Bone tissue engineering is an emerging interdisciplinary field in Science, combining expertise in medicine, material science and biomechanics. Hard tissue engineering research is focused mainly in two areas, osteo and dental clinical applications. There is a lot of exciting research being performed worldwide in developing novel scaffolds for tissue engineering. Although, nowadays the majority of the research effort is in the development of scaffolds for non-load bearing applications, primarily using soft natural or synthetic polymers or natural scaffolds for soft tissue engineering; metallic scaffolds aimed for hard tissue engineering have been also the subject of in vitro and in vivo research and industrial development. In this article, descriptions of the different manufacturing technologies available to fabricate metallic scaffolds and a compilation of the reported biocompatibility of the currently developed metallic scaffolds have been performed. Finally, we highlight the positive aspects and the remaining problems that will drive future research in metallic constructs aimed for the reconstruction and repair of bone.

The formation of hollow metal oxide nanoparticles through the oxidation process at low temperatures from 295 to 423 K has been studied by transmission electron microscopy for Cu, Al, and Pb. For Cu and Al, hollow oxide nanoparticles are obtained as a result of vacancy aggregation in the oxidation processes, resulting from the rapid outward diffusion of metal ions through the oxide layer during the oxidation process. On the other hand, Pb nanoparticles turn to solid PbO because the diffusivity difference $D_{\text{Pb}}<D_{\text{O}}$ in PbO does not lend itself to the formation of vacancy clusters. The oxide growth behavior of Cu and Al nanoparticles of a larger size at 423 K are summarized as follows: (i) for Al, the rapidly forming oxide layer on its surface stops growing once it reaches a critical thickness of about 1.5 nm, (ii) the growth of ${\text{Cu}}_2\text{O}$ continues until hollow ${\text{Cu}}_2\text{O}$ of a certain thickness is formed. This suggests the occurrence of two different diffusion processes in the formation of hollow oxides: the rapid outward diffusion of metal ions based on the Cabrera–Mott theory plays an important role in the formation of hollow Al-oxides, whereas the Kirkendall effect at the $\text{Cu}∕{\text{Cu}}_2\text{O}$ interface, where Cu diffuses much faster than oxygen, brings about the formation of hollow ${\text{Cu}}_2\text{O}$ .

The oxidation behaviour of Ni nanoparticles at temperatures from 573 to 673 K and the formation process of hollow oxide particles were studied by transmission electron microscopy. In the course of oxidation, a single large void was observed at one site of the interface between inner Ni and outer NiO layer due to vacancy clustering, which occurs during the oxidation process resulting from the rapid outward diffusion of Ni ions through the NiO layer. This suggests that supersaturated vacancies generated at the interface migrate to the site over a long-range distance and aggregate at the site. Ni nanoparticles were fully oxidized to become hollow NiO, in which nano-holes in the form of vacancy clusters were located at the off-centred positions. The de-centring of the voids in hollow NiO is probably due to the large mobility of vacancies inside Ni during oxidation.