Therapeutic bioactive microcarriers: co-delivery of growth factors and stem cells for bone tissue engineering.

Novel microcarriers made of sol-gel-derived bioactive glasses were developed for delivering therapeutic molecules effectively while cultivating stem cells for bone tissue engineering. Silica sols with varying concentration of Ca (0-30 mol.%) were formulated into microspheres ranging from 200 to 300 µm under optimized conditions. A highly mesoporous structure was created, with mesopore sizes of 2.5-6.3 nm and specific surface areas of 420-710 m(2)g(-1), which was highly dependent on the Ca concentration. Therapeutic molecules could be effectively loaded within the mesoporous microcarriers during microsphere formulation. Cytochrome C (cyt C), used as a model protein for the release study, was released in a highly sustainable manner, with an almost zero-order kinetics over a period of months; the amount released was ~2% at 9 days, and 15% at 40 days. A slight increase in the release rate was observed in the microcarrier containing Ca, which was related to the dissolution rate and pore size. The presence of Ca accelerated the formation of hydroxyapatite on the surface of the microcarriers. Cells cultured on the bioactive microcarriers were well adhered and distributed, and proliferated actively, confirming the three-dimensional substrate role of the microcarriers. An in vivo study performed in a rat subcutaneous model demonstrated the satisfactory biocompatibility of the prepared microspheres. As a therapeutic target molecule, basic fibroblast growth factor (bFGF) was incorporated into the microcarriers. A slow release pattern similar to that of cyt C was observed for bFGF. Cells adhered and proliferated to significantly higher levels on the bFGF-loaded microcarriers, demonstrating the effective role of bFGF in cell proliferative potential. It is believed that the developed mesoporous bioactive glass microspheres represent a new class of therapeutic cell delivery carrier, potentially useful in the sustainable delivery of therapeutic molecules such as growth factors, as well as in the support of stem cell proliferation and osteogenesis for bone tissue engineering.

Preparation and characterization of antibacterial P2O5-CaO-Na2O-Ag2O glasses.

60P2O5-20CaO-(20-x) Na2O-xAg2O and 60P2O5-30CaO-(10-x) Na2O-xAg2O glasses, x = 0, 0.5,1, and 2 mol % were prepared using normal glass melting technique. The antibacterial activity of pressed disks of powdered glass (undoped and silver-doped glass) was investigated against S.aureus, P.aeruginosa, and E.coli micro-organisms using agar disk-diffusion assays at 37 °C for 24 h. The antibacterial activity was deduced from the inhibition zone diameter (IZD), zone of no bacterial growth, measured under the stated experimental conditions. The antibacterial activity increases with the increase in IZD and vice versa. Dissolution of glass in water at 37 °C, pH changes of water during glass dissolution, and concentrations of silver ions released from silver-doped glasses into water during their dissolution were determined. An increase in the concentration of silver ions released from silver-doped glasses into water was observed with increasing time of glass dissolution and with increasing Ag2O content. The tested silver-free and silver-doped glasses demonstrated different antibacterial activity against the tested micro-organisms. For silver-free glasses, an increase in IZD was observed with the increase in the glass dissolution rate and with the decrease in pH of water. Also, the IZD showed an increase with increasing Ag2O content of silver-doped glasses.