Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with three different hardness of 5, 6 and 7kg/cm2. Theophylline controlled release granules were prepared and evaluated for the angle of repose, bulk density, tapped density, compressibility index and hausners ratio. All the formulation showed good flow properties. The compressed tablets were evaluated for the hardness, uniformity of weight, friability, drug content and invitro dissolution studies. All the formulations showed compliance with pharmacopial standards. There was no interaction between drug, polymer and other excipients. It was confirmed by FTIR studies. Among all the formulations F6 (i.e. polymer ratio1:2 and hardness 7kg/cm2) showed pr...
A 300 mg controlled-release theophylline formulation was developed as a tablet prepared by wet granu...
Purpose: To develop sustained release matrix tablets of diltiazem hydrochloride (DTZ) using karaya g...
The aim of the present study was to develop sustained release matrix tablets of phenytoin sodium an ...
Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with th...
The objectives of the present study are to develop novel sustained release matrix tablets of theophy...
WOS: 000392938000006The objectives of the present study are to develop novel sustained release matri...
The aim of present work was to develop theophylline sustained release tablets which could improve pa...
ABSTRACT: The effects of plastic, hydrophilic and hydrophobic types of polymers and impact of granul...
Matrix system is a well-established approach for prolonging the activity of otherwise short acting d...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
ABSTRACT: The objective of this study is to compare the drug release profile of an optimized multi-u...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
ABSTRACT: Controlled release matrix tablets of theophylline anhydrous were designed with different t...
AbstractThe deformation mechanism of pharmaceutical powders, used in formulating directly compressed...
A 300 mg controlled-release theophylline formulation was developed as a tablet prepared by wet granu...
Purpose: To develop sustained release matrix tablets of diltiazem hydrochloride (DTZ) using karaya g...
The aim of the present study was to develop sustained release matrix tablets of phenytoin sodium an ...
Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with th...
The objectives of the present study are to develop novel sustained release matrix tablets of theophy...
WOS: 000392938000006The objectives of the present study are to develop novel sustained release matri...
The aim of present work was to develop theophylline sustained release tablets which could improve pa...
ABSTRACT: The effects of plastic, hydrophilic and hydrophobic types of polymers and impact of granul...
Matrix system is a well-established approach for prolonging the activity of otherwise short acting d...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
ABSTRACT: The objective of this study is to compare the drug release profile of an optimized multi-u...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
This study aimed to improve the dissolution rate of aceclofenac and release the drug in a controlled...
ABSTRACT: Controlled release matrix tablets of theophylline anhydrous were designed with different t...
AbstractThe deformation mechanism of pharmaceutical powders, used in formulating directly compressed...
A 300 mg controlled-release theophylline formulation was developed as a tablet prepared by wet granu...
Purpose: To develop sustained release matrix tablets of diltiazem hydrochloride (DTZ) using karaya g...
The aim of the present study was to develop sustained release matrix tablets of phenytoin sodium an ...