Shear bond strength and SEM evaluation of composite bonded to Er:YAG laser-prepared dentin and enamel
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1 Dental Materials (2005) 21, Shear bond strength and SEM evaluation of composite bonded to Er:YAG laser-prepared dentin and enamel William J. Dunn a, *, John T. Davis b, Anneke C. Bush c a Director of Research and Biomaterials, Wilford Hall Medical Center, 1615 Truemper Street, Lackland Air Force Base, TX 78236, USA b Comprehensive Dentist, 341 MDOS/SGOD, 7300 Perimeter Road, Malstrom AFB, MT 59402, USA c Biostatistician and Epidemiologist, 59th Clinical Research Squadron, 1255 Wilford Hall Loop, Lackland Air Force Base, TX 78236, USA Received 26 May 2004; received in revised form 14 October 2004; accepted 16 November 2004 KEYWORDS Lasers; Ablation; Adhesion; Dentin bonding; Acid etching Summary Objectives. The purpose of this study was to evaluate dentin and enamel bond strength to resin composite following high-speed rotary or Er:YAG laser preparation using a total etch adhesive system. The microstructure of resin tooth interfaces was also investigated. Methods. Human dentin and enamel specimens were prepared with a high-speed handpiece (KaVo) or Er:YAG laser (DELight) at manufacturer s recommended settings and etched with either 37% H 3 PO 4, laser etched, or not etched. Composite rods (Z-250, 3M/ESPE) were bonded to specimens with an adhesive (Adper Scotchbond Multi- Purpose, 3M/ESPE). After thermocycling, specimens were tested in shear to failure. Results. Two-factor ANOVA detected significant differences in the main effects of preparation and etch type, and interaction (p!0.001). Post hoc analyses showed that in both dentin and enamel, only the acid-etched specimens had significantly higher mean bond strengths, with rotary-prepared specimens having significantly higher mean bond strengths versus laser prepared specimens. Within each preparation type, in both dentin and enamel, acid etch was better than laser etch, and laser etch was better than no etch. Scanning electron microscopy of laserablated specimens demonstrated significant surface scaling and subsurface fissuring beyond normal resin penetration depth. Significance. Adhesion to laser-ablated or laser-etched dentin and enamel was inferior to that of conventional rotary preparation and acid etching. Published by Elsevier Ltd on behalf of Academy of Dental Materials. * Corresponding author. Address: 3701 Point Clear Drive, Ocean Springs, MS 39564, USA. Tel.: C ; fax: C addresses: darkhorse@cableone.net (W.J. Dunn), William.dunn@keesler.af.mil (W.J. Dunn). Introduction In 1960, Maiman [1] developed the method of light amplification by the stimulated emission of /$ - see front matter Published by Elsevier Ltd on behalf of Academy of Dental Materials.
2 Bonding to Er:YAG laser prepared dentin and enamel 617 radiation, now commonly known by its acronym, LASER. Five years later, Goldman et al. [2] investigated the application of the laser beam on dental hard tissues. Clinicians were concerned about possible adverse pulpal responses [3], but subsequent investigations demonstrated that lasers cause little thermal damage [4,5], especially if used in conjunction with water spray [6]. Lasers have demonstrated some analgesic effect which could increase patient acceptance of certain procedures [7]. Advancements in laser technology have led to multiple dental applications such as periodontal soft tissue plastic surgery [8], gingivectomy [9], soft tissue crown lengthening [10], gingival retraction for prosthodontics [11], composite photopolymerization [12], frenectomy [13], tooth whitening [14], treatment of apthous ulcers [15], endodontic procedures [16], and caries removal with increased precision, improved hemostasis and sterility, with minimal post operative pain and swelling [6,7,17]. The first dental lasers cleared by the FDA were used exclusively for soft tissue procedures and included the carbon dioxide (CO 2 ) laser, Neodymium Yttrium Aluminum Garnet (Nd:YAG) laser, argon laser, and the semiconductor diode laser. The CO 2 laser was the first dental laser approved by the FDA and has been successfully used in soft tissue surgeries such as gingivectomies, frenectomies, removal of benign and malignant lesions, and excisional and incisional biopsies [18]. The Nd:YAG laser uses a fiberoptic delivery system that penetrates wet tissue more easily than the CO 2 laser. There has been interest in using the Nd:YAG laser on mineralized tissue to possibly enhance the bond strength of composite to dentin [19], but the Nd:YAG laser is still not approved for hard tissue applications. The argon laser can be used for soft tissue procedures and is approved for photopolymerization of light-activated materials [20]. Semiconductor diode lasers perform the same soft tissue procedures as the CO 2 and Nd:YAG lasers and have also been used to enhance the effects of bleaching discolored teeth [21]. Other approved systems include the Erbium Chromium Yttrium Scallium Gallium Garnet (Er, Cr:YSGG) laser and the Erbium doped,yttrium Aluminum Garnet (Er:YAG) laser. These systems can be used for soft tissue procedures but most of the interest in Erbium lasers has been focused on hard tissue applications such as caries removal and endodontic cleaning and shaping of the root canal system [22]. The Er:YAG laser, originally developed by Zharikov et al. [23] in 1975, was approved by the FDA in 1997 for caries removal, forming cavity preparations, and modifying dentin and enamel prior to etching [24]. The Er:YAG laser has compared favorably with the high-speed rotary dental handpiece in some scanning electron microscopic (SEM) and histological studies [6]. The Er:YAG laser has also been shown to be more comfortable for patients than conventional preparation with a high-speed rotary handpiece [7]. In endodontic studies the Er:YAG laser has demonstrated effective cleansing and antimicrobial properties [16,25]. Use of the Er:YAG laser has been suggested for nonsurgical periodontal therapy, soft tissue surgery [26], and possibly subgingival scaling [27]. Tooth preparation using the Er:YAG laser has not demonstrated any significant thermal elevation compared with a rotary dental handpiece [28]. Takamori [29] demonstrated that tooth preparation with the Er:YAG laser may lead to pulpal repair faster than with rotary preparation. The Er:YAG laser produces minimal thermal effect on the tooth during preparation in comparison to other dental lasers [3]. The cutting effect of the Er:YAG laser on enamel, dentin, carious dentin, and composite varies according to the water content of the material being prepared. The beam can ablate, or remove by melting or vaporization, carious dentin with an energy level of 250 mj at 2 Hz, sound dentin with 300 mj at 2 Hz, and enamel with 350 mj at 3 Hz [30]. In theory, this allows for the selective preparation of a particular type of substrate or material. For example, during operative procedures carious dentin would be selectively removed while sparing healthy dentin, or composite would be selectively removed without damaging tooth structure following orthodontic bracket removal [31]. Microleakage and bond strength studies following Er:YAG preparation report highly variable results [24,32 36]. Visuri et al. [32] reported a significantly higher shear bond strength of composite to dentin prepared with an Er:YAG laser. In contrast, Sakakibara et al. [24] and Ceballos et al. [35] reported a decrease in bond strength to laser-irradiated dentin, and Armengol et al. [30] and Kataumi et al. [33] found no difference between laserirradiated and non-irradiated specimens. Improvements in laser technology and the increased interest in their potential for hard tissue application warrant the further investigation of Er:YAG laser-prepared teeth and adhesion with resin-based composite. The purpose of this study was to evaluate dentin and enamel bond strength to resin-based composite following high-speed rotary handpiece preparation or Er:YAG laser preparation with a multi-step, total etch adhesive system. The microstructure of resin dentin and resin enamel interfaces was also investigated. The hypothesis tested was that there would be no difference in the mean shear bond strength between composite and
3 618 tooth surfaces prepared by high speed rotary instrumentation or laser ablation, etched with phosphoric acid, laser-etched, or not etched. Materials and methods Two hundred and forty human molar teeth were collected and stored in 0.5% chloramine-t solution no more than 6 months from time of extraction to inclusion in the study. The teeth were free of visible caries and other surface defects. For the dentin portion of the study the occlusal surfaces of 120 teeth were abraded with 120-grit silicon carbide (SiC) paper (Buehler Ltd, Lake Bluff, IL, USA) until a uniform layer of peripheral dentin was observed. Dentin specimens were then sequentially polished with 240, 400, and 600 grit SiC paper on a watercooled polishing lathe (Buehler Ltd). The roots were notched and embedded in type IV dental stone (WhipMix Corporation, Louisville, KY, USA) in acrylic molds (Mark V Laboratories, East Granby, CT, USA) with the polished occlusal surfaces extending 2-mm above the level of the stone. The dentin specimens were randomly divided into six groups (nz20), representing the six different surface treatments to be investigated. Group 1D: high-speed, #57 bur, no etch, Adper Scotchbond Multi-Purpose DBA Group 2D: high-speed, #57 bur, 37% H 3 PO 4 etch, Adper Scotchbond Multi-Purpose DBA Group 3D: high-speed, #57 bur, laser etch, Adper Scotchbond Multi-Purpose DBA Group 4D: Er:YAG laser preparation, no etch, Adper Scotchbond Multi-Purpose DBA Group 5D: Er:YAG laser preparation, 37% H 3 PO 4 etch, Adper Scothbond Multi-Purpose DBA Group 6D: Er:YAG laser preparation, laser etch, Adper Scotchbond Multi-Purpose DBA Approximately 0.5-mm of dentin was removed from the occlusal surface of specimens in groups receiving high-speed rotary preparation with a #57 straight fissure tungsten carbide bur (Brasseler USA, Savannah, GA) at approximately 200,000 rpm with air/water coolant. A high-speed handpiece (KaVo America, Lake Zurich, IL, USA) was secured to a surveying instrument to insure that tooth surfaces were prepared in a standard fashion, flat and parallel to the floor. The mounted dentin specimens in groups 4 6D were prepared with an Er:YAG dental laser (DELight laser system, Continuum, Santa Clara, CA, USA) in a focused, non-contact mode, at a setting of 30 Hz/140 mj, a spot size of 0.6-mm, W.J. Dunn et al. a working distance of 1-mm, and a repetition rate of 30 Hz. The DELight laser system is an Er:YAG laser that emits a pulsed laser beam with a wavelength of 2940 nm. After appropriate instrumentation with either the high-speed handpiece or the Er:YAG laser, Groups 3D and 6D were laser-etched in a focused, non-contact mode at a setting of 10 Hz/35 mj. The dentin surface was cooled throughout irradiation with water to avoid cracking and fusion. The laser beam was directed manually without using a fixed support to simulate clinical conditions. Following appropriate preparation with either the high speed handpiece or the Er:YAG laser, Groups 2D and 5D were chemically etched were etched with 37% phosphoric acid for 20 s, and then rinsed with sterile water for 20 s. Specimens were blotted with tissue, leaving a moist dentin surface for bonding, but with no pooling of water. Adper Scotchbond Multi-Purpose (3M ESPE, St Paul, MN, USA, lot# , exp. 12/2005), a multistep, total etch dentin bonding agent, was used as the adhesive for all specimens. The primer was applied for 20 s, and then gently blown with clean, dry, compressed air for 5 s until the primer rippled. The adhesive was then applied and photopolymerized for 20 s with an Optilux 501 light-curing unit (Demetron Research Corporation, Danbury, CT, USA). A power density of at least 600 mw/cm 2 was verified with a hand-held radiometer (Model 100, Demetron Research Corporation). A 3-mm long by 3-mm wide composite rod (Z-250 shade A1, 3M ESPE) was bonded to all dentin specimens using a split teflon mold with an inner diameter of 3-mm. The mold was secured to the specimen, and then two 1.5-mm increments of composite were polymerized separately for 40 s each. The teflon mold was removed and specimens were stored in water at 37 8C for 1 day, and then thermocycled for 500 cycles between 5 and 55 8C with a dwell time of 30 s each. The remaining 120 teeth were used to fabricate the enamel specimens. The roots were removed using an Isomet low speed precision saw (Buehler Ltd). The crowns were embedded in dental stone (WhipMix Corporation) in acrylic molds (Mark V Laboratories) with buccal enamel surfaces extending 2-mm above the level of the stone. The enamel specimens were randomly divided into six groups, similar to the dentin specimens, each representing a different surface treatment for enamel bonding. Group 1E: high-speed, #57 bur, no etch, Adper Scotchbond Multi-Purpose adhesive Group 2E: high-speed, #57 bur, 37% H 3 PO 4 etch, Adper Scotchbond Multi-Purpose adhesive
4 Bonding to Er:YAG laser prepared dentin and enamel 619 Group 3E: high-speed, #57 bur, laser etch, Adper Scotchbond Multi-Purpose adhesive Group 4E: Er:YAG laser preparation, no etch, Adper Scotchbond Multi-Purpose adhesive Group 5E: Er:YAG laser preparation, 37% H 3 PO 4 etch, Adper Scotchbond Multi-Purpose adhesive Group 6E: Er:YAG laser preparation, laser etch, Adper Scotchbond Multi-Purpose adhesive Approximately 0.5-mm of enamel was removed from buccal surfaces of specimens receiving highspeed rotary instrumentation with a #57 tungsten carbide straight fissure bur. The handpiece was secured to a paralleling device described earlier to ensure standardized, flat enamel surfaces parallel to the base of the stone. Surfaces were inspected for a flat bonding area of at least 4!4 mm with no dentin exposed. The dentin surfaces of groups 4E 6E were laser-prepared with the Er:YAG dental laser in a focused, non-contact mode, at a setting of 25 Hz/240 mj, a spot size of 0.6-mm, a working distance of 1-mm, and a repetition rate of 30 Hz. Groups 3E and 6E were laser-etched with the Er:YAG dental laser in a focused, non-contact mode at a setting of 10 Hz/35 mj. The surface was kept wet to avoid drying and cracking. Groups to be chemically etched were etched with 37% phosphoric acid for 20 s, rinsed with water for 20 s, and then dried with clean, compressed air for 10 s as recommended by the manufacturer. Adper Scotchbond Multi-Purpose was applied to specimens in Groups 2E and 5E in the same manner as the dentin samples, except surfaces for enamel specimens were kept dry. Composite rods were bonded to enamel specimens in the same manner as the dentin specimens. Enamel specimens were then stored in water at 37 8C for 1 day, and then thermocycled for 500 cycles between 5 and 55 8C with a dwell time of 30 s each. Shear bond testing was accomplished using a wire loop secured to a Universal Testing Machine (Model 1541S, Instron Corporation, Canton, MA, USA) at a crosshead speed of 0.5-mm/s. The force to failure was recorded for each specimen. The mean shear bond strength in megapascals (MPa) was determined for each group. Fractured specimens were observed with a stereomicroscope (Nikon SMZ-1B, Osaka, Japan) at 20! magnification for determination of failure modes, which were classified as cohesive, adhesive, or mixed. Data were subjected to a two-factor analysis of variance (ANOVA) to examine the effects of preparation type and etch type on each of the two substrates (enamel and dentin) separately. All statistical analyses were performed at az0.05. Twelve caries free human third molars were used for scanning electron microscopic (SEM) evaluation. Each tooth represented one of the six enamel or six dentin groups and was prepared and bonded with a composite rod according to the group s protocol as previously described. These specimens were cross-sectioned in a low speed precision saw (Isomet, Buehler Ltd) in a mesio-distal direction through the composite rod and then lightly polished with 600 and 1200 grit SiC paper under running water in a polishing lathe. The specimens were mounted on aluminum stubs, desiccated, sputter coated with gold/palladium, and examined in a scanning electron microscope (LEO, model #435VP, Cambridge, UK). In addition, several dentin and enamel specimens were acid-etched, lased, or acid-etched and lased and fixed in glutaraldehyde for SEM observation. Results Mean shear bond strength data of composite bonded to rotary-prepared or Er:YAG laser-prepared dentin and enamel, etched with either 37% phosphoric acid, laser-etched at 10 Hz/35 mj, or not etched, are presented in Table 1. For dentin specimens the ANOVA detected statistically significant main effects (p!0.001) as well as a significant interaction (p!0.001) between preparation type and etch type, so no direct conclusion can be drawn regarding the main effects of either factor. For enamel specimens the ANOVA also detected statistically significant main effects (p!0.001) in addition to a statistically significant interaction (p!0.001) between preparation type and etch type, so again, no direct conclusion may be drawn regarding the main effects of either factor. Tukey s post-hoc analyses of preparation type showed that among both the dentin and enamel specimens, only the acid-etched specimens had statistically significantly different (p!0.001) mean bond strengths, with the rotary-prepared specimens having much higher mean bond strengths versus the laser prepared specimens. There were no statistically significant differences within the other etch types with regard to preparation type, as might be expected by the significant interaction term. In other words, the acid-etched rotaryprepared specimens demonstrated higher mean bond strength than the acid-etched laser-prepared specimens. The laser-etched, rotary-prepared specimens were not statistically different from
5 620 W.J. Dunn et al. Table 1 Mean shear bond strength (MPa) of dentin and enamel groups. Group Preparation type Etchant Shear bond strength Standard deviation Dentin specimens 1D Rotary Acid D Laser D None D Laser Acid D Laser D None Enamel specimens 1E Rotary Acid E Laser E None E Laser Acid E Laser E None the laser-etched, laser-prepared specimens, nor were the non-etched, rotary-prepared specimens different from the non-etched, laser-prepared specimens. This observation was noted for both dentin and enamel. Tukey s post-hoc analyses demonstrated that within each preparation type, all of the differences among the three etch types were statistically different from each other (acid etch better than laser etch better than no etch). These differences were found to be significant (p!0.001). Fracture patterns of dentin and enamel specimens are presented in Table 2. Scanning electron microscopy of rotary-prepared, acid-etched dentin (Fig. 1A) revealed a smooth surface with tubule orifices devoid of smear plugs. The intertubular dentin is undisturbed. Cross section of the bonded composite rod to rotary-prepared, acid-etched dentin revealed intimate contact between composite and dentin, suggesting good hybridization. In contrast, SEM of a cross-section of laser-ablated, laser-etched dentin showed a highly irregular surface and fissuring. Areas of poor hybridization between composite and dentin suggest poor hybridization, or no hybridization. Laser-prepared dentin revealed surface scaling and flaking, along with peritubular cuffing (Fig. 1B). Acid-etching after laser ablation appeared to decrease some of the surface scaling and flaking (Fig. 1C). Laser ablated, acid-etched dentin demonstrated areas of detachment from both the resin adhesive and the unaffected subsurface dentin (Fig. 3). Scanning electron microscopic images of enamel surfaces bonded with composite revealed similar findings to that of dentin. Table 2 Group Fracture patterns of tooth specimens. Preparation Etchant Cohesive failure Adhesive failure Mixed failure type Dentin specimens 1D Rotary Acid 4 (20%) 6 (30%) 10 (50%) 2D Laser 8 (40%) 4 (20%) 8 (40%) 3D None 2 (10%) 14 (70%) 4 (20%) 4D Laser Acid 6 (30%) 6 (30%) 8 (40%) 5D Laser 11 (55%) 3 (15%) 6 (30%) 6D None 10 (50%) 5 (25%) 5 (25%) Enamel specimens 1E Rotary Acid 2 (10%) 11 (55%) 7 (35%) 2E Laser 12 (60%) 3 (15%) 5 (25%) 3E None 1 (5%) 13 (65%) 6 (30%) 4E Laser Acid 11 (55%) 3 (15%) 6 (30%) 5E Laser 12 (60%) 2 (10%) 6 (30%) 6E None 11 (55%) 2 (10%) 7 (35%)
6 Bonding to Er:YAG laser prepared dentin and enamel 621 Figure 1 Scanning electron microscopic images of dentin: (A) rotary-prepared and acid-etched (3500!), (B) laser-prepared (9000!), and (C) laser-prepared and then acid-etched (3500!). Figure 2 Scanning electron microscopic images of enamel (all 3500!): (A) rotary-prepared, acid-etched, (B) laser-ablated, and (C) laser-ablated then acid-etched. Lased dentin and enamel, subsequently acid-etched, demonstrated an improvement in contact intimacy between the composite material and the tooth surface interface. Acid-etched enamel is seen in Fig. 2A. A loss of surface area for resin penetration occurs during laser ablation of enamel (Fig. 2B). If laser-ablated enamel is subsequently acid-etched, a unique etch pattern is seen (Fig. 2C); this etch pattern resulted in specimens that had higher bond strength than laser ablation alone, but did not improve to the bond strength levels of conventional rotaryprepared, acid-etched enamel. Discussion Although some previous investigations have reported that the bond strength of composite to laser-irradiated dentin was higher than that of
7 622 acid-etched dentin, data from our study demonstrate that bond strengths are significantly weaker when tooth surfaces are prepared with the Er:YAG laser. The results of this study agree with the findings of Ceballos et al. [35], Kameyama et al. [37], Martinez-Insua et al. [38], and Aoki et al [39] In contrast, Keller and Hibst [40], Visuri et al. [32], and Stiesch-Scholz and Hanning [41] postulated that the lased dentin surface possessed an advantage because of an apparent enlarged surface area for adhesion based on the scaly and flaky surface appearance following Er:YAG irradiation. This scaly surface appearance of laser ablated dentin, along with the cuff-like appearance of peritubular dentin described by Aoki et al. [39], was also evident in the SEM images from the current study (Fig. 1b). The unusual appearance of laser-irradiated dentin can be explained by understanding the process of laser ablation. Li et al. [42] explained that the Er:YAG laser thermomechanically ablates hard tissues by causing micro-explosions within inorganic structures in teeth. Initially, the Er:YAG laser vaporizes water and other hydrated organic components until internal pressure causes the destructive explosion of the inorganic component before the melting point is reached. Aoki et al. [39] determined that intertubular dentin was selectively ablated more than peritubular dentin, leaving a cuff of more highly mineralized dentin around dentin tubule orifices. The higher water content of intertubular dentin compared to peritubular dentin can explain this. Ceballos et al. [35] proposed that the ablation of dentin fused collagen fibrils together resulting in a lack of interfibrillar space, restricting resin diffusion into the subsurface intertubular dentin. Cross sectional observation of resin bonded to laserablated dentin revealed a lack of penetration of the resin, and even peeling of the resin layer from the ablated dentin surface (Figs. 3 and 4), supporting the theory of resin restriction. The lack of resin penetration in laser-ablated dentin is the most likely explanation for lower bond strengths. Data from the current study substantiate the observation that laser ablated dentin results in significantly lower shear bond strength compared with rotaryprepared, acid-etched dentin. The bonding mechanism of resin to acid-etched dentin is well known and understood to be micromechanical. [43,44] Little is known about the adhesion of resin to laser irradiated dentin, but it appears that the formation of an interdiffusion zone, which is the basis for dentin hybridization in acid-etched dentin, is unlikely. Instead, laser ablated dentin probably acquires its bond strength solely from the penetration of resin tags into dentin tubules. Resin tag W.J. Dunn et al. Figure 3 Separation of resin adhesive and unaffected subsurface dentin from laser-ablated, then acid-etched dentin. formation accounts for only a fraction of the bond strength in normal hybridized dentin [45]. Fracture patterns of composite rods bonded to laser ablated dentin revealed a high incidence of cohesive dentin failures compared to rotary-prepared, acid-etched specimens (Table 2). These data are in agreement with the fracture pattern findings of Martinez-Insua et al. [38] and Kameyama et al. [37]. The cohesive dentin failures may be explained by the lack of penetration of resin into Er:YAG irradiated dentin, creating a weak subsurface zone just below the interface. The prospect of laser etching enamel surfaces was welcomed because of potential disadvantages with enamel acid etching. Acid demineralization with 37% phosphoric acid can make enamel surfaces more susceptible to caries, especially if resin impregnation is incomplete or defective [38]. It was thought that laser etching might reduce caries risk because demineralization would not occur, and that water and organic components would be Figure 4 Resin adhesive peeling away from the laserablated dentin surface.
8 Bonding to Er:YAG laser prepared dentin and enamel 623 reduced [46]. However, the extensive fissuring and subsurface cracking that occurs with the Er:YAG laser on enamel surfaces negates any possible advantages and precludes its use. Enamel specimens that were irradiated with the Er:YAG laser demonstrated significantly lower mean bond strengths compared to rotary-prepared, acidetched specimens. These results are in agreement with Martinez-Insua et al. [38]. Acid etching of enamel surfaces removes approximately 10 mg of the enamel surface and creates a microporous layer from 5 to 50 mg deep which is readily filled with resin [47]. The laser irradiated enamel surface (Fig. 2B) produced surface fissuring and a union or blending of the distinctive etch pattern normally seen in acidetched enamel (Fig. 2A). This blending effect likely prevented the penetration of resin into the enamel, resulting in lower enamel bond strength values. Interestingly, the subsequent addition of acid etchant to laser ablated enamel created a delicate etch pattern that assumed the appearance of a more retentive surface (Fig. 2C) than that created by laser etching alone. Bond strength data from the present study appear to support this observation (Table 1), but the values still do not reach those of acid-etched enamel. Fracture patterns of composite rods bonded to laser ablated enamel specimens reveal a high incidence of cohesive enamel failures, suggesting that the Er:YAG laser produces subsurface fissuring that goes beyond resin penetration. When dentin and enamel specimens were acid etched after they were laser irradiated, a significant improvement in shear bond strength from laser etching alone was observed. In contrast, Kameyama et al. [38] postulated that acid treatment following laser irradiation amplified the deleterious effects to dentin. Fig. 1C demonstrates that the subsequent use of phosphoric acid after laser irradiation eliminates some of the surface scaling and flaking that typifies the laser-ablated dentin surface (Fig. 1B). However, it appears that the thermomechanical effects of laser irradiation extend into the subsurface in both dentin and enamel, compromising the integrity of the tooth-restoration bonded interface and decreasing the resulting shear bond strength. Still, the highest bond strengths are obtained when dentin or enamel is prepared by a rotary handpiece and then etched with 37% phosphoric acid. Within the limits of this study, the null hypothesis that there would be no difference in mean shear bond strength between composite and tooth surfaces prepared by high speed rotary instrumentation or laser ablation, etched with acid, laser etched, or not etched, must be rejected. Our observations suggest that the deleterious effects of Er:YAG laser irradiation on dental hard tissue goes beyond normal resin penetration depth. Any purported advantage of Er:YAG laser treatment on dental hard tissues must be seriously challenged in light of the results of this study. Er:YAG laser irradiation has an adverse effect on dental hard tissues and is not a viable alternative to conventional acid etching. Further studies examining the effects of Er:YAG irradiation and the structural changes in teeth that result are required before Er:YAG laser use can be established as a reliable operative technique in dentistry. References [1] Maiman TH. Stimulated optical radiation in ruby. Nature 1960;187: [2] Goldman L, Glay A, Goldman J, Goldman B, Meyer R. Effect of laser beam impacts on teeth. J Am Dent Assoc 1965;70: 601. [3] Wigdor H, Abt E, Ashrafi S, Walsh Jr JT. The effects of lasers on dental hard tissues. J Am Dent Assoc 1993;124(2): [4] Orchardson R, Peacock EA, Whitters CJ. 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AGD Impact 2003; [23] Zharikov EV, Zhekvo VI, Kulesvskii LR, et al. Stimulated emission from Er 3C ions in Yttrium aluminum garnet crystals at lz2.94 mg. Soviet J Quantum Electron 1975;4: [24] Sakakibara Y, Ishimaru K, Takamizu M. A study on bond strength to dentin irradiated be Erbium:YAG laser. Jpn J Conservative Dent 1998;41: [25] Mehl A, Folwaczny M, Haffner C, Hickel R. Bactericidal effects of 2.94 mg Er:YAG-laser radiation on dental root canals. J Endod 1999;25(7): [26] Schwartz F, Sculean JA, Georg T, Reich E. Periodontal treatment with an Er:YAG laser compared to scaling and root planing. A controlled clinical study. J Periodont 2001; 72(3): [27] Aoki A, Ando Y, Watanabe H, Ishikawa I. In vitro studies on laser scaling of subgingival calculus with an Er:YAG laser. J Periodont 1994;65(12): [28] Armengol V, Jean A, Marion D. Temperature rise during Er:YAG and Nd:YAG laser ablation of dentin. J Endod 2000; 26(3): [29] Takamori K. A histopathological and immunohistochemical study of dental pulp and pulpal nerve fibers in rats after cavity preparation using Er:YAG laser. J Endod 2000;26(2): [30] Armengol V, Jean A, Rohanizadeh R, Hamel H. Scanning electron microscopic analysis of diseased and healthy dental hard tissues after Er:YAG laser irradiation: in vitro study. J Endod 1999;25(8): [31] Dumore T, Fried D. Selective ablation of orthodontic composite by using sub-microsecond IR laser pulses with optical feedback. Lasers Surg Med 2000;27(2): [32] Visuri SR, Gilbert JL, Wright DD, Wigdor HA, Walsh Jr JT. Shear strength of composite bonded to Er:YAG laserprepared dentin. J Dent Res 1996;75: W.J. Dunn et al. [33] Kataumi M, Nakajima M, Yamada T, Tagami J. Tensile Bond strength and SEM evaluation of Er:YAG laser irradiated dentin using dentin adhesive. Dent Mater J 1998;17: [34] Ceballos L, Osorio R, Toledano M, Marshall GW. Microleakage of composite restorations after acid or Er YAG laser cavity treatments. Dent Mater 2001;17: [35] Ceballos L, Toledano M, Osorio R, Tay FR, Marshall GW. Bonding to Er YAG-laser-treated dentin. J Dent Res 2002; 81(2): [36] Shigentani Y, Tate Y, Okamoto A, Iwaku M, Abu-Bakr N. A study of cavity preparation by Er:YAG laser-effects on the marginal leakage of composite resin restoration. Dent Mater J 2002;21(3): [37] Kameyama A, Kawada E, Takizawa M, Oda Y, Hirai Y. Influence of different acid conditioners on the tensile bond strength of 4-META/MMA-TBB resin to Er:YAG laser-irradiated bovine dentin. J Adhes Dent 2000;2: [38] Martinez-Insua A, da Silva Dominguez L, Guitian Rivera F, Santana-Penin UA. Differences in bonding to acid-etched or Er:YAG-laser-treated enamel and dentin surfaces. J Prosthet Dent 2000;84: [39] Aoki A, Ishikawa I, Yamada T, et al. Comparison between Er:YAG laser and conventional technique for root caries treatment in vitro. J Dent Res 1998;77: [40] Keller U, Hibst R. Experimental studies of the application of the Er:YAG laser on dental hard substances: II. Light microscopic and SEM investigations. Lasers Surg Med 1989; 9: [41] Stiesch-Scholz M, Hanning M. In vitro study of enamel and dentin marginal integrity of composite and compomer restorations placed in primary teeth after diamond or Er; YAG laser cavity preparation. J Adhes Dent 2000;2: [42] Li ZZ, Code JE, Van de Merwe WP. Er:YAG laser ablation of enamel and dentin of human teeth: determination of ablation rates at various fluences and pulse repetition rates. Lasers Surg Med 1992;12: [43] Van Meerbeek B, Inokoshi S, Braem M, Lambrechts P, Vanherle G. Morphological aspects of the resin dentin interdiffusion zone with different dentin adhesive systems. J Dent Res 1992;71: [44] Perdigao J, Swift Jr EJ, Denehy GE, Wefel JS, Donly KJ. In vitro bond strengths and SEM evaluation of dentin bonding systems to different dentin substrates. J Dent Res 1994;73: [45] Jassem HA, Retief DH, Jamison HC. Tensile and shear strengths of bonded and rebonded orthodontic attachments. Am J Orthod 1981;79: [46] Oho T, Morioka T. A possible mechanism of acquired acid resistance of human dental enamel by laser irradiation. Caries Res 1990;24: [47] Van Meerbeek B, Inoue S, Perdigao J, Lambrechts P, Vanherle G. Enamel and dentin adhesion. In: Summitt JB, Robbins JW, Schwartz RS, editors. Fundamentals of operative dentistry a contemporary approach. 2nd ed.. Carol Stream: Quintessence Publishing; p
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