Objective: This work evaluated the influence of the technological properties of polyvinylpyrrolidone (PVP), calcium phosphate (CP) and cross-linked sodium carboxymethylcellulose (CC) as well as the deposition of a solid dispersion, through the solvent evaporation method, on the technological parameters that define the properties of ibuprofen tablets. Methods: The powder flow rate through an orifice, bulk volume and tapped volume of powders, tablet hardness, disintegration time and dissolution profile of the tablets were determined on individual components, their physical mixtures, granules obtained by deposition and solvent evaporation, and tablets obtained at different compaction pressures. Results: The very poor flowability of CP and the ...
The low melting point, poor flow, physico-mechanical properties (particle size distribution, shape, ...
Objective: The present study aimed to formulate, develop and optimize orodispersible tablets of ibup...
NOTICE: this is the author’s version of a work that was accepted for publication in European Journal...
Purpose: To determine excipient and ibuprofen:excipient mixture sensitivity to reprocessing produced...
Objective: The aim of the present work was to prepare solid dispersion of ibuprofen with PEG 6000 to...
Objective: The aim of the present investigation was to design and evaluate orally disintegrating tab...
The objective of this thesis was to investigate a mechanical dry powder coating approach to improve ...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solventmethods using polyethylen...
A study of the comparative effects of different formulating additives and film coating on the proper...
A research report submitted to the Faculty of Health Sciences, University of the Witwatersrand , in ...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethyle...
Objective:The objective of this work was to enhance dissolution and tableting property of a poor sol...
Background: Tablets must be able to release the active drug in the gastrointestinal tract for absorp...
Objective: The present study was aimed to enhance the solubility of poorly water soluble drug Ibupro...
A matrix system was developed that releases ibuprofen (IB) over a 12-hour period and the influence o...
The low melting point, poor flow, physico-mechanical properties (particle size distribution, shape, ...
Objective: The present study aimed to formulate, develop and optimize orodispersible tablets of ibup...
NOTICE: this is the author’s version of a work that was accepted for publication in European Journal...
Purpose: To determine excipient and ibuprofen:excipient mixture sensitivity to reprocessing produced...
Objective: The aim of the present work was to prepare solid dispersion of ibuprofen with PEG 6000 to...
Objective: The aim of the present investigation was to design and evaluate orally disintegrating tab...
The objective of this thesis was to investigate a mechanical dry powder coating approach to improve ...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solventmethods using polyethylen...
A study of the comparative effects of different formulating additives and film coating on the proper...
A research report submitted to the Faculty of Health Sciences, University of the Witwatersrand , in ...
Ibuprofen solid dispersions were prepared by the solvent and fusion-solvent methods using polyethyle...
Objective:The objective of this work was to enhance dissolution and tableting property of a poor sol...
Background: Tablets must be able to release the active drug in the gastrointestinal tract for absorp...
Objective: The present study was aimed to enhance the solubility of poorly water soluble drug Ibupro...
A matrix system was developed that releases ibuprofen (IB) over a 12-hour period and the influence o...
The low melting point, poor flow, physico-mechanical properties (particle size distribution, shape, ...
Objective: The present study aimed to formulate, develop and optimize orodispersible tablets of ibup...
NOTICE: this is the author’s version of a work that was accepted for publication in European Journal...