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Christian Hellmich

Publications and source records attributed to Christian Hellmich.

2 recordsLinked to original sources

'Universal' microstructural patterns in cortical and trabecular, extracellular and extravascular bone materials: micromechanics-based prediction of anisotropic elasticity.

Bone materials are characterized by an astonishing variability and diversity. Still, because of 'architectural constraints' due to once chosen material constituents and their physical interaction, the fundamental hierarchical organization or basic building plans of bone materials remain largely unchanged during biological evolution. Such universal patterns of microstructural organization govern the mechanical interaction of the elementary components of bone (hydroxyapatite, collagen, water; with directly measurable tissue-independent elastic properties), which are here quantified through a multiscale homogenization scheme delivering effective elastic properties of bone materials: at a scale of 10nm, long cylindrical collagen molecules, attached to each other at their ends by approximately 1.5nm long crosslinks and hosting intermolecular water inbetween, form a contiguous matrix called wet collagen. At a scale of several hundred nanometers, wet collagen and mineral crystal agglomerations interpenetrate each other, forming the mineralized fibril. At a scale of 5-10microm, the extracellular solid bone matrix is represented as collagen fibril inclusions embedded in a foam of largely disordered (extrafibrillar) mineral crystals. At a scale above the ultrastructure, where lacunae are embedded in extracellular bone matrix, the extravascular bone material is observed. Model estimates predicted from tissue-specific composition data gained from a multitude of chemical and physical tests agree remarkably well with corresponding acoustic stiffness experiments across a variety of cortical and trabecular, extracellular and extravascular materials. Besides from reconciling the well-documented, seemingly opposed concepts of 'mineral-reinforced collagen matrix' and 'collagen-reinforced mineral matrix' for bone ultrastructure, this approach opens new possibilities in the exploitation of computer tomographic data for nano-to-macro mechanics of bone organs.

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Can the diverse elastic properties of trabecular and cortical bone be attributed to only a few tissue-independent phase properties and their interactions? Arguments from a multiscale approach.

As candidates for tissue-independent phases of cortical and trabecular bone we consider (i) hydroxyapatite, (ii) collagen, (iii) ultrastructural water and non-collagenous organic matter, and (iv) marrow (water) filling the Haversian canals and the intertrabecular space. From experiments reported in the literature, we assign stiffness properties to these phases (experimental set I). On the basis of these phase definitions, we develop, within the framework of continuum micromechanics, a two-step homogenization procedure: (i) at a length scale of 100-200 nm, hydroxyapatite (HA) crystals build up a crystal foam ("polycrystal"), and water and non-collagenous organic matter fill the intercrystalline space (homogenization step I); (ii) at the ultrastructural scale of mineralized tissues (5-10 microns), collagen assemblies composed of collagen molecules are embedded into the crystal foam, acting mechanically as cylindrical templates. At an enlarged material scale of 5-10 mm, the second homogenization step also accommodates the micropore space as cylindrical pore inclusions (Haversian and Volkmann canals, inter-trabecular space) that are suitable for both trabecular and cortical bone. The inputs for this micromechanical model are the tissue-specific volume fractions of HA, collagen, and of the micropore space. The outputs are the tissue-specific ultrastructural and microstructural (=macroscopic=apparent) elasticity tensors.A second independent experimental set (composition data and experimental stiffness values) is employed to validate the proposed model. We report a small mean prediction error for the macroscopic stiffness values. The validation suggests that hydroxyapatite, collagen, and water are tissue-independent phases, which define, through their mechanical interaction, the elasticity of all bones, whether cortical or trabecular.

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