Bioactive composites consist of pseudowollastonite and mullite synthesized from natural resources was developed for
bone implant applications. To realize such applications, a mechanical test of these composites and in vitro bioactivity in
SBF solution were studied. The present paper reports pseudowollastonite synthesized from the rice husk ash and limestone
reinforced with 10, 20 and 30 wt. % of mullite. Influence of sintering temperature, phase composition, morphology towards
mechanical properties of various pseudowollastonite-mullite (PSW-M) composites was examined prior to the bioactivity
test. It was found that pseudowollastonite with the addition of 20 wt. % of mullite sintered at 1150°C gave the best result
for diametral tensile strength (DTS) and hardness with the value of 8.8 ± 0.15 MPa and 3.79 ± 0.13 GPa, respectively.
The obvious increment in the mechanical strength was due to the formation of liquid phase CaAl2
O3
during sintering at
1150°C. In addition, the formation of fibrous apatite (HA) layer of amorphous calcium phosphate (ACP) with Ca/P ratio
1.8 on PSW20M sample confirmed the good bioactivity of the composite.
In this study, Adipose stem cells (ADSC) and bone marrow stem cells (BMSC), multipotent adult cells with the potentials for cartilage regenerations were induced to chondrogenic lineage and used for cartilage regenerations in surgically induced osteoarthritis in sheep model.
Recent advancement in cartilage tissue engineering has explored the potential of 3D culture to mimic the in vivo environment of human cartilaginous tissue. Three-dimensional culture using microspheres was described to play a role in driving the differentiation of mesenchymal stem cells to chondrocyte lineage. However, factors such as mechanical agitation on cell chondrogenesis during culture on the microspheres has yet to be elucidated. In this study, we compared the 2D and 3D culture of bone-marrow-derived mesenchymal stem cells (BMSCs) on gelatin microspheres (GMs) in terms of MSC stemness properties, immune-phenotype, multilineage differentiation properties, and proliferation rate. Then, to study the effect of mechanical agitation on chondrogenic differentiation in 3D culture, we cultured BMSCs on GM (BMSCs-GM) in either static or dynamic bioreactor system with two different mediums, i.e., F12: DMEM (1:1) + 10% FBS (FD) and chondrogenic induction medium (CIM). Our results show that BMSCs attached to the GM surface and remained viable in 3D culture. BMSCs-GM proliferated faster and displayed higher stemness properties than BMSCs on a tissue culture plate (BMSCs-TCP). GMs also enhanced the efficiency of in-vitro chondrogenesis of BMSCs, especially in a dynamic culture with higher cell proliferation, RNA expression, and protein expression compared to that in a static culture. To conclude, our results indicate that the 3D culture of BMSCs on gelatin microsphere was superior to 2D culture on a standard tissue culture plate. Furthermore, culturing BMSCs on GM in dynamic culture conditions enhanced their chondrogenic differentiation.