In this work dissolution profiles of furosemide tablets of nine commercial products marketed in Argentine were evaluated. All brands fulfill the specifications of dissolution test of USP. Comparison of dissolution profiles were carried out by model-dependent and model independent approaches. Results obtained via model-dependent approach show a first order drug release mechanism especially for Brand I (reference) and Brand IV. Results obtained via modelindependent approach show that there was not significant difference in Dissolution efficiency between the reference product and Brands II, III and IV and in Mean dissolution time between the reference product and Brands II, III, IV and V. Using fit factors, only Brands I and III were sim...
With recent advances in technology and research into drug delivery, the modernization of tests and g...
Generic drugs offer a cost-effective alternative to brand-name products. However, the main concern w...
During the last decades, the study of the in vitro dissolution of pharmaceuticals has been strongly ...
The rate and the extent of drug dissolution and its absorption depend on the characteristics of the ...
In this work dissolution profiles of furosemide tablets of nine commercial products marketed in Arge...
Furosemide is a widely used diuretic, indicated in the treatment of hypertension and edema. This act...
In this work, the dissolution profiles of nine meloxicam tablet brands marketed in Argentina have be...
The present work deals with the comparison of in vitro dissolution profiles of fenofibrate liquisoli...
The aim of the present study was to analyze comparatively the performance of the main methods propos...
The article analyzes comparatively the performance of the main methods proposed for the comparison o...
A drug dissolution profile is one of the most critical dosage form characteristics with immediate an...
The dissolution profiles of five different brands of norfloxacin (400 mg) tablets designated as A, B...
Abstract The aim of thisworkwas to compare the dissolution behaviour of six diclofenac sodium prolon...
Furosemide is a diuretic drug widely used in chronic renal failure. The drug has low solubility and ...
The in vitro dissolution is the physicochemical test most used to estimate the release of the drug f...
With recent advances in technology and research into drug delivery, the modernization of tests and g...
Generic drugs offer a cost-effective alternative to brand-name products. However, the main concern w...
During the last decades, the study of the in vitro dissolution of pharmaceuticals has been strongly ...
The rate and the extent of drug dissolution and its absorption depend on the characteristics of the ...
In this work dissolution profiles of furosemide tablets of nine commercial products marketed in Arge...
Furosemide is a widely used diuretic, indicated in the treatment of hypertension and edema. This act...
In this work, the dissolution profiles of nine meloxicam tablet brands marketed in Argentina have be...
The present work deals with the comparison of in vitro dissolution profiles of fenofibrate liquisoli...
The aim of the present study was to analyze comparatively the performance of the main methods propos...
The article analyzes comparatively the performance of the main methods proposed for the comparison o...
A drug dissolution profile is one of the most critical dosage form characteristics with immediate an...
The dissolution profiles of five different brands of norfloxacin (400 mg) tablets designated as A, B...
Abstract The aim of thisworkwas to compare the dissolution behaviour of six diclofenac sodium prolon...
Furosemide is a diuretic drug widely used in chronic renal failure. The drug has low solubility and ...
The in vitro dissolution is the physicochemical test most used to estimate the release of the drug f...
With recent advances in technology and research into drug delivery, the modernization of tests and g...
Generic drugs offer a cost-effective alternative to brand-name products. However, the main concern w...
During the last decades, the study of the in vitro dissolution of pharmaceuticals has been strongly ...