4. Discussion
The goal of our study was to better understand the links between the mechanical properties of the human cortical bone surface and human osteoclast mediated resorption. To date, the vast majority of in vitro studies on osteoclast mediated bone degradation have been performed using cortical bovine bone, dentin or biomaterials, which provide relatively homogeneous surfaces [27–29]. In contrast, the human haversian cortical bone microstructure is composed of osteonal units [30] derived from the remodeling process, implying osteoclast activity. The elastic modulus and mineral content were shown to be almost constant inside the same osteon, but variable across osteons [16, 31 and 32]. The hardest tissues inside the microstructure are interstitial tissues that are mainly composed of the remains of aging osteons [33].