by N ht n ot Q ui fo r Current Concepts and Techniques for Caries and Adhesion to Residual Dentin pyrig No Co t fo rP ub Excavationlication te ss e n c e Aline de Almeida Nevesa/Eduardo Coutinhob/Marcio Vivan Cardosoc/Paul Lambrechtsd/ Bart Van Meerbeeke Abstract: The advent of “Adhesive Dentistry” has simplified the guidelines for cavity preparation enormously. The design and extent of the current preparations are basically defined by the extent and shape of the caries lesion, potentially slightly extended by bevelling the cavity margins in order to meet the modern concept of minimally invasive dentistry. New caries excavation techniques have been introduced, such as the use of plastic and ceramic burs, improved caries-disclosing dyes, enzymatic caries-dissolving agents, caries-selective sono/air abrasion and laser ablation. They all aim to remove or help remove caries-infected tissue as selectively as possible, while being minimally invasive through maximum preservation of caries-affected tissue. Each technique entails a specific caries-removal endpoint and produces residual dentin substrates of different natures and thus different receptiveness for adhesive procedures. This paper reviews the newest developments in caries excavation techniques and their effect on the remaining dentin tissue with regard to its bonding receptiveness. Keywords: minimally invasive dentistry, dentin caries, caries excavation, bond strength of composite/dentin interfaces. J Adhes Dent 2011; 13; 7-22. doi: 10.3290/j.jad.a18443 T he potential to bond restorative materials to tooth structure has altered the general principles of cavity preparation. While new steps were added to cavity preparation procedures, especially for bonding, others – such as cutting retentive cavity geometries – were omitted. In light of the minimally invasive dentistry concept,112 the macroretentive “G.V.Black” cavities15 have been replaced by cavities limited to removal of carious dentin that are at most extended with some additional rounding off of sharp margin edges and/or bevelling, the latter to the direct benefit of the subsequent bonding process. a PhD student, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Leuven, Belgium. Literatur review, wrote manuscript in partial fulfillment for PhD. b PhD student, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Leuven, Belgium. Computer 3D-modeling of carious teeth, proofread manuscript. c Postdoctoral Research Fellow, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Leuven, Belgium. Contributed to content, proofread manuscript. d Full Professor, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Leuven, Belgium. Neves’ PhD supervisor, contributed to content, proofread manuscript. e Full Professor, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Leuven, Belgium. Neves’ PhD supervisor, defined manuscript outline, proofread manuscript. Correspondence: B. Van Meerbeek, Leuven BIOMAT Research Cluster, Department of Conservative Dentistry, School of Dentistry, Oral Pathology and Maxillo-Facial Surgery, Catholic University of Leuven, Kapucijnenvoer 7, B-3000, Leuven, Belgium. Tel: +32-16-337587, Fax: +32-16-332752. e-mail: bart.vanmeerbeek@med.kuleuven.be Vol 13, No 1, 2011 Submitted for publication: 08.07.09; accepted for publication: 24.10.09. However, the extent to which carious dentin should be removed in order to achieve a mechanically and biologically successful restoration is still a matter of debate. In particular, no definite diagnostic tool is today available to clinically define the caries-removal endpoint, enabling complete removal of infected tissue without overextending cavity preparation. In addition, the different techniques presently available for caries removal/cavity preparation produce residual dentin substrates of different natures and thus different receptiveness for adhesion. The extent of carious dentin excavation, the type of dentin substrate generated by each caries excavation technique, and the additional effect bonding agents exert on the residual dentin substrate are reviewed in this article, along with an in-depth discussion on aspects of dental caries histopathology. The latter is of direct importance for proper understanding of the rationale behind the different caries removal techniques. WHY SHOULD CARIOUS DENTIN BE REMOVED BEFORE THE ACTUAL RESTORATION IS PLACED? At the beginning of the past century, when the first operative dentistry guidelines were established, the term “caries excavation” was defined as a synonym for “cavity preparation”, which in turn consisted of “mechanical treatment of the injuries to the teeth produced by dental caries, as would best fit the remaining part of the tooth to receive a filling”.15 From this definition, it appears that caries excavation procedures were regarded as one of the many mandatory steps to prepare a tooth to receive the filling material. Furthermore, it has been described that the carious lesion should be excavated “until a hard pulpal floor 7 by N ht n fo r 8 Q ui was reached” and that “generally, when the cavity has been cut to form, no carious dentin will remain”. 15 In short, carious dentin should be removed until a sufficiently solid layer of dentin was reached to support condensation of the restorative material (“stability form”) and to provide adequate retention for the filling material (“retention form”), promoting a successful and long-term survival of the restoration. It is thus clear that when nonadhesive restorations were the only available option to directly restore decayed teeth, no distinct separation between caries removal and cavity preparation was made. In practical terms, it means that excavation of carious dentin was performed to remove necrotic, soft material in order to best accommodate the filling material. Perhaps it explains the general confusion still seen nowadays when dealing with the term “caries excavation” in view of the minimally invasive dentistry concept.112 As already mentioned, the ability to bond restorations has downgraded the rules for cavity preparation to simply and solely removing caries and, if needed, bevelling of the enamel cavity margins, while the main procedure of cavity preparation, or the excavation of caries, still lacks a more objective definition. This leads to the initial question: Does carious dentin need to be removed prior to restoration placement? Clinical follow-ups of bonded restorations placed over soft carious dentin81 provided evidence that once the cavity margins are laid in relatively sound tissue, adequate marginal sealing is guaranteed and further progression of the carious lesion can be arrested. Apparently, therefore, well-sealed margins determine the long-term success of adhesive restorations, in particular with respect to arresting the caries progress.81 After all, since bonding to carious dentin is generally not as good as that to sound dentin, the somewhat unexpected answer to this question is that carious dentin is still removed in order to provide adequate retention for the filling material (achieving better bonding), thus producing long-term successful restorations. As caries excavation is still an important step towards achieving good-quality bonded restorations, the next question arises: What is the current definition of the caries removal endpoint? Even now, there is still no better clinical criterion to define the caries excavation limit than the “normal” hardness feeling of sound dentin when probed by hand instruments.94 Although this so-called “cris dentinaire” is very subjective and dependent on the operator’s clinical background, it is still the gold-standard method to check residual caries. It was strongly corroborated after research showed that cariogenic bacteria were never found beyond the softening front of dentin.40 Further identification of a superficial infected dentin layer and a subjacent affected dentin layer41 has laid the foundation for a more rational approach for caries removal. Elimination of the heavily infected dentin and preservation of the residual affected dentin were thus defined as prerequisites for effectively arresting the carious process without harming the long-term survival of the pulp and the restoration.62 This has currently raised some discussion about moving toward more objective and hopefully more conservative approaches to selectively remove carious dentin.10,121 pyrig No Co t fo HISTOPATHOLOGY OF DENTIN CARIES rP ub lica Dentin is a mineralized tissue permeated by cellular extentio sions from odontoblasts, which are locatedtat periph- n esthe e s eFor eral zone of the pulp adjacent to the pre-dentin.110 n cthis ot Neves et al reason, dentin, as a vital tissue, is perfectly able to respond to any stimuli, even when invoked at the enamel surface, such as an acid challenge produced by an organized, acid-producing biofilm.106 The first detectable change in dentin in response to a cariogenic biofilm at the outer enamel surface is an area of sclerotic dentin subjacent to the demineralized enamel site (Figs 1A and 1B). The predominant feature of this reactive dentin is its increased translucency, which can be ascribed to intratubular mineral deposition.6 The translucent dentinal tubules will be those localized precisely beneath the demineralized enamel surface, and appear even before the enamel demineralization has reached the dentin-enamel junction (DEJ). Only when the caries lesion has progressed to a considerable length along the DEJ will the subjacent dentin be demineralized14 and become recognizable by a yellow to dark-brown discoloration (Figs 1C and 1D). At this point, bearing in mind that the dentin response to dental plaque is directly related to its metabolic activity77 and that different maturation stages can coexist in a fully-formed dental plaque depending on the self-cleaning ability of the surface, different phases of caries progression will co-exist within one lesion14 (Figs 2A and 2B). It is also well known that dentin caries will not spread laterally along the DEJ before dentin is cavitated and colonized by cariogenic bacteria.34 From this moment, the demineralized and thus unprotected organic dentin matrix (collagen) will be directly degraded through bacterial and host-mediated enzymes.65,107 Especially at peripheral parts of the cavity where the cariogenic biofilm is sheltered by the surrounding (undermined) enamel, the lesion may spread rapidly along the DEJ (“hidden” caries lesion) (Figs 2B and 2C). CARIES-EXCAVATION PROCEDURES Conventional Excavation with Burs Carbon-steel or tungsten-carbide burs Tungsten-carbide burs replaced carbon-steel burs once the process of hardening steel with tungsten carbide was introduced to the dental bur industry. Microscopic tungsten-carbide particles are held together in a matrix of cobalt or nickel at the head (working end) of the bur.120 The head has typical spiral-like cutting edges with or without additional cross cuts to improve cutting efficiency. Carbon-steel burs possess the same caries-removing properties as tungsten-carbide burs and are less expensive, but they are much more prone to corrosion and dulling.12 For caries removal, a round bur is recommended with diameters corresponding to the size of the carious lesion. Water irrigation is optional because generally low-speed (700 to 800 rpm) counter-angle handpieces are employed. It is generally advised to start carious dentin excavation from the periphery towards the center of the lesion in order to minimize the risk of infection in case of accidental The Journal of Adhesive Dentistry n fo r Fig 1A Proximal surface of a molar showing a non-cavitated lesion (black arrow) beneath the contact point (white arrow). The dotted line indicates the location of the mesiodistal section in Fig 1B. Fig 1B Mesiodistal section reveals an area of hypermineralized dentin (black arrow) beneath the area of enamel demineralization (white arrow). Fig 1C Occlusal surface of the same tooth showing a non-cavitated lesion on the central fossa (black arrow) and a cavitated lesion in the occluso-palatal groove (white arrow). The dotted line indicates the location of the mesiodistal section in Fig 1D. Fig 1D Mesiodistal section showing a yellowbrown discoloration under the demineralized enamel (black arrow). The white arrow depicts residual demineralized dentin originating from the occluso-palatal lesion (C: white arrow). ot Q ui by N ht opyretigal No CNeves t fo rP ub lica tio n te ss e n c e Fig 2A Volume-rendered slices based on xray micro-CT data of a molar showing a cavitated lesion in the central fossa. The numbers along the black lines in Fig 2B refer to each corresponding volume rendering based on xray micro-CT data of the tooth. From 1 to 6, increasing progression stages can be observed from the periphery to the center of the lesion. Fig 2B Occlusal surface of the same tooth element. The dotted red line indicates the location of the mesiodistal section in Fig 2C. The black lines indicate the location of the volume-rendered slices in Fig 2A. Fig 2C Mesiodistal section showing the lateral spread of the dentin lesion (white arrows) beyond the limit of the enamel cavitation (dotted lines). pulp exposure. Larger burs are recommended for this reason as well. Tungsten-carbide or carbon-steel burs in low-speed counter-angle handpieces are the most efficient method to excavate carious lesions in terms of time,24 and are therefore still the most widely used caries-excavation method. However, in terms of minimal invasiveness, bur-prepared cavities, combined with the use of a dental explorer to check for the caries removal endpoint, tend to overexcavate. This was Vol 13, No 1, 2011 found, for instance, when auto-fluorescence induced by bacterial metabolites was used to detect carious tissue.8 When studied by scanning electron microscopy (SEM), this method leaves a homogeneous smear layer with more or less uniform roughness, and dentinal tubules visibly obstructed with smear plugs.116 With regard to bonding receptiveness, the smearcovered surface does not interfere with etch-and-rinse adhesives, but has been shown to potentially reduce the bonding effectiveness of self-etching adhesives.91. 9 Q ui by N ht pyrig No Co t fo cavities prepared with conventional tungsten-carbide r P burs. ubto cariIn addition, not only the microtensile bond strength li ous dentin excavated with SmartPrep burs was lowerca forti both etch-and-rinse and self-etching adhesives, te 103 trans- on ssinterfaces mission electron microscopy (TEM) of the bonded e nc e n fo r Fig 3 CeraBurs with different diameters. From left to right: 10-, 14-, 18-, and 23-mm diameter. Polymeric burs In an attempt to develop a selective caries-removal rotating instrument, a “plastic” bur was made of a polyamide/ imide (PAI) polymer, possessing slightly lower mechanical properties than sound dentin. However, soon it became clear that if the bur touches sound or caries-affected dentin, it quickly becomes dull and produces undesirable vibration, making further cutting impossible. The blade design was developed to remove dentin by locally depressing the carious tissue and pushing it forward along the surface until it ruptures and is carried out of the cavity. With a prototype, single-use instrument, complete removal of carious tissue could be accomplished from extracted teeth when a 1% acid-red-propylene glycol solution was used as caries detector.17 The commercial version of these burs (SmartPrep, SSWhite Burs; Lakewood, NJ, USA) consisted of a polymer (PEKK – polyether-ketone-ketone) with a particular hardness of 50 KHN, which was higher than the hardness attributed to carious dentin (0 to 30 KHN), but lower than that of sound dentin (70 to 90 KHN).103 As opposed to conventional carbide burs, their cutting edges were not spiralled but straight. One disadvantage was that by keeping to the recommendation to excavate caries from the center to the periphery in order to avoid contact with sound tooth tissue, the bur would be prematurely and irreversibly damaged.28 Local anaesthesia was said not to be needed, based on the claim that these plastic burs would remove only the insensitive, soft, and necrotic carious dentin (caries-infected dentin), leaving the demineralized, noninfected sensitive layer (caries-affected dentin). Nevertheless, while the need for local anaesthesia during cavity preparation was in fact reduced, some patients still reported one or more episodes of pain sensation during treatment.3 The efficacy of the SmartPrep burs for caries removal was questioned in a histological study when excavated tooth sections were stained with Mallory-Azan.28 More residual caries was found in cavities excavated with SmartPrep burs than in 10 ot Neves et al disclosed remnants of carious tissue at the excavated dentin/composite interface. It was then suggested that the efficiency of the polymer burs could be enhanced if the hardness of the polymeric material could be increased. An improved version of the polymeric burs was more recently marketed (SmartBurs, SSWhite Burs; Lakewood, NJ, USA) and resulted, in primary teeth, in the highest coincidence between the caries removal endpoint obtained by auto-fluorescence of carious dentin and the actual degree of caries removal. A great amount of residual caries was nevertheless still found, especially in inactive caries-arrested lesions. This can probably be explained by the still rather low surface hardness of the SmartBurs (26.6 KHN) as compared to the hardness of arrested carious dentin (39.2 KHN).24 Ceramic burs A new line of slow-speed rotary cutting instruments made of ceramic materials is now commercially available for removal of carious dentin. The CeraBurs (Komet-Brasseler; Lemgo, Germany) are all-ceramic round burs made of alumina-yttria stabilized zirconia and are available in different diameter sizes (Fig 3). The manufacturer claims that besides its high cutting efficiency in infected, soft dentin, the use of this instrument for caries removal replaces both the explorer and the excavation spoon (commonly needed to evaluate the degree of decay removal) by simultaneously providing tactile sensation, self-evidently reducing preparation time. However, an in vitro investigation of the caries-removal efficiency (time consumption for excavation) and efficacy (ability to remove all carious material from the cavity) did not show any significant difference between the ceramic and conventional tungsten-carbide burs.27 Nevertheless, one important aspect to be emphasized – and which applies to all kinds of bur instruments – is its nonspecificity. Especially if no tactile instrument is used to check the cavity for its hardness, areas of underprepared dentin are likely to be left,59 as can be observed in the 3D volumetric reconstruction of a carious tooth when caries was excavated using ceramic burs (Fig 4). Further in vivo studies testing the effectiveness of these new burs are unfortunately still lacking. Caries-disclosing Dyes Early TEM and biochemical characterization of carious dentin revealed that the most superficial carious layer is necrotic, highly decalcified, and contains irregularly scattered granular crystals and irreversibly denatured collagen fibrils. Underneath this “caries-infected” dentin, the deeper “caries-affected” dentin layer exhibits decreased collagen crosslinks, but comprises needle-like apatite crystals, regularly attached to collagen fibrils with no signs of bacterial invasion.68,90 Based on this knowledge, the ideal caries-disclosing dye should stain solely the caries-infected, but not the caries-affected dentin. The Journal of Adhesive Dentistry n ot Q ui by N ht opyretigal No CNeves t fo rP ub lica tio n te ss e n c e fo r Fig 4A Occlusal surface of a tooth presenting dentin caries. Fig 4B Occlusal view after minimally invasive preparation and carious dentin excavation with Ceraburs. The dotted line depicts the location of the volume-rendered slice in Fig 4C. Fig 4C Volume-rendered slice based on x-ray micro-CT data of the section depicted by dotted line in Fig 4B. The arrow denotes an area of residual caries according to the mineraldensity calibration shown at the left side. The caries-removal endpoint was determined by the self-limiting property of the bur. 0.5% Basic fuchsin in a propylene glycol base One of the first caries-disclosing dyes was based on a solution of 0.5% basic fuchsin in propylene glycol and was claimed to stain exclusively the top, irreversibly destroyed carious layer, enabling differentiation from what could be left in the cavity.42 The mechanism of this differential staining was initially ascribed to the irreversible collagen denaturation of caries-infected dentin, caused by breakdown of the intermolecular crosslinks through bacterial lactic acid.69 Later, the differential stainability was attributed rather to differences in the degree of mineralization in the carious lesion than being specific for denatured collagen fibrils.119 The exact mechanism for the differential staining is however still unknown. The first combined clinical/laboratory study on the reliability of this caries-disclosing dye has pointed out that the extent of dentin excavated by the fuchsin-guided method was larger than the extent of demineralized dentin, as shown by conventional dental radiographs taken before histological sections were made.100 Later, others also showed that when caries was removed using conventional tactile probing to determine the caries removal endpoint, both in primary and permanent teeth, the cavity walls and floors were still fuchsin-stainable.119 Some concerns were also raised regarding possible carcinogenic effects of fuchsin for intra-oral Vol 13, No 1, 2011 use,119 and for this reason, alternative caries-disclosing dyes are sought. 1% Acid-red in propylene glycol base Although a 1% acid-red solution (Caries Detector, Kuraray; Tokyo, Japan) was launched as an alternative to fuchsin for intra-oral use,69 clinical inconsistencies have been reported when assessing the presence of stained tissue at the DEJ by means of the usual tactile probing method. Two studies have shown that more than half of the teeth judged clinically as having no caries at the DEJ could be stained with acid red.60,61 Microbiological assessment of the caries-stained and stain-free dentin at the DEJ failed to disclose differences in level of infection.61 Moreover, it has been demonstrated that a 1% acid-red solution can lead to staining of dentin clinically judged as “sound”, with a 30% false positive diagnosis of residual caries.18 At the pulpal floor, also more than half of the teeth diagnosed as having “hard” and “sound” pulpal floors still took up some stain.60 In fact, it has been reported that sound circumpulpal dentin takes up stain more easily, because of its lower degree of mineralization18,119 (Fig 5). For all these reasons, the use of caries-staining agents is still much criticized. 11 Q ui by N ht pyrig No Co t fo rP ub preFig 5A Mesiodistal section of a tooth lica senting occlusal dentin caries (black arrow) ti and an approximal lesion (white te arrow). DD = on ss e n c e demineralized dentin; HD= hypermineralized n ot Neves et al fo r dentin. Fig 5B Higher magnification of the dotted area in Fig 5A after staining with a 1% acidred-in-propylene-glycol solution. Note staining of circumpulpal dentin (black arrow) and areas of hypermineralized dentin (white arrow). Fig 6A Volume rendering based on x-ray micro-CT data (occlusal view) from a tooth presenting dentin caries (insert: stereomicroscopic view). Fig 6B Volume rendering based on x-ray micro-CT data of the same tooth after excavation with the aid of a pepsin-based gel and a specially designed plastic instrument (SFCVIII, 3M ESPE) (insert: stereomicroscopic view). Fig 6C Volume rendering based on x-ray micro-CT data of one slice (corresponding to the dotted line in Fig 6A before excavation, showing the extent of the lesion into dentin (blue = carious lesion; green = sound dentin). Fig 6D Volume rendering based on x-ray micro-CT data of one slice (corresponding to the dotted line in Fig 6B after excavation, showing the extent of the excavated dentin (blue = carious lesion; green = sound dentin). Comparing acid red to basic fuchsin, both in propylene glycol bases, acid-red produces a less intense and less bound stain with a more intense staining of the outer than the inner layer of carious dentin.119 Further in vitro studies have shown that the light pink staining from acid red, typically seen at the inner layer of carious dentin, was related to a low degree or absence of bacterial infection55 as well as to a low level of peritubular dentin dissolution and increased hardness.96,125 For these reasons, the lightly stained tissue should not be removed. Another concern is that the propylene glycol base of both staining agents can easily penetrate into normal dentin due its low molecular weight (76 MW), which could thus also explain the overstaining frequently reported for commercial products, such as Caries Detector.48 This finding has recently led to the introduction of a 1% acid-red dye in a polypropylene glycol base (Caries Check, Nippon Shika Yahuhin; Japan). The higher molecular weight of polypropylene glycol (300 MW) makes it more caries specific than a propylene-glycol-based dye. The fluorescence readings of residual dentin using DIAGNOdent (Kavo Dental; Jena, Germany) after caries removal guided by acid red in polypropylene-glycol-based dye were higher than those when caries was removed using a propylene-glycol-based dye, indicating that less dentin was removed with the former caries-disclosing dye.48,64 12 Clinically, both formulations of Caries Check (1% acid red or a 1% brilliant blue FCF in a polypropylene glycol base) also produced significantly lower DIAGNOdent readings after caries removal than an 1% acid red in propylene glycol.49 The blue version of the dye was introduced to facilitate identification of caries in heavily stained cavities, where the red color is more difficult to differentiate. Chemo-mechanical Excavation Sodium hypochlorite-based agents The first attempt to develop of a chemical solubilizer that would selectively act on carious dentin resulted in a sodium hypochlorite solution buffered with an amino-acidcontaining mixture of amino butyric acid, sodium chloride and sodium hydroxide.43 Even though sodium hypochlorite is a nonspecific deproteinizing agent, the capability to selectively remove carious dentin was attributed to the buffering effect of the amino acid mixture, originally intended to reduce the aggressiveness of sodium hypochlorite on sound dentin and to enhance the disrupting effect on degenerated collagen within carious dentin.108 After chlorination and cleavage of the partially degraded collagen fibrils in the carious lesion, the resultant friable collagen fibrils could be more easily removed with a spoon excavator.13 The Journal of Adhesive Dentistry by N ht ot n fo r Vol 13, No 1, 2011 Q ui However, this new caries-removing system, first commercialized as Caridex (National Patent Medical Products; New Brunswick, NJ, USA), was not fully successful in clinical practice. Not only its efficacy in caries removal was contested, but technical problems – such as the need of a specific apparatus to deliver the solution into the cavity, short shelf-life, longer treatment time, and higher treatment cost – were advanced as reasons why it was not adopted extensively by dental practitioners.11 Renewed interest in chemomechanical caries removing agents was associated with the emerging concept of minimally invasive dentistry. A new caries removing system, also based on sodium hypochlorite, was introduced in the form of a gel (Carisolv, MediTeam Dental; Sävedalem, Sweden) which contained 0.5% w/v sodium hypochlorite, 0.1M of an amino acid mixture (glutamic acid, leucine and lysine), and water. The gel is applied in the cavity, after which the carious dentin is scraped off using specially designed noncutting hand instruments. The method has been shown to effectively remove caries and was readily accepted by patients. However, compared with conventional drilling, a substantially longer treatment time was reported.38 In fact, the operative steps in chemomechanical caries excavation include: (1) application of the solution, (2) scrapping off the carious dentin with possible change of instrument size, (3) rinsing, and (4) repetition of the procedures until all caries is removed.38,73 However, if the use of local anaesthesia can be omitted, the total treatment time can be shortened.97. Carisolv has proven its efficacy in establishing the endpoint of caries excavation by removing carious dentin to the same extent as the auto-fluorescence signature of carious tissue when measured using confocal microscopy.8 However, histological evaluation using toluidine blue as a staining agent still revealed a higher percentage of teeth presenting bacteria invading the dentinal tubules. A great amount of residual bacteria was also detected at the DEJ, where direct access of the gel and the hand instruments is difficult.117 The presence of bacteria at the bottom of the cavity was explained by the relative absence of smear layer formation when Carisolv was used,9,98 and presumably resulted from “pushing” bacteria into the dental tubules.117 On the other hand, the viability of such residual bacteria should be very low, because Carisolv has some bactericidal activity due to formation of chloramine compounds. In fact, Carisolv has proven to be somewhat superior in reducing the counts of viable bacteria in residual dentin, as compared to conventional bur excavation.70 The chemical composition and microstructure of dentin after excavation with Carisolv does not seem to be significantly altered. The calcium and phosphorus content remain similar after excavation, while the hardness values of residual dentin left at the cavity bottom approximate those obtained for sound dentin.51,99 Actually, the chloride present in the gel does not seem able to interact with the collagen fibrils of sound dentin, since they are protected by mineral crystals.104 Although the etch pattern of dentin in Carisolv-excavated lesions is deeper than that in dentin from which caries was removed with a conventional bur guided by a caries-staining dye,117 the bonding effectiveness of adhesives to Carisolv- opyretigal No CNeves t fo treated dentin did not appear to be affected.20,36,47 r CarisolvPu excavated dentin has good bonding receptiveness, meaning bli cat that it is not covered by a smear layer, exhibits patent dentii 46 47 nal tubules and an irregular surface topography te with im- on ss e n ce have proved wetting potential.35 Acceptable bond strengths been reported after caries was excavated with Carisolv and a self-etching adhesive was employed.105 In other studies, bond strengths obtained with both etch-and-rinse and selfetching adhesives to dentin from which caries was excavated with Carisolv were even found to be similar to that of sound dentin.20,104 Pepsin-based caries excavation A new experimental gel consisting of pepsin in a phosphoric acid/sodium biphosphate buffer is being considered as an alternative chemomechanical caries excavation agent (SFC-VIII, 3M ESPE; Seefeld, Germany). The main advantage of this new enzyme-based solution is that it can be more specific by digesting only denatured collagen (after the triple-helix integrity is lost) than the sodium hypochlorite-based agents.1 According to the manufacturer, the phosphoric acid dissolves the inorganic component of carious dentin, while it at the same time gives pepsin access to the organic part of the carious biomass to selectively dissolve the denatured collagen. To avoid overexcavation, the SFC-VIII gel should be used in combination with a prototype plastic instrument having hardness between that of sound and infected dentin. Heavily pigmented, arrested dentin caries is known to be more resistant to pepsin digestion,109 but this does not seem to present a major drawback to the method. An x-ray micro-CT evaluation of carious teeth excavated with SFC-V revealed that the new enzymatic caries-removing gel was able to remove equivalent volumes of carious dentin as Carisolv.25 Figure 6 shows volume-rendering slices based on micro-CT data of a carious tooth before and after caries excavation with SFC-VIII aided by the prototype plastic instrument. SFC-VIII selectively removed carious dentin, leaving residual dentin with an acceptably high mineral density (1.18 to 1.44g/cm3). Figure 7 shows the prototype plastic instrument (Star v 1.8, 3M ESPE) before and after caries excavation. Others have found partially demineralized intertubular collagen fibrils and some tubule occlusion upon treatment of artificially-formed dentin caries with a pepsin-based caries-excavation agent.1 However, further laboratory studies and clinical trials are still lacking. Excavation by sono-abrasion Caries excavation by “sono-abrasion” is based on the use of cutting tips coupled to high-frequency, sonic, air-scaler handpieces under water cooling. The handpiece oscillates in the sonic region (< 6.5 kHz), while the tips perform an elliptical motion. A maximum 2-N torque force should be applied, otherwise the cutting efficiency is reduced due to damping of the oscillations.10 Sono-abrasion excavation with diamond-coated tips appeared as efficient (time required for excavation) as conventional hand excavation using dental spoons, but still taking more time than the carbide-bur excavation method.8 Re13 Q ui by N ht pyrig No Co t fo rP ub lica tio n te ss e n c e n ot Neves et al fo r Fig 7A Plastic single-use instrument intended to be used with the enzymatic pepsinbased gel (SFC-VIII, 3M ESPE). Fig 7B The same instrument after use in the tooth depicted in Fig 6, showing complete dulling after the excavation procedure. Fig 8A Cariex diamond-coated tips for enamel preparation. Fig 8B Cariex tungsten carbide tips for dentin excavation. garding caries removal, the effectiveness of sono-abrasion based on its auto-fluorescence signature has shown a tendency to underprepare carious cavities. Some authors speculated that the oscillation of the diamond-coated tip is transferred to only a slight vibration at the dentin surface, impairing effective tissue cutting and resulting only in a compacting effect on the carious dentin substrate.8 No chemical or structural changes were observed in sono-abraded dentin, the surface characteristics of which resembled those of conventionally bur-cut dentin.113 The surface topography of dentin after sono-abrasion excavation with diamond-coated tips revealed relatively little9 or even no evidence of smear layer formation.116 According to another study, any smear layer produced tends to be thinner than the one yielded by diamond/carbide burs,95 which may be advantageous for the bonding effectiveness of so-called mild self-etching adhesives in particular.39 More recently, the Cariex system (Kavo Dental; Biberach, Germany) was launched, including two sets of cutting tips: two diamond-coated tips with different diameters for enamel preparation and two tungsten-carbide tips with different diameters for dentin excavation (Fig 8). The effectiveness and efficacy of these new tungsten carbide tips in removing carious dentin have, however, not yet been explored. Air-abrasion Excavation Air-abrasion systems for cavity preparation use the kinetic energy of abrasive particles to cut tooth structure in a less invasive way, while rounding off internal and cavosurface angles to the direct benefit of the subsequent adhesive restoration. Pure aluminium oxide particles (alumina) have been most frequently used as the abrading agent, thanks 14 to their high cutting effectiveness, chemical stability, low cost, low affinity for water, and neutral color.16 Air-abrasion systems using 27-μm diameter alumina particles are currently available to remove tooth staining or to prepare shallow cavities. Aside from the type and size of the abrasive particles, other variables which also directly influence the cutting effectiveness of air-abrasion systems are the particle speed and the angle of surface approach, and naturally the properties of the substrate itself. The major drawback of air-abrasion excavation of carious dentin is that sound dentin is more efficiently removed than carious dentin.92 Although 27-μm alumina particles have proven to remove more carious dentin than particles with larger dimensions (50- and 125-μm diameter), cavities produced in sound dentin were still considerably deeper than in carious dentin.82 As carious dentin has a softer consistency, the energy of the particles is absorbed during the impact, reducing the cutting ability. Other types of particles were tested in order to improve the effectiveness of caries removal with air-abrasion systems. Spherical glass beads with different diameters improved removal of artificially softened dentin, but although at lower rates, sound enamel and dentin were still removed. Polycarbonate resin-crushed powder removed artificially softened dentin more selectively without cutting sound dentin or enamel,45 but further clinical investigations with these particles are still lacking. A mixture of alumina and hydroxyapatite in a volume ratio of 3:1, with particle sizes ranging from 3 to 60 μm, was shown to be as efficient as conventional hand excavation with dental spoons, and was positively rated when related to the auto-fluorescence signature of the lesion.8 An air-abrasion system that makes use of a The Journal of Adhesive Dentistry ot fo r Vol 13, No 1, 2011 by N ht Excavation Aided by Laser-induced Fluorescence Based on the above-mentioned fact that caries-induced changes lead to increased fluorescence of dentin at the n Fluorescence-aided Caries Excavation (“FACE”) This technique was developed as a direct method to clinically differentiate between infected and affected carious dentin. Based on the fact that several oral microorganisms produce orange-red fluorophores as by-products of their metabolism (porphyrins), infected carious tissue will fluoresce especially in the red fraction of the visible spectrum2 due to the presence of proto- and meso-porphyrins.76 In this way, continuous visual detection of orange-red fluorescence during caries excavation was thought to be convenient for clinicians. By feeding a slow-speed handpiece with a fiber-optic violet light source (370 to 420 nm) and allowing the operator to use a 530-nm yellow glass filter, areas exhibiting orangered fluorescence can be selectively identified and removed with the bur. Compared to Caries Detector or the visual-tactile method for establishing the caries removal endpoint, the FACE method showed the highest sensitivity, specificity, percentage correct score, and predictive values for residual caries detection, as evaluated using confocal microscopy.71 Histological examination after staining with ethidium bromide revealed fewer samples presenting bacteria in dentin when the FACE method was used than was the case with conventional bur excavation.72 Others failed to find differences in the number of infected samples between FACE and conventional bur excavation, but observed a significant reduction in the number of samples presenting residual bacteria after excavation with FACE, when compared to Carisolv or bur excavation guided by Caries Detector.73 The FACE method also proved to be very efficient, with less time needed to excavate caries and without a need to change instruments, apply chemical agents, orto test the cavity with an explorer.73 Another important aspect is that the increased caries-removal efficacy of FACE was apparently not associated with an increased cavity size or overexcavation.74 Q ui bioactive glass powder (Bioglass, Novamin Technology; Alachua, USA) with a particle diameter between 25 and 32 μm was also explored. Although still removing sound dentin, the risk of unnecessary sound dentin removal was reduced because of the difference in cutting rate between sound and carious dentin.93 The authors suggested that other bioactive glasses with different hardness should be evaluated for their caries-removal selectivity. The topography of residual dentin caries after removal with 50-μm alumina particles exhibits a porous, sponge-like appearance caused by the impact of the particles under compressed air. Remnants of alumina powder were also identified and tubules were fully occluded with surface debris.116 Although air abrasion produces a more irregular, imbricate surface pattern and a thinner smear layer when compared to bur-cut dentin, it does not seem to affect bonding performance of adhesives to dentin on the condition that it is still acid-etched if etch-and-rinse adhesives are employed.113 opyretigal No CNeves t fo 655-nm (red) wavelength,2 a laser-fluorescence r Pdevice ubdethat irradiates at this particular wavelength has been lica veloped to diagnose “hidden” occlusal carious lesions ti (DIAGNOdent, Kavo Dental; Biberach, Germany). te A photo- on ss e nthe ce diode attached to the tip of the handpiece measures feedback of fluorescence after initial irradiation, where the intensity of fluorescence at the occlusal surface is directly related to the degree of caries progression into dentin.76 Based on a diagnostic scale correlating the readings of fluorescence with the histological presence of caries, values above 30 should be considered a stage of caries progression demanding operative intervention.75 Beyond using laser-induced fluorescence for occlusal caries diagnosis, these readings are currently being investigated as a possible end-point guide to caries excavation. Based on a comparison with histological examination in the confocal microscope after staining with ethidium bromide, a DIAGNOdent reading of 15 was seen to best predict the presence of residual caries at the bottom of the cavity.71 Later, this value was correlated to the absence of detectable bacteria, and thus set as the endpoint for complete caries removal.54 It is interesting to note that when Caries Detector was used as caries removal endpoint, a threshold of 11 was found,19 corroborating previous findings that the staining method invariably leads to overexcavation. When combined with caries removal using an erbium laser, a DIAGNOdent threshold between 11 and 20 was shown to best predict removal of infected carious dentin.121 Others who used a threshold value of 30 for dentin caries have found acceptable sensitivity values (ability to correctly diagnose caries) for DIAGNOdent when used to determine the caries removal endpoint.118 One should, however, realize that the DIAGNOdent readings increase with the proximity to the pulp as well as with stained, sclerotic dentin,66 which thus could lead to a false-positive threshold for caries removal. Laser Excavation The word “laser” is an acronym for “Light Amplification by Stimulated Emission of Radiation”, which means that laser devices produce beams of coherent and high-intensity light. The indications for the use of lasers in dentistry are nowadays broad, varying from caries diagnosis, disinfection of periodontal pockets or root canals, photodynamic therapy of oral tumors, soft-tissue surgery, caries removal, and cavity preparation.114 Especially in the field of operative dentistry, erbium lasers have been pointed out as most promising due to their specificity in ablating enamel and dentin without side effects to the pulp and surrounding tissues when the approprate parameters are employed.114 The erbium-loaded yttrium-aluminum-garnet (Er:YAG) and the erbium,chromium: yttrium-scandium-gallium-garnet (Er,Cr:YSGG) lasers are the two types of erbium-based devices currently available on the market. Both devices present very similar wavelengths (2.78 μm for Er,Cr:YSGG and 2.94 μm for Er:YAG), although the Er,Cr:YSGG laser is discretely more absorbed by hydroxyapatite than Er:YAG.114 Despite this difference, both wavelengths are very close to the absorption peak of water in the infrared spectrum, which makes their interaction with dental hard tissues very similar. 15 by N ht n fo r 16 Q ui Fundamentally, the mechanism by which enamel and dentin are removed during Er:YAG irradiation consists of explosive subsurface expansion of water interstitially trapped in the dental hard tissues. During irradiation, the water molecules absorb the incident radiation, causing sudden heating and water evaporation. As a result, a high-stream pressure is formed, inducing a violent, yet controlled expansion and ejection of dental hard tissue components.50 In contrast, the Er,Cr:YSGG laser system, usually known as a “laserpowered hydrokinetic system”, delivers photons straight into an air-water spray directed to the target tissue. This phenomenon induces micro-explosive forces into water droplets, which is said to contribute significantly to the mechanism of hard-tissue removal.44 Unfortunately, no systematic studies comparing these two types of erbium lasers have been performed so far, especially considering their particular effects on cavity morphology and on the characteristics of the residual dentin after caries removal. Several advantages have been related to the use of laser irradiation in operative dentistry, such as a more conservative cavity design, an alleged antibacterial activity,111 and a significant decrease of enamel solubility, therefore also possibly playing a role in the prevention of recurrent caries.23 Moreover, laser ablation apparently provides more comfort to the patient due to the absence of vibration57 and a lower pain sensation. In fact, the need for local anaesthesia is reported to be lower when compared to the use of conventional rotary instruments.58 On the other hand, the major drawback related to their use in operative dentistry is the relatively long time needed for cavity preparation. The time required for a complete excavation is, in general, twice that with rotary instruments,4,12,58 Recently, one study succeeded in reducing the overall cavity preparation time by using considerably high energies (700 mJ).80 However, it should be noted that such high energies can also induce irreversible chemical and structural alteration to the dental hard tissues7 and even damage the pulp.114 Irrespective of the parameters used during laser irradiation, the effectiveness of carious dentin removal with erbium lasers has been questioned. SEM has shown that the laser produces an undefined and random excavation pattern in dentin, with deep overprepared and wide underprepared zones present in the same cavity. For optimal irradiation, a noncontact beam emission mode is usually recommended, thus rendering caries excavation more difficult to control due to the lack of tactile sensation.12 Moreover, the irregular dentin surface left after laser ablation hampers an accurate tactile feedback when an ordinary probe is used for detecting the status of excavation.12,116 Despite this, some studies have relied upon visual/tactile methods44,57 or staining with 1% acid-red solution to evaluate the thoroughness of caries removal,4 obtaining residual dentin hardness values similar to sound dentin. Histological observations have also disclosed the same degree of bacterial removal by an Er:YAG laser and conventional bur excavation.4 Additionally, better DIAGNOdent scores of residual dentin were obtained after excavation with an Er,Cr:YSGG laser than with Carisolv.63 Although Er:YAG laser ablation is not selective for carious dentin, it has been described that the popping sound emitted by these lasers when operating in dental hard tissues pyrig No Co t fo changes according to the presence or absence r Pof caries. ub This change in sound could assist the user in determining lica when caries removal is complete.114 This approach is, howtio ever, not very objective or practical, and is tsusceptible ess c eto n misinterpretation. An improvement in the caries-removal en ot Neves et al ability of erbium lasers is to combine it with laser-fluorescence technology for caries detection. In one unit (Key III, Kavo Dental), Er:YAG laser irradiation is controlled by the feedback response provided by the red-infrared diagnostic diode laser, resulting in a self-limiting laser ablation. Actually, the laser ablation is activated only if the fluorescence emitted from the dental tissue exceeds a pre-determined threshold.32 An initial threshold value of 7 for the laser fluorescence detection system removed all bacteria at the bottom of the cavity, as was detected histologically.32 This threshold value was corroborated by clinical studies in permanent31 and primary teeth,67 in which only clinically insignificant amounts of bacteria could be detected at the bottom of the excavated cavities. Beyond appropriate removal of infected dentin, this laser also precluded less sound dentin removal, resulting in smaller cavities compared to conventional bur excavation.33 Absence of smear layer is very often mentioned as an advantage of laser irradiation of tooth surfaces, in particular for bonding procedures.5,56,63 However, while relatively high bond strengths have been reported with either an etch-andrinse or a self-etching adhesive after caries removal with an Er:YAG laser,101 other authors found lower bond strengths to laser-irradiated dentin when compared to a conventionally bur-cut substrate.21,105,113 Such disappointing results have been related to the presence of subsurface microcracks produced in dentin during laser ablation, rendering it more prone to cohesive failures.21 Moreover, laser-irradiated dentin has also been reported to change the composition and conformation of the organic matrix of dentin,7 which may impair adhesive penetration and facilitate collagen degradation. ADHESION TO CARIOUS DENTIN Sound human dentin is most convenient to test the performance of dental adhesives by means of standard bondstrength protocols. This “model” dentin is, however, far from the clinically more relevant substrate remaining after caries removal, which exhibits “mixed” chemical and mechanical characteristics and includes caries-infected, caries-affected, sclerotic, eroded, and sound dentin.79 In general, the presence of carious dentin results in thicker hybrid layers and lower bond strengths.83,84,123,124 The bond strength of adhesives to carious dentin has been reported to be inversely proportional to the degree of caries progression, with caries-infected dentin presenting the lowest bond strength.30 The thickness of the hybrid layer is indirectly correlated to the degree of caries progression, with caries-infected dentin presenting thicker hybrid layers, followed by caries-affected and sound dentin.52,123,124 Like in sound dentin, hybrid layers in caries-affected dentin are thicker using etch-and-rinse than self-etching adhesives.52,123 For caries-infected dentin, however, the thickThe Journal of Adhesive Dentistry by N ht ot n fo r Vol 13, No 1, 2011 Q ui ness of the hybrid layer tends to be similar, irrespective of the adhesive approach.52 Thicker hybrid layers in caries-affected dentin are explained by the increased porosity of intertubular dentin, which promotes diffusion of resin monomers.53,83 The lower bonding effectiveness to caries-infected dentin is related to its extremely low cohesive strength, due to its low degree of mineralization and the collagen-matrix disorganization.83 Although resulting in thicker hybrid layers, this type of dentin allows only superficial monomer penetration, keeping many dentin tubules completely free from tag formation.52,123,124 Considering the poor interaction with the substrate, bonding to caries-infected dentin is seldom indicated, except when aiming to prevent further caries progression in uncooperative patients while implementing behavior control. The lower bonding effectiveness to caries-affected dentin than to sound dentin is related to the alterations that occur in this substrate as a consequence of caries progression. First, the reduction in mineral content and loss of crystallinity of the remaining mineral phase, coupled to the changes in the secondary structure of collagen,115 result in a dentin substrate with a lower hardness89 and modulus of elasticity than those of sound dentin,78 performing poorer in mechanical tests. Secondly, the deposition of mineral casts, namely of β-tricalcium phosphates (whitlockites),26,115 in the dentin tubules during caries progression also alters the etch pattern and thus the penetration capacity of resin monomers into the tubules. When bonding using the moist bonding technique with etch-and-rinse adhesives, some studies were able to achieve similar bond strengths to residual dentin after caries excavation (guided by Caries Detector) as to sound dentin.83,85,86 While one of these studies83 with sound dentin achieved a relatively “low” bond strength (20 to 30 MPa) compared to what is achieved nowadays with modern adhesives (40 to 50 MPa),29 the others may have achieved these favorable results by using a rather aggressive threshold to establish the endpoint of caries removal, that is, by having produced a substrate that is more receptive for bonding than that obtained in other studies. It was also demonstrated that acetone-based etch-and-rinse adhesives bonded better to caries-affected dentin than did ethanol-based adhesives, although both were able to produce acceptable bond strengths to non-stained (with Caries Detector) dentin left after excavation.86 Although other studies were not able to produce similar results in bond strength to sound as to caries-affected dentin for many materials tested,22,88,102,122 it became clear that the chemical composition of the adhesive could strongly influence the bond strength to caries-affected dentin. Apparently, the immediate bond strength of etchand-rinse adhesives to caries-affected dentin is higher than that of self-etching adhesives.22,37,122 However, no differences in bond strength of etch-and-rinse and self-etching adhesives to carious dentin was observed after the specimens were stored for 6 months in water.37 In summary, although the bond strength at caries-affected dentin interfaces is lower than that at sound dentin interfaces, they are both continually improving and have now reached relatively high values. Table 1 offers an overview of opyretigal No CNeves t fo rP ub lica tio n te ss e n c e Fig 9 Pooled data from Table 1 (Nakajima et al;84-86 Yoshiyama et al;122-124 Tachibana et al105) regarding carious dentin surfaces that were prepared with 600-grit SiC-paper and when Caries Detector was used as caries removal endpoint following two different thresholds: non-stained vs lightly pink-stained dentin. The more “aggressive” threshold (non-stained) shows only slightly higher bond strength values than the more conservative threshold (light pink). The 3-step etch-and-rinse adhesives achieved the highest values, followed by the 2-step etch-and-rinse and the 2step self-etching adhesives. Horizontal lines represent the mean values and bars represent the upper and lower standard deviations. bond-strength values in relation to different caries removal endpoints employed, different methods used to produce the carious substrate, and different types of adhesives used. Figure 9 summarizes the bond strength values depicted in Table 1, when the caries removal endpoint was obtained with two different thresholds for staining (no staining vs lightpink staining) and after the carious dentin substrate was produced with a standardized surface-preparation method using 600-grit SiC paper. Figure 10 depicts the bond strength results for the studies presented in Table 1 that used a conventional bur and Carisolv to excavate caries. In both cases, essentially no differences in bond strength between etch-and-rinse and self-etching approach were found. Altogether, irrespective of the caries excavation method chosen, it remains clinically recommended to finish the cavity margins in clean/sound tooth tissue in order to achieve the best performance of adhesives, while being at the same time least invasive with regard to caries excavation and most conservative with regard to sound-tissue preservation. REFERENCES 1. Ahmed AA, Garcia-Godoy F, Kunzelmann KH. Self-limiting caries therapy with proteolytic agents. Am J Dent 2008;21:303-312. 2. Alfano RR, Yao SS. Human teeth with and without dental caries studied by visible luminescent spectroscopy. J Dent Res 1981;60:120-122. 17 pyrig No Co t Table 1 Bond strength related to the different caries removal endpoints, type of caries-affected substrate, andfo adhesive rP ub material used lica tio n te Method of caries Type of caries-affected Type of adhesive (brand name) μTBS Reference e s s c en excavation endpoint substrate Neves et al by N ht Q ui fo r Non-stained dentin remaining after using Caries Detector 220-grit SiC paper 600-grit SiC paper 320-grit SiC paper Conventional bur Er,Cr:YSGG Laser Carisolv Light-pink staining remaining after using Caries Detector 18 600-grit SiC paper 2-step etch-and-rinse (Prime & Bond NT, Dentsply) 2-step etch-and-rinse (Scotchbond 1, 3M ESPE) 2-step self-etch (Clearfil SE Bond, Kuraray) 1-step self-etch (Prompt L-Pop, 3M ESPE) 3-step etch-and-rinse (Scotchbond MP, 3M ESPE) 3-step etch-and-rinse (ART Bond, VITA) 2-step etch-and-rinse (One-Step, Bisco) 2-step etch-and-rinse (Single Bond, 3M ESPE) 2-step etch-and-rinse (Single Bond, 3M ESPE) 2-step etch-and-rinse (Single Bond, 3M ESPE) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step self-etch (Clearfil Liner Bond 2, Kuraray) 2-step self-etch (Clearfil Liner Bond 2, Kuraray) 2-step self-etch (Clearfil Protect Bond, Kuraray) 2-step self-etch (Tenure ABS System, Denmat) 2-step self-etch (FluoroBond, Shofu) 3-step etch-and-rinse (Scotchbond MP, 3M ESPE) 3-step etch-and-rinse (All Bond 2, Bisco) 2-step self-etch (Clearfil Liner Bond 2, Kuraray) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step etch-and-rinse (Scotchbond 1, 3M ESPE) 2-step etch-and-rinse (Optibond Solo Plus, Kerr) 2-step self-etch (Clearfil Protect Bond, Kuraray) 2-step self-etch (AdheSE, Ivoclar Vivadent) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step self-etch (Mac-Bond II, Tokuyama) 2-step self-etch (UniFil Bond, GC) 41.3±10.7 ot n Staining with 0.5% fuchsin Ceballos et al22 36.3±12.2 21.5±5.5 13.4±1.9 48.2±3.9 Nakajima et al85 30.2±13.4 Nakajima et al84 45±7.2 Nakajima et al86 40.2±11.1 28.8±6.3 Yoshiyama et al123 27.1±6.5 Yoshiyama et al122 30.3±11.9 Tachibana et al105 30±10 Yoshiyama et al124 29.7±10.3 Nakajima et al84 29.4±7.5 Nakajima et al87 25.3±5 Yoshiyama et al123 17.5±2.1 Yoshiyama et al122 18.49±4.04 Nakajima et al83 13.01±3.64 13.97±4.3 29±10.3 Tachibana et al105 18.4±11 21.5±10 34.5±6.8 Erhardt et al37 29.2±4.3 Say et al102 28.7±5 Erhardt et al37 24.2±7 21.5±5.3 Doi et al30 20.2±5.8 19.6±6 The Journal of Adhesive Dentistry Q ui by N ht opyretigal No CNeves t fo Table 1 Bond strength related to the different caries removal endpoints, type of caries-affected substrate, and adhesive rP ub material used (continued) lica tio n Method of caries Type of caries-affected Type of adhesive (brand name) μTBS Referencet e e s s c en excavation endpoint substrate fo r 600-grit SiC paper Conventional bur Er:YAG laser Visual-tactile method Hand excavation Conventional bur Carisolv Smart Prep bur 2-step etch-and-rinse (Optibond Solo Plus, Kerr) 2-step self-etch (Clearfil Protect Bond, Kuraray) 2-step etch-and-rinse (Optibond Solo Plus, Kerr) 2-step self-etch (Clearfil Protect Bond, Kuraray) 2-step etch-and-rinse (Optibond Solo Plus, Kerr) 2-step self-etch (Clearfil Protect Bond, Kuraray) 2-step etch-and-rinse (Prime & Bond NT, Dentsply) 2-step self-etch (Tenure ABS System, Denmat) 2-step etch-and-rinse (Single Bond, 3M ESPE) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step etch-and-rinse (Prime & Bond NT, Dentsply) 2-step self-etch (Clearfil SE Bond, Kuraray) 2-step self-etch (One Coat Bond, Coltene) 2-step self-etch (Tenure ABS System, Denmat) 2-step etch-and-rinse (Single Bond, 3M ESPE) 2-step self-etch (Clearfil SE Bond, Kuraray) 25.7±5.9 ot n Diagnodent value = 20 Sattabanasuk et al101 35.4±9.7 21.3±7.5 12.2±3.1 26.6±9.4 32.5±7.1 25.06±10.16 Sonoda et al104 22.33±6.9 24.8±15.9 Silva et al103 31.4±12.7 26.99±11.69 Sonoda et al104 28.7±6.9 Burrow et al20 27.4±6.4 31.1±9.21 Sonoda et al104 13.9±7.1 Silva et al103 10.5±6.6 Fig 10 Pooled data from Table 1 (Burrow et al;20 Sattabanasuk et al;101 Silva et al;103 Tachibana et al105) comparing the bond strength results when caries was excavated with a conventional bur (left) or Carisolv (right). Similar mean bond strength values were recorded for etch-and-rinse and self-etching adhesives in both cases. Horizontal line represents the mean values and bars represent the upper and lower standard deviations. Vol 13, No 1, 2011 19 by N ht 31. n fo r 20 30. Q ui 3. Allen KL, Salgado TL, Janal MN, Thompson V. Removing carious dentin using a polymer instrument without anesthesia versus a carbide bur with anesthesia. J Am Dent Assoc 2005;136:643-651. 4. Aoki A, Ishikawa I, Yamada T, Otsuki M, Watanabe H, Tagami J, Ando Y, Yamamoto H. Comparison between Er:YAG laser and conventional technique for root caries treatment in vitro. J Dent Res 1998;77:1404-1414. 5. 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;25:543-546. 6. Arnold WH, Konopka S, Gaengler P. Qualitative and quantitative assessment of intratubular dentin formation in human natural carious lesions. Calcif Tiss Int 2001;69:268-273. 7. Bachmann L, Diebolder R, Hibst R, Zezell DM. Changes in chemical composition and collagen structure of dentine tissue after erbium laser irradiation. Spectrochim Acta A 2005;61:2634-2639. 8. Banerjee A, Kidd EA, Watson TF. In vitro evaluation of five alternative methods of carious dentine excavation. Caries Res 2000;34:144-150. 9. Banerjee A, Kidd EA, Watson TF. Scanning electron microscopic observations of human dentine after mechanical caries excavation. J Dent 2000;28:179-186. 10. Banerjee A, Watson TF, Kidd EA. Dentine caries excavation: A review of current clinical techniques. Br Dent J 2000;188:476-482. 11. Barwart O, Moschen I, Graber A, Pfaller K. Invitro study to compare the efficacy of N-monochloro-D, L-2-aminobutyrate (NMAB, GK-101E) and water in caries removal. J Oral Rehab 1991;18:523-529. 12. Bayne SC, Thompson JY, Studervant CM, Taylor DF. Instruments and equipment for tooth preparation. In: Roberson TM, Heymann HO, Swift-Jr EJ (eds). Studervant’s Art & Science of Operative Dentistry. St. Louis: Mosby, 2002:307-344. 13. Beeley JA, Yip HK, Stevenson AG. Chemo-mechanical caries removal: A review of the techniques and latest developments. Br Dent J 2000;188:427-430. 14. Bjorndal L, Thylstrup A. A structural analysis of approximal enamel caries lesions and subjacent dentin reactions. Eur J Oral Sci 1995;103:25-31. 15. Black GV. Cavity preparation. In: Black GV (ed). A work on operative dentistry. Chicago: Medico-Dental Publishing Company, 1908:105-116. 16. Black RE. Technique for non-mechanical preparation of cavities and prophylaxis. J Am Dent Assoc 1945;32:955-965. 17. Boston DW. New device for selective dentin caries removal. Quintessence Int 2003;34:678-685. 18. Boston DW, Liao J. Staining of non-carious human coronal dentin by caries dyes. Oper Dent 2004;29:280-286. 19. Boston DW, Sauble JE. Evaluation of laser fluorescence for differentiating caries dye-stainable versus caries dye-unstainable dentin in carious lesions. Am J Dent 2005;18:351-354. 20. Burrow MF, Bokas J, Tanumiharja M, Tyas MJ. Microtensile bond strengths to caries-affected dentine treated with Carisolv. Austr Dent J 2003;48:110-114. 21. Cardoso MV, Coutinho E, Ermis RB, Poitevin A, Van Landuyt K, De Munck J, Carvalho RC, Lambrechts P, Van Meerbeek B. Influence of Er,Cr:YSGG laser treatment on the microtensile bond strength of adhesives to dentin. J Adhes Dent 2008;10:25-33. 22. Ceballos L, Camejo DG, Victoria Fuentes M, Osorio R, Toledano M, Carvalho RM, Pashley DH. Microtensile bond strength of total-etch and selfetching adhesives to caries-affected dentine. J Dent 2003;31:469-477. 23. Cecchini RC, Zezell DM, de Oliveira E, de Freitas PM, de Paula CE. Effect of Er:YAG laser on enamel acid resistance: Morphological and atomic spectrometry analysis. Lasers Surg Med 2005;37:366-372. 24. Celiberti P, Francescut P, Lussi A. Performance of four dentine excavation methods in deciduous teeth. Caries Res 2006;40:117-123. 25. Clementino-Luedemann TN, Ilie AD, Hickel R, Kunzelmann KH. Micro-computed tomographic evaluation of a new enzyme solution for caries removal in deciduous teeth. Dent Mater J 2006;25:675-683. 26. Daculsi G, LeGeros RZ, Jean A, Kerebel B. Possible physico-chemical processes in human dentin caries. J Dent Res 1987;66:1356-1359. 27. Dammaschke T, Vesnic A, Schäfer E. In vitro comparison of ceramic burs and conventional tungsten carbide bud burs in dentin caries excavation. Quintessence Int 2008;39:495-499. 28. Dammascke T, Rodenberg TN, Schafer E, Ott KH. Efficiency of the polymer bur SmartPrep compared with conventional tungsten carbide bud bur in dentin caries excavation. Oper Dent 2006;31:256-260. 29. De Munck J, Van Landuyt K, Peumans M, Poitevin A, Lambrechts P, Braem M, Van Meerbeek B. A critical review of the durability of adhesion to tooth tissue: Methods and results. J Dent Res 2005;84:118-132. pyrig No Co t fo bond strength Doi J, Itota T, Torii Y, Nakabo S, Yoshiyama M. Micro-tensile r P dentin. of self-etching primer adhesive systems to human coronal carious ub J Oral Rehab 2004;31:1023-1028. lica Dommisch H, Peus K, Kneist S, Krause F, Braun A, Hedderich J, Jepsen S, ti Eberhard J. Fluorescence-controlled Er:YAG laser for caries removal in per- on t es2008;116:170manent teeth: A randomized clinical trial. Eur J Oral Sci se nc e 176. ot Neves et al 32. Eberhard J, Eisenbeiss AK, Braun A, Hedderich J, Jepsen S. Evaluation of selective caries removal by a fluorescence feedback-controlled Er:YAG laser in vitro. Caries Res 2005;39:496-504. 33. Eberhard J, Bode K, Hedderich J, Jepsen S. Cavity size difference after caries removal by a fluorescence-controlled Er:YAG laser and by conventional bur treatment. Clin Oral Invest 2008;12:311-318. 34. Ekstrand KR, Ricketts DN, Kidd EA. Do occlusal carious lesions spread laterally at the enamel-dentin junction? Clin Oral Invest 1998;2:15-20. 35. Emanuel R, Broome JC. Surface energy of chemomechanically prepared dentin. Quintessence Int 1988;19:369-372. 36. Erhardt MC, Amaral CM, de Castro AK, Ambrosano GM, Pimenta LA. In vitro influence of Carisolv on shear bond strength of dentin bonding agents. Quintessence Int 2004;35:801-807. 37. Erhardt MC, Toledano M, Osorio R, Pimenta LA. Histomorphologic characterization and bond strength evaluation of caries-affected dentin/resin interfaces: Effects of long-term water exposure. Dent Mater 2008;24: 786-798. 38. Ericson D, Zimmerman M, Raber H, Götrick B, Bornstein R, Thorell J. Clinical evaluation of efficacy and safety of a new method for chemo-mechanical removal of caries: A multi-centre study. Caries Res 1999;33:171-177. 39. Ermis RB, De Munck J, Cardoso MV, Coutinho E, Van Landuyt KL, Poitevin A, Lambrechts P, Van Meerbeek B. Bond strength of self-etch adhesives to dentin prepared with three different diamond burs. Dent Mater 2008;24:978-985. 40. Fusayama T, Okuse K, Hosoda H. Relationship between hardness discoloration and microbial invasion in carious dentin. J Dent Res 1966; 45:1033-1046. 41. Fusayama T, Kurosaki N. Structure and removal of carious dentine. Int Dent J 1972;22:401-411. 42. Fusayama T, Terachima S. Differentiation of 2 layers of carious dentin by staining. J Dent Res 1972;51:866. 43. Goldman M, Kronman JH. Preliminary report on a chemo-mechanical means of removing caries. J Am Dent Assoc 1976;93:1149-1153. 44. Hadley J, Young DA, Eversole LR, Gornbein JA. A laser-powered hydrokinetic system - for caries removal and cavity preparation. J Am Dent Assoc 2000;131:777-785. 45. Horiguchi S, Yamada T, Inokoshi S, Tagami J. Selective caries removal with air abrasion. Oper Dent 1998;23:236-243. 46. Hosoya Y, Kawashita Y, Marshall GW, Jr., Goto G. Influence of Carisolv for resin adhesion to sound human primary dentin and young permanent dentin. J Dent 2001;29:163-171. 47. Hosoya Y, Shinkawa H, Marshall GW. Influence of Carisolv on resin adhesion for two different adhesive systems to sound human primary dentin and young permanent dentin. J Dent 2005;33:283-291. 48. Hosoya Y, Taguchi T, Tay FR. Evaluation of a new caries detecting dye for primary and permanent carious dentin. J Dent 2007;35:137-143. 49. Hosoya Y, Taguchi T, Arita S, Tay FR. Clinical evaluation of polypropylene glycol-based caries detecting dyes for primary and permanent carious dentin. J Dent 2008;36:1041-1047. 50. Hossain M, Nakamura Y, Yamada Y, Kimura Y, Nakamura G, Matsumoto K. Ablation depths and morphological changes in human enamel and dentin after Er:YAG laser irradiation with or without water mist. J Clin Laser Med Surg 1999;17:105-109. 51. Hossain M, Nakamura Y, Tamaki Y, Yamada Y, Jayawardena JA, Matsumoto K. Dentinal composition and knoop hardness measurements of cavity floor following carious dentin removal with Carisolv. Oper Dent 2003;28:346-351. 52. Hsu KW, Marshall SJ, Pinzon LM, Watanabe L, Saiz E, Marshall GW. SEM evaluation of resin-carious dentin interfaces formed by two dentin adhesive systems. Dent Mater 2008;24:880-887. 53. Inoue G, Tsuchiya S, Nikaido T, Foxton RM, Tagami J. Morphological and mechanical characterization of the acid-base resistant zone at the adhesive-dentin interface of intact and caries-affected dentin. Oper Dent 2006;31:466-472. 54. Iwami Y, Shimizu A, Narimatsu M, Hayashi M, Takeshige F, Ebisu S. Relationship between bacterial infection and evaluation using a laser fluorescence device, Diagnodent. Eur J Oral Sci 2004;112:419-423. The Journal of Adhesive Dentistry by N ht ot 84. n fo r Vol 13, No 1, 2011 83. Q ui 55. Iwami Y, Shimizu A, Narimatsu M, Kinomoto Y, Ebisu S. The relationship between the color of carious dentin stained with a caries detector dye and bacterial infection. Oper Dent 2005;30:83-89. 56. Jepsen S, Açil Y, Peschel T, Kargas K, Eberhard J. Biochemical and morphological analysis of dentin following selective caries removal with a fluorescence-controlled Er:YAG laser. Laser Surg Med 2008;40:350-357. 57. Keller U, Hibst R. Effects of Er:YAG laser in caries treatment: A clinical pilot study. Laser Surg Med 1997;20:32-38. 58. Keller U, Hibst R, Geurtsen W, Schilke R, Heidemann D, Klaiber B, Raab WHM. Erbium: YAG laser application in caries therapy. Evaluation of patient perception and acceptance. J Dent 1998;26:649-656. 59. Kidd EA, Ricketts DN, Beighton D. Criteria for caries removal at the enamel-dentine junction: A clinical and microbiological study. Br Dent J 1996;180:287-291. 60. Kidd EA, Joystonbechal S, Smith MM, Allan R, Howe L, Smith SR. The use of a caries detector dye in cavity preparation. Br Dent J 1989;167:132134. 61. Kidd EA, Joystonbechal S, Beighton D. Microbiological validation of assessments of caries activity during cavity preparation. Caries Res 1993; 27:402-408. 62. Kidd EA. How ‘clean’ must a cavity be before restoration? Caries Res 2004;38:305-313. 63. Kinoshita J, Kimura Y, Matsumoto K. Comparative study of carious dentin removal by Er, Cr:YSGG laser and Carisolv. J Clin Laser Med Surg 2003;21:307-315. 64. Kinoshita J, Shinomiya H, Itoh K, Matsumoto K. Light intensity evaluation of laser-induced fluorescence after caries removal using an experimental caries staining agent. Dent Mater J 2007;26:307-311. 65. Kleter GA, Damen JJM, Buijs MJ, Ten Cate JM. Modification of amino acid residues in carious dentin matrix. J Dent Res 1998;77:488-495. 66. Krause F, Braun A, Eberhard J, Jepsen S. Laser fluorescence measurements compared to electrical resistance of residual dentine in excavated cavities in vivo. Caries Res 2007;41:135-140. 67. Krause F, Braun A, Lotz G, Kneist S, Jepsen S, Eberhard J. Evaluation of selective caries removal in deciduous teeth by a fluorescence feedbackcontrolled Er:YAG laser in vivo. Clin Oral Invest 2008;12:209-215. 68. Kuboki Y, Ohgushi K, Fusayama T. Collagen biochemistry of the two layers of carious dentin. J Dent Res 1977;56:1233-1237. 69. Kuboki Y, Liu CF, Fusayama T. Mechanism of differential staining in carious dentin. J Dent Res 1983;62:713-714. 70. Lager A, Thornqvist E, Ericson D. Cultivatable bacteria in dentine after caries excavation using rose-bur or Carisolv. Caries Res 2003;37:206211. 71. Lennon AM, Buchalla W, Switalski L, Stookey GK. Residual caries detection using visible fluorescence. Caries Res 2002;36:315-319. 72. Lennon AM. Fluorescence-aided caries excavation (FACE) compared to conventional method. Oper Dent 2003;28:341-345. 73. Lennon AM, Buchalla W, Rassner B, Becker K, Attin T. Efficiency of 4 caries excavation methods compared. Oper Dent 2006;31:551-555. 74. Lennon AM, Attin T, Buchalla W. Quantity of remaining bacteria and cavity size after excavation with FACE, caries detector dye and conventional excavation in vitro. Oper Dent 2007;32:236-241. 75. Lussi A, Megert B, Longbottom C, Reich E, Francescut P. Clinical performance of a laser fluorescence device for detection of occlusal caries lesions. Eur J Oral Sci 2001;109:14-19. 76. Lussi A, Hibst R, Paulus R. Diagnodent: An optical method for caries detection. J Dent Res 2004;83:80-83. 77. Marsh P, Martin MV. Dental plaque. In: Marsh P, Martin MV (eds). Oral microbiology. Oxford: Wright, 1999:58-81. 78. Marshall GW, Habelitz S, Gallagher R, Balooch M, Balooch G, Marshall SJ. Nanomechanical properties of hydrated carious human dentin. J Dent Res 2001;80:1768-1771. 79. Marshall GW, Jr., Marshall SJ, Kinney JH, Balooch M. The dentin substrate: Structure and properties related to bonding. J Dent 1997;25:441458. 80. Matsumoto K, Wang XG, Zhang CF, Kinoshita JI. Effect of a novel Er:YAG laser in caries removal and cavity preparation: A clinical observation. Photomed Laser Surg 2007;25:8-13. 81. Mertz-Fairhurst EJ, Curtis JW, Ergle JW, Rueggeberg FA, Adair SM. Ultraconservative and cariostatic sealed restorations: Results at year 10. J Am Dent Assoc 1998;129:55-66. 82. Motisuki C, Lima LM, Bronzi ES, Spolidorio DMP, Santos-Pinto L. The effectiveness of alumina powder on carious dentin removal. Oper Dent 2006;31:371-376. opyretigal No CNeves t o S, Ciucchi Nakajima M, Sano H, Burrow MF, Tagami J, Yoshiyama M,fEbisu r P of B, Russell CM, Pashley D. Tensile bond strength and SEM evaluation ub caries-affected dentin using dentin adhesives. J Dent Res 1995;74:1679lica 1688. tio Nakajima M, Ogata M, Okuda M, Tagami J, Sano H, Pashley Bonding n te DH. to caries-affected dentin using self-etching primers. Am J Dent e s s c en 1999;12:309-314. 85. Nakajima M, Sano H, Zheng L, Tagami J, Pashley D. Effect of moist vs. Dry bonding to normal vs. caries-affected dentin with scotchbond multi-purpose plus. J Dent Res 1999;78:1298-1303. 86. Nakajima M, Sano H, Urabe I, Tagami J, Pashley DH. Bond strengths of single-bottle dentin adhesives to caries-affected dentin. Oper Dent 2000; 25:2-10. 87. Nakajima M, Kitasako Y, Okuda M, Foxton RM, Tagami J. Elemental distributions and microtensile bond strength of the adhesive interface to normal and caries-affected dentin. J Biomed Mater Res B 2005;72:268-275. 88. Nakajima M, Hosaka K, Yamauti M, Foxton RM, Tagami J. Bonding durability of a self-etching primer system to normal and caries-affected dentin under hydrostatic pulpal pressure in vitro. Am J Dent 2006;19:147-150. 89. Ogawa K, Yamashita Y, Ichijo T, Fusayama T. The ultrastructure and hardness of the transparent layer of human carious dentin. J Dent Res 1983;62:7-10. 90. Ohgushi K, Fusayama T. Electron microscopic structure of 2 layers of carious dentin. J Dent Res 1975;54:1019-1026. 91. Oliveira SS, Pugach MK, Hilton JF, Watanabe LG, Marshall SJ, Marshall GW, Jr. The influence of the dentin smear layer on adhesion: A self-etching primer vs. a total-etch system. Dent Mater 2003;19:758-767. 92. Paolinelis G, Watson TF, Banerjee A. Microhardness as a predictor of sound and carious dentine removal using alumina air abrasion. Caries Res 2006;40:292-295. 93. Paolinelis G, Banerjee A, Watson TF. An in vitro investigation of the effect and retention of bioactive glass air-abrasive on sound and carious dentine. J Dent 2008;36:214-218. 94. Penning C, Van Amerongen J, de Kloet HJ, Van Loveren C, Verhoef A. Excaveren. In: Penning C, Van Amerongen J, de Kloet HJ, Van Loveren C, Verhoef A (eds). Cariëslaesies: Diagnose en behandeling. Houten: Prelum, 2007:73-88. 95. Pioch T, Garcia-Godoy F, Duschner H, Koch MJ, Staehle HJ, Dörfer CE. Effect of cavity preparation instruments (oscillating or rotating) on the composite-dentin interface in primary teeth. Dent Mater 2003;19:259-263. 96. Pugach MK, Strother J, Darling CL, Fried D, Gansky SA, Marshall SJ, Marshall GW. Dentin caries zones: Mineral, structure, and properties. J Dent Res 2009;88:71-76. 97. Rafique S, Fiske J, Banerjee A. Clinical trial of an air-abrasion/chemomechanical operative procedure for the restorative treatment of dental patients. Caries Res 2003;37:360-364. 98. Sakoolnamarka R, Burrow MF, Kubo S, Tyas MJ. Morphological study of demineralized dentine after caries removal using two different methods. Austr Dent J 2002;47:116-122. 99. Sakoolnamarka R, Burrow MF, Swain MV, Tyas MJ. Microhardness and Ca:P ratio of carious and carisolv treated caries-affected dentine using an ultra-microidentation system and energie dispersive analysis of x-rays: A pilot study. Austr Dent J 2005;50:246-250. 100. Sato Y, Fusayama T. Removal of dentin by fuchsin staining. J Dent Res 1976;55:678-683. 101. Sattabanasuk V, Burrow MF, Shimada Y, Tagami J. Resin adhesion to caries-affected dentine after different removal methods. Austr Dent J 2006;51:162-169. 102. Say EC, Nakajima M, Senawongse P, Soyman M, Ozer F, Tagami J. Bonding to sound vs caries-affected dentin using photo- and dual-cure adhesives. Oper Dent 2005;30:90-98. 103. Silva N, Carvalho RM, Pegoraro LF, Tay FR, Thompson VP. Evaluation of a self-limiting concept in dentinal caries removal. J Dent Res 2006;85:282286. 104. Sonoda H, Banerjee A, Sheriff M, Tagami J, Watson TF. An in vitro investigation of microtensile bond strengths of two dentine adhesives to cariesaffected dentine. J Dent 2005;33:335-342. 105. Tachibana A, Marques MM, Soler JM, Matos AB. Erbium, chromium: Yttrium, scandium, gallium garnet laser for caries removal: Influence on bonding of a self-etching adhesive system. Lasers Med Sci 2008;23:435441. 106. Thylstrup A, Qvist V. Principal enamel and dentine reactions during caries progression. In: Thylstrup A, Leach SA, Qvist V (eds). Dentine and dentine reactions in the oral cavity. Oxford: IRL Press, 1987:3-16. 21 by N ht n fo r 22 Q ui 107. Tjaderhane L, Larjava H, Sorsa T, Uitto VJ, Larmas M, Salo T. The activation and function of host matrix metalloproteinases in dentin matrix breakdown in caries lesions. J Dent Res 1998;77:1622-1629. 108. Tonami K, Araki K, Mataki S, Kurosaki N. Effects of chloramines and sodium hypochlorite on carious dentin. J Med Dent Sci 2003;50:139-146. 109. Tonami K, Ericson D. Protein profile of pepsin-digested carious and sound human dentine. Acta Odontol Scand 2005;63:17-20. 110. Torneck DR. Dentin-pulp complex. In: Ten Cate B (ed). Oral histology. St. Louis: Mosby, 1998:150-196. 111. Turkun M, Turkun LS, Celik EU, Ates M. Bactericidal effect of Er,Cr:YSGG laser on streptococcus mutans. Dent Mater J 2006;25:81-86. 112. Tyas MJ, Anusavice KJ, Frencken JE, Mount GJ. Minimal intervention dentistry: A review - fdi commission project. International Dental Journal 2000;50:1-12. 113. Van Meerbeek B, De Munck J, Mattar D, Van Landuyt K, Lambrechts P. Microtensile bond strengths of an etch&rinse and self-etch adhesive to enamel and dentin as a function of surface treatment. Oper Dent 2003;28:647-660. 114. Walsh LJ. The current status of laser applications in dentistry. Austr Dent J 2003;48:146-155. 115. Wang Y, Spencer P, Walker MP. Chemical profile of adhesive/caries-affected dentin interfaces using raman microspectroscopy. J Biomed Mater Res A 2007;81A:279-286. 116. Yazici AR, Özgunaltay G, Dayangac B. A scanning electron microscopic study of different caries removal techniques on human dentin. Oper Dent 2002;27:360-366. 117. Yazici AR, Atilla P, Özgunaltay G, Muftuoglu S. In vitro comparison of the efficacy of Carisolv and conventional rotary instrument in caries removal. J Oral Rehab 2003;30:1177-1182. 118. Yazici AR, Baseren M, Gokalp S. The in vitro performance of laser fluorescence and caries-detector dye for detecting residual carious dentin during tooth preparation. Quintessence Int 2005;36:417-422. pyrig No Co t fo detector dyes in 119. Yip HK, Stevenson AG, Beeley JA. The specificity of caries rP cavity preparation. Br Dent J 1994;176:417-421. ub 120. Yip HK, Samaranayake LP. Caries removal techniques and instrumentalica tion: A review. Clin Oral Invest 1998;2:148-154. tio 121. Yonemoto K, Eguro T, Maeda T, Tanaka H. Application tof Diagnodent as a n e guide for removing carious dentin with Er:YAG laser. J Dent ss2006;34:269e nc e 276. ot Neves et al 122. Yoshiyama M, Urayama A, Kimochi T, Matsuo T, Pashley DH. Comparison of conventional vs self-etching adhesive bonds to caries-affected dentin. Oper Dent 2000;25:163-169. 123. Yoshiyama M, Tay FR, Doi J, Nishitani Y, Yamada T, Itou K, Carvalho RM, Nakajima M, Pashley DH. Bonding of self-etch and total-etch adhesives to carious dentin. J Dent Res 2002;81:556-560. 124. Yoshiyama M, Tay FR, Torii Y, Nishitani Y, Doi J, Itou K, Ciucchi B, Pashley DH. Resin adhesion to carious dentin. Am J Dent 2003;16:47-52. 125. Zheng L, Hilton JF, Habelitz S, Marshall SJ, Marshall GW. Dentin caries activity status related to hardness and elasticity. European J Oral Sci 2003;111:243-252. Clinical relevance: The bonding performance to carious dentin is directly related to the caries-excavation method and to the caries removal endpoint. Despite this, the bond strength achieved today to carious dentin using modern adhesives has shown major improvement. The Journal of Adhesive Dentistry Copyright of Journal of Adhesive Dentistry is the property of Quintessence Publishing Company Inc. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use.