The progress from batch to continuous manufacture of pharmaceuticals has highlighted the requirement for dosing solid feed material directly, efficiently and accurately into continuous flow systems. Solids are currently dissolved in batch vessels before feeding into a flow system. This study focuses on gaining scientific understanding on rate kinetics of solid dissolution and parameters affecting solid dosing in current batch systems as a starting point; the knowledge gained will inform future continuous solid dosing work. Paracetamol was the model compound and the mixtures of water/ IPA the solvent systems. An in situ UV spectrometer was used to quantify the concentration of solute in solution during dissolution. In this paper, we present ...
Dissolution of tablets into their component parts is an important method by which orally-administere...
The use of Process Analytical Technology (PAT) recommended by the Food and Drug Administration (FDA)...
The objective of this study was to compare the in vitro dissolution profile of a new rapidly absorbe...
The progress from batch to continuous manufacture of pharmaceuticals has highlighted the requirement...
Dissolution testing of solid dosage forms is well-established as a standard technique to assess drug...
The use of Process Analytical Technology (PAT) recommended by the Food and Drug Administration (FDA)...
Solution crystallization processes are widely treated as binary systems consisting of a solute and a...
Synthetic biodegradable polymers are widely used as materials for the targeted drug delivery and con...
This work concerns solid-liquid mass transfer in stirred tanks and is focused on the analysis of exp...
ABSTRACT: Ten brands of commercial paracetamol suspensions were investigated for their dissolution c...
Pharmaceutical synthesis involves work up, reaction, crystallization, filtration and further downst...
The dissolution processes of active pharmaceutical ingredient (API) crystals have been extensively s...
In this study, an automated intelligent decision support (IDS) framework was applied to monitor the ...
AbstractThe solid-state form of an active pharmaceutical ingredient (API) in an oral dosage form pla...
Introduction: Paracetamol is analgesic and antipyretic, which is usually in the form of an immediate...
Dissolution of tablets into their component parts is an important method by which orally-administere...
The use of Process Analytical Technology (PAT) recommended by the Food and Drug Administration (FDA)...
The objective of this study was to compare the in vitro dissolution profile of a new rapidly absorbe...
The progress from batch to continuous manufacture of pharmaceuticals has highlighted the requirement...
Dissolution testing of solid dosage forms is well-established as a standard technique to assess drug...
The use of Process Analytical Technology (PAT) recommended by the Food and Drug Administration (FDA)...
Solution crystallization processes are widely treated as binary systems consisting of a solute and a...
Synthetic biodegradable polymers are widely used as materials for the targeted drug delivery and con...
This work concerns solid-liquid mass transfer in stirred tanks and is focused on the analysis of exp...
ABSTRACT: Ten brands of commercial paracetamol suspensions were investigated for their dissolution c...
Pharmaceutical synthesis involves work up, reaction, crystallization, filtration and further downst...
The dissolution processes of active pharmaceutical ingredient (API) crystals have been extensively s...
In this study, an automated intelligent decision support (IDS) framework was applied to monitor the ...
AbstractThe solid-state form of an active pharmaceutical ingredient (API) in an oral dosage form pla...
Introduction: Paracetamol is analgesic and antipyretic, which is usually in the form of an immediate...
Dissolution of tablets into their component parts is an important method by which orally-administere...
The use of Process Analytical Technology (PAT) recommended by the Food and Drug Administration (FDA)...
The objective of this study was to compare the in vitro dissolution profile of a new rapidly absorbe...