AbstractContext: Microcrystalline cellulose (MCC) is the most widely used excipient for the production of pellets but it retards the release of poorly water soluble drugs. Objective: The present investigation reports incorporation of camphor, cross carmellose sodium (CCS) and spray dried lactose (SDL) into MCC pellets to enhance the dissolution rate of telmisartan. Materials and methods: A full factorial design (32) was used in the study. Concentration of camphor and CCS was selected as independent variables whereas percentage porosity and percentage drug release at 60min were selected as dependent variables. Pellets were produced by extrusion–spheronization technique and evaluated for percentage yield, particle size analysis, flow characte...
ABSTRACTDisintegration performance was measured by analysing both water ingress and tablet swelling ...
Thesis (MSc (Pharmaceutics))--North-West University, Potchefstroom Campus, 2013.There are mainly two...
Objective: The main purpose of this investigation was to prepare self-microemulsifying drug delivery...
Context: Microcrystalline cellulose (MCC) is the most widely used excipient for the production of pe...
Objective: In the present investigation, an attempt was made to improve the surface characters and s...
Objective: In the present investigation, an attempt was made to improve the surface characters and s...
ABSTRACT: Silicified microcrystalline cellulose pellets with hydroxypropyl methylcellullose (HPMC) a...
Microcrystalline Cellulose (MCC) pellets containing highly water soluble compound A was formulated ...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid using the extrusi...
Objective: The motivation behind the current examination was to build the solvency and dissolution r...
The aim of the present study was to investigate the effects of drug solubility, inert pellet size a...
AbstractThe poor dissolution characteristics of water-insoluble drugs are a major challenge for phar...
The objective of the study was to prepare mefenamic acid (MA) sustained release matrix pellets and i...
Abstract: The aim of the present study was to formulate and evaluate Almotriptan pellets. Almotripta...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid for a high and lo...
ABSTRACTDisintegration performance was measured by analysing both water ingress and tablet swelling ...
Thesis (MSc (Pharmaceutics))--North-West University, Potchefstroom Campus, 2013.There are mainly two...
Objective: The main purpose of this investigation was to prepare self-microemulsifying drug delivery...
Context: Microcrystalline cellulose (MCC) is the most widely used excipient for the production of pe...
Objective: In the present investigation, an attempt was made to improve the surface characters and s...
Objective: In the present investigation, an attempt was made to improve the surface characters and s...
ABSTRACT: Silicified microcrystalline cellulose pellets with hydroxypropyl methylcellullose (HPMC) a...
Microcrystalline Cellulose (MCC) pellets containing highly water soluble compound A was formulated ...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid using the extrusi...
Objective: The motivation behind the current examination was to build the solvency and dissolution r...
The aim of the present study was to investigate the effects of drug solubility, inert pellet size a...
AbstractThe poor dissolution characteristics of water-insoluble drugs are a major challenge for phar...
The objective of the study was to prepare mefenamic acid (MA) sustained release matrix pellets and i...
Abstract: The aim of the present study was to formulate and evaluate Almotriptan pellets. Almotripta...
Objective: To study microcrystalline cellulose II (MCCII) as new pelletization aid for a high and lo...
ABSTRACTDisintegration performance was measured by analysing both water ingress and tablet swelling ...
Thesis (MSc (Pharmaceutics))--North-West University, Potchefstroom Campus, 2013.There are mainly two...
Objective: The main purpose of this investigation was to prepare self-microemulsifying drug delivery...