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Fatigue crack propagation path across the dentinoenamel junction complex in human teeth
Author(s) -
Dong X. D.,
Ruse N. D.
Publication year - 2003
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.10541
Subject(s) - materials science , dentin , enamel paint , composite material , fracture toughness , human tooth , scanning electron microscope , toughness , fracture mechanics
The human tooth structures should be understood clearly to improve clinically used restorative materials. The dentinoenamel junction (DEJ) plays a key role in resisting crack propagation in teeth. The aim of this study was to determine the fracture toughness of the enamel‐DEJ‐dentin complex and to investigate the influence of the DEJ on the fatigue crack propagation path across it by characterizing fatigue‐fractured enamel‐DEJ‐dentin complexes using optical and scanning electron microscopy. The results of this study showed that the fracture toughness of the enamel‐DEJ‐dentin complex was 1.50 ± 0.28 Mpa·m 1/2 . Based on the results of this investigation, it was concluded that the DEJ complex played a critical role in resisting crack propagation from enamel into dentin. The DEJ complex is, approximately, a 100 to 150 μm broad region at the interface between enamel and dentin. The toughening mechanism of the DEJ complex may be explained by the fact that crack paths were deflected as cracks propagated across it. Understanding the mechanism of crack deflection could help in improving dentin‐composite as well as ceramic‐cement interfacial qualities with the aim to decrease the risk of clinical failure of restorations. Both can be viewed as being composed from a layer of material of high strength and hardness bonded to a softer but tougher substratum (dentin). The bonding agent or the luting cement layer may play the critical role of the DEJ in improving the strength of these restorations in clinical situations. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res 66A: 103–109, 2003

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