In the current study Indomethacin (IM) fast dissolving tablets (FDTs) were prepared by direct compression technique in order to enhance its dissolution rate. The tablets were formulated using two different approaches; super-disintegration and effervescence. A combination formulation of above approaches was also developed to further improve its properties. The super-disintegrants used in the formulae were sodium starch glycolate (Primogel), cross-povidone (Kollidon) and cross-carmellose (Ac-di-sol). Sodium bicarbonate and citric acid combination was employed as effervescent ingredients. The prepared powder mixtures of IM were subjected to evaluation of various pre-compression parameters and tablets were evaluated for weight variat...
Objective: The purpose of the present study was to enhance solubility and dissolution characteristic...
The aim of the present research is to develop the fast dissolving tablets and to study the effect of...
Oral administration of indomethacin has been limited by its poor water solubility. Cyclodextrins hav...
In the current study Indomethacin (IM) fast dissolving tablets (FDTs) were prepared by direct compre...
Objective: The main objective of this study was to investigate the potential of in situ crystallizat...
Indomethacin is a non-steroidal anti-inflammatory drug mainly used for musculo skeletal & joint diso...
Oral drug delivery is the most widely used route of drug administration among all the routes that ha...
AbstractThe aim of this study was to prepare and characterize solid dispersions of water insoluble n...
Indomethacin is an anti inflammatory drug which is used to relieve pain and inflammatory conditions....
Indomethacin is an anti inflammatory drug which is used to relieve pain and inflammatory conditions....
The present studies are aimed for overcoming these common problems by introducing solid dispersion ...
PURPOSE: For poorly soluble, highly permeable (Class II) drugs, such as indomethacin, the rate of or...
The intrinsic cohesive nature of micronized poorly water-soluble drug particles often promotes the f...
The objective of this study was to improve the dissolution rate of a hydrophobic non-steroidal anti-...
A formula containing Compactrol, Ac-Di-Sol, Aerosil 200 and talc was used to prepare directly-compre...
Objective: The purpose of the present study was to enhance solubility and dissolution characteristic...
The aim of the present research is to develop the fast dissolving tablets and to study the effect of...
Oral administration of indomethacin has been limited by its poor water solubility. Cyclodextrins hav...
In the current study Indomethacin (IM) fast dissolving tablets (FDTs) were prepared by direct compre...
Objective: The main objective of this study was to investigate the potential of in situ crystallizat...
Indomethacin is a non-steroidal anti-inflammatory drug mainly used for musculo skeletal & joint diso...
Oral drug delivery is the most widely used route of drug administration among all the routes that ha...
AbstractThe aim of this study was to prepare and characterize solid dispersions of water insoluble n...
Indomethacin is an anti inflammatory drug which is used to relieve pain and inflammatory conditions....
Indomethacin is an anti inflammatory drug which is used to relieve pain and inflammatory conditions....
The present studies are aimed for overcoming these common problems by introducing solid dispersion ...
PURPOSE: For poorly soluble, highly permeable (Class II) drugs, such as indomethacin, the rate of or...
The intrinsic cohesive nature of micronized poorly water-soluble drug particles often promotes the f...
The objective of this study was to improve the dissolution rate of a hydrophobic non-steroidal anti-...
A formula containing Compactrol, Ac-Di-Sol, Aerosil 200 and talc was used to prepare directly-compre...
Objective: The purpose of the present study was to enhance solubility and dissolution characteristic...
The aim of the present research is to develop the fast dissolving tablets and to study the effect of...
Oral administration of indomethacin has been limited by its poor water solubility. Cyclodextrins hav...