LASER EFFECTS ON DENTAL HARD TISSUES J.D.B FEATHERSTONE AND D.G.A. NELSON Department of Oral Biology, Eastman Dental Center, 625 Elmwood Avenue, Rochester, New York 14620 Adv Dent Res l(l):21-26, October, 1987 ABSTRACT he use of lasers in dentistry has been considered for over 20 years. Higher-energy density lasers were shown to fuse enamel but were potentially unsafe. Subsequently, low-energy density laser radiation was shown to affect artificial caries lesion formation. Recent studies have shown that carbon dioxide lasers can successfully be used at low-energy densities to fuse enamel, dentin, and apatite. Our studies have shown that specific wavelengths are highly efficient. These wavelengths are directly related to the infrared absorption regions of apatite. We have conducted studies with enamel and dentin, using pulsed CO 2 laser radiation in the 9.32-jim to 10.49-|xm region with energy densities in the 10 to 50 J.cm~2 range. This laser treatment caused surface fusion and inhibition of subsequent lesion progression and markedly improved the bonding strength of a composite resin to dentin. Similar studies have shown no pulpal damage or permanent deleterious effect on soft tissues. This improved understanding of the scientific rationale for the interaction of CO 2 lasers with teeth can lead to several clinical applications. This will depend, however, on the development of a technology to direct a specific frequency laser beam precisely to a desired site. T INTRODUCTION Studies on the possible application of lasers to dentistry began over 20 years ago. Many of the studies that have been carried out have been based simply on empirical use of available lasers and an examination by various techniques of their effect on dental hard or soft tissues. Studies by Stern and Sognnaes (1964) and Stern et ah (1966) utilized a ruby laser (wavelength 693.4 nm) and did demonstrate that exposure of human enamel to the laser increased the resistance of that enamel to subsurface demineralization in vitro. Vahl (1968) used electron microscopy and x-ray diffraction to study the effects of laser radiation on enamel. These studies clearly demonstrated ultrastructural and crystallographic changes in response to laser radiation. Later studies by Yamamoto and Ooya (1974) and Yamamoto and Sato (1980) showed the potential of a Nd:YAG laser (wavelength 1060 nm) to fuse dental Presented at the Conference on Diagnostic and Therapeutic Technology in Dentistry, September 29-October 1,1986, conducted by the National Institute of Dental Research This study was supported in part by a Fogarty International Research Fellowship, F05 TW03162. enamel and to make it highly resistant to subsequent dissolution. In the above studies and in other studies carried out with visible light lasers during that same period, non-specific laser radiation was utilized with very inefficient energy interaction with the tooth substance. Often high-energy densities — for example, 104 J.cm~2 — were used together with relatively long interaction times in the range of 50 msec to 2 sec. Later studies utilizing the carbon dioxide laser utilized much lowerenergy density levels, with a much more efficient transfer of energy, and these are described below. An obvious possible utilization of lasers in dentistry is for the fusion of enamel for cavity preparation. Goldman et al. (1965) and Gordon (1967) studied this possibility and came to the conclusion that the enormous amount of heat generated locally caused cracking and distortion of the enamel, and that the technique did not warrant further study. Interaction of lasers with the soft tissues is another obvious possible application in terms of both surgery and wound healing. Any surgical application of lasers which is currently in use in other parts of the body has obvious application to the oral cavity. It is beyond the scope of this paper to discuss that aspect. However, studies have been carried out to investigate the possibility of improved wound healing after the 21 22 FEATHERSTONE & NELSON Adv Dent Res October 1987 use of lasers. Surinchak et al (1983) and Hunter et at. (1984) utilized He:Ne laser irradiation at 632.8 nm and low-energy densities (1-2 J.cm~2) but demonstrated no advantage with respect to wound healing compared with conventional surgery. These aspects deserve further attention, but the potential does not appear to be good. on human dental enamel and dentin in the infrared region from 9.3 through 10.6 jjim. Low-energy densities in the region 10-50 J.cm"2 and short interaction times in the region of 100-200 nsec have been used. Carbon Dioxide Laser The abovementioned studies all utilized lasers with energy frequency values that do not interact efficiently with enamel. In those cases, the energy density of the laser irradiation was large enough not only to cause changes in the enamel surface structurally and morphologically but also to cause an apparent large change in the physical properties of the enamel. Pitting and melting of the surface enamel and fusion of the crystals occurred. Dental enamel, cementum, and dentin contain carbonated apatite which has absorption bands in the infrared region due to phosphate, carbonate, and hydroxyl groups in the crystal structure. The carbon dioxide laser produces radiation which falls in the infrared region and coincides closely with some of the absorption bands of apatite (Nelson and Featherstone, 1982; Nelson and Williamson, 1982). Stern et al (1972), Kantola et al (1973), and Lenz et al (1982) carried out studies utilizing carbon dioxide lasers and demonstrated ultrastructural crystallographic effects with this laser. In most previous studies using the carbon dioxide laser, continuous wave lasers were used, and typical interaction times varied from 50 msec to 2 sec. Kuroda and Fowler (1984) and Fowler and Kuroda (1986) reported structural and phase changes in surface enamel when treated with the carbon dioxide laser or when heated. All of these studies suggest that the carbon dioxide laser could be the system of choice for possible dental applications. In studies carried out in our laboratories during the last five years, we have considered that the wavelength of the laser light is extremely important. Dental enamel absorbs very little light in the visible region, so the use of visible light lasers requires high-energy densities as discussed above. Further, pulsed lasers rather than continuous lasers provide a way for increasing the peak power density while keeping the pulse energy density constant. This means that fusion, melting, and recrystallization of enamel crystals are confined to a 5-10-|i,m thin surface region without affecting the underlying enamel at depths of 50 |xm or greater and — very importantly — the underlying dentin or pulp. Dental hard tissue has intense absorption bands in the 9.0 through 11.0 juim region because of the apatite crystals, and this implies that infrared radiation from the carbon dioxide laser should be much more efficiently absorbed than radiation from the visible spectrum. We summarize here some of the recent investigations of our group (Nelson et al, 1986a; Nelson et al 1987). These studies have concentrated on the use of low-energy pulsed CO2 laser radiation Full experimental details have been presented elsewhere (Nelson et al, 1986a; Nelson et al, 1987). The present paper is designed to summarize these studies and to present the principal conclusions from them. MATERIALS AND METHODS Artificial Caries-like Lesion Formation Non-carious crowns of human molars or pre-molars were removed from the roots, cleaned according to previously reported methods (Featherstone et al, 1983), and painted with acid-resistant varnish, leaving two 1 x 3-mm rectangular windows side by side at equal heights from the cemento-enamel junction. The teeth were then cut in half so that one window could be retained as an unlased control, with the other exposed to laser treatment (see below). A total of 106 teeth was utilized in the studies. The control teeth, or the lased teeth (with the windows re-painted), were immersed in artificial caries-producing buffer, pH 5.0, at 37°C, containing 0.04 mol/L lactic acid, 0.1 mmol/ L methane hydroxy diphosphonate (MHDP), 40 mL per tooth, for periods from two hr up to 14 days. The demineralizing buffers were analyzed for calcium and phosphate at the end of the dissolution period. The teeth were cut in half through the window for subsequent examination by microhardness testing, polarized light microscopy, and scanning electron microscopy (see below). Laser Treatment We used a Lumonics TEA103-1 Multimode Line Tunable CO 2 Gas Laser (Lumonics Research Ltd., Ottawa, Canada) that produced 100-200 nsec pulses with a maximum pulse energy of 5J. Four specific lines were chosen by means of an Optical Engineering Model 16A carbon dioxide laser spectrum analyzer (Optical Engineering, Inc., Santa Rosa, CA) at the following wavelengths (wave numbers): 9.32 |im (1073 cm- 1 ), 9.57 |mm (1045 cm" 1 ), 10.27 \im (973 cm" 1 ), and 10.59 |xm (945 cm" 1 ). The pulses were ellipticallypolarized with unequal components in the perpendicular and parallel polarization directions. The spot size was varied from 2-5 mm in diameter with a concave mirror so that pulse energy densities of approximately 10-50 J.cm~2 and peak power densities of 107-108 Won- 2 could be obtained. Scanning Electron Microscopy The SEM examination was carried out by Dr. Dennis Nelson and Dr. W. Jongebloed (University of Groningen) and is reported in detail elsewhere (Nelson et al, 1987), but is included here for completeness. Individual enamel specimens were treated with one of four different laser wavelengths as above, with Vol. 1 No. 1 LASER EFFECTS ON DENTAL TISSUE an energy density of 50 J.cm 2 for 400 pulses. This part of the study was carried out so that we could assess the surface enamel changes which occurred under the conditions utilized in the lesion formation experiments. Dentin was also irradiated with 1073 cm 2 line for 20 pulses. These samples were sputtered with a layer of gold 10-12 nm thick and examined in a JEOL 35C Scanning Electron Microscope (JEOL, Japan) at 25 kV. Microhardness Testing The lased and control halves of each tooth were embedded and polished with the cut face exposed, according to standard procedures in our laboratory (Featherstone et al., 1983). The hardness profiles were determined at 25-|a.m intervals across the lesion section into the underlying normal enamel, and converted via the empirical relationship previously reported (Featherstone et al., 1983). A computer program was used for calculation of the average profiles for each group, based on the means at each depth. Polarized Light Microscopy Thin sections were cut to a thickness of approximately 80 |xm and examined by polarized light microscopy in water, Thoulet's solution, and quinoline, according to standard procedures. [This portion of the study was conducted by Dr. James Wefel (University of Iowa), and the details are reported elsewhere (Nelson et al., 1987).] The thin sections used were immediately adjacent to the hemi-sections used for the microhardness testing. 100 100 150 200 250 300 Depth (microns) Fig. 1 —Composite mineral profile of 14-day-old lesions obtained from cross-sectional microhardness data for enamel lased with the 9.32-n.m (1073 c m 1 ) line ( • ) compared with the non-lased controls (x). Each point is the average of 15 microhardness indentations, with the p value (paired t test at each depth) shown above each set of points. Bars show standard deviations (from Nelson et al., 1986a; published courtesy of Karger AG). | low energy [ j high energy Chemical Analysis The demineralization solutions were analyzed for calcium by atomic absorption, and phosphate by the molybdate method. RESULTS Hardness Profiles The irradiation of intact human dental enamel by carbon dioxide laser inhibited subsequent artificial caries-like lesion formation. This was, however, variable according to the wavelength used and according to the energy density used. The most effective laser line at the pulse energy1 density of 10 J.cm"2 was the R12 line at 1073 cm" . This produced significantly less demineralization and shallower lesions than did the controls (Fig. 1). Although the 1045-, 973-, and 945-cm ' lines also produced effects, they were not as pronounced, with pre-treatments consisting of 400 pulses of 10 J.cm 2 energy density laser beam. For each of the experiments performed, the area of mineral loss was calculated from the data between 25-200 |xm depth and expressed as a percentage of the total demineralization in the control calculated in the same way. This gives an estimate of the average reduction in artificial lesion formation given by a particular laser pre-treatment. Fig. 2 presents the results 1073 1045 973 945 wavenumber (cm'^l Fig. 2 —Mean percentage reduction in artificial lesion formation (14-day immersion) in enamel when compared with the control group for 400-pulse laser pre-treatment at 10 J.cm 2 (dark shading) and 50 J.cm 2 (single cross-hatching). Error bars are standard deviations (from Nelson ct al., 1986a; published courtesy of Karger AG). expressed using this2 parameter for the low-energy treatment (10 J.cm" ) and the higher energy treatment of 50 J.cm 2 at each of the four wavelengths studied. The 50 J.cm 2 energy treatment was more effective than the low-energy treatment at each wavelength. The most effective wavelength at reducing subsequent subsurface caries-like lesion progression 24 Adv Dent Res October 1987 FEATHERSTONE & NELSON was the 9.32 |xm (1073 cm"1) line, with lesions approximately 50 percent less demineralized than those of the controls. Each of the four wavelengths tested did, however, have an effect, as illustrated in Fig. 2. Further details of the effect on the subsurface profiles are presented elsewhere (Nelson et al., 1986a). Scanning Electron Microscopy Scanning electron microscopy (for details, refer to Nelson et al., 1987) revealed that extensive surface roughening of enamel occurred when laser irradiation at 50 J.cm~2 was used. This surface roughening was wavelength-dependent, with the 9.32- and 9.57ixm lines producing the greatest effect (Figs. 3 a,b), and the 10.59-|xm producing the smoothest effect (Figs. 3 c,d). At higher magnifications, it was shown that there was a central melt region (at the center of beam contact with the surface), which, although rough, was covered by a thin, smooth, fused surface layer (Figs. 3 d,b). Fractured cross-sections (Figs. 3 e,f) revealed a region, up to 5 |xm deep from the enamel surface, where the melting and fusion of the crystals had occurred. Polarized Light Microscopy Polarized light microscopy confirmed the considerable reduction in lesion depth as a result of preradiation by the laser treatment. It also confirmed thin well-fused surface zones up to 10 |xm thick as a result of laser treatment with the 973-, 1045-, and 1073-cm1 lines (see Nelson et al, 1987, for further details). This effect at the surface was not shown in the control, unlased lesions. Chemical Analysis The mineral loss as determined by chemical analysis was of the same order as the change in mineral profiles recorded by microhardness testing. The details are given elsewhere (Nelson et al., 1986a). DISCUSSION The studies summarized here, together with the earlier studies utilizing carbon dioxide lasers, summarized in the "Introduction", clearly show that lowenergy infrared laser irradiation of enamel markedly inhibits the progress of subsurface caries-like lesions. Fig. 3 —(a) Low-magnification SEM of human dental enamel lased with an energy density of 50 J.cm~2 using the 1073-cm ' line. Bar = 300 |xm. (b) Higher magnification of (a). Bar = 50 |im. (c) Enamel lased with the 945-cm 1 line. Bar = 300 p.m. (d) Higher magnification of (c). Bar = 50 jim. (e) Cross-fracture through lased enamel (1073-cm ] line). Bar = 3 |j.m. (f) Higher magnification of cross-fracture. Notice completely fused crystallites (fc) near the surface, partially fused crystallites (pf), and normal crystallites (nc). Bar = 1 jjtm. (from Nelson et al., 1987; published courtesy of Karger AG) Vol. 1 No. 1 LASER EFFECTS ON DENTAL TISSUE The present studies have shown that this inhibition is wavelength-dependent and that the carbon dioxide laser is a very much more efficient treatment system than the visible wavelength lasers previously utilized by other workers. The effect of the laser on the enamel surface was to produce a surface melt which one would normally associate with momentary temperature rises in the region of 800-1100°C. This is sufficient for fusing and melting of enamel crystals, which are carbonated-apatite. The pulsed laser utilized in the present studies, although having pulses only 100-200 nsec in length, was sufficient to cause this surface temperature rise. In order to confirm this, we subsequently carried out experiments to measure this temperature rise, using a Modline Temperature Measuring System (Ircon, Inc., Niles, IL) which showed that temperatures rose to approximately 1050°C at the enamel surface for the 1073-cm 1 and approximately 800°C for the 945-cm"1 line. We have subsequently carried out infrared analysis of the surface enamel after laser treatment with the 1073-cm 1 line for 400 pulses at 50 J . c m 2 (Nelson et ah, 1987). The carbonate content was dramatically reduced, and the surface phases were hydroxyapatite and tetracalcium diphosphate monoxide. This is comparable with effects reported after heat treatment or laser treatment (Fowler and Kuroda, 1986). This surface melt zone is no deeper than 5 \im, beneath which there is a region of interaction 10-40 jim deep, where the temperature rise is insufficient for the sintering process but sufficient for some compositional changes to the crystals. Hargreaves et ah (1984) reported experiments that demonstrated a minimal temperature rise in the pulp cavity as a result of laser irradiation of the surface enamel. Hence, it appears possible for surface enamel, or dentin, or carious enamel, or carious dentin, to be treated with specifically directed low-energy pulsed carbon dioxide laser without biological damage to the inner tooth. The reasons for the observed inhibition of lesion formation by laser pre-treatment are still not clear, although there are several possible explanations. It has been suggested by other authors (Stern et ah, 1966; Lenz et ah, 1982) that the surface is sealed by the laser and is less permeable for the subsequent diffusion of ions into and from the enamel. We believe that the laser-induced compositional changes of the enamel surface reduce its solubility and that changes below the surface, not detected by methods utilized to date, will reduce the solubility also at the subsurface. [Many of these changes have been discussed by Fowler and Kuroda (1986).] There may also be an effect of laser irradiation on the organic matrix (Yamamoto and Sato, 1980) which may affect the solubility. With regard to permeability, a recent report by Borggreven et ah (1980) suggested that laser irradiation actually increased the permeability of bovine dental enamel. At this stage, the relative importance of these various aspects has yet to be determined. However, what is known is that specific-frequency 25 carbon dioxide laser irradiation is efficiently transformed from light into heat at the enamel surface and in the immediate subsurface, causing crystal transformation and subsequent inhibition of subsurface lesion formation. It is of considerable interest to compare the infrared absorption spectrum of dental enamel and the Raman spectrum of dental enamel with the laser lines used in the present study (Fig. 4). It can be seen that three of the lines used in the present study nearly coincide with the phosphate and carbonate absorption bands, but that one (the 945-cm 1 line) is slightly displaced. This overlap of frequencies of absorption should theoretically coincide with highly efficient uptake of energy by the apatite crystals, followed by transformation into other forms of energy. This phenomenon deserves further theoretical consideration (Lin and George, 1984). On the basis of the above data, it may be expected that the carbon dioxide laser would also have a dramatic effect on dentin. This has indeed been shown to be the case, in that lased dentin readily melted at the surface, with low-energy pulsed carbon dioxide irradiation similar to that reported here for enamel (Nelson et ah, 1986b). Cooper et ah (1986) from our group recently reported studies where they irradiated the surface of dentin and followed this by bonding of an appliance. The bond strength was increased by 300 percent compared with that to non-lased dentin. Other possible applications relating to dentin have been investigated in a preliminary manner by Zakariasen (1986), who looked at the fusion of apatite or enamel into root canal preparations. These are all preliminary studies which deserve further experimentation to look at the potential of the carbon dioxide laser at specific frequencies for clinical applications. 2000 1600 1200 Wavenumber (cm" 1 ) 800 400 Fig. 4-Diagrammatic representation of the infrared spectrum of dental enamel (A), the Raman spectrum of dental enamel (B, Nelson and Williamson, 1982), and the tunable infrared laser spectrum (C) superimposed. The dotted lines represent the four laser lines used in the present study (from Nelson et al., 1986a; published courtesy of Karger AG). 26 FEATHERSTONE & NELSON For clinical applications, the optimal wavelength of carbon dioxide laser radiation must be determined, together with the optimal energy density and optimal pulse frequency. It would also be necessary that the beam be directed very precisely by means of a fiberoptic system which is currently in its developmental stages (Beckman and Fuller, 1983). The treatment of caries lesions, the treatment of pits and fissures (Stewart et ah, 1985), and the pre-treatment of occlusal surfaces are all possibilities which could be explored further in the future. If the technology becomes available at a reasonable cost to take advantage of these conditions which can be determined in the laboratory experimentally, then there may well be a future for the clinical application of lasers in dentistry. ACKNOWLEDGMENTS The input and assistance of the following people into these reported studies are gratefully acknowledged: L.F. Cooper, R. Glena, M. Shariati, C.P. Shields, J. Mclntyre, W.L. Jongebloed, J. Wefel, A. Mowery, T.F. George, and J.T. Lin. The Laboratory for Laser Energetics, University of Rochester, is gratefully thanked for the loan of the laser equipment. REFERENCES BECKMAN, H. and FULLER, T.A. (1983): Carbon Dioxide Laser Fiber Optics in Endoscopy. In: New Frontiers in Laser Medicine and Surgery, K. Atsumi, Ed., Amsterdam: Excerpta Medica, pp. 76-80. BORGGREVEN, J.M.P.M.; VAN DIJK, J.W.E.; and DRIESSENS, F.C.M. (1980): Effect of Laser Irradiation on the Permeability of Bovine Dental Enamel, Arch Oral Biol 25:831-832. COOPER, L.F.; MYERS, M.L.; NELSON, D.G.A.; and MOWERY, A.S. (1986): Shear Strength of Composite Resin Bonded to Laser Pretreated Dentin, / Dent Res 65:239. FEATHERSTONE, J.D.B.; TEN CATE, J.M.; SHARIATI, M; and ARENDS, J. (1983): Comparison of Artificial Caries-like Lesions by Quantitative Microradiography and Microhardness Profiles, Caries Res 17:385-391. FOWLER, B.O. and KURODA, S. (1986): Changes in Heated and in Laser-irradiated Human Tooth Enamel and Their Probable Effects on Solubility, Calcif Tissue Int 38:197-208. GOLDMAN, L.; GRAY, J.A.; GOLDMAN, J.; GOLDMAN, B.; and MEYER, R. (1965): Effect of Laser Beam Impacts on Teeth, J Am Dent Assoc 70:601-606. GORDON, T.E. (1967): Single-surface Cutting of Normal Tooth with Ruby Laser, / Am Dent Assoc 74:398-402. HARGREAVES, J.A. and PISKO-DUBIERSKI, R.P. (1984): Changes Adv Dent Res October 1987 in Surface Enamel using Three Different Methods of Laser Application, / Dent Res 63:506. HUNTER, J.; LEONARD, L.; WILSON, R.; SNIDER, G.; and DIXON, J. (1984): Effects of Low Energy Laser on Wound Healing in a Porcine Model, Lasers in Surgery and Medicine 3:285-290. KANTOLA, S.; LAINE, E.; and TARNA, T. (1973): Laser-induced Effects on Tooth Structure. VI. X-ray Diffraction Study of Dental Enamel Exposed to a CO2 Laser, Ada Odontol Scand 31:369-379. KURODA, S. and FOWLER, B.O. (1984): Compositional, Structural and Phase Changes in in vitro Laser-irradiated Human Tooth Enamel, Calcif Tissue Int 36:361-369. LENZ, P.; GLIDE, H.; and WALZ, R. (1982): Studies on Enamel Sealing with the CO2 Laser, Dtsch Zahnarztl Z 37:469^178. LIN, J. and GEORGE, T.F. (1983): Laser-generated Electron Emission from Surfaces: Effect of the Pulse Shape on Temperature and Transient Phenomena, / Appl Phys 54:382-387. NELSON, D.G.A. and WILLIAMSON, B.E. (1982): Low-Temperature Laser Raman Spectroscopy of Synthetic Carbonated Apatites and Dental Enamel, Aust J Chem 35:715-727. NELSON, D.G.A. and FEATHERSTONE, J.D.B. (1982): Preparation, Analysis, and Characterization of Carbonated Apatites, Calcif Tissue Int 34:S69-S81. NELSON, D.G.A.; SHARIATI, M.; GLENA, R.; SHIELDS, C.P.; and FEATHERSTONE, J.D.B. (1986a): Effect of Pulsed Low Energy Infrared Laser Irradiation on Artificial Caries-like Lesion Formation, Caries Res 20:289-299. NELSON, D.G.A.; JONGEBLOED, W.L.; and FEATHERSTONE, J.D.B. (1986b): Laser Irradiation of Human Dental Enamel and Dentine, N Z Dent J 82:74-77. NELSON, D.G.A.; WEFEL, J.S.; JONGEBLOED, W.L.; and FEATHERSTONE, J.D.B. (1987): Morphology, Histology and Crystallography of Human Dental Enamel Treated With Pulsed Low Energy IR Laser Radiation, Caries Res (in press). STERN, R.H. and SOGNNAES, R.F. (1964): Laser Beam Effect on Dental Hard Tissues, / Dent Res 43:873. STERN, R.H.; SOGNNAES, R.F.; and GOODMAN, F. (1966): Laser Effect on in vitro Enamel Permeability and Solubility, / Am Dent Assoc 78:838-843. STERN, R.H.; VAHL, J.; and SOGNNAES, R.F. (1972): Lased Enamel: Ultrastructural Observations of Pulsed Carbon Dioxide Laser Effects, / Dent Res 51:455-460. STEWART, L.; POWELL, G.L.; and WRIGHT, S. (1985): Hydroxyapatite Attached by Laser: A Potential Sealant for Pits and Fissures, Oper Dent 10:2-5. SURINCHAK, J.S.; ALAGO, M.L.; BELLAMY, R.F.; STUCK, B.E.; and BELKIN, M. (1983): Effects of Low-Level Energy Lasers on the Healing of Full-Thickness Skin Defects, Lasers in Surgery and Medicine 2:267-274. VAHL, J. (1968): Electron Microscopical and X-ray Crystallographic Investigations of Teeth Exposed to Laser Rays, Caries Res 28:1018. YAMAMOTO, H. and OOYA, K. (1974): Potential of Ytrium-Aluminum-Garnet Laser in Caries Prevention, / Oral Pathol 38:7-15. YAMAMOTO, H. and SATO, K. (1980): Prevention of Dental Caries by Nd:YAG Laser Irradiation, / Dent Res 59:2171-2177. ZAKARIASEN, K.L.; McMURRAY, F.M.; PATTERSON, S.K.; DEDERICH, D.N.; and TULIP, J. (1986): Apical Leakage Associated With Lased and Unlased Apical Plugs, / Dent Res 65:253.
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