Amorphization of Pharmaceuticals by Co- grinding with Neusilin
ثبت نشده
چکیده
Amorphization of crystalline drugs can be achieved through several methods. The most common method is melting and solidifi cation by rapid cooling over liquid nitrogen or slow cooling at room temperature. Other methods for drug amorphization include milling, solvent evaporation, spray drying, and lyophilization. Solid state amorphization can be achieved through high energy milling or co-grinding drugs with excipients leading to micronized particles with particle size distributions at submicron levels. These amorphous forms are in a higher energetic state compared to its crystalline counterpart and therefore, provide an advantage in terms of solubility, dissolution and bioavailability. Such amorphized forms of crystalline drugs leads to a marked improvement in their dissolution rates and bioavailability.
منابع مشابه
Amorphization of itraconazole by inorganic pharmaceutical excipients: comparison of excipients and processing methods.
The aim of this study was to investigate the effects of solid carriers and processing routes on the properties of amorphous solid dispersions of itraconazole. Three solid carriers with a range of surface properties were studied, (1) a mesoporous silicate, magnesium aluminum silicate (Neusilin US2), (2) a nonporous silicate of corresponding composition (Veegum) and (3) a non-silicate, inorganic ...
متن کاملEnhancement of the dissolution rate and bioavailability of fenofibrate by a melt-adsorption method using supercritical carbon dioxide
BACKGROUND The aim of this study was to enhance the bioavailability of fenofibrate, a poorly water-soluble drug, using a melt-adsorption method with supercritical CO(2). METHODS Fenofibrate was loaded onto Neusilin(®) UFL2 at different weight ratios of fenofibrate to Neusilin UFL2 by melt-adsorption using supercritical CO(2). For comparison, fenofibrate-loaded Neusilin UFL2 was prepared by so...
متن کاملDissolution Rate Enhancement of Clarithromycin Using Ternary Ground Mixtures: Nanocrystal Formation
Clarithromycin (CLA), a broad-spectrum macrolide, is a poorly soluble drug with dissolution rate limited absorption. The aim of this investigation was to prepare CLA nanoparticles from a ternary ground mixture in the presence of sodium lauryl sulfate (SLS) and polyvinyl pyrrolidone (PVP) as co-grinding water-soluble compounds, in order to improve the drug dissolution rate. Different weight rati...
متن کاملA Study on Improvement of Solubility of Rofecoxib and its effect on Permeation of Drug from Topical Formulations
Rofecoxib, a practically insoluble cox-2 selective nonsteroidal antiinflammatory agent was subjected to improvement in solubility by preparing its binary mixtures with beta cyclodextrin using various methods such as physical mixing, co-grinding, kneading with aqueous methanol and co-evaporation from methanol-water mixture. Characterization of the resulting binary mixtures by differential scanni...
متن کاملDissolution Rate Enhancement of Clarithromycin Using Ternary Ground Mixtures: Nanocrystal Formation
Clarithromycin (CLA), a broad-spectrum macrolide, is a poorly soluble drug with dissolution rate limited absorption. The aim of this investigation was to prepare CLA nanoparticles from a ternary ground mixture in the presence of sodium lauryl sulfate (SLS) and polyvinyl pyrrolidone (PVP) as co-grinding water-soluble compounds, in order to improve the drug dissolution rate. Different weight rati...
متن کامل