ENHANCEMENT OF SOLUBILITY OF TELMISARTAN USING VARIOUS METHODS AND CARRIERS

Solid dispersions of olmesartan in Crosspovidone using various ratios of drug: carrier were. prepared by solvent

Solid dispersion of sulfamethoxazole by employing starch citrate as solubility enhancer prepared by utilizing physical mixing, solvent evaporation and kneading

Thus prepared solid dispersions were evaluated for percentage yield, drug content, saturation solubility and in-vitro dissolution studies.. The result obtained from above

To enhance the solubility of poorly soluble drug and improvement dissolution for local action, FP was prepared as solid dispersions by solvent evaporation

Whereas in solid dispersions prepared by solvent evaporation method, dissolution of pure Olmesartan is very low in comparison with the solid dispersion samples

Dissolution enhancement of Fenofibrate solid dispersion prepared using hydrophillic carriers by solvent evaporation method. Journal of Medical and Pharmaceutical

Prepared solid dispersions were compared for dissolution rate studies in discriminating medium and release obtained are depicted in Table 3 and Fig.1.. Adsorption

The existing analysis was piloted to develop the dissolution and solubility of second generation fluoroquinolones using solid dispersions formulation by