The polymorphism of new and old active pharmaceutical ingredients (APIs) is of great importance due to performance, stability and processability aspects. The objective of this study was to investigate the polymorphism of deflazacort (DEF), a glucocorticoid discovered >40 years ago, since this phenomenon has not been previously investigated for this API. Using different methods for solid form screening, it was determined for the first time that DEF is able to exist as three forms: a crystalline (DEF-1); a hydrated X-ray amorphous (DEF-t-bw) and an anhydrous amorphous phase (DEF-g) obtained from manually grinding DEF-1. The in vitro and in vivo dissolution rates (DRs) of DEF-1 and DEF-t-bw, which were measured using the rotating disk method i...
In the present study various crystalline forms of glipizide were prepared in order to enhance dissol...
ABSTRACT Spironolactone (SPR) is a steroidal drug administered as a potassium-sparing diuretic for h...
The aim of this study was to develop and validate a dissolution test for the quality control of defl...
Polymorphism of drugs has been the subject of intense interest in the pharmaceutical industry for ov...
ABSTRACT − Polymorphism has been recognized to be a critical issue throughout the drug product devel...
A comparison of the polymorphic forms of 3 commercial sources of fusidic acid using FTIR and XRPD te...
This study reports the appearance and characterization of multiple new polymorphic forms of indometh...
Amorphization is a well-established strategy to enhance the dissolution properties of poorly water-s...
Formulators are charged with the responsibility of formulating a product which is physically and che...
Triamcinolone acetonide acetate (TAA) is a widely applied drug for rheumatoid arthritis and for the ...
International audienceThis study aims to investigate the polymorphism, physical stability, and amorp...
The formation and physical stability of amorphous sulfathiazole obtained from polymorphic forms I an...
Drugs with low water solubility are predisposed to poor and variable oral bioavailability and, there...
Solid dispersions are one of the most effective methods for improving the dissolution rate of poorly...
International audienceStability ranking of different crystalline polymorphs of pharmaceuticals is im...
In the present study various crystalline forms of glipizide were prepared in order to enhance dissol...
ABSTRACT Spironolactone (SPR) is a steroidal drug administered as a potassium-sparing diuretic for h...
The aim of this study was to develop and validate a dissolution test for the quality control of defl...
Polymorphism of drugs has been the subject of intense interest in the pharmaceutical industry for ov...
ABSTRACT − Polymorphism has been recognized to be a critical issue throughout the drug product devel...
A comparison of the polymorphic forms of 3 commercial sources of fusidic acid using FTIR and XRPD te...
This study reports the appearance and characterization of multiple new polymorphic forms of indometh...
Amorphization is a well-established strategy to enhance the dissolution properties of poorly water-s...
Formulators are charged with the responsibility of formulating a product which is physically and che...
Triamcinolone acetonide acetate (TAA) is a widely applied drug for rheumatoid arthritis and for the ...
International audienceThis study aims to investigate the polymorphism, physical stability, and amorp...
The formation and physical stability of amorphous sulfathiazole obtained from polymorphic forms I an...
Drugs with low water solubility are predisposed to poor and variable oral bioavailability and, there...
Solid dispersions are one of the most effective methods for improving the dissolution rate of poorly...
International audienceStability ranking of different crystalline polymorphs of pharmaceuticals is im...
In the present study various crystalline forms of glipizide were prepared in order to enhance dissol...
ABSTRACT Spironolactone (SPR) is a steroidal drug administered as a potassium-sparing diuretic for h...
The aim of this study was to develop and validate a dissolution test for the quality control of defl...