The aim of present study was to prepare sustained release tablet of Theophylline so as to prolong its elimination time and at the same time to keep cost of the formulation minimum. In this study ethyl cellulose and Eudragit are used in the formulation to sustain the release of Theophylline. Ethyl cellulose and Eudragit are added at the granulation step to form a sustained release coating around each granule. Different batches were designed one after another on trial and error basis to get the optimum drug release upto 12 hours. Keywords: Theophylline, ethyl cellulose, Eudragit, sustained release, coating, tablet
The objective of the present study was to develop an oral timed-released press-coated tablet contain...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with th...
ABSTRACT: The objective of this study is to compare the drug release profile of an optimized multi-u...
WOS: 000392938000006The objectives of the present study are to develop novel sustained release matri...
The objectives of the present study are to develop novel sustained release matrix tablets of theophy...
A 300 mg controlled-release theophylline formulation was developed as a tablet prepared by wet granu...
Objective: The main objective of this research work was to design, prepare and evaluate extended rel...
A 300 mg controlled-reelase theophylline formulation was developed as a tablet prepared by wet granu...
The dissolution behavior of five commercially available brands of sustained release theophylline ta...
The objective of this study is to compare the drug release profile of an optimized multi-unit dose (...
In this study, the effect of ethylcellulose (EC) and 6 types of hydroxypropylmethylcellulose (Methoc...
The aim of present work was to develop theophylline sustained release tablets which could improve pa...
Matrix system is a well-established approach for prolonging the activity of otherwise short acting d...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
The objective of the present study was to develop an oral timed-released press-coated tablet contain...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with th...
ABSTRACT: The objective of this study is to compare the drug release profile of an optimized multi-u...
WOS: 000392938000006The objectives of the present study are to develop novel sustained release matri...
The objectives of the present study are to develop novel sustained release matrix tablets of theophy...
A 300 mg controlled-release theophylline formulation was developed as a tablet prepared by wet granu...
Objective: The main objective of this research work was to design, prepare and evaluate extended rel...
A 300 mg controlled-reelase theophylline formulation was developed as a tablet prepared by wet granu...
The dissolution behavior of five commercially available brands of sustained release theophylline ta...
The objective of this study is to compare the drug release profile of an optimized multi-unit dose (...
In this study, the effect of ethylcellulose (EC) and 6 types of hydroxypropylmethylcellulose (Methoc...
The aim of present work was to develop theophylline sustained release tablets which could improve pa...
Matrix system is a well-established approach for prolonging the activity of otherwise short acting d...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
The objective of the present study was to develop an oral timed-released press-coated tablet contain...
Purpose: To formulate theophylline microspheres with cellulose acetate using solvent evaporation met...
Theophylline controlled release matrix tablets were prepared with guar gum in two ratios and with th...