In the present work different parameters, which influence the release of diclofenac sodium (2-[(2,6-dichlorophenyl)amino]benzeneacetic acid mono sodium salt) from lipophilic matrix prolonged release tablets, were investigated. Solubility characteristics of diclofenac sodium in aqueous media with various ionic strengths, ionic compositions and pH in the range of 1 to 10 were determined. According to the obtained results different experimental conditions of the dissolution test on the drug release profiles were studied, i.e. different dissolution apparatus, various rotation speeds of the stirring elements, different buffer media with a pH in the range of 5.8 to 10.0 and various ionic strengths. The amount of released diclofenac sodium was det...
none4The release of diclofenac (20%, w/w) was studied from lipidic solid dispersions using three dif...
none3The formation of pharmaceutical salts is widely recognized as a tool to improve the solubility ...
The main accusative of the present work was to develop sustained release matrix tablets of Diclofena...
Sodium diclofenac (SD) release from dosage forms has been studied under different conditions. Howeve...
Numerous methods have been applied to improve drug release of pharmaceuticals, among which the liqui...
The purpose of this study was to investigate the effects of polymer type and composition on drug rel...
The mechanism of diclofenac sodium release from non-disintegrating bioadhesive tablets was studied. ...
Objective: The current study aimed to develop a matrix type sustained release Diclofenac tablet, usi...
The aim of this study is to develop and optimize an osmotically controlled drug delivery system of d...
Abstract The aim of thisworkwas to compare the dissolution behaviour of six diclofenac sodium prolon...
The influence of solid dispersions (SD) on diclofenac solubility was determined by studying diclofen...
The present study was performed to illustrate the effect of pH on dissolution profile of diclofenac ...
Objectives: The impact of hydroxypropylmethyl cellulose(HPMC K 100M) alone and in combination with t...
Purpose: To comparatively evaluate the effect of two hydroxylpropyl methylcellulose (HPMC) molecular...
The present study describes the development and validation of an in vitro dissolution method for eva...
none4The release of diclofenac (20%, w/w) was studied from lipidic solid dispersions using three dif...
none3The formation of pharmaceutical salts is widely recognized as a tool to improve the solubility ...
The main accusative of the present work was to develop sustained release matrix tablets of Diclofena...
Sodium diclofenac (SD) release from dosage forms has been studied under different conditions. Howeve...
Numerous methods have been applied to improve drug release of pharmaceuticals, among which the liqui...
The purpose of this study was to investigate the effects of polymer type and composition on drug rel...
The mechanism of diclofenac sodium release from non-disintegrating bioadhesive tablets was studied. ...
Objective: The current study aimed to develop a matrix type sustained release Diclofenac tablet, usi...
The aim of this study is to develop and optimize an osmotically controlled drug delivery system of d...
Abstract The aim of thisworkwas to compare the dissolution behaviour of six diclofenac sodium prolon...
The influence of solid dispersions (SD) on diclofenac solubility was determined by studying diclofen...
The present study was performed to illustrate the effect of pH on dissolution profile of diclofenac ...
Objectives: The impact of hydroxypropylmethyl cellulose(HPMC K 100M) alone and in combination with t...
Purpose: To comparatively evaluate the effect of two hydroxylpropyl methylcellulose (HPMC) molecular...
The present study describes the development and validation of an in vitro dissolution method for eva...
none4The release of diclofenac (20%, w/w) was studied from lipidic solid dispersions using three dif...
none3The formation of pharmaceutical salts is widely recognized as a tool to improve the solubility ...
The main accusative of the present work was to develop sustained release matrix tablets of Diclofena...