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Despite substantial clinical interest in the frac- ture resistance of human dentin, there is little mechanistic information in archival literature that can be usefully used to model such fracture. In fact, although the fracture event in dentin, akin to other mineralized tissues like bone, is widely believed to be locally strain-controlled, there has never been any scientific proof to support this belief. The present study seeks to address this issue through the use of a novel set of in vitro experiments in Hanks' balanced salt solution involv- ing a double-notched bend test geometry, which is designed to discern whether the critical failure events involved in the onset of fracture are locally stress- or strain-controlled. Such experiments are further used to characterize the notion of "plasticity" in dentin and the interaction of cracks with the salient microstructural features. It is observed that fracture in dentin is indeed locally strain-controlled and that the presence of dentinal tubules does not substantially affect this process of crack initiation and growth. The results pre- sented are believed to be critical steps in the development of a micromechanical model for the fracture of human dentin that takes into consideration the influence of both the mi- crostructure and the local failure mode. © 2003 Wiley Peri- odicals, Inc. J Biomed Mater Res 67A: 484 - 495, 2003

Dentin structure and properties are known to vary with orientation and location. The present study explored the variation in the ultimate tensile strength (UTS) of dentin with location in the tooth. Hourglass specimens were prepared from dentin located in the center, under cusps, and in the cervical regions of human molar teeth. These were tested in tension at various distances from the pulp. Median tensile strengths ranged from 44.4 MPa in the inner dentin near the pulp, to 97.8 MPa near the dentino-enamel junction (DEJ). This increase in the median UTS with distance from the pulp to the DEJ was statistically significant (P

Using an atomic force microscope (AFM) with an attachment specifically designed for indentation, we measured the mechanical properties of demineralized human dentin under three conditions: in water, in air after desiccation, and in water after rehydration. The static elastic modulus (E(h)r = 134 kPa) and viscoelastic responses (tau(epsilon) = 5.1 s and tau(sigma) = 6.6 s) of the hydrated, demineralized collagen scaffolding were determined from the standard linear solid model of viscoelasticity. No significant variation of these properties was observed with location. On desiccation, the samples showed considerably larger elastic moduli (2 GPa), and a hardness value of 0.2 GPa was measured. Upon rehydration the elastic modulus decreased but did not fully recover to the value prior to dehydration (381 kPa).

Dentin conditioners provide a microporous surface for penetration by bonding agents. This study used an atomic force microscope (AFM) to examine the initial steps in the conditioning process of dentin using three demineralizing agents, 0.5 M EDTA, and dilute solutions of phosphoric (3mM, 6mM) and citric (5 mM) acids, in order to establish the relationships between demineralization and changes in surface morphology. Polished dentin disks had a 10-nm-thick gold pattern applied which served as a height reference. Samples(n = 3/agent) were examined at baseline and at 2-s intervals for up to 120 s for each agent. EDTA (0.5 M) was used as received; other conditioners were diluted to slow the rates of demineralization for detailed study. The surfaces of the peritubular and intertubular regions were altered differently. Initially subsidence rates were equal and linear, but after a 100-nm depth change the intertubular rates decreased. For phosphoric acid and citric acid, the movement of the intertubular surface was uniform and the surfaces remained smooth. However, the intertubular surfaces were rough for the EDTA treatment. The surface subsidence reached a plateau after a depth change of about 0.5μm, which resulted from a limit to the contraction of the demineralized and hydrated collagen scaffold. © 1995 John Wiley & Sons, Inc.