In order to enhance in vitro dissolution and content uniformity of poorly soluble drug glimepiride by preparing solid dispersions using modified solvent fusion method, solid dispersions of drug were prepared by modified fusion solvent method using PEG 6000 and PVP K25 (as carrier). Eight batches (F1-F8) were prepared by Factorial design (23) by taking three ...

In this work, we report synthesis and characterization of Bi2O3 nanoparticles loaded on mesoporous MCM-41 nanoparticles by a simple solid-state dispersion (SSD) method. Monoclinic bismuth oxide nanoparticles were prepared by polyacrylamide gel method and used as loading materials on the prepared mesoporous MCM-41 as a supporting material. Fourier transform infrared spectroscopy (FT-IR), X-ray p...

In the present work, the solid-state dispersion method has been used to stabilize ZnOon Todorokite (TD). ZnO/TD catalysts have been characterized by SEM and XRD. Optimum process conditions were determined for the removal of Cr(VI) from water using the Taguchi fractional design method. Four controllable factors containing pH, photocatalyst amount, irradiation intensity, and <em...

This research aimed to develop a supercritical fluid (SCF) technique for preparing a particulate form of itraconazole (ITZ) with good dissolution and bioavailability characteristics. The ITZ particulate solid dispersion was formulated with hydroxypropyl methylcellulose, Pluronic F-127, and L-ascorbic acid. Aggregated particles showed porous structure when examined by scanning electron microscop...

The purpose of this study is to develop and characterize the nature of a solid dispersion system of nifedipine in a polymer matrix consisting of PVP K30 and poloxamer 407. Dispersions consist of drug, polymeric carrier and surfactant carrier. Binary solid dispersions consisting of nifedipine and PVP K30 were developed by solvent evaporation method. Poloxamer 407, surfactant carrier was incorpor...

INTRODUCTION Prednisolone is a class II substance according to the Biopharmaceutics Classification System. It is a poorly water soluble agent. The aim of the present study was to improve dissolution rate of a poorly water-soluble drug, prednisolone, by a solid dispersion technique. METHODS Solid dispersion of prednisolone was prepared with PEG 6000 or different carbohydrates such as lactose a...

the present study deals with characterization of dispersions of a poorly water-soluble drug, celecoxib (clx) in polyvinyl caprolactame–polyvinyl acetate–polyethylene glycol graft copolymer (soluplus® (sol)) prepared by different techniques. dispersions of clx in sol at different ratios (2:1, 1:1, 1:2, 1:4 and 1:6) were prepared by spray drying, conventional solvent evaporation and melting metho...

In the present study, solid dispersion nanoparticles with a hydrophilic polymer and surfactant were developed using the supercritical antisolvent (SAS) process to improve the dissolution and oral absorption of megestrol acetate. The physicochemical properties of the megestrol acetate solid dispersion nanoparticles were characterized using scanning electron microscopy, differential scanning calo...