Solid dispersions can be used to improve dissolution of poorly soluble drugs and PVP is a common polymeric carrier in such systems. The mechanisms controlling release of drug from solid dispersions are not fully understood and proposed theories are dependent on an understanding of the dissolution behaviour of both components of the dispersion. This study uses microviscometry to measure small changes in the viscosity of the dissolution medium as the polymer dissolves from ibuprofen-PVP solid dispersions. The microviscometer determines the dynamic and kinematic viscosity of liquids based on the rolling/falling ball principle. Using a standard USP dissolution apparatus, the dissolution of the polymer from the solid dispersion was easily measur...
The dissolution mechanism of rubbery polymers was analyzed by dividing the penetrant concentration f...
The dissolution of semicrystalline poly(vinyl alcohol) (PVA) in water was investigated using spectro...
The development of a meaningful dissolution procedure for drug products with limited water solubilit...
Solid dispersions in water-soluble carriers have attracted considerable interest as a means of impro...
An attempt was made in this study to relate the release of a highly water-soluble model drug from ta...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
Dissolution molecular mechanism of solid dispersions still remains unclear despite thousands of repo...
Microcrystalline cellulose (MCC) and cross-linked polyvinylpyrrolidone (PVP-CL) were examined as pol...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
In this study, planar induced fluorescence (PLIF) was used for the first time to evaluate variabilit...
The objective of this research was to investigate the impact of polymer blends and solid dispersion ...
Research in the area of controlled drug release is increasingly important in the pharmaceutical indu...
Solid dispersions and physical mixtures made up of the poorly water-soluble drug UC 781, a polymer a...
The aim of this work was to investigate the factors influencing the dissolution characteristics of d...
The dissolution mechanism of rubbery polymers was analyzed by dividing the penetrant concentration f...
The dissolution of semicrystalline poly(vinyl alcohol) (PVA) in water was investigated using spectro...
The development of a meaningful dissolution procedure for drug products with limited water solubilit...
Solid dispersions in water-soluble carriers have attracted considerable interest as a means of impro...
An attempt was made in this study to relate the release of a highly water-soluble model drug from ta...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The objective of this study was to compare the dissolution behavior of tablets prepared from solid d...
Dissolution molecular mechanism of solid dispersions still remains unclear despite thousands of repo...
Microcrystalline cellulose (MCC) and cross-linked polyvinylpyrrolidone (PVP-CL) were examined as pol...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
In this study, planar induced fluorescence (PLIF) was used for the first time to evaluate variabilit...
The objective of this research was to investigate the impact of polymer blends and solid dispersion ...
Research in the area of controlled drug release is increasingly important in the pharmaceutical indu...
Solid dispersions and physical mixtures made up of the poorly water-soluble drug UC 781, a polymer a...
The aim of this work was to investigate the factors influencing the dissolution characteristics of d...
The dissolution mechanism of rubbery polymers was analyzed by dividing the penetrant concentration f...
The dissolution of semicrystalline poly(vinyl alcohol) (PVA) in water was investigated using spectro...
The development of a meaningful dissolution procedure for drug products with limited water solubilit...