In this study, different grades of hydroxyl propyl methyl cellulose (HPMC) were used to develop floating microspheres of Cefpodoxime Proxetil in order to demonstrate the effect of different viscosities on drug release profile. The Cefpodoxime Proxetil microspheres were prepared by non aqueous solvent evaporation method using different grades of HPMC such as HPMC K15M ( 15cps), HPMCK4M(4000cps), HPMC100LV(100cps) and ethyl cellulose. The prepared microspheres were characterized by polymer compactibility (FTIR Scan), percentage yield, Buoyancy percentage, Drug Entrapment Efficiency (DEE) and invitro drug release was performed by USP Apparatus type I. The prepared floating microspheres were found to produce the percentage yield of 50.5-72.21%...
Abstract: The purpose of the present study was to develop an optimized gastroretentive drug delivery...
Purpose: To prepare and evaluate floating microspheres of curcumin for prolonged gastric residence t...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...
The purpose of this research work was to increase the residence time of drug Cefuroxime axetil by fo...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
AbstractObjectiveTo develop floating microspheres of cefpodoxime proxetil (CP) in order to achieve a...
Objective: The objective of research work was to formulate and evaluate the floating drug delivery s...
Now a day oral route is the easiest and most prominent route for drug delivery. More than 40% of new...
Present investigation describes statistically the influence of viscosity of hydroxypropyl methylcell...
Hydrophilic matrix tablets are a compressed well mixed composite of drug substance and excipients in...
Systematic studies were conducted using two different polymers in different concentrations to prepar...
Objective: This study was undertaken to formulate a floating drug delivery system of theophylline hy...
A single unit sustainable drug release system was developed using hydroxypropyl methylcellulose (HPM...
Hydrophilic matrix tablets are a compressed well mixed composite of drug substance and excipients in...
The purpose of this study was to investigate the effect of various in vitro test conditions, on the ...
Abstract: The purpose of the present study was to develop an optimized gastroretentive drug delivery...
Purpose: To prepare and evaluate floating microspheres of curcumin for prolonged gastric residence t...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...
The purpose of this research work was to increase the residence time of drug Cefuroxime axetil by fo...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
AbstractObjectiveTo develop floating microspheres of cefpodoxime proxetil (CP) in order to achieve a...
Objective: The objective of research work was to formulate and evaluate the floating drug delivery s...
Now a day oral route is the easiest and most prominent route for drug delivery. More than 40% of new...
Present investigation describes statistically the influence of viscosity of hydroxypropyl methylcell...
Hydrophilic matrix tablets are a compressed well mixed composite of drug substance and excipients in...
Systematic studies were conducted using two different polymers in different concentrations to prepar...
Objective: This study was undertaken to formulate a floating drug delivery system of theophylline hy...
A single unit sustainable drug release system was developed using hydroxypropyl methylcellulose (HPM...
Hydrophilic matrix tablets are a compressed well mixed composite of drug substance and excipients in...
The purpose of this study was to investigate the effect of various in vitro test conditions, on the ...
Abstract: The purpose of the present study was to develop an optimized gastroretentive drug delivery...
Purpose: To prepare and evaluate floating microspheres of curcumin for prolonged gastric residence t...
The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic ...