Search

Magnetic materials inside bone scaffolds are known to be a promoting factor for bone healing especially when the therapy is accompanied by application of external magnetic stimulation. In this study we employed a new route to synthesize iron oxide nanoparticles inside hydroxyapatite/chitosan bone scaffolds. Hydroxyapatite and chitosan are both natural compounds and were prepared from bovine cortical bone and shrimp shell, respectively. The morphology and composition of the synthesized materials were characterized employing scanning electron microscopy and FTIR spectroscopy. The iron oxide mean particle size inside the scaffold matrix was estimated to be in the range of 10–40 nm by particle size analyzer and transmission electron microscopy. The X-ray powder diffraction pattern indicated that the magnetite crystal size was about 23.5 nm. Magnetic measurements specified that the saturated magnetic intensity ( M s ) was approximately 3.04 emu/g and the coercive force was 128.39 Oe. The results revealed that the as-prepared magnetite was super-paramagnetic. [ABSTRACT FROM AUTHOR]

The main goal of this research was the preparation and evaluation of the mechanical properties, in vitro biodegradability and cytocompatibility, of natural chitosan/hydroxyapatite/nano magnetite (nano-Fe 3 O 4 ) composite. Different ratios of these components were investigated, including chitosan/hydroxyapatite: 4/4 (S1), chitosan/hydroxyapatite: 4/6 (S2), and chitosan/hydroxyapatite: 6/4 (S3). Mechanical properties of fabricated composites were examined using bending and compression tests before immersion, and after 2 and 9 weeks of immersion in the Ringer's solution. Scanning electron microscope (SEM) was employed for observing the bending fracture surface and analyzing the degradation morphology. Human mesenchymal stem cells (hMSC) were also cultured on the samples in order to assess the cytocompatibility. The obtained results revealed that S1 had the highest bending strength before immersion, while S3 had the highest bending strength after 9 weeks immersion. Compressive strength of S2 was greater than that of S1 and S3 not only before immersion, but also after 9 weeks immersion. Although the bio-minerals were deposited on the surface of all samples during the immersion in Ringer's solution, S2 appeared to have the highest quantity of bio-minerals. According to the weight loss percentage (ΔW(%)), the biodegradation resistance of S1 was the lowest. Finally, the cytocompatibility of S1 was greater than that of S2 and S3. [ABSTRACT FROM AUTHOR]