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Kinetics of Water-Induced Amorphous Phase Separation in Amorphous Solid Dispersions via Raman Mapping

Adrian Krummnow, Andreas Danzer, Kristin Voges, Samuel O. Kyeremateng, Matthias Degenhardt, Gabriele Sadowski

2023Pharmaceutics14 citationsDOIOpen Access PDF

Abstract

The poor bioavailability of an active pharmaceutical ingredient (API) can be enhanced by dissolving it in a polymeric matrix. This formulation strategy is commonly known as amorphous solid dispersion (ASD). API crystallization and/or amorphous phase separation can be detrimental to the bioavailability. Our previous work (Pharmaceutics 2022, 14(9), 1904) provided analysis of the thermodynamics underpinning the collapse of ritonavir (RIT) release from RIT/poly(vinylpyrrolidone-co-vinyl acetate) (PVPVA) ASDs due to water-induced amorphous phase separation. This work aimed for the first time to quantify the kinetics of water-induced amorphous phase separation in ASDs and the compositions of the two evolving amorphous phases. Investigations were performed via confocal Raman spectroscopy, and spectra were evaluated using so-called Indirect Hard Modeling. The kinetics of amorphous phase separation were quantified for 20 wt% and 25 wt% drug load (DL) RIT/PVPVA ASDs at 25 °C and 94% relative humidity (RH). The in situ measured compositions of the evolving phases showed excellent agreement with the ternary phase diagram of the RIT/PVPVA/water system predicted by PC-SAFT in our previous study (Pharmaceutics 2022, 14(9), 1904).

Topics & Concepts

Amorphous solidPharmaceuticsRaman spectroscopyKineticsDissolutionChemical engineeringPhase (matter)Materials scienceCrystallizationTernary operationBioavailabilityChemistryAnalytical Chemistry (journal)ChromatographyOrganic chemistryOpticsMedicineQuantum mechanicsBioinformaticsBiologyEngineeringPhysicsPharmacologyProgramming languageComputer scienceDrug Solubulity and Delivery SystemsAnalytical Chemistry and ChromatographyMicrofluidic and Capillary Electrophoresis Applications
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