Study of indentation of a sample equine bone using finite element simulation and single cycle reference point indentation.
Abstract: In an attempt to study the mechanical behavior of bone under indentation, methods of analyses and experimental validations have been developed, with a selected test material. The test material chosen is from an equine cortical bone. Stress-strain relationships are first obtained from conventional mechanical property tests. A finite element simulation procedure is developed for indentation analyses. The simulation results are experimentally validated by determining (1) the maximum depth of indentation with a single cycle type of reference point indentation, and (2) the profile and depth of the unloaded, permanent indentation with atomic force microscopy. The advantage of incorporating in the simulation a yield criterion calibrated by tested mechanical properties, with different values in tension and compression, is demonstrated. In addition, the benefit of including damage through a reduction in Young's modulus is shown in predicting the permanent indentation after unloading and recovery. The expected differences in response between two indenter tips with different sharpness are predicted and experimentally observed. Results show predicted indentation depths agree with experimental data. Thus, finite element simulation methods with experimental validation, and with damage approximation by a reduction of Young's modulus, may provide a good approach for analysis of indentation of cortical bone. These methods reveal that multiple factors affect measured indentation depth and that the shape of the permanent indentation contains useful information about bone material properties. Only further work can determine if these methods or extensions to these methods can give useful insights into bone pathology, for example the bone fragility of thoroughbred racehorses.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication Date: 2014-11-29 PubMed ID: 25528690DOI: 10.1016/j.jmbbm.2014.11.020Google Scholar: Lookup
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- Journal Article
- Research Support
- N.I.H.
- Extramural
- Research Support
- U.S. Gov't
- Non-P.H.S.
Summary
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This is a study aiming to understand the mechanical behaviour of bone under stress using finite element simulation and experimental validation. The chosen sample is from equine cortical bone. The study validated its findings through simulations and experiments, showing this method’s potential to provide useful insights into bone pathology like bone fragility.
Methods and Materials
- The study elected equine cortical bone as the test material. The choice of material was influenced by its close resemblance to human bone and its applicability to studying bone pathologies like bone fragility.
- The researchers utilised conventional mechanical property tests to first deduce the stress-strain relationships of the equine cortical bone.
- They developed finite element simulation procedures for indentation analyses, which is a technique used to determine the mechanical properties of materials through the application of a concentrated load.
Validation of Simulation Results
- The validity of the simulations was substantiated through experiments involving two operations: (1) Determining the maximum depth of indentation using a procedure called single cycle type of reference point indentation. (2) Identifying the profile and depth of the unloaded, permanent indentation using atomic force microscopy, a tool to measure forces at the nanoscale.
- The inclusion of a yield criterion in the simulation, calibrated by the tested mechanical properties with distinct values in tension and compression, was exemplified.
- Demonstration of the value of damage consideration through a reduction in a mechanical property known as Young’s modulus (which measures the stiffness of a material) was given in predicting the permanent indentation after unloading and recovery.
Results and Conclusion
- Results showed that the predicted indentation depths agree with experimental data, reinforcing the effectiveness of the finite element simulation methods along with experimental validation.
- The study also revealed that indentation depth is affected by multiple factors and the shape of the permanent indentation contains valuable information about the bone material properties.
- In conclusion, these methods could potentially offer valuable insights into bone pathology. Nevertheless, further research is required to ascertain whether these methods and extensions can give valuable insights into specific bone pathologies like the bone fragility of thoroughbred racehorses.
Cite This Article
APA
Hoffseth K, Randall C, Hansma P, Yang HT.
(2014).
Study of indentation of a sample equine bone using finite element simulation and single cycle reference point indentation.
J Mech Behav Biomed Mater, 42, 282-291.
https://doi.org/10.1016/j.jmbbm.2014.11.020 Publication
Researcher Affiliations
- Department of Mechanical Engineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA. Electronic address: kevhoffseth@engineering.ucsb.edu.
- Department of Mechanical Engineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
- Department of Physics, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
- Department of Mechanical Engineering, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
MeSH Terms
- Animals
- Biomechanical Phenomena
- Finite Element Analysis
- Horses
- Materials Testing / instrumentation
- Materials Testing / methods
- Mechanical Phenomena
- Metacarpal Bones
- Stress, Mechanical
Grant Funding
- R01 GM055354 / NIGMS NIH HHS
Citations
This article has been cited 2 times.- Chang A, Easson GW, Tang SY. Clinical measurements of bone tissue mechanical behavior using reference point indentation.. Clin Rev Bone Miner Metab 2018 Sep;16(3):87-94.
- Diez-Perez A, Bouxsein ML, Eriksen EF, Khosla S, Nyman JS, Papapoulos S, Tang SY. Technical note: Recommendations for a standard procedure to assess cortical bone at the tissue-level in vivo using impact microindentation.. Bone Rep 2016 Dec;5:181-185.
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