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Bioactive borosilicate glasses having weight composition (74-X) SiO2, 16 Na2O, 10 B2O3 and (X) V2O5 (wt%), where (X = 0, 0.1, 0.3, 0.5, 1, 2.5, 4 wt %) were synthesized using the conventional melting procedure. Bioactive glass samples were melted in a platinum crucible of 50 ml capacity at 1400 °C in the globular furnace with air as the furnace atmosphere and kept hold for 2 h. These glasses were characterised and tested by using several experiment techniques like XRD, FTIR, SEM and EDX. The bioactivity of the borosilicate samples was determined by submerging them in simulated body fluid (SBF) for different time intervals. The developed hydroxy apatite (HA) was identified by FTIR, XRD, SEM and EDX technique. The obtained results demonstrate that the in-vitro bioactivity of the samples increases with the increase in V2O5 doping in samples. Various properties like density, compressive strength and electrical properties are determined. Physical and mechanical properties are improved after V2O5 doping. Electrical properties are improved after SBF doping, and the result shows the ion movement due to increased bioactivity. The in-vitro hemocompatibility and cellular compatibility on MG-63 cell lines were carried out. It was found that samples were compatible with human blood. Cellular proliferation is increased with increasing concentration of V2O5. However beyond 0.5% V2O5 doping the value of bioactivity decreases at higher concentrations of samples in culture media. [ABSTRACT FROM AUTHOR]

Bioglass® (45S5) was prepared by conventional melting process and hydroxyapatite (HA) was prepared by sol-gel method. The bioglass (45S5) and hydroxyapatite (Ca10(PO₄)₆(OH)₂) samples were mixed in a particular proportion to prepare composite by using hydraulic pressing. Based on thermogravimetric and differential thermal analysis, the composite were sintered with a suitable heat treatment process at 1000-1050 °C. The in-vitro bioactivity of samples was determined in simulated body fluid for 1, 3, 7, 14 and 21 days. The bioactivity was examined in vitro with respect to the ability of hydroxyapatite layer formation on the surface of samples when they were immersed in simulated body fluid (SBF). DTA/TGA, XRD, SEM and mechanical studies were conducted for different characteristic measurement of biocomposites. The result shows the enhancement in bioactivity and mechanical properties of (45S5-HA) biocomposites for clinical implantation.

We developed ZnO‐assisted 1393 bioactive glass‐based scaffold with suitable mechanical properties through foam replica technique and observed to be suitable for bone tissue engineering application. However, the developed scaffolds' ability to facilitate cellular infiltration and integration was further assessed through in vivo studies in suitable animal model. Herein, the pure 1393 bioactive glass (BG) and ZnO‐assisted 1393 bioactive glass‐ (ZnBGs; 1, 2, 4 mol% ZnO substitution for SiO2 in pure BG is named as Z1BG, Z2BG, Z3BG, respectively) based scaffolds were prepared through sol–gel route, followed by foam replica techniques and characterized by a series of in vitro and some in vivo tests. Different cell lines like normal mouse embryonic cells (NIH/3T3), mouse bone marrow stromal cells (mBMSc), peripheral blood mononuclear cells, that is, lymphocytes and monocytes (PBMC) and U2OS (carcinogenic human osteosarcoma cells) were used in determination and comparative analysis of the biological compatibility of the BG and ZnBGs. Also, the alkaline phosphatase (ALP) activity, and osteogenic gene expression by primer‐specific osteopontin (OPN), osteocalcin (OCN), and glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH) genes were performed to study osteogenic differentiability of the stromal cells in different BGs. Moreover, radiological and histopathological tests were performed in bone defect model of Wister rats to evaluate the in vivo bone regeneration and healing. Interestingly, these studies demonstrate augmented biological compatibility, and superior osteogenic differentiation in ZnBGs, in particular Z3BG than the pure BG in most cases. [ABSTRACT FROM AUTHOR]