Premium
Fracture toughness of human dentin
Author(s) -
Iwamoto Nanako,
Ruse N. Dorin
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.10005
Subject(s) - dentin , materials science , composite material , molar , anisotropy , fracture toughness , perpendicular , dentinal tubule , transverse plane , fracture (geology) , anatomy , geometry , optics , dentistry , medicine , physics , mathematics
The purpose of this study was to determine the fracture toughness ( K IC ) of human dentin and to test the null hypothesis that K IC is not affected by the orientation of dentinal tubules relative to the plane of crack propagation. Triangular prisms (4 × 4 × 4 × 8 mm) were obtained from human molars and tested using the notchless triangular prism (NTP) specimen K IC test. Dentin prisms were prepared so that the plane of crack propagation would have three different orientations relative to the orientation of dentinal tubules: perpendicular ( PE ), parallel aligned ( PAA ), and parallel transverse ( PAT ). The prepared specimens were secured in the specimen holder and loaded in tension until fracture or crack arrest. The maximum load recorded was used to calculate K IC . There was no significant difference between the K IC of PAA specimens (1.97 ± 0.17 MPa/m 1/2 ) and PAT (2.02 ± 0.18 MPa/m 1/2 ). The K IC for the PE specimens (1.13 ± 0.36 MPa/m 1/2 ) was significantly lower. The SEM images of the fractured surfaces showed distinct differences that were correlated with the determined K IC values. The fractured surfaces of PAA and PAT specimens were rougher compared to PE specimens. Both the hyper mineralized peritubular dentin and the orientation of collagen fibrils surrounding the tubules could be responsible for the significant differences in K IC . The results of this study identified a significant anisotropy of dentin with respect to its K IC . © 2003 Wiley Periodicals, Inc. J Biomed Mater Res 66A: 507–512, 2003