The aim of this study was to investigate the impact of formulation excipients and solubilizing additives on dissolution, supersaturation, and membrane transport of an active pharmaceutical ingredient (API). When a poorly water-soluble API is formulated to enhance its dissolution, additives, such as surfactants, polymers, and cyclodextrins, have an effect not only on dissolution profile but also on the measured physicochemical properties (solubility, p<i>K</i><sub>a</sub>, permeability) of the drug while the excipient is present, therefore also affecting the driving force of membrane transport. Meloxicam, a nonsteroidal anti-inflammatory drug, was chosen as a poorly water-soluble model drug and formulated in order to enhance its dissolution ...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The purpose of this study was to investigate the potential of applying amorphous solid dispersions (...
Almost 40% of the new chemical entities at present self find out poorly water soluble drugs. Badly w...
The aim of this study was to investigate the impact of formulation excipients and solubilizing addit...
The aim of this research was to investigate the driving force of membrane transport through size-exc...
During the dissolution of amorphous solid dispersions (ASDs), various phase transformations can occu...
An experimental/computational approach has been successfully applied in order to study the effect of...
Supersaturating formulations are increasingly being used to improve the absorption of orally adminis...
The goal of this work was to comprehensive study the transport properties of controlled-release syst...
In order to understand the role of the formulation components in topical drug delivery it is necessa...
The tendency of highly supersaturated solutions of poorly water-soluble drugs to undergo liquid–liqu...
This paper considers fundamental aspects determining the processes of drug compound dissolution and ...
Dissolution is commonly the rate limiting step to the absorption of poorly water-soluble drugs. Sur...
The solution behavior and membrane transport of multidrug formulations were herein investigated in a...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The purpose of this study was to investigate the potential of applying amorphous solid dispersions (...
Almost 40% of the new chemical entities at present self find out poorly water soluble drugs. Badly w...
The aim of this study was to investigate the impact of formulation excipients and solubilizing addit...
The aim of this research was to investigate the driving force of membrane transport through size-exc...
During the dissolution of amorphous solid dispersions (ASDs), various phase transformations can occu...
An experimental/computational approach has been successfully applied in order to study the effect of...
Supersaturating formulations are increasingly being used to improve the absorption of orally adminis...
The goal of this work was to comprehensive study the transport properties of controlled-release syst...
In order to understand the role of the formulation components in topical drug delivery it is necessa...
The tendency of highly supersaturated solutions of poorly water-soluble drugs to undergo liquid–liqu...
This paper considers fundamental aspects determining the processes of drug compound dissolution and ...
Dissolution is commonly the rate limiting step to the absorption of poorly water-soluble drugs. Sur...
The solution behavior and membrane transport of multidrug formulations were herein investigated in a...
Tablets exhibiting extended drug release have in many therapeutical applications shown both complian...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
The purpose of this study was to investigate the potential of applying amorphous solid dispersions (...
Almost 40% of the new chemical entities at present self find out poorly water soluble drugs. Badly w...