched	0.316	0.313	0.335	0.321
Sand-blasted and acid-etched	0.538	0.493	0.499	0.510

Table 2
Incubation period and biofilm formation (log₁₀ CFU/mg) on titanium discs with different surface treatments.

Hours	Smooth	Sand-blasted	Acid-etched	Sand-blasted and acid-etched	p
12	7.348±7.155 AB	7.622±7.156 C	7.241±6.971 A	7.477±7.084 BC	0.001
24	8.153±7.561 AB	8.309±7.802 B	8.103±7.724 A	8.255±7.628 AB	0.016
48	8.468±8.1375 A	8.619±8.149 AB	8.623±8.163 AB	8.728±8.038 B	0.013
168	8.941±8.384 NS	9.014±8.354 NS	8.878±8.520 NS	8.984±8.571 NS	0.358

• NS: not significant. Means followed by same letters in the line are not statistically different (Student-Newman-Keuls test, p≤ 0.05).

Figure 1
Photomicrograph of smooth titanium surface (control – S), sand-blasted with aluminum oxide (B), etched with nitric acid (E) and sand-blasted with aluminum oxide and etched with nitric acid (BE) after 12 hours of biofilm formation.

It has been reported that bacterial biofilm formation on dental restorative materials is a clinical problem, and on dental implants it has been associated to peri-implantitis^{2,8,13,14,22,23}. The microcosm technique or “artificial mouth” developed by Wong and Sissons¹⁵ has already been explored for the assessment of antimicrobial substances and in the field of cariology^16-18,24-28. However, few studies exist on adhesion and biofilm formation on titanium surfaces and on peri-implantitis²⁹.

In the present study, microcosm was used to simulate the oral environment as to the multi-strain behavior of the bacteria found in human saliva, especially in periodontal patients. Another advantage of using microcosm is the feasibility of biofilm study on a large scale through the use of artificial saliva (DMM) and appropriate nutritional conditions for biofilm growth. By using titanium discs with different topographies, biofilm growth periods, and multiplication conditions in an “artificial mouth”, it is possible to observe the adhesion, concentration and biomass of microorganisms in different time periods and on different surfaces.

Saliva was collected from periodontal patients because it was reported that the microbiota in peri-implantitis is similar to the one found in periodontal disease, as well as its pathogenesis³⁰. This correlation between biofilm accumulation and presence of periodontal pathogens at the level of bone loss and around the peri-implant tissue has been well reported^30-37. However, peri-implantitis does not occur without previous adhesion and subsequent microbial colonization. Adhesion depends on the type of microorganism, on the physicochemical properties of the implant surface and on the presence of oral fluids between the microorganisms and the surfaces^38-42, as well as on the control procedures associated with oral hygiene^43,44.

Initial biofilm formation may be influenced by the implant surface and the adhesion of microorganisms seems to be directly proportional to surface roughness^35,43,45-51. Other studies also confirm the relationship between surface roughness and the efficiency for osseointegration^52-55. Thus, the rougher the surface, the larger the accumulation of biofilm^46,48, and the greater the chances for clinical failure due to the interplay between these factors.

This issue was investigated by Teughels et al.⁵⁶ and Mioralli⁵⁷, who reported on rough surfaces with larger accumulation and plaque retention and development of more mature plaques, characterized by the increase in the number of colonies, mobile organisms and spirochetes. Ameen et al.⁵⁸ tested the energy components on the surface of several materials to verify the strength of cell adhesion and demonstrated that the surface free energy is more important than roughness for induction of adhesion and cell proliferation.

In the present study, the average surface roughness is summarized in Table 1. Considering the association of roughness and microbial growth (Tables 1 and 2), growth remained constant throughout the study period (12, 24, 48 and 168 hours). Nonetheless, at 12 hours, smooth surfaces (S) and acid-etched surfaces (E) showed the lowest CFUs (7.348 and 7.241, respectively), a fact that can be attributed to the initial adhesion and biofilm formation limited to less rough surfaces, as mentioned by Amoroso et al.² that evaluated in vitro the bacterial adhesion of Porphyromonas gengivalis on titanium discs and the relationship between roughness and free surface energy. They observed that a surface with R_a=0.15 µm, classified as very smooth, showed significant less bacterial adhesion than rougher surfaces (R_a=0.22 µm and 0.45 µm), which are similar to implants surfaces (around R_a=0.35 µm).

In the present study, biofilm formation was smaller at 12 and 24 hours on less rough surfaces (S and E surfaces), in line with the findings of Bürgers et al.²¹, who used sand-blasted titanium discs etched with nitric acid to assess the in vitro bacterial adhesion of Streptococcus sanguinis, confirming that the initial bacterial adhesion on titanium surfaces is primarily influenced by surface roughness.

At the end of the present experiment (168 hours), there was no statistical significance (p˃0.05) between CFUs on the evaluated surfaces. Although the control surface (R_a=0.21 µm) presented one third of the roughness value of B surface (R_a=0.624 µm) the biofilm formation was statistically identical for all surface treatments. The relationship between surface treatment with nitric acid etching (E) and the lower amount of microorganisms in the first two assessment periods (12 and 24 hours) may be associated with a decrease in roughness, compared to groups where sand-blasted was used, due to the acid etching process, or to a possible antimicrobial property of the nitric acid. Some studies aimed to maximize the quantity and quality of the bone-implant interface, reported that several changes in the implant surface have been proposed, most of them based on the assumption that a better and quicker osseointegration may be achieved by changing the topography or roughness of the implant^52,53,59.

Since the R_a values found in the present study were different between the groups, biological results may not have been influenced by roughness according to the experimental periods assessed (48 to 168 hours) but rather by factors such as irregular surface topography, surface contamination by aluminum (Al) particles or possible changes in the surface energy of the metal by the surface treatments used.

4 Conclusions

The microcosm technique showed that microbial growth occured regardless of the surface treatment used, and that biofilm formation was smaller within the first 12 hours on less rough surfaces, suggesting that initial adhesion is directly proportional to surface roughness.

Acknowledgements

We thank Titanium Fix for providing the titanium specimens used in this study and FAPERGS PqG 12/2523-5 to partial financial support.

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Publication Dates

• Publication in this collection
  Jul-Aug 2015

History

• Received
  30 May 2014
• Reviewed
  03 July 2015