Add to ORKGThe biopharmaceutical properties of eight lorazepam tablet formulations, marketed in Italy, were studied and compared. A few significant differences in behaviour were found even among similar formulations. In vitro dissolution patterns vazied on varying pH, technological properties, excipients employed and active ingredient concentrations
The drug lorazepam is a benzodiazepine by class and is used in many healthcare settings as a sedativ...
The pharmacokinetics of lorazepam premedication were studied in 16 patients using two different form...
The dissolution rates of eight products containing Levodopa in three strengths and made by two diffe...
The in vitro properties of ten flurazepam capsule formulations marketed in Italy were studied. All s...
The present investigation was done on lorazepam orodispersible tablets using super disintegrants. Th...
A growing concern for the biopharmaceutical characterization of pharmaceutical products increased th...
AbstractThe aim of this study was to investigate the degree of correlation between the weight and th...
The aim of the present study was to analyze comparatively the performance of the main methods propos...
AIMS: This study explores the impact of paediatric patient related factors and choice of formulation...
Objective: The aim of this study was to examine zolpidem (ZLP) orally disintegrating tablets (ODTs) ...
The purpose of this study was to evaluate the biopharmaceutical drug properties suitable for orally ...
In this work, the dissolution profiles of nine meloxicam tablet brands marketed in Argentina have be...
Class of 2005 AbstractObjectives: To determine whether the quantity of active ingredient and content...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
The in vitro dissolution is the physicochemical test most used to estimate the release of the drug f...
The drug lorazepam is a benzodiazepine by class and is used in many healthcare settings as a sedativ...
The pharmacokinetics of lorazepam premedication were studied in 16 patients using two different form...
The dissolution rates of eight products containing Levodopa in three strengths and made by two diffe...
The in vitro properties of ten flurazepam capsule formulations marketed in Italy were studied. All s...
The present investigation was done on lorazepam orodispersible tablets using super disintegrants. Th...
A growing concern for the biopharmaceutical characterization of pharmaceutical products increased th...
AbstractThe aim of this study was to investigate the degree of correlation between the weight and th...
The aim of the present study was to analyze comparatively the performance of the main methods propos...
AIMS: This study explores the impact of paediatric patient related factors and choice of formulation...
Objective: The aim of this study was to examine zolpidem (ZLP) orally disintegrating tablets (ODTs) ...
The purpose of this study was to evaluate the biopharmaceutical drug properties suitable for orally ...
In this work, the dissolution profiles of nine meloxicam tablet brands marketed in Argentina have be...
Class of 2005 AbstractObjectives: To determine whether the quantity of active ingredient and content...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
The in vitro dissolution is the physicochemical test most used to estimate the release of the drug f...
The drug lorazepam is a benzodiazepine by class and is used in many healthcare settings as a sedativ...
The pharmacokinetics of lorazepam premedication were studied in 16 patients using two different form...
The dissolution rates of eight products containing Levodopa in three strengths and made by two diffe...