Aim: To enhance the aqueous solubility of olanzapine by using the Solid dispersion technique. Solid dispersions of Olanzapine were prepared by the dispersion method using using PGS and SSG as carriers. Drug:carrier ratios such as 1:1, 1:2, 1:4, 1:6, 1:8 and 1:10 were tried for optimization. Characterization was done by phase solubility, in vitro release, saturation solubility, permeation, wetta...

The aim of the present work was to develop immediate release dosage form of the solid dispersion of glimperide (GLIM) for potential enhancement in the bioavailability. The solid dispersions of GLIM were prepared with PEG6000, PVP K30 and Poloxamer 188, in 1:1, 1:3 and 1:5 %w/w ratio by using solvent wetting and solvent melt method. The in vitro dissolution parameters (%DE10min, %DE30min, %DE60m...

In this paper CuFe2O4, nanocrystalline powders were prepared. Also, the supported Cu ferrite was obtained by impregnation of the supports with Cu and Fe nitrates solutions, for calcination temperature 450 ºC. The samples were characterized by X-ray powder diffraction (XRD) and Fourier transform-infrared spectroscopy (FT-IR). Photocatalytic degradation of acid red 206 in water was studied. CuFe2...

In this paper CuFe2O4, nanocrystalline powders were prepared. Also, the supported Cu ferrite was obtained by impregnation of the supports with Cu and Fe nitrates solutions, for calcination temperature 450 ºC. The samples were characterized by X-ray powder diffraction (XRD) and Fourier transform-infrared spectroscopy (FT-IR). Photocatalytic degradation of acid red 206 in water was studied. CuFe2...

In this research, zeolite-TiO2 nanocomposite was prepared for degradation of dibenzothiophene as a typical aromatic organosulfur compound of transportation fuels.The synthesized TiO2 was immobilized on the surface of clinoptilolite by Solid State Dispersion (SSD) method. The nanocomposite was then characterized by XRD, FTIR, TEM and SEM techniques. Photodegradation of ...

Cefpodoxime Proxetil (Poorly water soluble drug), when prepared as solid dispersion showed improved solubility and dissolution. So the main purpose of this investigation was to increase the solubility and dissolution rate of Cefpodoxime Proxetil by the preparation of its solid dispersion with urea using solvent evaporation method. Physical mixtures and solid dispersions of Cefpodoxime Proxetil ...

The issues of solubility for the targeted drug delivery new affects, many existing drug. minimum 40% novel from pharmaceutical industries are showing poor ability solubilization in water. Hence to increase such waters and their bioavailabilities major challenges scientists. So overcome problems dissolution, development solid dispersion with carriers having good water is beneficiary. methods fou...

Aceclofenac is an analgesic and anti-inflammatory agent used in the management of osteoarthritis, rheumatoid arthritis and ankylosing spondylitis. The objective of the present work was to investigate the effect of different types of carriers such as polyvinyl pyrrolidone (PVP), polyethylene glycol (PEG) 6000 and sodium lauryl sulphate (SLS) as solubilizer on in vitro dissolution of aceclofenac....