Superconductivity in doped FeTe1-xSx (x= 0.00 to 0.25) single crystals

We report self flux growth and characterization of FeTe1-xSx (x= 0.00 to 0.25) single crystal series. Surface X-ray diffraction (XRD) exhibited crystalline nature with growth in (00l) plane. Micro-structural (electron microscopy) images of representative crystals showed the slab-like morphology and near stoichiometric composition. Powder XRD analysis (Rietveld) of single crystals exhibited tetragonal structure with P4/nmm space group and decreasing a and c lattice parameters with increase in x. Electrical resistivity measurements (R-T) showed superconductivity with Tconset at 9.5K and 8.5K for x =0.10 and x =0.25 respectively. The un-doped crystal exhibited known step like anomaly at around 70K. Upper critical field Hc2(0), as calculated from magneto transport for x =0.25 crystal is around 60Tesla and 45Tesla in H//ab and H//c directions. Thermal activation energy [U0(H)] calculated for x =0.10 and 0.25 crystals followed weak power law, indicating single vortex pinning at low fields. Mossbauer spectra for FeTe1-xSx crystals at 300K and 5K are compared with non superconducting FeTe. Both quadrupole splitting (QS) and isomer shift (IS) for S doped crystals were found to decrease. Also at 5K the hyperfine field for x =0.10 superconducting crystal is decreased substantially from 10.6Tesla (FeTe) to 7.2Tesla. For x =0.25 crystal, though small quantity of un-reacted Fe is visible at room temperature, but unlike x =0.10, the low temperature (5K) ordered FeTe hyperfine field is nearly zero.Comment: 20 Pages Text + Figs: Accepted Mat. Res. Exp, Mat. Rex. Exp. (2018

DEVELOPMENT AND EVALUATION OF CLOBETASOL–LOADED SOLID LIPID NANOPARTICLES FOR TOPICAL TREATMENT OF PSORIASIS

Objective: The current research was structured to achieve a maximum topical delivery for the drug clobetasol-17-propionate (CP) and to predict the effects of various independent variables like lipid: drug ratio, surfactant, and homogenization time on particulate characters and performance solid lipid nanoparticles (SLNs). Methods: CP loaded SLNs were formulated by Emulsification–Homogenization method and optimized using 33 full factorial designs (Design-Expert software 11.0). Drug loaded SLNs were evaluated for various parameters like particle size, surface charge, polydispersity index, entrapment efficiency, surface morphology, thermal analysis, in vitro drug release through skin (Franz diffusion cell), drug deposition study and stability. Results: The optimized formulation (SLNs) attains a minimal Particle size of 133.3±3.66 nm, Poly dispersibility index of 0.179±0.081, % entrapment efficiency of 78.1±1.11 and Zeta potential of-36.2±0.11mV. Skin permeation study of CP loaded SLNs suspension showed prolonged drug release up to 24h. Maximum drug deposition was obtained after developing the drug into SLNs (48.22µg/ml) when compared to the pure drug (19.12µg/ml). Conclusion: SLNs were promising colloidal particulate carriers by which prolonged drug release and improved skin permeation was achieved for the drug Clobetasol 17- propionate

Management of Peri Implant deficiency with PRP and bone grafts – A Case Report

The objective of this paper is to report a case that has been successfully managed by incorporating Platelet Rich Plasma ( PRP) with a combination of autogenous bone graft and a commercial xenograft (BIO-OSS).                                                  Platelet rich plasma seems to enhance early bone healing (3 months) when used along with Auto grafts and Xeno graft mixture. A Substantial increase in the area of bone was observed post operatively. In our case, Clinically,  no major complications were noted after 3months when assessed using parameters like implant mobility, pain, infection, implant exposure. Therefore, the use of Platelet rich plasma along with auto graft and xeno graft mixture in peri implants deficient regions appears to be beneficial in  clinical situations. &nbsp

Analysis of an unswept propfan blade with a semiempirical dynamic stall model

The time history response of a propfan wind tunnel model with dynamic stall is studied analytically. The response obtained from the analysis is compared with available experimental data. The governing equations of motion are formulated in terms of blade normal modes which are calculated using the COSMIC-NASTRAN computer code. The response analysis considered the blade plunging and pitching motions. The lift, drag and moment coefficients for angles of attack below the static stall angle are obtained from a quasi-steady theory. For angles above static stall angles, a semiempirical dynamic stall model based on a correction to angle of attack is used to obtain lift, drag and moment coefficients. Using these coefficients, the aerodynamic forces are calculated at a selected number of strips, and integrated to obtain the total generalized forces. The combined momentum-blade element theory is used to calculate the induced velocity. The semiempirical stall model predicted a limit cycle oscillation near the setting angle at which large vibratory stresses were observed in an experiment. The predicted mode and frequency of oscillation also agreed with those measured in the experiment near the setting angle

PROCESS AND PARAMETERS AFFECTING DRUG RELEASE PERFORMANCE OF PREPARED CROSS-LINKED ALGINATE HYDROGEL BEADS FOR EZETIMIBE

Objective: The objective of this study was to formulate an oral sustained release delivery system of ezetimibe mucoadhesive beads by ionic gelation technique based on sodium alginate used as a hydrophilic carrier in combination with carbopol 934P which acts as a rate modifier.Methods: Microbeads of ezetimibe were prepared using an easy method of ionotropic gelation by little modification while in addition of drug. The prepared beads were characterised for mean particle size, entrapment efficiency, swelling capacity, and in vitro release. They were also subjected to various studies such as Fourier Transform Infrared Spectrophotometer (FTIR) Spectroscopy for drug polymer reaction, Scanning Electron Microscopy for surface morphology, and Differential Scanning Calorimetric Analysis to determine the physical state of the drug in the beads.Results: The microspheres of ezetimibe were formulated successfully. The addition of drug concentration gives higher drug loading and higher conc. of Alcl+3 yields small diameter beads and lower drug entrapment. Analysis of the release profiles showed that the data corresponds to zero order release and the diffusion-controlled mechanism as suggested by Higuchi concept.Conclusion: It can be concluded that beads produced by the sequential method had higher drug entrapment. Beads produced by simultaneous yields larger beads in diameter. The concept was cleared that drug release was dependent upon the quantity of polymer and increase in conc. of. aluminium chloride retarded the drug release in the sequential method. Prepared beads enhance the dissolution of ezetimibe and the oral bioavailability and also reduce the fluctuations in the oral bioavailability