Journal List > J Periodontal Implant Sci > v.40(6) > 1082252

Kim, Kwon, Chung, Shin, and Herr: The effect of Er:YAG laser irradiation on the surface microstructure and roughness of hydroxyapatite-coated implant

Abstract

Purpose

The present study was performed to evaluate the effect of erbium:yttrium-aluminium-garnet (Er:YAG) laser irradiation on the change of hydroxyapatite (HA)-coated implant surface microstructure according to the laser energy and the application time.

Methods

The implant surface was irradiated by Er:YAG laser under combination condition using the laser energy of 100 mJ/pulse, 140 mJ/pulse and 180 mJ/pulse and application time of 1 minute, 1.5 minutes and 2 minutes. The specimens were examined by surface roughness evaluation and scanning electron microscopic observation.

Results

In scanning electron microscope, HA-coated implant surface was not altered by Er:YAG laser irradiation under experimental condition on 100 mJ/pulse, 1 minute. Local areas with surface melting and cracks were founded on 100 mJ/pulse, 1.5 minutes and 2 minutes. One hundred forty mJ/pulse and 180 mJ/pulse group had surface melting and peeling area of HA particles, which condition was more severe depending on the increase of application time. Under all experimental condition, the difference of surface roughness value on implant surface was not statistically significant.

Conclusions

Er:YAG laser on HA-coated implant surface is recommended to be irradiated below 100 mJ/pulse, 1 minute for detoxification of implant surface without surface alteration.

INTRODUCTION

Today, endosseous dental implants are an established treatment alternative for edentulous and partial edentulous patients. Various surface characteristics ranging from relatively smooth machined surfaces to more roughened surfaces are available and survival rate of implant is increased [1]. However, as better results and higher success rate have been reported annually, implant-related complications have been also increasing.
The term peri-implant disease is collectively used to describe biological complication in implant dentistry, including periimplant mucositis and peri-implantitis. While peri-implant mucositis includes reversible inflammatory reactions located solely in the mucosa adjacent to an implant, peri-implantitis was defined as an inflammatory process that affects all tissues around an osseointegrated implant in function resulting in a loss of the supporting alveolar bone. Diagnosis of peri-implant infections is based on peri-implant probing depth, evaluation of peri-implant keratinized mucosa, presence of bleeding on probing and suppuration, radiographic evaluation, evaluation of implant mobility, and analysis of peri-implant sulcus fluid [2].
The main etiological factor of peri-implant diseases is the accumulation of dental plaque that shows a very similar composition if compared to bacterial biofilms found in periodontal pockets [3-5]. These bacteria present on implant surfaces may lead to an inflammation spreads apically and results in bone loss. Peri-implant tissues are easily susceptible to any bacteria or mechanical attack because a supracrestal connective area that is highly acellular and with a great number of collagen fibers [6]. Therefore, the removal of bacterial biofilms seems to be a prerequisite in the therapy of peri-implantitis especially when a regenerative procedure is planned [7-9].
In recent years, several treatment strategies (i.e., mechanical, chemical) have been proposed for the treatment of peri-implant infection [10]. Mechanical debridement is usually performed using plastic curettes or rubber cups [11-13]. But mechanical methods alone have been proven to be insufficient in the elimination of bacteria on roughened implant surfaces [11]. Although air powder flow was also successfully used for implant surface decontamination in vitro, there are limitations in the application because it can lead to microscopically visible alterations of the implant surface and be associated with an increased risk of emphysema [13-15]. Chemical methods with citric acid, chlorhexidine gluconate, hydrogen peroxide, tetracycline chloridrate, stannous fluoride were suggested even if they leave microscopic residues or resulted in a loss of implant surface roughness when viewed on scanning electron microscopy [10,16,17].
Nowadays, laser is widely used in dentistry and many authors suggested its use for treatment of peri-implant infections. Various advantageous characteristics, such as easy handling, hemostatic effects and bactericidal effects against periodontopathic pathogens have been suggested to improve treatment outcomes. However, several potential risks complicate their clinical use. The neodymium-doped: yttrium-aluminum-garnet (Nd:YAG) laser is not suitable for implant therapy since it easily ablates titanium irrespective of output energy [18,19]. Only the CO2 laser, the diode laser, and the erbium:yttrium-aluminium-garnet (Er:YAG) laser may be suitable for the irradiation of titanium surfaces because the implant body temperature did not increase significantly during its application. But neither CO2 nor diode lasers were effective in removing plaque biofilms from titanium implants [20-23]. On the other hand, Er:YAG laser, emitting at a wavelength of 2.94 µm, seemed to be capable of effectively removing plaque and calculus from both smooth and rough implant surfaces without injuring their surfaces [24-27].
In the earlier studies, the effects of Er:YAG laser on the different kinds of implant surfaces have been evaluated to find the most ideal laser application conditions, and this study was performed on that extension. The purpose of this study was to evaluate the effect of Er:YAG laser irradiation on the microstructural change of hydroxyapatite (HA)-coated implant surface according to the laser energy and the application time.

MATERIALS AND METHODS

Implants

Ten HA-coated implants (SCREW-VENT, Zimmer Dental Inc., Carlsbad, CA, USA) of a diameter of 4.7 mm and a length of 16 mm were used in this study. One was the control group and the others were the test group.

Laser apparatus

The applied laser system was an Er:YAG laser (KEY3, KaVo, Biberach, German) emitting pulsed infrared radiation at an wavelength of 2.94 µm with a truncated cone tip. Er:YAG laser has variable pulse frequency (1-15 pps) and pulse energy (60-260 mJ).

Surface evaluation

To evaluate the implant surface topography qualitatively, we used scanning electron microscope (SEM; S-2300, Hitachi, Tokyo, Japan). And mechanical contact profilometer (Form Talysurf Laser 635, Taylor Hobson, Leicester, UK) with a contact stylus instrument made of diamond was used to present roughness data in the form of numeric standard roughness parameters.

Specimen assignment

The control group didn't have laser irradiation and the test group was irradiated with the different energy and time conditions. Test group was divided into 3 subgroups (group I, II, III) by laser application energy (100, 140, and 180 mJ/pulse). Three different irradiation time (1, 1.5, and 2 minutes) was applied on each subgroups.

Surface roughness measurement before laser application

At first, implant container was made using impression putty so as to fix the implant in position. After the measurement point had been marked by water-proof maker pen on the container, implant surface roughness was measured three times each on the 3rd, 8th, and 13th valley by mechanical contact profilometer. With a profilometer, the average roughness (Ra), one of the height-descriptive two-dimensional parameters profiles was measured and recorded with a diamond-tipped stylus of 5 µm radius running horizontally to the long axis of the implant.

Laser application and surface roughness re-measurement

Nine implants were assigned to 3 test groups, three implants per one group. Laser on the setting of 100 mJ/pulse, 10 Hz was irradiated on the three implants of group I during 1 minute, 1.5 minutes and 2 minutes each. In the same time protocol, energy of 140 mJ/pulse was irradiated to group II and 180 mJ/pulse, 10 Hz to group III. Each laser irradiation area was 2×2 mm2 on the 2nd-4th, 7th-9th, and 12th-14th valleys of the implant. The laser beam was irradiated under water irrigation and the fiber tips were guided parallel to the implant surface in near contact mode which allows the working distance between the tip of the laser and the exposed surface to be approximately 0.5 mm. The angle between the fiber tips and implant surface was 90 degree and the laser handpiece was moved along the horizontal, vertical and oblique pathways repeatedly to provide even laser exposure to the surface. The laser-irradiated implants were dehydrated and surface roughness was re-measured on the same area.

SEM observation

The specimens were sputter-coated with a thin layer of gold for 10 minutes and examined using SEM with magnification of 500 and 2,000. By examining the SEM images, the changes of implant surface were evaluated.

Statistical analysis

A software package was used for the statistical analysis (SPSS 17.0, SPSS Inc., Chicago, IL, USA). Mean values and standard deviations were then calculated for the implant surface roughness. Group comparison was performed by the Wilcoxon's signed rank sum test and differences between before and after the laser irradiation were considered to be significant when P<0.05.

RESULTS

SEM evaluation

Control group

One HA-coating implant that didn't have any surface treatment was evaluated using SEM with magnification of 500 and 2,000. It showed irregular rough surface with various sized crystalline HA (Fig. 1).

Test groups

In group I (100 mJ/pulse), there was no remarkable surface change on condition of 1 minute (Fig. 2). But on condition of 1.5 and 2 minutes, surface melting and cracks were observed on magnification of 2,000. In addition, surface was partially flattened (Figs. 3 and 4).
Group II (140 mJ/pulse) showed more significant change than group I and was shown a severe surface melting and peeling of HA particles. In addition, the surface had deep and wide cracks (Figs. 5, 6, 7).
In the group III (180 mJ/pulse), surface melting and peeling area of HA particles were observed wider and deeper than group II. As a result of this, there was a tendency showing that the surface roughness had been gradually reduced. This tendency was more significant with increased irradiation time (Figs. 8, 9, 10).

Surface roughness measurement

The mean surface roughness of pretreatment 9 specimens was 2.507±0.352 µm. The amount of change between before and after the laser irradiation was each 0.319, 0.817, 0.945, 0.989, 0.302, 0.645, 0.212, -0.329 and -0.414 µm respectively from No. 1 to No. 9. The average roughness values were increased in all group I and II, irrespective of the irradiation energy and time. But in group III, while the roughness value was increased at 1 minute, it was decreased at 1.5 and 2 minutes. But this all changes were not statistically significant (P>0.05) (Table 1, Fig. 11).

DISCUSSION

This study was evaluated the effect of Er:YAG laser irradiation on the microstructural change of HA-coated implant surface according to the laser energy and the application time. While HA-coated implant surface showed no significant change by Er:YAG laser irradiation under experimental condition of 100 mJ/pulse, 1 minute, surface melting and cracks were founded on condition of 100 mJ/pulse, 1.5 and 2 minutes. 140 mJ/pulse and 180 mJ/pulse group had surface melting and peeling area of HA particles. But in all experimental groups, the roughness value change was not statistically significant.
The main etiological factor of peri-implant diseases is the accumulation of dental plaque. Therefore it is essential to remove the dental plaque and decontaminate implant surface for treatment of peri-implant disease. To achieve this, many mechanical and chemical methods were developed but nothing was satisfactory [10-17,28,29]. Nowadays, laser is widely used in dentistry. Especially Er:YAG laser possesses bactericidal decontamination effectiveness and seemed to be capable of effectively removing plaque and calculus without injuring titanium surfaces and adjacent bone [27,30]. And Er:YAG laser was showed biocompatibility more than ultrasonic scaler on implant surface [26]. Therefore Er:YAG laser was used in this study. Kreisler et al. [19] demonstrated that titanium plasma sprayed, sandblasted and acid-etched, HA-coated and machine-polished surface were influenced by the Er:YAG laser and the power output must be limited to avoid surface damage. Therefore the respective surface determined the energy necessary to induce surface alterations. Also the working angle, application mode, time and water cooling influenced on surface alterations.
In this study, HA-coated implant produced by a plasma-spraying technique on pure titanium is used [31]. It was rough surface between 2.0-3.0 µm in (Sa) value and Albrektsson and Wennerberg [32] and Cook [33] suggested that it was supposed to promote osseointegration in contrast to a pure titanium surface. But it was a much greater affinity of lipopolysaccharides (LPS) than pure titanium and the risk of increased peri-implantitis because of high charged surface [9,34]. And HA-coated implant surface was damaged by metal curet, plastic curet, ultrasonic scaler and air powder flow [13].
Kreisler et al. [27,30] reported mean bacterial reductions of 98% and no excessive temperature elevations at pulse energy of 60 and 120 mJ and a 10 Hz. And Schwarz et al. [26] reported no significant alteration of HA-coated implant surface at pulse energy of 100 mJ, 10 Hz and 2 minutes. Overall the test group I is irradiated pulse energy of 100 mJ and 10 Hz that is effective detoxification and no significant surface alteration.
The angle of the application tip is another important factor for decreasing root substance removal. Folwaczny et al. [35] reported that the angle of the application tip to the root surface has a strong influence on the amount of root substance removed during Er:YAG laser irradiation and the effect is maximum at an angle of 90 degrees. In this study for maximum energy application, the irradiation angle was 90 degrees and the distance from the implant surface was 0.5 mm.
The laser beam was irradiated under maximum water irrigation to minimize thermal influence. Eriksson and Albrektsson [36] reported that a temperature threshold levels for heat-induced bone tissue injury is 47℃. The use of water coolant minimizes heat generation by cooling the irradiated area and absorbing excessive laser energy. In addition, a water spray facilitates hard tissue ablation by keeping the target moist [37,38].
In this study, local areas with surface melting and cracks were founded at 100 mJ/pulse, 1.5 minutes. On the other hand, result of Schwarz et al. [26] is no surface alteration at 100 mJ/pulse, 2 minutes. The different of this is resulted from irradiated area. While it was irradiated on round titanium discs of 10 mm diameter in Schwarz's study, it was irradiated on implant surface area of 2×2 mm2 in our study.
In this study, there was significant surface change between control and test group in SEM image but the difference of roughness value (Ra) on implant surface was not statistically significant. In all test groups except for Nos. 8 and 9, roughness value was slightly increased after laser treatment. The reason is presumed instrument and parameter of roughness measurement. The principle of mechanical contact profilometers is that a pick-up with a stylus is traversed over the surface at a constant velocity. Its disadvantages are that there is no precise information about which regions were actually measured and the surface will be damaged from the load applied on the tip. And it cannot be used for non-destructive evaluations of implants since the tip cannot evaluate threaded parts [39]. Also, the two-dimensional (Ra) or three-dimensional (Sa) parameter of average height deviation is known to be quite stable and insensitive to occasional high peaks or deep valleys and the most commonly used parameter in evaluating implant surface roughness. However, 3D topographic analysis using optical interferometer is superior to 2D analysis because the former (Sa) is more accurate, representative and flexible. Therefore the use of 3D evaluations is recommended for implant surface evaluation [40]. In future study, we will use the instrument and parameter for exact roughness value comparison.
Only the topographic characterization was studied related to the microstructure change in this study. Though surface roughness has been regarded as predominant factor in cell adhesion and osteogenesis during the implant healing phases, no correlation was reported between the profilometry data and bone contact percentage. So additional study is needed that can evaluate the effect of Er:YAG laser on the cell attachment and bacteria removal on the implant surface.
The present study was performed to evaluate the effect of Er:YAG laser irradiation on the change of HA-coated implant surface microstructure according to the laser energy and the application time. In SEM, HA-coated implant surface was not altered by Er:YAG laser irradiation under experimental condition on 100 mJ/pulse, 1 minute, but local areas with surface melting and cracks were founded on 100 mJ/pulse, 1.5 and 2 minutes. In addition, 140 and 180 mJ/pulse group had surface melting and peeling area of HA particles, which condition was more severe depending on the increase of application time. In conclusion, Er:YAG laser on HA-coated implant surface is recommended to be irradiated below 100 mJ/pulse, 1 minute for detoxification of implant surface without surface alteration.

Figures and Tables

Figure 1
Control specimen. Hydroxyapatite (HA)-coated implant surface without any conditioning (×500). (A) Irregular rough surface with various shaped crystalline HA (×2,000).
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Figure 2
Hydroxyapatite-coated implant surface irradiated under 100 mJ/pulse for 1 minute (×500). (A) Note no remarkable change (×2,000).
jpis-40-276-g002
Figure 3
Hydroxyapatite-coated implant surface irradiated under 100 mJ/pulse for 1.5 minutes (×500). (A) Cracks and surface melting were observed and the surface was partially flattened (×2,000).
jpis-40-276-g003
Figure 4
Hydroxyapatite-coated implant surface irradiated under 100 mJ/pulse for 2 minutes (×500). (A) Cracks and surface melting were observed and the surface was more flattened than Fig. 3A (×2,000).
jpis-40-276-g004
Figure 5
Hydroxyapatite (HA)-coated implant surface irradiated under 140 mJ/pulse for 1 minute (×500). (A) Surface melting and peeling of HA particles were observed. In addition, surface had deep and wied cracks (×2,000).
jpis-40-276-g005
Figure 6
Hydroxyapatite (HA)-coated implant surface irradiated under 140 mJ/pulse for 1.5 minutes (×500). (A) Surface melting and peeling of HA particles are observed. And surface had deep and wide cracks (×2,000).
jpis-40-276-g006
Figure 7
Hydroxyapatite (HA)-coated implant surface irradiated under 140 mJ/pulse for 2 minutes (×500). (A) Surface melting and peeling area of HA particles are observed wider than Fig. 6A (×2,000).
jpis-40-276-g007
Figure 8
Hydroxyapatite (HA)-coated implant surface irradiated under 180 mJ/pulse for 1 minute (×500). (A) Surface melting and peeling area of HA particles are observed wider and deeper than 140 mJ/pulse group (×2,000).
jpis-40-276-g008
Figure 9
Hydroxyapatite-coated implant surface irradiated under 180 mJ/pulse for 1.5 minutes (×500). (A) It was shown similar surface with Fig. 8A (×2,000).
jpis-40-276-g009
Figure 10
Hydroxyapatite-coated implant surface irradiated under 180 mJ/pulse for 2 minutes (×500). (A) It was shown similar surface with Fig. 8A and surface was more and more flattened (×2,000).
jpis-40-276-g010
Figure 11
Surface roughness values before and after surface detoxification by laser treatment.
jpis-40-276-g011
Table 1
Surface roughness values measured 3 valleys (3th, 8th, 13th valley from the platform) before and after surface detoxification by laser treatment (mean±SD).
jpis-40-276-i001

Ra: roughness.

Notes

No potential conflict of interest relevant to this article was reported.

References

1. Pjetursson BE, Tan K, Lang NP, Bragger U, Egger M, Zwahlen M. A systematic review of the survival and complication rates of fixed partial dentures (FPDs) after an observation period of at least 5 years. Clin Oral Implants Res. 2004. 15:667–676.
crossref
2. Esposito M, Hirsch JM, Lekholm U, Thomsen P. Biological factors contributing to failures of osseointegrated oral implants. (I). Success criteria and epidemiology. Eur J Oral Sci. 1998. 106:527–551.
crossref
3. Mombelli A, Buser D, Lang NP. Colonization of osseointegrated titanium implants in edentulous patients. Early results. Oral Microbiol Immunol. 1988. 3:113–120.
crossref
4. Becker W, Becker BE, Newman MG, Nyman S. Clinical and microbiologic findings that may contribute to dental implant failure. Int J Oral Maxillofac Implants. 1990. 5:31–38.
5. Apse P, Ellen RP, Overall CM, Zarb GA. Microbiota and crevicular fluid collagenase activity in the osseointegrated dental implant sulcus: a comparison of sites in edentulous and partially edentulous patients. J Periodontal Res. 1989. 24:96–105.
crossref
6. Quaranta A, Maida C, Scrascia A, Campus G, Quaranta M. Er:Yag Laser application on titanium implant surfaces contaminated by Porphyromonas gingivalis: an histomorphometric evaluation. Minerva Stomatol. 2009. 58:317–330.
7. Baier RE, Meyer AE. Implant surface preparation. Int J Oral Maxillofac Implants. 1988. 3:9–20.
8. Sennerby L, Lekholm U. The soft tissue response to titanium abutments retrieved from humans and reimplanted in rats. A light microscopic study. Clin Oral Implants Res. 1993. 4:23–27.
crossref
9. Meffert RM, Langer B, Fritz ME. Dental implants: a review. J Periodontol. 1992. 63:859–870.
crossref
10. Zablotsky MH, Diedrich DL, Meffert RM. Detoxification of endotoxin-contaminated titanium and hydroxyapatite-coated surfaces utilizing various chemotherapeutic and mechanical modalities. Implant Dent. 1992. 1:154–158.
crossref
11. Fox SC, Moriarty JD, Kusy RP. The effects of scaling a titanium implant surface with metal and plastic instruments: an in vitro study. J Periodontol. 1990. 61:485–490.
crossref
12. Matarasso S, Quaremba G, Coraggio F, Vaia E, Cafiero C, Lang NP. Maintenance of implants: an in vitro study of titanium implant surface modifications subsequent to the application of different prophylaxis procedures. Clin Oral Implants Res. 1996. 7:64–72.
crossref
13. Augthun M, Tinschert J, Huber A. In vitro studies on the effect of cleaning methods on different implant surfaces. J Periodontol. 1998. 69:857–864.
crossref
14. Kreisler M, Kohnen W, Christoffers AB, Gotz H, Jansen B, Duschner H, et al. In vitro evaluation of the biocompatibility of contaminated implant surfaces treated with an Er : YAG laser and an air powder system. Clin Oral Implants Res. 2005. 16:36–43.
crossref
15. Van de Velde E, Thielens P, Schautteet H, Vanclooster R. Subcutaneous emphysema of the oral floor during cleaning of a bridge fixed on an IMZ implant. Case report. Rev Belge Med Dent. 1991. 46:64–71.
16. Mouhyi J, Sennerby L, Pireaux JJ, Dourov N, Nammour S, Van Reck J. An XPS and SEM evaluation of six chemical and physical techniques for cleaning of contaminated titanium implants. Clin Oral Implants Res. 1998. 9:185–194.
crossref
17. Krozer A, Hall J, Ericsson I. Chemical treatment of machined titanium surfaces. An in vitro study. Clin Oral Implants Res. 1999. 10:204–211.
crossref
18. Romanos GE, Everts H, Nentwig GH. Effects of diode and Nd:YAG laser irradiation on titanium discs: a scanning electron microscope examination. J Periodontol. 2000. 71:810–815.
crossref
19. Kreisler M, Gotz H, Duschner H. Effect of Nd:YAG, Ho:YAG, Er:YAG, CO2, and GaAIAs laser irradiation on surface properties of endosseous dental implants. Int J Oral Maxillofac Implants. 2002. 17:202–211.
20. Schwarz F, Sculean A, Berakdar M, Szathmari L, Georg T, Becker J. In vivo and in vitro effects of an Er:YAG laser, a GaAlAs diode laser, and scaling and root planing on periodontally diseased root surfaces: a comparative histologic study. Lasers Surg Med. 2003. 32:359–366.
crossref
21. Tucker D, Cobb CM, Rapley JW, Killoy WJ. Morphologic changes following in vitro CO2 laser treatment of calculus-ladened root surfaces. Lasers Surg Med. 1996. 18:150–156.
crossref
22. Moritz A, Schoop U, Goharkhay K, Schauer P, Doertbudak O, Wernisch J, et al. Treatment of periodontal pockets with a diode laser. Lasers Surg Med. 1998. 22:302–311.
crossref
23. Bach G, Neckel C, Mall C, Krekeler G. Conventional versus laser-assisted therapy of periimplantitis: a five-year comparative study. Implant Dent. 2000. 9:247–251.
24. Ando Y, Aoki A, Watanabe H, Ishikawa I. Bactericidal effect of erbium YAG laser on periodontopathic bacteria. Lasers Surg Med. 1996. 19:190–200.
crossref
25. Friedmann A, Antic L, Bernimoulin JP, Purucker P. In vitro attachment of osteoblasts on contaminated rough titanium surfaces treated by Er:YAG laser. J Biomed Mater Res A. 2006. 79:53–60.
crossref
26. Schwarz F, Rothamel D, Sculean A, Georg T, Scherbaum W, Becker J. Effects of an Er:YAG laser and the Vector ultrasonic system on the biocompatibility of titanium implants in cultures of human osteoblast-like cells. Clin Oral Implants Res. 2003. 14:784–792.
crossref
27. Kreisler M, Al Haj H, d'Hoedt B. Temperature changes at the implant-bone interface during simulated surface decontamination with an Er:YAG laser. Int J Prosthodont. 2002. 15:582–587.
28. Porras R, Anderson GB, Caffesse R, Narendran S, Trejo PM. Clinical response to 2 different therapeutic regimens to treat peri-implant mucositis. J Periodontol. 2002. 73:1118–1125.
crossref
29. Rimondini L, Cicognani Simoncini F, Carrassi A. Micromorphometric assessment of titanium plasma-sprayed coating removal using burs for the treatment of peri-implant disease. Clin Oral Implants Res. 2000. 11:129–138.
crossref
30. Kreisler M, Kohnen W, Marinello C, Gotz H, Duschner H, Jansen B, et al. Bactericidal effect of the Er:YAG laser on dental implant surfaces: an in vitro study. J Periodontol. 2002. 73:1292–1298.
crossref
31. Geesink RG, de Groot K, Klein CP. Bonding of bone to apatite-coated implants. J Bone Joint Surg Br. 1988. 70:17–22.
crossref
32. Albrektsson T, Wennerberg A. Oral implant surfaces: Part 1--review focusing on topographic and chemical properties of different surfaces and in vivo responses to them. Int J Prosthodont. 2004. 17:536–543.
33. Cook SD. Hydroxyapatite-coated total hip replacement. Dent Clin North Am. 1992. 36:235–238.
34. Artzi Z, Carmeli G, Kozlovsky A. A distinguishable observation between survival and success rate outcome of hydroxyapatite-coated implants in 5-10 years in function. Clin Oral Implants Res. 2006. 17:85–93.
crossref
35. Folwaczny M, Thiele L, Mehl A, Hickel R. The effect of working tip angulation on root substance removal using Er:YAG laser radiation: an in vitro study. J Clin Periodontol. 2001. 28:220–226.
crossref
36. Eriksson AR, Albrektsson T. Temperature threshold levels for heat-induced bone tissue injury: a vital-microscopic study in the rabbit. J Prosthet Dent. 1983. 50:101–107.
crossref
37. Burkes EJ Jr, Hoke J, Gomes E, Wolbarsht M. Wet versus dry enamel ablation by Er:YAG laser. J Prosthet Dent. 1992. 67:847–851.
crossref
38. Visuri SR, Walsh JT Jr, Wigdor HA. Erbium laser ablation of dental hard tissue: effect of water cooling. Lasers Surg Med. 1996. 18:294–300.
crossref
39. Wennerberg A, Albrektsson T. Suggested guidelines for the topographic evaluation of implant surfaces. Int J Oral Maxillofac Implants. 2000. 15:331–344.
40. Dong SP, Mainsah E, Sullivan PJ, Stout KJ. Stout KJ, Dong WP, editors. Instruments and measurement techniques of 3-dimensional surface topography. Three dimensional surface topography: measurement, interpretation, and applications: a survey and bibliography. 1994. London: Penton Press;3–63.
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ORCID iDs

Jong-Hyuk Chung
https://orcid.org/http://orcid.org/0000-0002-2678-1525

Seung-Il Shin
https://orcid.org/http://orcid.org/0000-0001-8762-6169

Yeek Herr
https://orcid.org/http://orcid.org/0000-0001-9243-7119

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