Special Section on Laser Applications in Life Sciences

Selective removal of carious human dentin using a nanosecond pulsed laser operating at a wavelength of 5.85  μm

[+] Author Affiliations
Katsunori Ishii

Osaka University, Graduate School of Engineering, Building A1-411, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan

Tetsuya Kita

Osaka University, Graduate School of Engineering, Building A1-411, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan

Kazushi Yoshikawa

Osaka Dental University, Department of Operative Dentistry, Hanazono-cho 8-1, Kuzuha, Hirakata, Osaka 573-1121, Japan

Kenzo Yasuo

Osaka Dental University, Department of Operative Dentistry, Hanazono-cho 8-1, Kuzuha, Hirakata, Osaka 573-1121, Japan

Kazuyo Yamamoto

Osaka Dental University, Department of Operative Dentistry, Hanazono-cho 8-1, Kuzuha, Hirakata, Osaka 573-1121, Japan

Kunio Awazu

Osaka University, Graduate School of Engineering, Building A1-411, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan

Osaka University, Graduate School of Frontier Biosciences, Yamadaoka 1-3, Suita, Osaka 565-0871, Japan

Osaka University, The Center for Advanced Medical Engineering and Informatics, Yamadaoka 2-2, Suita, Osaka 565-0871, Japan

J. Biomed. Opt. 20(5), 051023 (Jan 16, 2015). doi:10.1117/1.JBO.20.5.051023
History: Received October 14, 2014; Accepted December 9, 2014
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Open Access Open Access

Abstract.  Less invasive methods for treating dental caries are strongly desired. However, conventional dental lasers do not always selectively remove caries or ensure good bonding to the composite resin. According to our previous study, demineralized dentin might be removed by a nanosecond pulsed laser operating at wavelengths of around 5.8μm. The present study investigated the irradiation effect of the light on carious human dentin classified into “remove,” “not remove,” and “unclear” categories. Under 5.85-μm laser pulses, at average power densities of 30W/cm2 and irradiation time of 2 s, the ablation depth of “remove” and “not remove,” and also the ablation depth of “unclear” and “not remove,” were significantly different (p<0.01). The ablation depth was correlated with both Vickers hardness and Ca content. Thus, a nanosecond pulsed laser operating at 5.85μm proved an effective less-invasive caries treatment.

Figures in this Article

Dentistry aspires to ultraconservative management concept, described as minimally invasive treatment and teeth preservation, also referred to as minimal intervention (MI).1 Available clinical technologies for excavating teeth and removing caries include burs, excavators, air-abrasives, chemo-mechanical agents, ultrasonics, and lasers. Most of these techniques help to create cavities, but they are not self-selective for caries-infected dentin.2,3 Therefore, to realize MI, new techniques of minimally invasive and selective treatment of caries are required.

Er:YAG and Er, Cr:YSGG lasers have already been applied in a water absorption and rapid evaporation technique for tooth ablation.47 However, to efficiently harness the laser energies, this technique requires strict control by the dentist. In addition, the quantity of excavation is less easily controlled by an Er:YAG laser than by conventional mechanical excavation methods,8 and the irradiated dentin surface may not strongly bond to the composite resin.9,10 A recent systematic review concluded that laser treatments are not yet viable as a general dental practice option for caries excavation.11,12 However, because lasers introduce no noise or vibration, viable laser treatments would increase the comfort levels.13,14 If the excavation selectivity and tensile bonding strength of laser techniques could be improved, lasers could become an essential instrument of excavation.

In general, there are three sets of absorption bands at the wavelengths of about 3, 6, and 9 μm in dentin. The 6 μm absorption band is attributable to the dominant organic materials of carious dentin, which is the so-called as the amide 1 and amide 2 bands.15 In our previous studies, we investigated the fundamental ablation properties of bovine dentin under a wavelength-tunable nanosecond pulsed laser operating at 5.6 to 6.6μm.1618 We found that selective removal of demineralized dentin, due to a difference in the amount of ablation for sound and demineralized dentin, could be achieved with less damage to sound dentin, especially at the wavelengths of around 5.8μm.15 However, real carious human dentin varies according to the type and progression of caries. Subsequently, the ablation properties of carious human dentin were investigated at the wavelengths of around 5.8μm.19 The wavelength of the highest selective removal of carious dentin was then refined to 5.85μm; however, the ablation selectivity was highly variable, and appeared to depend on the hardness rather than the absorption.20

In most cases, removal of grossly softened caries-infected dentin is recommended.21 Thus, it is important to investigate the relationship between the hardness and ablation characteristics of carious dentin. The present study exploits the hardness difference between human carious and sound dentin to selectively remove the former by laser irradiation at the wavelength of 5.85μm. Laser ablations were carried out at the optimally absorbed wavelength of 5.85μm and the strongly absorbed wavelength of 6.00μm. The relationships between ablation depth and hardness of carious human dentin (quantified by the Vickers hardness and the Ca content) were then evaluated. The dentin-resin bonding strength can potentially be improved by shortening the pulse width of a conventional dental Er:YAG laser to 1 ns. To determine whether this approach is compatible with dental adhesive procedures, we also evaluated the tensile bonding strength between the irradiated human sound dentin surface and a composite resin.

Sample Preparations

Human carious teeth (molar) were extracted and sectioned parallel to the occlusal surface, exposing the carious dentin lesion. The dentin plates were soaked in normal saline solution until required for ablation depth and hardness evaluation (see Sec. 2.4). Prior to experiment, the saline was wiped from the plates. The dentin areas including carious lesions were classified into “remove (carious),” “not remove (sound),” and “unclear (difficult to determine)” categories, based on their optical appearances and palpation by two conservative dentistry specialists with over 8 years of clinical experience. Figure 1 shows the typical absorption spectra of sound and carious human dentin in the mid-infrared range. The absorption spectra were measured by a Fourier transform infrared spectrometer (MB3000, ABB, Switzerland) coupled to an infrared microscope (μMax, Pike Technologies). The spectra were normalized at a peak wavelength of 6μm.

Graphic Jump LocationF1 :

Absorption spectra of sound and carious human dentins. Both dentins exhibit the characteristic amide 1 and 2 absorption peaks around 6μm. The absorption peak assigned to the PO vibration (around 9 to 10μm) is weaker in carious than in sound dentin.

The tensile bonding strength (see Sec. 2.5) was evaluated on human sound teeth (molar). The teeth were sectioned parallel to the occlusal surface, exposing approximately (10×10)mm2 of the dentin area, with the dental tubules running perpendicular to the irradiated surface. The surfaces of the plates were ground on a silicon carbide waterproof abrasive paper with 600-grit in the wet condition. The polished plates were soaked in normal saline solution. Prior to experiment, the saline was removed from the plates by a dental air blower.

The human teeth samples were removed at the Department of Oral and Maxillofacial Surgery in the Osaka Dental University Hospital (Osaka, Japan). All samples were anonymized and stored after obtaining informed consent. This study was approved by the ethics committee at the Osaka Dental University (Approved No. 100502).

Light Sources

The nanosecond pulsed laser beam was produced by difference-frequency generation (DFG).15,22 The DFG laser was jointly developed by RIKEN and Kawasaki Heavy Industries, Ltd. (both based in Japan). The wavelength-tunable range, pulse duration, and repetition rate of the pulse is 5.5 to 10μm, 5 ns, and 10 Hz, respectively. To achieve a mid-infrared output, two AgGaS2 crystals were inserted between a Q-switched Nd:YAG laser (Tempest 10, New Wave Research Inc.) operating at a wavelength of 1064 nm and a wavelength-tunable Cr:forsterite laser operating at 1150 to 1350 nm. The Cr:forsterite laser was pumped by a Q-switched Nd:YAG laser (Tempest 300, New Wave Research Inc.) operating at 1064 nm and its wavelength was tuned by rotating the rear mirror of an optical resonator.

Caries excavation (Sec. 2.5) was also performed using a conventional dental laser, namely, the Er:YAG laser (Erwin® AdvErL, Morita, Japan). The wavelength, pulse duration, and repetition rate of this laser is 2.94μm, 200μs, and 10 Hz, respectively.

Irradiation Conditions

When evaluating the ablation depth and hardness (Sec. 2.4), the carious human dentin samples were horizontally arranged on an XYZ-stage and the laser beam was irradiated by a parabolic mirror with a focal length of 100 mm. The beam diameters (full width at half maximum values of the beam profile) were determined as 100 to 150μm by the knife-edge method. The wavelengths were set to 5.85 and 6.00μm, and the average power density was set to 30W/cm2. The irradiation time was set to 2 s using an electric shutter (F77-4, Suruga Seiki, Japan). No water spray was applied.

In the caries excavation (Sec. 2.5), the human sound dentin samples were horizontally arranged on a motorized stage (SG SP 20-20, Sigma Koki, Japan), which was linearly moved at a constant rate. The scanning speed was calculated as the beam size divided by the irradiation time per spot (1 s). The approximate area irradiated by the DFG laser (wavelength=5.85μm, average power density=30W/cm2, no water spray) and the Er:YAG laser (pulse energy=100mJ, water spray applied at 2ml/min) was (4.5×4.5)mm2. The irradiation conditions of the Er:YAG laser were those used in clinical settings.

Evaluations of Ablation Depth and Hardness

Following the irradiation experiments, the ablation depths were measured using a confocal laser microscope (OLS3000, Olympus, Japan). The Vickers hardness around the irradiation spots was measured by a dynamic ultramicrohardness tester (DUH-211, Shimadzu, Japan) with a maximum indentation load and a depth of 196 mN and 3μm, respectively. Next, the samples were gold-coated by an ion sputtering system (E-1010, Hitachi, Japan), applied for 60 s at 15 mA discharge current. The irradiated regions were then observed using a scanning electron microscope (SEM) (JCM-5700, JEOL, Japan). Additionally, the Ca contents were measured at 10 positions and averaged over the irradiation spots by an energy dispersive x-ray spectrometer (JED-2300, JEOL, Japan) coupled to SEM at an accelerating voltage of 20 kV at 37-fold magnification.

Evaluations of Tensile Bonding Strength

The compatibility of the irradiated normal dentin surface with adhesive restoration procedures was evaluated in tensile bonding strength tests. The preirradiated samples were mounted on a brass jig, leaving an exposed circular region with a diameter of 3 mm for the testing. A self-etching primer (Clearfil Mega Bond, Kuraray Noritake Dental, Japan) was applied to the irradiated dentin surface, and a composite resin (Clearfil AP-X, Kuraray Noritake Dental, Japan) was then bonded to the surface. The samples were retained in water at 37°C for 24 h, and their tensile bonding strengths were then measured by a universal testing machine (IM-20, Intesco, Japan) at a crosshead speed of 0.3mm/min until failure occurred. The fractured surfaces of the samples were observed using a laser microscope (VK-X100, Keyence, Japan) at 50-fold magnification to evaluate the failure modes. When cohesive failure accounted for 70% or more of the fractured surface, the mode was regarded as cohesive failure. When cohesive failure rate was <70%, the mode was regarded as mixed failure. When 70% or more of the interface was exposed, the mode was regarded as interfacial (pretesting) failure.

Statistical Analysis

Statistical analysis was performed using the statistical functions of Excel 2013 (Microsoft Office, Microsoft Corporation). Continuous variables were expressed as mean and standard deviation. Fisher’s extract tests were used to compare dichotomous variables in two groups and unpaired Student’s t tests were used to assess differences in continuous variables. The tests were two-sided and a P-value <0.01 was determined to be statistically significant.

Selective Removal by 5.85-μm Laser Pulses

Figure 2 shows the SEM images of the surface morphologies of sound and carious dentin irradiated at 5.85 and 6.00μm. The 5.85-μm pulses removed considerably more carious dentin than sound dentin. On the other hand, the irradiation spots under 6.00-μm pulses were similarly sized on sound and carious dentin, indicating that demineralized dentin was not selectively removed at this wavelength. Cracking, which is undesirable in restoration treatment, was absent in both dentins.

Graphic Jump LocationF2 :

Scanning electron microscopy images of irradiation spots at 5.85 and 6.00μm. The 5.85μm laser light removed a large amount of carious dentin while retaining the sound dentin. The 6.00μm light was less selective (the irradiation spots in sound and carious dentins are similarly sized).

Figure 3 shows the averaged differences in ablation depth for the dentin categories “remove,” “not remove,” and “unclear,” irradiated at 5.85 and 6.00μm. Under 5.85μm irradiation, the number of sample spots classified as “remove,” “not remove,” and “unclear” were 121, 88, and 46, respectively [Fig. 3(a)]; under 6.00μm irradiation, they were 46, 72, and 25, respectively [Fig. 3(b)]. In Fig. 3(a), the ablation depth of “remove” and “not remove,” and also the ablation depth of “unclear” and “not remove,” were significantly different (p<0.01). The ablation depths showed a large standard deviation (approximately 40μm) in the “remove” and “not remove” categories. By contrast, in Fig. 3(b), the ablation depths were not significantly different among the three dentin categories.

Graphic Jump LocationF3 :

Differences in ablation depth among three categories of carious lesions, “remove,” “not remove,” and “unclear” at (a) 5.85μm and (b) 6.00μm. At 5.85μm, the ablation depths significantly differed between “remove” and “not remove,” and between “unclear” and “not remove.”

Relationship Between Ablation Depth and Dentin Hardness

Figure 4 plots the relationships between ablation depth and Vickers hardness of carious dentins. Under 5.85μm irradiation, the numbers of sample spots classified as “remove,” “not remove,” and “unclear” were 22, 18, and 16, respectively [Fig. 4(a)]; under 6.00μm irradiation, they were 14, 15, and 14, respectively [Fig. 4(b)]. Figure 4(a) shows a clear negative correlation between ablation depth and Vickers hardness. Specifically, ablation was reduced (enhanced) at high (low) Vickers hardness. The coefficient of determination in a linear approximation (R2) was 0.38. However, the ablation depth-hardness correlation disappeared under 6.00μm irradiation [R2=0.09; see Fig. 4(b)]. The Vickers hardness threshold at which the category switched from “remove” to “not remove” was around 30 to 40.

Graphic Jump LocationF4 :

Relationships between Vickers hardness and ablation depth at (a) 5.85μm and (b) 6.00μm. The Vickers hardness is correlated with ablation depth at 5.85μm, but not at 6.00μm. In (a), large ablation is associated with low Vickers hardness.

Figure 5 plots the relationships between ablation depth and Ca content of carious dentins. In Fig. 5(a) (5.85μm), the sample spots classified as “remove,” “not remove,” and “unclear” numbered 99, 70, and 30, respectively; in Fig. 5(b) (6.00μm), they numbered 32, 56, and 11, respectively. The results of this analysis approximately mirror those of the Vickers hardness, but no clear threshold separates the “remove” and “not remove” categories.

Graphic Jump LocationF5 :

Relationships between Ca content and ablation depth at (a) 5.85μm and (b) 6.00μm. The Ca content is correlated with ablation depth at 5.85μm, but not at 6.00μm. In (a), large ablation is associated with low Ca content.

Tensile Bonding Strength Measurements

Figure 6 shows the tensile bonding strengths of nonirradiated samples, samples irradiated by the 5.85μm-DFG laser, and samples irradiated by the Er:YAG laser. In all cases, five samples were irradiated. The tensile bonding strength was significantly higher under the optimized DFG laser conditions than that under standard Er:YAG laser conditions (p<0.01). The failure modes of nonirradiated conditions, DFG laser conditions, and Er:YAG laser conditions were evaluated as cohesion failure, mixed failure, and interfacial failure, respectively.

Graphic Jump LocationF6 :

Tensile bonding strengths under different irradiation conditions. The bonding strength was much higher under 5.85-μm DFG laser irradiation than under Er:YAG laser irradiation.

Since Stern first reported laser ablation of dental hard tissue approximately 50 years ago,23,24 tooth excavation by laser has been trialed at numerous wavelengths. The first lasers approved for hard dental tissue use were the Er:YAG and Er, Cr:YSGG lasers operating at 2.94 and 2.79μm, respectively.47 Excellent high-speed precise ablation of dental caries has been achieved by pulsed CO2 lasers with the wavelengths of 9.6 and 9.3μm.2531 Dental target selectivity using CO2 lasers, Nd:YAG laser, and lasers with the wavelengths of 355, 377, and 400 nm has also been reported.3236

The present study of selective laser-based ablation for carious dentin is entirely novel. The mid-infrared wavelength of 5.85μm has not been previously considered for medical applications. Laser light of 5.85μm applied to demineralized or carious dentin without water spray is mainly absorbed by collagen. The absorption coefficient (μa) of carious dentin is similar to that of collagen and demineralized dentin, and is estimated as 500 to 1000cm1 at 5.85μm.15,37 The thermal relaxation time τtherm38 and stress relaxation time τstress39 are given by Display Formula

τtherm=δp24α=14αμa2,(1)
Display Formula
τstress=δpcs=1μacs,(2)
where δp is the optical penetration depth, α is the thermal diffusivity, and cs is the speed of sound. The α of dentin was assumed as 1.83×103,40 while cs of demineralized dentin was taken as 1.60×105cm/s.41 Using these parameters, the τtherm and τstress of carious dentin at 5.85μm were calculated as 0.14 to 0.55 ms and 6.3 to 12.5 ns, respectively. In the present study, the DFG laser was pulsed at 5 ns, sufficiently shorter than τtherm. Since the interval (0.1 s) exceeds the τtherm of carious dentin, the interaction time τint corresponds to the pulse duration. The degree of thermal damage can be assessed by considering the thermal confinement condition (τint<τtherm). In the present study, thermal confinement was satisfied and photomechanical interactions were induced because τint and τstress were comparable. Indeed, the ablation craters were extremely clean and appeared to be free of cracks induced by thermally induced stresses.

Thermal damage to the irradiated dentin surface is thought to contribute to reduced tensile bonding strength.42,43 In this study, the tensile bonding strength between the composite resin and dentin surface was significantly higher under the DFG laser irradiation (12.5 MPa) than under irradiation by the standard dental Er:YAG laser (4.8 MPa). Different failure modes were also observed between the DFG laser and the Er:YAG laser. The interfacial failure by the Er:YAG laser is likely to be due to a smear layer caused by the thermal damage.44 By contrast, the mixed failure by the DFG laser indicates less smear layer. Therefore, the advantages of short laser pulses are twofold; less thermal damage to the dentin surface and enhanced tensile bonding. On the other hand, the tensile bonding strength was significantly lower under the DFG laser irradiation than under nonirradiation (28.0 MPa). However, reportedly, bonding strength higher than 10 MPa is considered clinically sufficient.45,46 Therefore, the tensile bonding strength under the DFG laser irradiation, satisfied the clinical demand, is not thought to be a severe problem.

Water absorbs over a broad wavelength range around 6μm, attributed to its OH bending vibration mode.47 The shoulder of this band is located at 5.85μm. The μa and optical penetration depth δp of water are approximately 540cm1 and 18.5μm, respectively. Thus, the light absorption at 5.85μm is affected by the oral hydric environment and the amount of water spray, and the selectivity and accuracy of laser absorptions are inconsistent. In clinical applications at 5.85μm, no or less water spray is preferred for stable and selective ablation. In the mid-infrared range, specifically at wavelengths that are strongly absorbed by dental hard tissue, microsecond pulses likely require less water cooling to prevent peripheral thermal damage.31 The pulse width applied in the present study (5 ns) is significantly shorter than the thermal diffusion time of carious dentin, so it is expected to incur minimal thermal damage and allow less water spray.

Laser caries treatment should also account for the thermal effects on dental pulp vitality. Short pulses and the high absorption coefficient of the dentin reduce the accumulation of heat in the dentin. Because the present study satisfies the thermal confinement condition, the temperature rise can be limited to the optical penetration region of the dentin, preventing thermal damage to wider areas. The δp of carious dentin at 5.85μm is approximately 10 to 20μm; that is, the light penetrates only the dentin surface and remains far from the dental pulp. Based on these optical tissue properties, no thermal effects on dental pulp vitality are expected. However, this hypothesis requires verifying in further experiments accounting for pathological or biochemical effects.

Because demineralization elutes hydroxyapatite from the dentin, carious dentin chiefly comprises organic material. Reportedly, the constituent ratio of organic to mineral material continuously alters as the caries progresses, with corresponding changes in hardness.4851 In this study, carious human dentins were diagnosed by their optical appearances and palpation by dentists. The three categories of carious lesions “remove,” “not remove,” and “unclear” were categorized by the Vickers hardness. The threshold of Vickers hardness separating the “remove” and “not remove” categories was around 30 to 40, suggesting that the Vickers hardness provides an index parameter for selective removal of carious dentin. In fact, some studies have reported a relationship between caries progression and hardness, and the effectiveness of hardness in caries diagnosis.52,53 In the ablation experiment undertaken at 5.85μm, areas categorized as “remove” and “unclear” were removed more rapidly than the areas categorized as “not remove”; that is, the technique preferentially ablated soft carious dentin. These findings are likely explained by the relationship between the counteracting force of photomechanical ablation and the hardness of carious dentin. High absorption energy density increases the counteracting force. High μa of the target increases the absorption energy density. As the organic material maximally absorbs at 6.00μm, consequently, the counteracting force is higher at 6.00μm than at 5.85μm. The increased counteracting force is likely responsible for the nonselective excavation at 6.00μm. On the other hand, the counteracting force at 5.85μm was below the mechanical strength of hard carious dentin but exceeded that of soft carious dentin. Consequently, soft carious dentin was ablated while the hard dentin remained intact.

The relationship between the mechanical strength of carious dentin and the counteracting force of laser irradiation is crucial in selective ablation of carious dentin by mid-infrared laser pulses. The irradiation conditions of this study (wavelength=5.85μm, average power density=30W/cm2, and irradiation time=2s) provided the appropriate counteracting force for selective removal. Conversely, the irradiation condition for selective removal is underspecified if the mechanical strength versus irradiation force relationship is met. In our previous works, we selectively removed demineralized bovine at several combinations of wavelengths and energies.15,17 Selective removal was achieved by either high absorption wavelengths and low average power densities or low absorption wavelengths and high average power densities. Therefore, provided that μa is not altered much from its value at 5.85μm, carious dentin should be selectively removable at other wavelength ranges, such as 3μm and 6 to 10μm. However, extremely-high or extremely-low absorption ranges are inadvisable because low-power irradiation reduces the ablation rate, whereas high-power irradiation reduces the selectivity. In addition, wavelengths that are strongly absorbed by water should be avoided because the ablation properties would then strongly depend on the wetness conditions. Consequently, the suitable wavelength range is limited in practice.

Despite the difficulty of high-power oscillations or generations at 5.85μm, a compact dental laser device could be constructed using nonlinear optical techniques and quantum cascade laser (QCL) techniques under low-repetition and short-pulse control, which are currently available. However, these techniques are problematic. The low repetition rate of the DFG laser caused a low ablation rate in our current experiment. To increase the ablation rate, we must increase either the peak power or the repetition rate. Nonlinear optical techniques with Q-switched pulsed lasers can generate short pulses at high peak power, but current repetition rates are regulated only at tens of hertz. Conversely, QCL techniques realize high repetition operation, but are unsuited for high peak power operation. Therefore, if QCL techniques are to be useful in dental treatment, they require higher average power oscillation and pulse control techniques. Short laser pulses at 5.85μm can also be delivered by the optical hollow fiber technique,54 which has already been applied in a dental Er:YAG laser device. Further innovation is required to render the tip of the optical hollow fiber nontoxic and highly transmitting.

Although selective removal of caries-infected dentin is ultimately required in the MI approach to caries treatment, hardness may not reliably indicate infection. Thus, to ensure that carious dentin ablation complies with the MI concept, the relationship between the degree of infection and ablation selectivity must be investigated in further study.

Carious human dentin was selectively removed by applying nanosecond pulsed laser light at 5.85μm. This treatment caused minimal damage to sound dentin, whereas material with low Vickers hardness and low Ca content was largely removed. Future study will investigate the relationship between degree of infection and ablation selectivity, attempt to improve the ablation rate, and develop a compact device for clinical application.

This study was supported by KAKENHI Grant Nos. 24241029 and 25870414.

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Fried  D. et al., “Thermal and chemical modification of dentin by 9–11-μmCO2 laser pulses of 5–100-μs duration,” Lasers Surg. Med.. 31, , 275 –282 (2002). 0196-8092 CrossRef
Goodis  H. E. et al., “Pulpal safety of 9.6  μm TEA CO2 laser used for caries prevention,” Lasers Surg. Med.. 35, , 104 –110 (2004). 0196-8092 CrossRef
Rosa  A. D. et al., “Peripheral thermal and mechanical damage to dentin with microsecond and sub-microsecond 9.6  μm, 2.79  μm, and 0.355  μm laser pulses,” Lasers Surg. Med.. 35, , 214 –228 (2004). 0196-8092 CrossRef
Chan  K. H., Hirasuna  K., Fried  D., “Rapid and selective removal of composite from tooth surfaces with a 9.3  μmCO2 laser using spectral feedback,” Lasers Surg. Med.. 43, , 824 –832 (2011). 0196-8092 CrossRef
Harris  D. M. et al., “Selective ablation of surface enamel caries with a pulsed Nd:YAG dental laser,” Lasers Surg. Med.. 30, , 342 –350 (2002). 0196-8092 CrossRef
Wheeler  C. R. et al., “Irradiation of dental enamel with Q-switched λ=355-nm laser pulses: surface morphology, fluoride adsorption, and adhesion to composite resin,” Lasers Surg. Med.. 32, , 310 –317 (2003). 0196-8092 CrossRef
Rechmann  P., Hennig  T., “Selective ablation of dental calculus with frequency-doubled alexandrite laser,” Proc. SPIE. 2623, , 180 –188 (1996). 0277-786X CrossRef
Schoenly  J. E., Seka  W., Rechmann  P., “Investigation into the optimum beam shape and fluence for selective ablation of dental calculus at λ=400  nm,” Lasers Surg. Med.. 42, , 51 –61 (2010). 0196-8092 CrossRef
Heya  M. et al., “Observation of dynamic absorption properties of wet gelatin around λ=6.05  μm using a mid-infrared free electron laser,” Jpn. J. Appl. Phys.. 46, (3A ), 1208 –1216 (2007). 0021-4922 CrossRef
Choi  B., Welch  A. J., “Analysis of thermal relaxation during laser irradiation of tissue,” Lasers Surg. Med.. 29, , 351 –359 (2001). 0196-8092 CrossRef
Esenaliev  R. O. et al., “Studies of acoustical and shock waves in the pulsed laser ablation of biotissue,” Lasers Surg. Med.. 13, , 470 –484 (1993). 0196-8092 CrossRef
Brown  W. S., Dewey  W. A., Jacobs  H. R., “Thermal properties of teeth,” J. Dent. Res.. 49, , 752 –755 (1970). 0022-0345 CrossRef
Yasuda  G. et al., “Determination of elastic modulus of demineralized resin-infiltrated dentin by self-etch adhesives,” Eur. J. Oral. Sci.. 115, , 87 –91 (2007). 0909-8836 CrossRef
Armengol  V. et al., “Comparative in vitro study of the bond strength of composite to enamel and dentin obtained with laser irradiation or acid etch,” Lasers Med. Sci.. 14, , 207 –215 (1999). 1435-604X CrossRef
Staninec  M. et al., “Adhesion of composite to enamel and dentin surfaces irradiated by IR laser pulses of 0.5–35  μs duration,” J. Biomed. Mater. Res. B Appl. Biomater.. 79B, , 193 –201 (2006). 0021-9304 CrossRef
Ceballo  L. et al., “Bonding to Er-YAG-laser-treated dentin,” J. Dent. Res.. 81, , 119 –122 (2002). 0022-0345 CrossRef
Matsumura  H. et al., “Shear bond strength of resin composite veneering material to gold alloy with varying metal surface preparations,” J. Prosthet. Dent.. 86, , 315 –319 (2001). 0022-3913 CrossRef
Behr  M. et al., “The bond strength of the resin-to-zirconia interface using different bonding concepts,” J. Mech. Behav. Biomed. Mater.. 4, , 2 –8 (2011). 1751-6161 CrossRef
Marley  N. A., Gaffney  J. S., Cunningham  M. M., “Lambert absorption coefficients of water in the frequency range of 3000–934 cm–1,” Appl. Opt.. 33, , 8041 –8054 (1994). 0003-6935 CrossRef
Featherstone  J. D. et al., “Comparison of artificial caries-like lesions by quantitative microradiography and microhardness profiles,” Caries Res.. 17, , 385 –391 (1983). 0008-6568 CrossRef
Arends  J., ten Bosch  J. J., “Demineralization and remineralization evaluation techniques,” J. Dent. Res.. 71, , 924 –928 (1992). 0022-0345 
Kodaka  T. et al., “Correlation between microhardness and mineral content in sound human enamel (short communication),” Caries Res.. 26, , 139 –141 (1992). 0008-6568 CrossRef
Angker  L. et al., “Correlating the mechanical properties to the mineral content of carious dentine—a comparative study using an ultra-micro indentation system (UMIS) and SEM-BSE signals,” Arch. Oral Biol.. 49, , 369 –378 (2004). 0003-9969 CrossRef
Shimizu  A. et al., “Newly developed hardness testing system, “Cariotester”: measurement principles and development of a program for measuring Knoop hardness of carious dentin,” Dent. Mater. J.. 32, , 643 –647 (2013). 0287-4547 CrossRef
Banerjee  A. et al., “A confocal micro-endoscopic investigation of the relationship between the microhardness of carious dentine and its autofluorescence,” Eur. J. Oral Sci.. 118, , 75 –79 (2010). 0909-8836 CrossRef
Matsuura  Y. et al., “Infrared-laser delivery system based on polymer-coated hollow fibers,” Opt. Laser Technol.. 33, , 279 –283 (2001). 0030-3992 CrossRef

Katsunori Ishii received his PhD degree in engineering from Graduate School of Engineering, Osaka University, Japan, in March 2008. Since 2009, he has been an assistant professor in the Medical Beam Physics Laboratory (Professor Kunio Awazu), Graduate School of Engineering, Osaka University, Japan. His research interest is the basics in laser surgery and medicine, including laser-tissue interaction, tissue optics, medical laser applications, and infrared light techniques. He is a lifetime member of SPIE.

Tetsuya Kita received his master’s degree in engineering from the Graduate School of Engineering, Osaka University, Japan, in March 2013. His study covered the field of midinfrared laser and laser dentistry.

Kazushi Yoshikawa received his PhD degree in dentistry from the Graduate School of Dentistry, Osaka Dental University, Japan, in March 1996. Since 2008, he has been an associate professor in the Department of Operative Dentistry, Osaka Dental University, Japan.

Kenzo Yasuo received his PhD degree in dentistry from the Graduate School of Dentistry, Osaka Dental University, Japan, in March 2012. Since 2012, he has been an assistant professor in the Department of Operative Dentistry, Osaka Dental University, Japan.

Kazuyo Yamamoto received his PhD degree in dentistry from the Graduate School of Dentistry, Osaka Dental University, Japan, in March 1991. Since 2005, he has been a full professor in the Department of Operative Dentistry, Osaka Dental University, Japan.

Kunio Awazu received his master’s degree and PhD degree of engineering from the Graduate School of Engineering, Kobe University, Japan, in March 1984 and April 1996, respectively. He received a Dr. Med. Sci. degree from Juntendo University, Japan, in March 1997. He spent 3 years (1993 to 1995) at the University of Texas MD Anderson Cancer Center, USA. Since 2005, he has been a full professor in the Medical Beam Physics Laboratory, Graduate School of Engineering, Osaka University.

© The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.

Citation

Katsunori Ishii ; Tetsuya Kita ; Kazushi Yoshikawa ; Kenzo Yasuo ; Kazuyo Yamamoto, et al.
"Selective removal of carious human dentin using a nanosecond pulsed laser operating at a wavelength of 5.85  μm", J. Biomed. Opt. 20(5), 051023 (Jan 16, 2015). ; http://dx.doi.org/10.1117/1.JBO.20.5.051023


Figures

Graphic Jump LocationF1 :

Absorption spectra of sound and carious human dentins. Both dentins exhibit the characteristic amide 1 and 2 absorption peaks around 6μm. The absorption peak assigned to the PO vibration (around 9 to 10μm) is weaker in carious than in sound dentin.

Graphic Jump LocationF2 :

Scanning electron microscopy images of irradiation spots at 5.85 and 6.00μm. The 5.85μm laser light removed a large amount of carious dentin while retaining the sound dentin. The 6.00μm light was less selective (the irradiation spots in sound and carious dentins are similarly sized).

Graphic Jump LocationF3 :

Differences in ablation depth among three categories of carious lesions, “remove,” “not remove,” and “unclear” at (a) 5.85μm and (b) 6.00μm. At 5.85μm, the ablation depths significantly differed between “remove” and “not remove,” and between “unclear” and “not remove.”

Graphic Jump LocationF4 :

Relationships between Vickers hardness and ablation depth at (a) 5.85μm and (b) 6.00μm. The Vickers hardness is correlated with ablation depth at 5.85μm, but not at 6.00μm. In (a), large ablation is associated with low Vickers hardness.

Graphic Jump LocationF5 :

Relationships between Ca content and ablation depth at (a) 5.85μm and (b) 6.00μm. The Ca content is correlated with ablation depth at 5.85μm, but not at 6.00μm. In (a), large ablation is associated with low Ca content.

Graphic Jump LocationF6 :

Tensile bonding strengths under different irradiation conditions. The bonding strength was much higher under 5.85-μm DFG laser irradiation than under Er:YAG laser irradiation.

Tables

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Mullejans  R. et al., “Cavity preparation using a superpulsed 9.6-λm CO2 laser—a histological investigation,” Lasers Surg. Med.. 30, , 331 –336 (2002). 0196-8092 CrossRef
Fried  D. et al., “Thermal and chemical modification of dentin by 9–11-μmCO2 laser pulses of 5–100-μs duration,” Lasers Surg. Med.. 31, , 275 –282 (2002). 0196-8092 CrossRef
Goodis  H. E. et al., “Pulpal safety of 9.6  μm TEA CO2 laser used for caries prevention,” Lasers Surg. Med.. 35, , 104 –110 (2004). 0196-8092 CrossRef
Rosa  A. D. et al., “Peripheral thermal and mechanical damage to dentin with microsecond and sub-microsecond 9.6  μm, 2.79  μm, and 0.355  μm laser pulses,” Lasers Surg. Med.. 35, , 214 –228 (2004). 0196-8092 CrossRef
Chan  K. H., Hirasuna  K., Fried  D., “Rapid and selective removal of composite from tooth surfaces with a 9.3  μmCO2 laser using spectral feedback,” Lasers Surg. Med.. 43, , 824 –832 (2011). 0196-8092 CrossRef
Harris  D. M. et al., “Selective ablation of surface enamel caries with a pulsed Nd:YAG dental laser,” Lasers Surg. Med.. 30, , 342 –350 (2002). 0196-8092 CrossRef
Wheeler  C. R. et al., “Irradiation of dental enamel with Q-switched λ=355-nm laser pulses: surface morphology, fluoride adsorption, and adhesion to composite resin,” Lasers Surg. Med.. 32, , 310 –317 (2003). 0196-8092 CrossRef
Rechmann  P., Hennig  T., “Selective ablation of dental calculus with frequency-doubled alexandrite laser,” Proc. SPIE. 2623, , 180 –188 (1996). 0277-786X CrossRef
Schoenly  J. E., Seka  W., Rechmann  P., “Investigation into the optimum beam shape and fluence for selective ablation of dental calculus at λ=400  nm,” Lasers Surg. Med.. 42, , 51 –61 (2010). 0196-8092 CrossRef
Heya  M. et al., “Observation of dynamic absorption properties of wet gelatin around λ=6.05  μm using a mid-infrared free electron laser,” Jpn. J. Appl. Phys.. 46, (3A ), 1208 –1216 (2007). 0021-4922 CrossRef
Choi  B., Welch  A. J., “Analysis of thermal relaxation during laser irradiation of tissue,” Lasers Surg. Med.. 29, , 351 –359 (2001). 0196-8092 CrossRef
Esenaliev  R. O. et al., “Studies of acoustical and shock waves in the pulsed laser ablation of biotissue,” Lasers Surg. Med.. 13, , 470 –484 (1993). 0196-8092 CrossRef
Brown  W. S., Dewey  W. A., Jacobs  H. R., “Thermal properties of teeth,” J. Dent. Res.. 49, , 752 –755 (1970). 0022-0345 CrossRef
Yasuda  G. et al., “Determination of elastic modulus of demineralized resin-infiltrated dentin by self-etch adhesives,” Eur. J. Oral. Sci.. 115, , 87 –91 (2007). 0909-8836 CrossRef
Armengol  V. et al., “Comparative in vitro study of the bond strength of composite to enamel and dentin obtained with laser irradiation or acid etch,” Lasers Med. Sci.. 14, , 207 –215 (1999). 1435-604X CrossRef
Staninec  M. et al., “Adhesion of composite to enamel and dentin surfaces irradiated by IR laser pulses of 0.5–35  μs duration,” J. Biomed. Mater. Res. B Appl. Biomater.. 79B, , 193 –201 (2006). 0021-9304 CrossRef
Ceballo  L. et al., “Bonding to Er-YAG-laser-treated dentin,” J. Dent. Res.. 81, , 119 –122 (2002). 0022-0345 CrossRef
Matsumura  H. et al., “Shear bond strength of resin composite veneering material to gold alloy with varying metal surface preparations,” J. Prosthet. Dent.. 86, , 315 –319 (2001). 0022-3913 CrossRef
Behr  M. et al., “The bond strength of the resin-to-zirconia interface using different bonding concepts,” J. Mech. Behav. Biomed. Mater.. 4, , 2 –8 (2011). 1751-6161 CrossRef
Marley  N. A., Gaffney  J. S., Cunningham  M. M., “Lambert absorption coefficients of water in the frequency range of 3000–934 cm–1,” Appl. Opt.. 33, , 8041 –8054 (1994). 0003-6935 CrossRef
Featherstone  J. D. et al., “Comparison of artificial caries-like lesions by quantitative microradiography and microhardness profiles,” Caries Res.. 17, , 385 –391 (1983). 0008-6568 CrossRef
Arends  J., ten Bosch  J. J., “Demineralization and remineralization evaluation techniques,” J. Dent. Res.. 71, , 924 –928 (1992). 0022-0345 
Kodaka  T. et al., “Correlation between microhardness and mineral content in sound human enamel (short communication),” Caries Res.. 26, , 139 –141 (1992). 0008-6568 CrossRef
Angker  L. et al., “Correlating the mechanical properties to the mineral content of carious dentine—a comparative study using an ultra-micro indentation system (UMIS) and SEM-BSE signals,” Arch. Oral Biol.. 49, , 369 –378 (2004). 0003-9969 CrossRef
Shimizu  A. et al., “Newly developed hardness testing system, “Cariotester”: measurement principles and development of a program for measuring Knoop hardness of carious dentin,” Dent. Mater. J.. 32, , 643 –647 (2013). 0287-4547 CrossRef
Banerjee  A. et al., “A confocal micro-endoscopic investigation of the relationship between the microhardness of carious dentine and its autofluorescence,” Eur. J. Oral Sci.. 118, , 75 –79 (2010). 0909-8836 CrossRef
Matsuura  Y. et al., “Infrared-laser delivery system based on polymer-coated hollow fibers,” Opt. Laser Technol.. 33, , 279 –283 (2001). 0030-3992 CrossRef

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