This presentation narrates the comparative analysis of the dissolution data nimesulide microparticles prepared with ethylcellulose, hydroxypropyl methylcellulose, chitosan and Poly(D,L-lactide-co-glycolide) as polymers. The analysis of release profiles showed that the variations noted in the release behavior of nimesulide from various microparticulate formulations are due to the nature of used polymer. In addition, maximum retardation in the nimesulide release was observed with HPMC (floating particles). Thus HPMC miacroparticles may be preferably employed for sustained release dosage form development
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...
Systematic studies were conducted using two different polymers in different concentrations to prepar...
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...
Purpose: To formulate prolonged-release floating microparticles that would minimise the irritant eff...
The aim of this study was to formulate ethyl cellulose (EC) microparticles for sustained release of ...
The synthetic polymers and their combinations were employed to retard the release of nimesulide from...
Nimesulide was formulated as sustained release microcapsules using biodegradable polymer Poly(D,L-l...
Purpose: To formulate prolonged-release floating microparticles that would minimise the irritant eff...
The aim of this study was to develop a single combined once-daily sustained release microencapsulat...
The present study involves the preparation of nimesulide-chitosan microparticles (NCM) as sustained ...
The aim of this study was to develop a single combined once-daily sustained release microencapsulate...
The objective of this project is to determine the effect of formulation parameters on the in vitro d...
The pharmaceutical innovations, such as the use of polymers to control drug release, create possibil...
In this study, polymeric blend microparticles are prepared with tunable drug releasing behavior, imp...
Nimesulide was formulated as novel dual coated microparticles using chitosan (CTN) and ethyl cellulo...
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...
Systematic studies were conducted using two different polymers in different concentrations to prepar...
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...
Purpose: To formulate prolonged-release floating microparticles that would minimise the irritant eff...
The aim of this study was to formulate ethyl cellulose (EC) microparticles for sustained release of ...
The synthetic polymers and their combinations were employed to retard the release of nimesulide from...
Nimesulide was formulated as sustained release microcapsules using biodegradable polymer Poly(D,L-l...
Purpose: To formulate prolonged-release floating microparticles that would minimise the irritant eff...
The aim of this study was to develop a single combined once-daily sustained release microencapsulat...
The present study involves the preparation of nimesulide-chitosan microparticles (NCM) as sustained ...
The aim of this study was to develop a single combined once-daily sustained release microencapsulate...
The objective of this project is to determine the effect of formulation parameters on the in vitro d...
The pharmaceutical innovations, such as the use of polymers to control drug release, create possibil...
In this study, polymeric blend microparticles are prepared with tunable drug releasing behavior, imp...
Nimesulide was formulated as novel dual coated microparticles using chitosan (CTN) and ethyl cellulo...
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...
Systematic studies were conducted using two different polymers in different concentrations to prepar...
The purpose of this study was to prepare and characterize nimodipine loaded microspheres using ethyl...