0000000000043200

AUTHOR

Malte Bille Rask

showing 2 related works from this author

Influence of PVP/VA copolymer composition on drug–polymer solubility

2015

In this study, the influence of copolymer composition on drug-polymer solubility was investigated. The solubility of the model drug celecoxib (CCX) in various polyvinylpyrrolidone/vinyl acetate (PVP/VA) copolymer compositions (70/30, 60/40, 50/50 and 30/70 w/w) and the pure homopolymers polyvinylpyrrolidone (PVP) and polyvinyl acetate (PVA) was predicted at 25 °C using a thermal analysis method based on the recrystallization of a supersaturated amorphous dispersion (recrystallization method). These solubilities were compared with a prediction based on the solubility of CCX in the liquid monomeric precursors of PVP/VA, N-vinylpyrrolidone (NVP) and vinyl acetate (VA), using the Flory-Huggins …

Recrystallization (geology)PolymersChemistry PharmaceuticalPharmaceutical Science02 engineering and technologyFlory–Huggins solution theory030226 pharmacology & pharmacy03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDrug StabilityPolymer chemistrymedicineVinyl acetateCopolymerSolubilityPolyvinyl acetatePolyvinylpyrrolidonePovidone021001 nanoscience & nanotechnologyMonomerSolubilitychemistryCelecoxibThermodynamicsPolyvinylsCrystallization0210 nano-technologyHydrophobic and Hydrophilic Interactionsmedicine.drugEuropean Journal of Pharmaceutical Sciences
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A Promising New Method to Estimate Drug-Polymer Solubility at Room Temperature

2016

The established methods to predict drug-polymer solubility at room temperature either rely on extrapolation over a long temperature range or are limited by the availability of a liquid analogue of the polymer. To overcome these issues, this work investigated a new methodology where the drug-polymer solubility is estimated from the solubility of the drug in a solution of the polymer at room temperature using the shake-flask method. Thus, the new polymer in solution method does not rely on temperature extrapolations and only requires the polymer and a solvent, in which the polymer is soluble, that does not affect the molecular structure of the drug and polymer relative to that in the solid st…

Work (thermodynamics)Materials sciencePolymersChemistry PharmaceuticalPharmaceutical Science02 engineering and technologyFlory–Huggins solution theory030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineDrug StabilityTransition TemperatureOrganic chemistrySolubilityThermal analysisChromatography High Pressure LiquidAcetaminophenchemistry.chemical_classificationPolymerAtmospheric temperature range021001 nanoscience & nanotechnologySolutionsSolventHildebrand solubility parameterChloramphenicolPharmaceutical PreparationsSolubilityChemical engineeringchemistryCelecoxib0210 nano-technologyJournal of Pharmaceutical Sciences
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