Extrafibrillar matrix yield stress and failure envelopes for mineralised collagen fibril arrays.

Bone metabolic diseases such as osteoporosis constitute a major socio-economic challenge. A detailed understanding of the structure-property relationships of bone's underlying hierarchical levels has the potential to improve diagnosis and the ability to treat those diseases, especially with regards to the onset of failure. Therefore, elastic and yield properties of mineralised turkey leg tendon (MTLT), a mineralised tissue that is similar to bone but has a simpler multiscale structure, were investigated. Elastic properties were identified using a multiscale micromechanical model. The input parameters include constituent mechanical properties, volume fractions and inclusion aspect ratios and these were obtained from a wide variety of literature sources. The determined elastic properties were used to formulate micromechanically informed yield surfaces and to identify yield properties of MTLT at the nanometre length scale where failure is first reported to occur. This was done in conjunction with experimental results from the compression of micropillars extracted from individual mineralised collagen fibres. This data was then used to identify micromechanically informed failure envelopes. The shear yield stress of the extrafibrillar matrix, associated with interfibrillar sliding, was identified as 137.65 MPa. The ratio between tensile and compressive yield stress in the Drucker-Prager yield criterion was 0.65. For both criteria apparent yield stress of the mineralised collagen fibril decreased to 25.3-31.4% when varying fibril orientation from 0° to 90°. This study identified yield properties of extrafibrillar matrix using an aligned mineralised tissue. The ability to obtain yield stress data and unloading stiffness from micropillar compression tests of MTLT at the level of the mineralised collagen fibril array and downscaling these into the EM mitigates against possible errors associated with macroscopic stiffness predictions and proved to be an invaluable advantage compared to similar modelling approaches. Results may help to improve computational models that may then be used in pre-clinical testing or development of personalised treatment strategies.

Mechanical properties of cortical bone and their relationships with age, gender, composition and microindentation properties in the elderly.

The growing incidence of skeletal fractures poses a significant challenge to ageing societies. Since a major part of physiological loading in the lower limbs is carried by cortical bone, it would be desirable to better understand the structure-mechanical property relationships and scale effects in this tissue. This study aimed at assessing whether microindentation properties combined with chemical and morphological information are usable to predict macroscopic elastic and strength properties in a donor- and site-matched manner. Specimens for quasi-static macroscopic tests in tension, compression, and torsion and microindentation were prepared from a cohort of 19 male and 20 female donors (46 to 99 years). All tests were performed under fully hydrated conditions. The chemical composition of the extra-cellular matrix was investigated with Raman spectroscopy. The results of the micro-mechanical tests were combined with morphological and compositional properties using a power law relationship to predict the macro-mechanical results. Microindentation properties were not gender dependent, remarkably constant over age, and showed an overall small variation with standard deviations of approximately 10 %. Similar results were obtained for chemical tissue composition. Macro-mechanical stiffness and strength were significantly related to porosity for all load cases (p<0.05). In case of macroscopic yield strain and work-to-failure this was only true in torsion and compression, respectively. The correlations of macro-mechanical with micro-mechanical, morphological, and chemical properties showed no significance for cement line density, mineralisation, or variations in the microindentation results and were dominated by porosity with a moderate explanatory power of predominately less than 50 %. The results confirm that age, with minor exceptions gender, and small variations in average mineralisation have negligible effect on the tissue microindentation properties of human lamellar bone in the elderly. Furthermore, our findings suggest that microindentation experiments are suitable to predict macroscopic mechanical properties in the elderly only on average and not on a one to one basis. The presented data may help to form a better understanding of the mechanisms of ageing in bone tissue and of the length scale at which they are active. This may be used for future prediction of fracture risk in the elderly.