In vitro antimicrobial activity of ZnO based glass-ceramics against pathogenic bacteria.

The antibacterial activity of ZnO (0-15.53 mol%) based SiO2-CaO-P2O5-Na2O-CaF2 bioactive glass-ceramics synthesized by controlled crystallisation were studied against eight micro-organisms using modified Kirby Bauer method. The antibacterial activity of the specimens was statistically evaluated using one-way analysis of variance and P < 0.05 was used as the level of significance. In vitro dissolution tests were performed in stimulated body fluid for 48 h at 37 °C for different time intervals to correlate the dissolution behaviour of test samples with antibacterial effects. The results illustrate that specimen BZn15.53 having the highest concentration of ZnO (15.53 mol%) demonstrated the strongest effect against Staph.aureus, S. epidermidis, B. subtilis and K. pneumonia. The effectiveness of BZn15.53 in inhibiting bacteria was due to accumulation of Zn(+2) ions around the surface of the bacteria cell release that caused the death of the cell, besides the presence of hydroxyapatite phase was also responsible for damaging the cell membrane of bacteria.

Electrochemical corrosion study of chitosan-hydroxyapatite coated dental implant.

Chitosan (Ch) is a naturally occurring biocompatible and bio-degradable material with high corrosion protective capacities for metals in various corrosive media. Hydroxyapatite (HA) is a significant biodegradable and bioactive material. In the present work, chitosan-hydroxyapatite (Ch-HA) composite coatings with various concentrations of chitosan were made on 316L stainless steel (316L SS) using sol-gel dip coating technique. The coatings were characterized by X-ray diffraction (XRD), FTIR, SEM, and electrochemical measurements. The surface morphology results (SEM) of coated implants exposed the fairly dense microstructures having uniformity without cracks and pores indicating that coating was successfully deposited. From electrochemical analyses, it was observed that the value of corrosion current density and the corrosion rate decreased from 6.03 to 0.15 and 5.56-0.13 respectively indicating that 1.5gCh-HA is the best coating concentration. The electrochemical results demonstrated an improvement in the corrosion resistance of 316L SS than the bare one. The decrease in slope and loop area of cyclic voltammograms reveals about improvement in corrosion resistance. This increment in corrosion resistance of the Ch-HA coated SS implant in the artificial saliva is as 1.5gCh-HA > 2gCh-HA >1gCh-HA >0.5gCh-HA. Furthermore, Ch-HA coatings revealed appropriate adhesion with 316L SS substrate for its use in dental implants.

The structural, biological and dielectric properties of Sr, Mg and Zn doped silicate ceramics.

The current work examines the structural and biological characteristics of doped Zn, Mg, and Sr. Na2O-CaO-Si2O-P2O5 silicate ceramics synthesized by the solid state method. The undoped sample showed amorphous behavior after sintering at the 800 OC while doping of SrO, MgO and ZnO induce crystal growth; and a single phase of Parawollastonite (JCPDS# 00-043-1460) was identified in both doped samples. The strontium doped sample showed the highest value of the dielectric as compared to other three samples. The Sr doped sample had higher dielectric value because the size of Sr2+ is greater than Ca+2 so it will possess the higher polarizing power. Conductivity of Zn and Sr doped samples increased with increase in frequency and Mg doped decrease with increase in frequency. Bioactivity test confirmed that doped samples were more bioactive as compared to undoped samples, and Sr doped sample showed superior bioactivity as compared to other samples.

To study the synthesis and characterization of SrO-MgO-SiO2 system in biological and dielectric applications.

Ternary ceramic samples comprising SrO-MgO-SiO2 with varying element concentrations were synthesized using the solid-state method and sintered at 800°C. To characterize the properties of the samples, several analysis techniques were employed. X-ray Diffraction (XRD) was utilized for structural analysis, FTIR spectroscopy was used to identify bonds, SEM provided morphological analysis, biocompatibility was assessed through Vitro testing, microhardness was evaluated using Vickers testing, and dielectric analysis was performed to investigate electrical properties. The XRD spectra confirmed the presence of a ternary phase known as Magnesium Strontium Di-silicate [MgSr2Si2O7], with no impurity peaks detected. FTIR spectroscopy indicated the formation of Magnesium silicate, displaying vibrational bands corresponding to SiO4 and MgO, which further confirmed the existence of MgSr2Si2O7 in the samples. The Vitro test results revealed that all samples exhibited biocompatible behavior, with moderate pH and weight loss. SEM images provided insights into the morphology of the system and confirmed the development of an appetite layer on the sample surfaces. The particle size of the samples was measured to be approximately 116.48±9 nm. Vickers hardness testing yielded microhardness values ranging from 378.1 to 400.2 HV. Dielectric constant measurements demonstrated that the AC conductivity of the SrO-MgO-SiO2 system increased as the percentage of Mg doping increased.

Structural, biological investigation of metal (Fe, Cu, Ag)-ceramic composites.

In the present study, five composites based on metals (Ag, Fe, Cu) and ceramic; named as 0.2 Ag, 0.2 Cu, 0.2 Fe, 0.1Ag-0.1Cu, and 0.1Ag-0.1Fe were prepared by the solid-state sintering method. Two different phases of wollastonite: ß-wollastonite (JCPDS No.: 01-076-0186), and α-wollastonite (JCPDS No.:00-031-0300) were identified in all composite. The in vitro bioactivity assay performed in simulated body fluid showed the bioactive behavior of all composites except one having >0.1% Ag concentration. The antibacterial activity test was performed against two pathogenic bacteria Staph. Aureus and Staph. Epidermidis using the agar well diffusion method. Results of antibacterial assays showed that all samples showed antibacterial activity except the 0.2 Fe sample. It was observed that the addition of Ag and Cu provided the inhibitory ability to composites, 0.1Ag-0.1Cu and 0.1Ag-0.1Fe composites are regarded as an optimum composite having better bioactive and antibacterial efficacy as compared to all other composites.

Synthesis of monophasic Ag doped hydroxyapatite and evaluation of antibacterial activity.

The present study aims to synthesized biomaterial that has antibacterial properties. Currently the surgical implants associated infections are a major cause of implant failure. Synthesis of silver doped hydroxyapatite as an antibacterial agent has potential importance to overcome post-surgical infections in a variety of clinical applications. Five silver doped hydroxyapatite Ca10-xAgx(PO4)6(OH)2 (x = 0, 0.1, 0.3, 0.5, 0.7 M) samples were synthesized by precipitation method and sintered at 900 °C to obtain well crystallized structure. No minor phase developed with silver addition, hexagonal hydroxyapatite (JCPDS# 09-432) was the single phase identified in all silver doped hydroxyapatite samples. The lattice parameter a and c changed with increase in silver concentration. The results of in vitro bioactivity revealed the bone bonding ability of silver doped hydroxyapatite samples. The antibacterial test showed that silver doped hydroxyapatite was sensitive to Staphylococcus aureus bacteria. Addition of silver significantly (P < 0.005) increased the antibacterial activity.

Synthesis, characterization of CaF2 doped silicate glass-ceramics.

This paper reports the fabrication and characterization of silicate glass-ceramics doped with (0-12mol%) CaF2. TGA-DSC analysis was carried out to determine the crystallization temperature and stability of glass measured by two glass parameters; Hruby parameter KH=(Tx-Tg)/(TL-Tx) and Weinberg parameter KW=(Tc-Tg)/TL. It was found that with CaF2 doping improved sinterability at low temperature and provided stability to the glass. The XRD pattern exhibits a single phase of combeite and doping of CaF2 cause increase in crystallite size. Microstructure of samples was also improved with CaF2 addition, pores were significantly reduced. After 15days immersion in simulated body fluid all samples developed apatite layer onto its surface. Hence, the addition of CaF2 provided bioactive glass-ceramic material having a low processing temperature.

Effect of Ti(+4) on in vitro bioactivity and antibacterial activity of silicate glass-ceramics.

A novel glass-ceramic series in (48-x) SiO2-36 CaO-4 P2O5-12 Na2O-xTiO2 (where x=0, 3.5, 7, 10.5 and 14mol %) system was synthesized by crystallization of glass powders, obtained by melt quenching technique. The differential scanning calorimetric analysis (DSC) was used to study the non-isothermal crystallization kinetics of the as prepared glasses. The crystallization behaviour of glasses was analyzed under non-isothermal conditions, and qualitative phase analysis of glass-ceramics was made by X-ray diffraction. The in vitro bioactivity of synthesized glass-ceramics was studied in stimulated body fluid at 37°C under static condition for 24days. The formation of hydroxyl-carbonated apatite layer; evident of bioactivity of the material, was elucidated by XRD, FTIR, AAS, SEM and EDX analysis. The result showed that partial substitution of TiO2 with SiO2 negatively influenced bioactivity; it decreased with increase in concentration of TiO2. As Ti(+4) having stronger field strength as compared to Si(+4) so its replacement became the cause for reduction in degradation that in turn improved the chemical stability. The compressive strength was also enhanced with progress addition of TiO2 in the system. The antibacterial properties were examined against Staphylococcus Epidermidis. Strong antibacterial efficacy was observed with the addition of TiO2 in the system.