Mefenamic acid (MA) is a widely used non-steroidal antiinflammatory (NSAID) drug. The adverse effects typical of NSAIDs are also present in the case of MA, partly due to its low water solubility. The aim of this study was to increase the water solubility of MA in order to influence its absorption and bioavailability. Solid dispersions of MA were prepared by the melting method using polyethylene glycol 6000 and different types (laurate, D-1216; palmitate, P-1670; stearate, S-1670) and amounts of sucrose esters as carriers. The X-ray diffraction results show that MA crystals were not present in the products. Dissolution tests carried out in artificial intestinal juice showed that the product containing 10 % D-1216 increased water solubility a...
The objective of this study was to enhance the solubility as well as to mask the intensely bitter ta...
The objective of this study was to develop an immediate release dose form containing 250 mg Mefenami...
The objective of this study was to develop an immediate release (IR), crystalline solid dispersion (...
Mefenamic acid (MA) is a widely used non-steroidal anti-inflammatory (NSAID) drug. The adverse effec...
The objective of the present work was to study the effect of different polymers on the solubility an...
Mefenamic acid, based on the Biopharmaceutics Classification System (BCS), is a class II drug that h...
Mefenamic acid, a non-steroidal anti-inflammatory drug generally used for the treatment of pain, has...
Solid dispersions refer to the group of solid products consisting of at least a hydrophilic carrier ...
Mefenamic acid was esterified with starchwith[1:1] Molar ratio, as drug substituted with natural pol...
Mefenamic acid (MA) spherical agglomerates (SAs) were prepared with various polymethacrylates having...
PubMed ID: 21284557Mefenamic acid (MA) spherical agglomerates (SAs) were prepared with various polym...
The influence of solid dispersions (SD) on diclofenac solubility was determined by studying diclofen...
The present studies were undertaken to develop solvent-free solid dispersions (SDs) for poorly solub...
Research has been carried out on the Preparation of Mefenamic Acid Solid Dispersion System Using Pol...
Patience who suffered from menstrual pain disease is generally prescribed the non-steroidal anti-inf...
The objective of this study was to enhance the solubility as well as to mask the intensely bitter ta...
The objective of this study was to develop an immediate release dose form containing 250 mg Mefenami...
The objective of this study was to develop an immediate release (IR), crystalline solid dispersion (...
Mefenamic acid (MA) is a widely used non-steroidal anti-inflammatory (NSAID) drug. The adverse effec...
The objective of the present work was to study the effect of different polymers on the solubility an...
Mefenamic acid, based on the Biopharmaceutics Classification System (BCS), is a class II drug that h...
Mefenamic acid, a non-steroidal anti-inflammatory drug generally used for the treatment of pain, has...
Solid dispersions refer to the group of solid products consisting of at least a hydrophilic carrier ...
Mefenamic acid was esterified with starchwith[1:1] Molar ratio, as drug substituted with natural pol...
Mefenamic acid (MA) spherical agglomerates (SAs) were prepared with various polymethacrylates having...
PubMed ID: 21284557Mefenamic acid (MA) spherical agglomerates (SAs) were prepared with various polym...
The influence of solid dispersions (SD) on diclofenac solubility was determined by studying diclofen...
The present studies were undertaken to develop solvent-free solid dispersions (SDs) for poorly solub...
Research has been carried out on the Preparation of Mefenamic Acid Solid Dispersion System Using Pol...
Patience who suffered from menstrual pain disease is generally prescribed the non-steroidal anti-inf...
The objective of this study was to enhance the solubility as well as to mask the intensely bitter ta...
The objective of this study was to develop an immediate release dose form containing 250 mg Mefenami...
The objective of this study was to develop an immediate release (IR), crystalline solid dispersion (...