The evaluation of four conditioners for glass ionomer cements using field-emission scanning electron microscopy
Introduction
One of the features of glass ionomer cements (GICs) is that they are able to bond physico-chemically to tooth structure without any pretreatment of the surface [1], [2], [3]. However, conditioning of the tooth surface prior to the application of GICs has been reported to improve the bond strength [1], [4], [5], [6], [7], [8]. The objective of conditioning is to remove surface contaminants and the smear layer, which may limit the bond of the GIC to tooth structure, particularly the dentine [9], [10], [11]. It has been shown that laboratory bond strength results may be affected by the method of applying the conditioners, concentration of conditioners, duration of conditioning, material used and the nature of the pre-prepared surface [6], [12], [13], [14], [15], [16].
When a conditioning agent has been used in conjunction with a GIC, bond strength studies have been used as a preliminary evaluation of the adhesive strength. The microtensile bond strengths of GICs to human dentine using the conditioners in this study have been reported in a previous article [16], and the results seemed material dependent. On the other hand, studies on the ultramorphological structure of the adhesive interface are able to provide information regarding the interaction of a GIC with the tooth substrate [17]. Two preparation techniques have generally been used for scanning electron microscopy (SEM); the fractured specimen technique and the acid-base treatment technique [18]. With the use of a Field-Emission Scanning Electron Microscope (FE-SEM), better characterization of the ultramorphological interface is possible due to the enhanced resolution and reduced voltage which lessens damage to specimen surfaces [19], [20], [21]. However, few studies with GIC using the FE-SEM have been reported using these two techniques.
The Atomic Force Microscope (AFM) is a high resolution instrument which has been widely used to observe dentine in a wet environment [22], [23], [24], [25], [26], [27]. This tool allows the examination of specimens without the need for irreversible specimen processing which has the potential to cause distortion and subsequent artefacts [28]. However, limited AFM data are available which describe the morphology of dentine surfaces treated with commercial dentine conditioners used for GICs.
The aim of this study was to evaluate the GIC-dentine interface morphology after the use of four conditioners (Ketac Conditioner, ESPE Germany; Dentin Conditioner, GC International, Japan; Cavity Conditioner, GC International, Japan; and an experimental conditioner K-930, GC International, Japan) in conjunction with two resin-modified GICs (RM-GICs) (Photac-Fil Quick, ESPE, Germany; and capsulated Fuji II LC, GC International, Japan) and one self-cured GIC (capsulated Fuji IX GP, GC International, Japan) using a FE-SEM and AFM.
Section snippets
Sample preparation for FE-SEM
Twenty-four dentine discs were obtained from superficial occlusal dentine of freshly extracted human third molars kept in a saline solution containing thymol. The specimens were polished and finished with wet-600 grit SiC paper, and randomly allocated to three groups of eight discs; one group of eight discs for each of the GICs (Table 1). Each group of eight discs was randomly divided into four subgroups of two discs; one subgroup was used for each conditioner and treated according to the
FE-SEM images
The FE-SEM observations of the GIC-dentine interfaces are illustrated in the scanning electron micrographs shown in Fig. 1, Fig. 2, Fig. 3, Fig. 4.
For the non-conditioned specimens, all samples showed intimate adaptation of the GICs to the underlying dentine. All fractured specimens showed the smear layer had occluded the dentinal tubules [Fig. 1(a)]. All acid-base treated specimens showed a cement matrix-dentine interdiffusion zone or ‘ion exchange layer’. This layer was resistant to the
Discussion
Although the mechanism of adhesion of self-cured GICs to tooth structure is not completely understood, it is believed that it is achieved through adsorption and diffusion and ionic exchange between the mineral components of tooth structure and the organic components of the GIC [29], [30], [31], [32]. The initial stage is a weak hydrogen bond due to polar attraction between the cut tooth and freshly placed cement. At this stage, the acidity of the cement allows it to act as a self-demineralizing
Acknowledgements
This research was supported by the University of Melbourne, School of Dental Science Research Committee Grant. The assistance of Jocelyn Carpenter, School of Botany, The University of Melbourne, with FE-SEM imaging is also greatly appreciated.
References (45)
- et al.
Dentine smear layer: an asset or liability for bonding?
Dental Materials
(1989) - et al.
Glass ionomer bond strength and treatment of dentin with polyacrilic acid
Journal of Prosthetic Dentistry
(1991) - et al.
Bond strength to dentine of two light-activated glass polyalkenoate (ionomer) cements
Journal of Dentistry
(1994) - et al.
Microtensile bond strengths of glass ionomer (polyalkenoate) cements to dentine using four conditioners
Journal of Dentistry
(2000) - et al.
Effect of phosphoric acid concentration on wet bonding to etched dentin
Dental Materials
(1996) - et al.
Morphological field-emission SEM study of the effect of six phosphoric acid etching agents on human dentin
Dental Materials
(1996) - et al.
Atomic force microscope study of dimensional changes in dentine during drying
Archives of Oral Biology
(1993) - et al.
Atomic microscopy of acid effects on dentin
Dental Materials
(1993) - et al.
Dentin demineralization: effects of dentin depth, pH and different acids
Dental Materials
(1997) - et al.
Surface fine structure of treated dentine investigated with tapping mode atomic force micrscopy (TMAFM)
Journal of Dentistry
(1999)
X-ray photoelectron spectroscopy study of the dentin-glass ionomer cement interface
Dental Materials
The bonding of glass ionomer cement to metal and tooth substrate
British Dental Journal
The clinical development of the glass-ionomer cements. I. Formulations and properties
Australian Dental Journal
Cavity sealing ability of composite and glass ionomer cement restorations. An assessment in vivo
British Dental Journal
Increased bonding of a glass ionomer cement by means of FeCl3
Scandinavian Journal of Dental Reserach
Improved adhesion of a glass ionomer cement to dentin and enamel
Journal of Dental Reserach
Effect of dentinal pretreatment on bond strength between glass ionomer cement and dentin
Operative Dentistry
Dentin surface treatment and bond strength of glass ionomer cement
American Journal of Dentistry
Effect of surface treatment on microleakage and tensile bond strength of glass polyalkenoate cement
Japanese Journal of Conservative Dentistry
Smear layer: morphological considerations
Operative Dentistry
Smear layer: physiological considerations
Operative Dentistry
Influence of dentine surface treatments on the bond strength of dentin lining cements
Operative Dentistry
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