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Anomalous Water-Sorption Kinetics in ASDs.
Dominik Borrmann1, Andreas Danzer1, Gabriele Sadowski1
1Laboratory of Thermodynamics, Department of Chemical and Biochemical Engineering, TU Dortmund University, Emil-Figge-Str. 70, 44227 Dortmund, Germany.
Anomalous water sorption in amorphous solid dispersions (ASDs) is due to slow polymer swelling. A diffusion-relaxation model accurately predicted this behavior, revealing more pronounced effects in ASDs than in pure polymers.
Area of Science:
- Materials Science
- Physical Chemistry
- Pharmaceutical Sciences
Background:
- Anomalous water-sorption kinetics in amorphous solid dispersions (ASDs) are primarily attributed to the slow swelling of the polymer matrix.
- Understanding these kinetics is crucial for predicting drug release from ASDs.
Purpose of the Study:
- To predict the anomalous water-sorption kinetics in poly(vinyl-pyrrolidone)-co-vinyl-acetate (PVPVA) and indomethacin (IND) ASDs using a diffusion-relaxation model.
- To elucidate the underlying mechanisms causing anomalous water sorption in these ASDs.
Main Methods:
- Utilized a diffusion-relaxation model incorporating the Williams-Landel-Ferry (WLF) and Arrhenius equations.
- Model predictions were based on the viscosities of pure PVPVA, pure IND, and water-sorption kinetics of pure PVPVA.
- Compared model predictions with experimental data for qualitative and quantitative agreement.
Main Results:
- The diffusion-relaxation model successfully predicted various types of anomalous water-sorption behavior in ASDs.
- ASDs exhibited more pronounced anomalous two-stage water-sorption than pure PVPVA.
- Higher viscosity of glassy ASD-water mixtures compared to PVPVA-water mixtures was identified as the cause for slower swelling.
Conclusions:
- The developed modeling approach accurately captures anomalous water-sorption kinetics in ASDs.
- The study highlights the significant impact of polymer swelling dynamics on water sorption in ASDs.
- This modeling strategy can be applied to predict diffusion- or swelling-controlled drug release from ASDs.
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