Mechanics of cortical bone: exploring the micro- and nano-scale
File(s)
Author(s)
Rodriguez Florez, Naiara
Type
Thesis
Abstract
This PhD aimed at characterising mechanical, structural and compositional properties
of cortical bone at the micro- and nano-scale employing various techniques applied to
mouse models of ageing and disease.
Nanoindentation was used to probe bone at the micro-scale. Nanoindentation properties
of the same control mouse bones were measured using a range of preparation, testing
and analysis options. This was the first time that such systematic study was conducted.
It was concluded that although the measured values were influenced by experimental
and analysis choices, nanoindentation was capable of capturing relative trends in bone’s
mechanical properties.
Nanoindentation was then coupled to a poroelastic approach to measure age-related
changes in mouse bone permeability. Permeability is key to understanding fluid flow in
bone, which may indicate how bone cells sense changes in the mechanical
environment. These first permeability measurements in mouse bone demonstrated that
the permeability caused by fluid flowing through bone’s lacunar-canalicular porosity
decreases with age.
Porosity is expected to also affect bone’s ability to resist fracture at the micro-scale.
The influence of intra-cortical porosity on crack propagation was explored via extended
finite element methods. A novel technique was suggested to propagate cracks through
holes and applied to 2D models of the porosity of osteogenesis imperfecta mouse bone.
Results showed that vascular canals affect crack propagation and might contribute to
the brittleness of osteogenesis impefecta bone.
Skeletal pathologies often cause alterations in bone’s building blocks leading to
deteriorated whole-bone toughness. Mineral properties of brittle and ductile mouse
bone (models of osteogenesis imperfecta and rickets respectively) were evaluated.
Results revealed that deviations in size, composition and organisation of bone mineral
reduce bone’s mechanical integrity both in brittle and ductile pathologic bone.
The outcomes of this thesis provide a deeper understanding of bone material, which is
required for future improvements in treatments for skeletal diseases.
of cortical bone at the micro- and nano-scale employing various techniques applied to
mouse models of ageing and disease.
Nanoindentation was used to probe bone at the micro-scale. Nanoindentation properties
of the same control mouse bones were measured using a range of preparation, testing
and analysis options. This was the first time that such systematic study was conducted.
It was concluded that although the measured values were influenced by experimental
and analysis choices, nanoindentation was capable of capturing relative trends in bone’s
mechanical properties.
Nanoindentation was then coupled to a poroelastic approach to measure age-related
changes in mouse bone permeability. Permeability is key to understanding fluid flow in
bone, which may indicate how bone cells sense changes in the mechanical
environment. These first permeability measurements in mouse bone demonstrated that
the permeability caused by fluid flowing through bone’s lacunar-canalicular porosity
decreases with age.
Porosity is expected to also affect bone’s ability to resist fracture at the micro-scale.
The influence of intra-cortical porosity on crack propagation was explored via extended
finite element methods. A novel technique was suggested to propagate cracks through
holes and applied to 2D models of the porosity of osteogenesis imperfecta mouse bone.
Results showed that vascular canals affect crack propagation and might contribute to
the brittleness of osteogenesis impefecta bone.
Skeletal pathologies often cause alterations in bone’s building blocks leading to
deteriorated whole-bone toughness. Mineral properties of brittle and ductile mouse
bone (models of osteogenesis imperfecta and rickets respectively) were evaluated.
Results revealed that deviations in size, composition and organisation of bone mineral
reduce bone’s mechanical integrity both in brittle and ductile pathologic bone.
The outcomes of this thesis provide a deeper understanding of bone material, which is
required for future improvements in treatments for skeletal diseases.
Version
Open Access
Date Issued
2015-01
Date Awarded
2015-05
Copyright Statement
Attribution NoDerivatives 4.0 International Licence (CC BY-ND)
Advisor
Shefelbine, Sandra
Saiz Gutierrez, Eduardo
Nowlan, Niamh
Sponsor
Basque Country (Spain)
Publisher Department
Bioengineering
Publisher Institution
Imperial College London
Qualification Level
Doctoral
Qualification Name
Doctor of Philosophy (PhD)