Add to ORKGThe effects of agitation rate, buffer molarity,and mesh size on the dissolution rate of verapamil hydrochloride from sustained release matrix tablets were studied using USP Apparatus 3. Eudragit® and Carbopol® were used as rate-retarding polymers in tablets prepared by wet granulation.The study was conducted to determine whether the drugs exhibit similar release characteristics when tested under the same dissolution conditions. It was found that the dissolution rate of verapamil hydrochloride was affected by the variables assessed in these studies
The aim of this work was to evaluate the preparation process and in vitro release performances of HP...
Drug delivery systems are a magic tool for existing drug to enhance the safety and efficacy of the d...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid for a high and lo...
The effects of agitation rate, buffer molarity,and mesh size on the dissolution rate of verapamil hy...
The objectives of this study were to compare dissolution profiles of a verapamil (VRP) formulation m...
Tablets manufactured in-house were compared to a marketed sustained-release product of verapamil to ...
Matrix tablets of Verapamil Hydrochloride were formulated as sustained release tablet employing sodi...
This work has focused on the effects of different hydroxypropylmethylcellulose (HPMC) types and HPMC...
Abstract. Among different variables that influence drug release from hydrated hydrophilic matrices, ...
Tématem této bakalářské práce je studium kinetiky uvolňování účinné látky verapamil hydrochloridu z ...
The purpose of the present research work was to observe the effects of drug solubility on the releas...
The objectives of this study were to prepare microcapsules containing verapamil and propranolol and ...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
PubMed ID: 15231431The purpose of this study is to obtain a drug release at a constant rate with a m...
Floating sustained release Verapamil HCl capsules were prepared using different polymers. Hydroxypro...
The aim of this work was to evaluate the preparation process and in vitro release performances of HP...
Drug delivery systems are a magic tool for existing drug to enhance the safety and efficacy of the d...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid for a high and lo...
The effects of agitation rate, buffer molarity,and mesh size on the dissolution rate of verapamil hy...
The objectives of this study were to compare dissolution profiles of a verapamil (VRP) formulation m...
Tablets manufactured in-house were compared to a marketed sustained-release product of verapamil to ...
Matrix tablets of Verapamil Hydrochloride were formulated as sustained release tablet employing sodi...
This work has focused on the effects of different hydroxypropylmethylcellulose (HPMC) types and HPMC...
Abstract. Among different variables that influence drug release from hydrated hydrophilic matrices, ...
Tématem této bakalářské práce je studium kinetiky uvolňování účinné látky verapamil hydrochloridu z ...
The purpose of the present research work was to observe the effects of drug solubility on the releas...
The objectives of this study were to prepare microcapsules containing verapamil and propranolol and ...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
PubMed ID: 15231431The purpose of this study is to obtain a drug release at a constant rate with a m...
Floating sustained release Verapamil HCl capsules were prepared using different polymers. Hydroxypro...
The aim of this work was to evaluate the preparation process and in vitro release performances of HP...
Drug delivery systems are a magic tool for existing drug to enhance the safety and efficacy of the d...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid for a high and lo...