Nimesulide is a non-steroidal anti-inflammatory drug. Here, the present study was planned to prepare and evaluate the solid dispersions of Nimesulide. Solid dispersions of Nimesulide were prepared by using various hydrophilic carriers like PVP K-40, PEG 4000, PEG-6000 in various ratios by solvent evaporation method. The solubility of Nimesulide in different solvents; water, acetone and ethanol was enhanced in the form of solid dispersions. The prepared solid dispersions were subjected to solubility studies (in water, 0.1 N HCL and phosphate buffer pH 7.4. Stability studies were carried out at 40±2 ° C and at 75±5 % RH. The phosphate buffer pH 7 Showed highest solubility for the drug. The cumulative amount of drug release of Nimesulide: PVP ...
Introduction: Indomethacin is a nonsteroidal anti-inflammatory drug used for the treatment of many i...
The objective of this study was to develop sustained release tablets of Montelukast sodium by direct...
The bioavailability of a drug is usually determined by its aqueous solubility and lipid permeability...
Development of solid dispersions of poorly water soluble drugs is one of the most widely used approa...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethyle...
Indomethacin (IM) is one of the most widely used non-steroidal anti-inflammatory active pharmaceutic...
Abstract: The concept of Fast Dissolving Drug Delivery System emerged from the desire to provide pat...
peer reviewedNimesulide is a nonsteroidal antiinflammatory drug that exhibits a very poor water solu...
The limited solubility of drugs has always been a challenging task for pharmaceutical industries eng...
Candesartan cilexetil is a poorly soluble antihypertensive agent with low bioavailability. It is a p...
Ibuprofen is a non-steroidal anti-inflammatory drug with poor water solubility. The most frequent ca...
In the present research work, an attempt was made to improve the solubility and dissolution rate of ...
The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent...
The synthetic polymers and their combinations were employed to retard the release of nimesulide from...
An attempt was made to prepare fast dissolving tablets of anti-inflammatory drug Nimesulide preparin...
Introduction: Indomethacin is a nonsteroidal anti-inflammatory drug used for the treatment of many i...
The objective of this study was to develop sustained release tablets of Montelukast sodium by direct...
The bioavailability of a drug is usually determined by its aqueous solubility and lipid permeability...
Development of solid dispersions of poorly water soluble drugs is one of the most widely used approa...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethyle...
Indomethacin (IM) is one of the most widely used non-steroidal anti-inflammatory active pharmaceutic...
Abstract: The concept of Fast Dissolving Drug Delivery System emerged from the desire to provide pat...
peer reviewedNimesulide is a nonsteroidal antiinflammatory drug that exhibits a very poor water solu...
The limited solubility of drugs has always been a challenging task for pharmaceutical industries eng...
Candesartan cilexetil is a poorly soluble antihypertensive agent with low bioavailability. It is a p...
Ibuprofen is a non-steroidal anti-inflammatory drug with poor water solubility. The most frequent ca...
In the present research work, an attempt was made to improve the solubility and dissolution rate of ...
The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent...
The synthetic polymers and their combinations were employed to retard the release of nimesulide from...
An attempt was made to prepare fast dissolving tablets of anti-inflammatory drug Nimesulide preparin...
Introduction: Indomethacin is a nonsteroidal anti-inflammatory drug used for the treatment of many i...
The objective of this study was to develop sustained release tablets of Montelukast sodium by direct...
The bioavailability of a drug is usually determined by its aqueous solubility and lipid permeability...