Abstract
Many drugs present solubility challenges which adversely affect
bioavailability
• Drug-polymer solid dispersions can improve solubility by maintaining
the drug in an amorphous state
• This study investigated computational modelling for use in preformulation studies of drug-PVP solid dispersions
• Computational modelling was able to provide insight to temperature
dependence of miscibility and to calculate key mixing parameters
bioavailability
• Drug-polymer solid dispersions can improve solubility by maintaining
the drug in an amorphous state
• This study investigated computational modelling for use in preformulation studies of drug-PVP solid dispersions
• Computational modelling was able to provide insight to temperature
dependence of miscibility and to calculate key mixing parameters
Original language | English |
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Number of pages | 1 |
Publication status | Published - 5 Sept 2016 |
Externally published | Yes |
Event | 7th APS International PharmSci 2016 - University of Strathclyde, Glasgow, United Kingdom Duration: 5 Sept 2016 → 7 Sept 2016 |
Conference
Conference | 7th APS International PharmSci 2016 |
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Country/Territory | United Kingdom |
City | Glasgow |
Period | 5/09/16 → 7/09/16 |