Document Type : Regular Article


1 Chemical Engineering Department, Faculty of Engineering, Azarbaijan Shahid Madani University, Tabriz, Iran

2 Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran



Bone tissue engineering require approaches to provide a suppression/promotion environment for bone growth. Scaffold biomaterials have profound regulatory effects on the functionality of mesenchymal stem cells (MSCs). In the present study, three-component bioceramic of selenium/reduced graphene oxide/hydroxyapatite (Se/RGO/HA) was developed and its performance to repair bone defects was compared to HA. The Se/RGO/HA nanocomposite scaffold was synthesized using the chemical bath technique, characterized by X-ray diffraction spectra, Field emission scanning electron microscope, Energy dispersion X-ray spectrometer, and Fourier transform infrared spectroscopy analyses. Human adipose-derived MSCs (hAD-MSCs) were used to investigate the in-vitro osteogenic properties of Se/RGO/HA scaffold. The effect of combined scaffold on cell proliferation was analyzed by MTT assay. Cell adhesion behaviors was evaluated using optical microscopy and SEM. The osteogenic properties of Se/RGO/HA scaffold was examined by the measurement of alkaline phosphatase (ALP) activity and western blotting technique.
The hAD-MSCs proliferation for HA, Se/RGO/HA nanocomposite were 2±0.1 and 1.1±0.05 respectively. The Se/RGO/HA nanocomposite had cytotoxic effect of on the KHOS-240S cancer cells . Additionally, good cell attachment and osteoblast-like morphology were characterized on the designed scaffold. The ALP activity and mineralization potential of cells seeded on Se/RGO/HA were higher than those seeded on HA. The Osteocalsin protein for Se/RGO/HA and HA were 64±1 and 12±0.1 respectively. Furthermore, the expression of Osteocalcin, a bone-specific protein, was synergistically increased by incorporation of Se and RGO into HA. In conclusion, the presence of RGO inside the Se could significantly increase positive effects of HA on the osteogenic potential of hAD-MSCs.


Main Subjects