Case Reports in Dentistry

Case Reports in Dentistry / 2014 / Article

Case Report | Open Access

Volume 2014 |Article ID 927429 |

Karen Müller Ramalho, Patrícia Moreira de Freitas, Ana Cecília Correa-Aranha, Marina Stella Bello-Silva, Roberta Marques da Graça Lopes, Carlos de Paula Eduardo, "Lasers in Esthetic Dentistry: Soft Tissue Photobiomodulation, Hard Tissue Decontamination, and Ceramics Conditioning", Case Reports in Dentistry, vol. 2014, Article ID 927429, 6 pages, 2014.

Lasers in Esthetic Dentistry: Soft Tissue Photobiomodulation, Hard Tissue Decontamination, and Ceramics Conditioning

Academic Editor: Manoela Domingues Martins
Received08 May 2014
Accepted30 Jun 2014
Published23 Jul 2014


The increasing concern and the search for conservative dental treatments have resulted in the development of several new technologies. Low and high power lasers can be cited as one of these new technologies. Low power lasers act at cellular level leading to pain reduction, modulation of inflammation, and improvement of tissue healing. High power lasers act by increasing temperature and have the potential to promote microbial reduction and ablation of hard and soft tissues. The clinical application of both low and high power lasers requires specific knowledge concerning laser interaction with biological tissues, so that the correct irradiation protocol can be established. The present case report describes the clinical steps of two metal-ceramic crowns development in a 60-year-old patient. Three different laser wavelengths were applied throughout the treatment with different purposes: Nd:YAG laser (1,064 nm) for dentin decontamination, diode (660 nm) for soft tissue biomodulation, and Er:YAG laser (2,940 nm) for inner ceramic surface conditioning. Lasers were successfully applied in the present case report as coadjutant in the treatment. This coadjutant technology can be a potential tool to assist treatment to reach the final success.

1. Introduction

In the last few years, the demand for esthetic dentistry has increased significantly. Regarding complex restorations or great alteration in tooth color, indirect composite and ceramic restorations are claimed to be a superior alternative to direct composite resin fillings.

New technologies have been introduced in dentistry and have contributed to the clinical success of restorative procedures. Among these technologies, high and low power lasers have been widely studied and reported as offering many benefits in different steps of restorative treatment [1].

Clinical indications of high power lasers on indirect and direct restorative dentistry include microbial reduction, final caries removal, enamel/dentin etching, internal ceramic conditioning, and crown lengthening. Studies have reported their promising results when used for the treatment/irradiation of the inner surface of ceramic restorations [24], as well as for the microbial reduction at the dentin surface and subsurface [59]. On the other hand, low power lasers are used for modulation of inflammatory process, pain reduction, and soft tissue biomodulation [1017].

The present clinical case aims to describe the use of three different wavelengths—low power diode laser (660 nm), Nd:YAG laser (1,064 nm), and Er:YAG laser (2,940 nm)—throughout clinical steps of a ceramic crown placement.

Lasers are contemporary coadjutant tools to conventional dental procedures, which could favor the treatment in order to reach successful final results. This clinical case shows the importance and positive results of using laser technology. Important clinical details and the benefits related to the use of this technology are also addressed.

2. Case Presentation

A 60-year-old patient, female, was referred to a private clinic claiming for esthetic restorations of the right inferior molars. The radiographic exam was conducted and revealed two metal-ceramic crowns on both first and second right lower molars with unsatisfactory marginal sealing (Figure 1(a)). The replacement of the inadequate metal-ceramic crowns by indirect ceramic restorations was then indicated.

The patient presented severe teeth grinding and, although metallic crowns seem to be the best indication in this case, patient refused to receive metallic crowns and opted for esthetic ones.

The first clinical step was to remove both crowns and place provisional acrylic-resin crowns. In the following session, endodontic treatment was conducted in the lower right first molar. Following root canals impression of the first molar and the placement of a new metallic post, tooth preparation was conducted, leaving enough space for the ceramic crown (approximately 2 mm from antagonist tooth) (Figure 1(b)). The metallic post of the second molar was maintained.

Instructions of hygiene were given to the patient throughout the prosthetic treatment.

After tooth preparation, laser phototherapy with low power laser was performed in all clinical sessions (total of six sessions) on the surrounding periodontal tissue, until the final luting of the ceramic crown was conducted (Figures 1(c), 1(d) and 2(b)). Time interval between laser phototherapy applications varies between two and three days. Laser phototherapy was conducted punctually with a semiconductor laser (InGaAIP—DMC, São Carlos, SP, Brazil), working at 660 nm, using an energy density of 3.57 J/cm2 per point and output power of 50 mW. The spot area was 0.028 cm2 (Figures 1(c), 1(d)–Figure 2(b)). Each point received a total energy of 0.1 J. A total of 6 points were performed per tooth (2 seconds per point), consisting of 3 points in buccal gingiva and 3 in lingual gingiva. Laser phototherapy with low power laser was carried out aiming to promote soft tissue biomodulation, since both hard and soft tissues should be completely healthy at the end of treatment, so that a fully esthetic outcome could be achieved. Likewise, no inflammatory signals should be present in gingival tissue before final luting procedure.

The ceramic color was selected (Figure 1(e)) and teeth impression was taken with vinyl polysiloxane impression material (Virtual, Ivoclar Vivadent, Schaan, Liechtenstein). In the following session, the ceramic restorations were proved. Prior to the final luting, the decontamination of tooth surfaces was done using a high power laser. The irradiation was performed using the Nd:YAG laser (Smarty A10, DEKA, Firenze, Italy) (Figure 2(a)), 1,064 nm, with the following parameters: 1.5 W, 15 Hz, and 100 mJ. The laser application was made using a 320 μm diameter optical fiber (Figure 1(f)).

Before luting, the temporary restorations were removed and the prepared teeth were cleaned to remove any temporary cement. Both teeth were rinsed with water and air-dried. Next, the shade and fit of the ceramic restorations were checked.

The teeth surfaces and the inner surface of the ceramic restorations were treated and prepared for adhesive luting. Teeth surfaces were conditioned with 35% phosphoric acid (Scotchbond Etchant Phosphoric Acid, 3M ESPE, St. Paul, USA), during 15 seconds, followed by abundant rinse. The inner surfaces of the ceramic restorations (LAVA Zirconia, 3M/ESPE, St. Paul, MN, EUA) (Figures 1(g) and 1(h)) were irradiated with the Er:YAG laser (Key Laser 2, KaVo, Biberach, Germany) (Figure 2(c)) emitting photons at a wavelength of 2.94 μm. The energy per pulse and repetition rate of this equipment range from 60 to 500 mJ and 1 to 15 Hz, respectively. The handpiece number 2052 was used and parameters were set at 250 mJ, 10 Hz, and 2.5 W (Figures 1(i), 1(j), and 1(k)). The irradiation was done under water cooling (5 mL/min), at 12–15 mm distance from the ceramic surface, for 30 seconds (enough time for the entire inner surface to be irradiated). The surfaces were gently dried for 2 seconds.

A thin layer of primer (Multilink Primer A/B—Ivoclar Vivandent, Schaan, Liechtenstein) was applied on the inner surface of the ceramic restoration using a disposable brush and left to react for 3 minutes. Subsequently, it was gently air-dried. The Multilink primer liquids A and B (Ivoclar Vivandent, Schaan, Liechtenstein) were mixed in a 1 : 1 ration and applied with a disposable brush in the entire tooth surface, starting with the enamel, and applied with slight pressure for 15 seconds, according to the manufacturer’s instructions. Thirty seconds of reaction time was considered for enamel and 15 seconds for dentin. The applied primer was subsequently air-dried.

The luting cement was dispensed in a double-push syringe, in which the two pastes were mixed in a 1 : 1 ration and then applied on the inner surface of the restorations. The restorations were seated in place and hold (Figure 1(l)). The excesses were immediately removed. The margins of restorations were covered with glycerin gel and the light activation was carried out for polymerization of the luting cement. Finally, the occlusion was checked.

3. Discussion

The use of low and high power lasers in dentistry has been, to some extent, adopted as an adjuvant treatment due to its clinical benefits. Successful esthetic treatments involve not only restorative procedures, but also the presence of a healthy surrounding periodontal tissue. After 1971, when Mester [18] first reported the biological effects of low power lasers and the beneficial use of laser phototherapy, this treatment modality has been considered an alternative, noninvasive method to enhance healing of chronic wounds, modulate the inflammatory process, and promote pain relief [16, 1924]. At the cellular level, the absorption of light by specific chromophore photoreceptors occurs, and once absorbed, the light can modulate cell biochemical reactions and stimulate mitochondrial activity [25]. This primary answer will lead to secondary responses such as increase in ATP synthesis, collagen production, increase in cell proliferation and migration, and biomodulation of inflammatory process [10, 26]. Therefore, the use of laser phototherapy associated with a rigorous routine of hygiene adopted by the patient will lead to a healthy periodontal tissue and contribute not only to a more adequate luting by avoiding inflammatory process and bleeding during impression, but also to a more advanced final esthetic result and longevity of the indirect restoration. Clinical studies have reported laser phototherapy effects on the modulation of periodontal inflammatory process, verifying that patients in whom the conventional treatment was associated with laser phototherapy presented better results than nonirradiated patients [17, 27].

One of the factors that can be related to the success of the treatment provided is the frequency of the laser phototherapy sessions. Several studies have shown that a single irradiation is not as effective as successive ones [28, 29]. Transitory effects in cells resultant from laser phototherapy were also demonstrated in the literature, suggesting that the number of sessions is important to maintain the laser effect on cells [30]. The fluence is also of great importance, since it has been reported that increased effects could be achieved when using laser parameters between 4 and 8 J/cm2 [31, 32]. The use of high doses of energy has been considered as a potential inhibitor of cellular proliferation [12]. In the present case report, after teeth preparation, laser phototherapy was applied in gingival tissue surrounding the prepared teeth in all following sessions. Instructions of hygiene were also given to the patient, so that, at the day in which the impression was taken, the gingiva was completely healthy.

The morphology of dentin facilitates accumulation and proliferation of bacteria in dentinal tubules. Sometimes, a provisionary crown does not allow a perfect sealing and dentin contamination can occur. So, it is important that before final luting of a definite crown, dentin decontamination should be performed. The dentin decontamination will be an important step for the success of a prosthetic treatment. There are several studies in the literature that described the potential of Nd:YAG laser in dentin bacteria decontamination [59, 3335]. In general, dental lasers provide greater accessibility of formerly unreachable parts of dentin due to their better penetration into dentinal tissues [35] and a high disinfecting capability of Nd:YAG was reported [59, 3335]. In the present clinical case, the Nd:YAG laser was used before final luting with the aim to promote microbial reduction on dentin substrate. So, the luting of the definitive crown was performed in a decontaminated substrate, aspect that certainly sums to the final success of the treatment.

It is well known that, for adhesive indirect restorations, several steps are required to ensure optimal adhesion of the restoration to the tooth structure and to provide predictable clinical results. These steps include not only the treatment of the dental hard tissues with acid etching and bonding agent, but also the pretreatment of the ceramic inner surface. The mechanical limitations presented by resin composites gave rise to the development of the ceramic systems, which relate esthetics with adequate function and greater resistance to occlusal forces [36]. Zirconia-based ceramics have been increasingly introduced in prosthetic dentistry for the production of fixed partial dentures and crowns in combination with CAD/CAM techniques [37].

Adhesive cementation requires ceramic internal surface treatment, so that micromechanical retentions can be produced and favor adhesion [38]. A further chemical bond is mediated by the silane agent, which favors the union between the ceramic inorganic and the cement organic phases. Because zirconia-based ceramics present an increase in their crystalline content and a decrease in their glass content, conventional surface treatments are not effective enough to produce such alterations. Acid etching and sandblasting have been widely used to promote micromechanical retention in several types of ceramics and are the conventional procedures clinically performed. However, none of these methods are able to produce sufficient surface changes on ceramics for adequate bonding to resin cement [37]. Currently, tribochemical silica-coating (Rocatec System) is considered the most effective method to provide better luting of high crystalline ceramics to dental substrate. This method covers the ceramic surface with a 0.15 μm silica layer and favors its interaction with the silane agent [39]. Recent studies have reported that Rocatec System provides higher bond strength than the conventionally used sandblasting [4042]. More recently, high power lasers have been investigated for potential use on ceramic conditioning. There are still few studies in the literature about laser treatment of dental ceramics; however, the results indicate that high power lasers can provide similar or even higher bond strength values than those obtained with Rocatec System when adequate irradiation parameters were used [3, 4, 43]. Despite the promising results regarding laser conditioning of high-crystalline ceramics, several studies in the literature do not report this increase in bond strength. For this reason, it is important to emphasize that this improved adhesion to laser conditioned ceramics can only be observed by using adequate laser parameters. Some studies used lower energy or irradiated ceramic surface for a shorter period of time [44, 45]. In this study, the inner surface of the ceramic crowns was irradiated for approximately 30 seconds. The energy of 250 J per pulse and the pulse repetition rate of 10 Hz were used.

As observed in the present clinical case, lasers can be useful for several clinical procedures in dentistry. The association of both low and high power lasers can bring many benefits on biological tissues, improve prosthetic procedures, and provide the patient with a more comfortable and predictable treatment.

4. Conclusion

Low and high power lasers can contribute positively to all steps of the indirect restorative treatment period. It is important to highlight that, due to their different interactions with biological tissues, the knowledge on their correct use is of extreme importance for clinical success.

Conflict of Interests

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


  1. C. P. Eduardo, P. M. Freitas, and L. Gaspar, “The state of the art of lasers in esthetics and prosthodontics,” The Journal of Oral Laser Applications, vol. 5, no. 3, pp. 135–143, 2005. View at: Google Scholar
  2. A. M. Spohr, G. A. Borges, L. H. Burnett Jr., E. G. Mota, and H. M. S. Oshima, “Surface modification of In-Ceram Zirconia ceramic by Nd:YAG laser, Rocatec system, or aluminum oxide sandblasting and its bond strength to a resin cement,” Photomedicine and Laser Surgery, vol. 26, no. 3, pp. 203–208, 2008. View at: Publisher Site | Google Scholar
  3. B. L. da Silveira, A. Paglia, L. H. Burnett Jr., R. S. A. Shinkai, C. D. P. Eduardo, and A. M. Spohr, “Micro-tensile bond strength between a resin cement and an aluminous ceramic treated with Nd: YAG laser, rocatec system, or aluminum oxide sandblasting,” Photomedicine and Laser Surgery, vol. 23, no. 6, pp. 543–548, 2005. View at: Publisher Site | Google Scholar
  4. C. de Paula Eduardo, M. S. Bello-Silva, S. G. Moretto, P. F. Cesar, and P. M. de Freitas, “Microtensile bond strength of composite resin to glass-infiltrated alumina composite conditioned with Er,Cr:YSGG laser,” Lasers in Medical Science, vol. 27, no. 1, pp. 7–14, 2012. View at: Publisher Site | Google Scholar
  5. R. Franzen, M. Esteves-Oliveira, J. Meister et al., “Decontamination of deep dentin by means of erbium, chromium:yttrium- scandium-gallium-garnet laser irradiation,” Lasers in Medical Science, vol. 24, no. 1, pp. 75–80, 2009. View at: Publisher Site | Google Scholar
  6. T. Klinke, W. Klimm, and N. Gutknecht, “Antibacterial effects of Nd: YAG laser irradiation within root canal dentin,” Journal of Clinical Laser Medicine and Surgery, vol. 15, no. 1, pp. 29–31, 1997. View at: Google Scholar
  7. A. Moritz, O. Doertbudak, N. Gutknecht, K. Goharkhay, U. Schoop, and W. Sperr, “Nd:YAG laser irradiation of infected root canals in combination with microbiological examinations,” The Journal of the American Dental Association, vol. 128, no. 11, pp. 1525–1530, 1997. View at: Publisher Site | Google Scholar
  8. N. Gutknecht, A. Moritz, G. Conrads, T. Sievert, and F. Lampert, “Bactericidal effect of the Nd:YAG laser in in vitro root canals,” Journal of Clinical Laser Medicine and Surgery, vol. 14, no. 2, pp. 77–80, 1996. View at: Google Scholar
  9. S. Gouw-Soares, N. Gutknecht, G. Conrads, F. Lampert, E. Matson, and C. P. Eduardo, “The bactericidal effect of Ho:YAG laser irradiation within contaminated root dentinal samples,” Journal of Clinical Laser Medicine and Surgery, vol. 18, no. 2, pp. 81–87, 2000. View at: Google Scholar
  10. M. J. Conlan, J. W. Rapley, and C. M. Cobb, “Biostimulation of wound healing by low-energy laser irradiation: a review,” Journal of Clinical Periodontology, vol. 23, no. 5, pp. 492–496, 1996. View at: Publisher Site | Google Scholar
  11. F. P. Eduardo, D. U. Mehnert, T. A. Monezi et al., “Cultured epithelial cells response to phototherapy with low intensity laser,” Lasers in Surgery and Medicine, vol. 39, no. 4, pp. 365–372, 2007. View at: Publisher Site | Google Scholar
  12. T. Karu, “Photobiology of low-power laser effects,” Health Physics, vol. 56, no. 5, pp. 691–704, 1989. View at: Publisher Site | Google Scholar
  13. R. F. Lyons, R. P. Abergel, R. A. White, R. M. Dwyer, J. C. Castel, and J. Uitto, “Biostimulation of wound healing in vivo by a helium-neon laser,” Annals of Plastic Surgery, vol. 18, no. 1, pp. 47–50, 1987. View at: Publisher Site | Google Scholar
  14. A. N. Pereira, C. de Paula Eduardo, E. Matson, and M. M. Marques, “Effect of low-power laser irradiation on cell growth and procollagen synthesis of cultured fibroblasts,” Lasers in Surgery and Medicine, vol. 31, no. 4, pp. 263–267, 2002. View at: Publisher Site | Google Scholar
  15. A. Schindl, M. Schindl, H. Schön, R. Knobler, L. Havelec, and L. Schindl, “Low-intensity laser irradiation improves skin circulation in patients with diabetic microangiopathy,” Diabetes Care, vol. 21, no. 4, pp. 580–584, 1998. View at: Publisher Site | Google Scholar
  16. N. Shimizu, M. Yamaguchi, T. Goseki et al., “Inhibition of prostaglandin E2 and interleukin 1-beta production by low-power laser irradiation in stretched human periodontal ligament cells,” Journal of Dental Research, vol. 74, no. 7, pp. 1382–1388, 1995. View at: Publisher Site | Google Scholar
  17. C. de Paula Eduardo, P. M. de Freitas, M. Esteves-Oliveira et al., “Laser phototherapy in the treatment of periodontal disease: a review,” Lasers in Medical Science, vol. 25, no. 6, pp. 781–792, 2010. View at: Publisher Site | Google Scholar
  18. E. Mester, T. Spiry, B. Szende, and J. G. Tota, “Effect of laser rays on wound healing,” The American Journal of Surgery, vol. 122, no. 4, pp. 532–535, 1971. View at: Publisher Site | Google Scholar
  19. P. Moore, T. D. Ridgway, R. G. Higbee, E. W. Howard, and M. D. Lucroy, “Effect of wavelength on low-intensity laser irradiation-stimulated cell proliferation in vitro,” Lasers in Surgery and Medicine, vol. 36, no. 1, pp. 8–12, 2005. View at: Publisher Site | Google Scholar
  20. Y. Sakurai, M. Yamaguchi, and Y. Abiko, “Inhibitory effect of low-level laser irradiation on LPS-stimulated prostaglandin E2 production and cyclooxygenase-2 in human gingival fibroblasts,” European Journal of Oral Sciences, vol. 108, no. 1, pp. 29–34, 2000. View at: Publisher Site | Google Scholar
  21. G. Tam, “Low power laser therapy and analgesic action,” Journal of Clinical Laser Medicine and Surgery, vol. 17, no. 1, pp. 29–33, 1999. View at: Google Scholar
  22. J. Tunér and L. Hode, “It's all in the parameters: a critical analysis of some well-known negative studies on low-level laser therapy,” Journal of Clinical Laser Medicine & Surgery, vol. 16, no. 5, pp. 245–248, 1998. View at: Google Scholar
  23. P. Wedlock, R. A. Shephard, C. Little, and F. Mcburney, “Analgesic effects of cranial laser treatment in two rat nociception models,” Physiology and Behavior, vol. 59, no. 3, pp. 445–448, 1996. View at: Publisher Site | Google Scholar
  24. M. Ando, Y. Okita, Y. Sasako, J. Kobayashi, O. Tagusari, and S. Kitamura, “Surgery for aortic regurgitation caused by Behcet's disease: a clinical study of 11 patients,” Journal of Cardiac Surgery, vol. 14, no. 2, pp. 116–121, 1999. View at: Publisher Site | Google Scholar
  25. T. Karu, “Primary and secondary mechanisms of action of visible to near-IR radiation on cells,” Journal of Photochemistry and Photobiology B, vol. 49, no. 1, pp. 1–17, 1999. View at: Publisher Site | Google Scholar
  26. C. E. N. de Araújo, M. S. Ribeiro, R. Favaro, D. M. Zezell, and T. M. T. Zorn, “Ultrastructural and autoradiographical analysis show a faster skin repair in He-Ne laser-treated wounds,” Journal of Photochemistry and Photobiology B: Biology, vol. 86, no. 2, pp. 87–96, 2007. View at: Publisher Site | Google Scholar
  27. T. Qadri, L. Miranda, J. Tunér, and A. Gustafsson, “The short-term effects of low-level lasers as adjunct therapy in the treatment of periodontal inflammation,” Journal of Clinical Periodontology, vol. 32, no. 7, pp. 714–719, 2005. View at: Publisher Site | Google Scholar
  28. M. Kreisler, A. B. Christoffers, B. Willershausen, and B. D'Hoedt, “Effect of low-level GaAlAs laser irradiation on the proliferation rate of human periodontal ligament fibroblasts: an in vitro study,” Journal of Clinical Periodontology, vol. 30, no. 4, pp. 353–358, 2003. View at: Publisher Site | Google Scholar
  29. T. Kubasova, L. Kovacs, Z. Somosy, P. Unk, and A. Kókai, “Biological effect of He-Ne laser: investigations on functional and micromorphological alterations of cell membranes, in vitro,” Lasers in Surgery and Medicine, vol. 4, no. 4, pp. 381–388, 1984. View at: Publisher Site | Google Scholar
  30. A. Pejcic, D. Kojovic, L. Kesic, and R. Obradovic, “The effects of low level laser irradiation on gingival inflammation,” Photomedicine and Laser Surgery, vol. 28, no. 1, pp. 69–74, 2010. View at: Publisher Site | Google Scholar
  31. M. Schaffer, H. Bonel, R. Sroka et al., “Magnetic resonance imaging (MRI) controlled outcome of side effects caused by ionizing radiation, treated with 780 nm-diode laser: Preliminary results,” Journal of Photochemistry and Photobiology B, vol. 59, no. 1-3, pp. 1–8, 2000. View at: Publisher Site | Google Scholar
  32. R. Sroka, M. Schaffer, C. Fuchs et al., “Effects on the mitosis of normal and tumor cells induced by light treatment of different wavelengths,” Lasers in Surgery and Medicine, vol. 25, no. 3, pp. 263–271, 1999. View at: Google Scholar
  33. T. M. Odor, N. P. Chandler, T. F. Watson, T. R. Pitt Ford, and F. McDonald, “Laser light transmission in teeth: a study of the patterns in different species,” International Endodontic Journal, vol. 32, no. 4, pp. 296–302, 1999. View at: Publisher Site | Google Scholar
  34. J. Vaarkamp, J. J. ten Bosch, and E. H. Verdonschot, “Propagation of light through human dental enamel and dentine,” Caries Research, vol. 29, no. 1, pp. 8–13, 1995. View at: Publisher Site | Google Scholar
  35. U. Schoop, W. Kluger, A. Moritz, N. Nedjelik, A. Georgopoulos, and W. Sperr, “Bactericidal effect of different laser systems in the deep layers of dentin,” Lasers in Surgery and Medicine, vol. 35, no. 2, pp. 111–116, 2004. View at: Publisher Site | Google Scholar
  36. K. J. Anusavice, Philips' Science of Dental Materials, W.B. Saunders, Philadelphia, Pa, USA, 10th edition, 1996.
  37. I. Denry and J. R. Kelly, “State of the art of zirconia for dental applications,” Dental Materials, vol. 24, no. 3, pp. 299–307, 2008. View at: Publisher Site | Google Scholar
  38. M. Aida, T. Hayakawa, and K. Mizukawa, “Adhesion of composite to porcelain with various surface conditions,” The Journal of Prosthetic Dentistry, vol. 73, no. 5, pp. 464–470, 1995. View at: Publisher Site | Google Scholar
  39. M. Kern and V. P. Thompson, “Sandblasting and silica coating of a glass-infiltrated alumina ceramic: volume loss, morphology, and changes in the surface composition,” The Journal of Prosthetic Dentistry, vol. 71, no. 5, pp. 453–461, 1994. View at: Publisher Site | Google Scholar
  40. A. Della Bona, K. J. Anusavice, and J. A. A. Hood, “Effect of ceramic surface treatment on tensile bond strength to a resin cement,” International Journal of Prosthodontics, vol. 15, no. 3, pp. 248–253, 2002. View at: Google Scholar
  41. L. F. Valandro, A. D. Bona, M. A. Bottino, and M. P. Neisser, “The effect of ceramic surface treatment on bonding to densely sintered alumina ceramic,” The Journal of Prosthetic Dentistry, vol. 93, no. 3, pp. 253–259, 2005. View at: Publisher Site | Google Scholar
  42. M. Özcan and P. K. Vallittu, “Effect of surface conditioning methods on the bond strength of luting cement to ceramics,” Dental Materials, vol. 19, no. 8, pp. 725–731, 2003. View at: Publisher Site | Google Scholar
  43. R. Li, Y. Ren, and J. Han, “Effects of pulsed Nd:YAG laser irradiation on shear bond strength of composite resin bonded to porcelain,” Hua Xi Kou Qiang Yi Xue Za Zhi, vol. 18, no. 6, pp. 377–379, 2000. View at: Google Scholar
  44. A. Erdem, G. Akar, and T. Kose, “Effects of different surface treatments on bond strength between resin cements and zirconia ceramics,” Operative Dentistry, vol. 39, no. 3, pp. E118–E127, 2014. View at: Publisher Site | Google Scholar
  45. Y. Lin, X. Song, Y. Chen, Q. Zhu, and W. Zhang, “Effect of Er:YAG laser irradiation on bonding property of zirconia ceramics to resin cement,” Photomedicine and Laser Surgery, vol. 31, no. 12, pp. 619–625, 2013. View at: Publisher Site | Google Scholar

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