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Startseite » Bioavailability enhancement » Water-Induced Phase Separation of Spray-Dried Amorphous Solid Dispersions

Water-Induced Phase Separation of Spray-Dried Amorphous Solid Dispersions

25. September 2020
Increasing water content in solvent during ASD drying

Increasing water content in solvent during ASD drying

Spray drying is widely used in the manufacturing of amorphous solid dispersion (ASD) systems due to its fast drying rate, enabling kinetic trapping of the drug in amorphous form. Spray-drying conditions, such as solvent composition, can have a profound impact on the properties of spray-dried dispersions. In this study, the phase behavior of spray-dried dispersions from methanol and methanol–water mixtures was assessed using ritonavir and copovidone [poly(vinylpyrrolidone-co-vinyl acetate) (PVPVA)] as dispersion components. The resultant ASDs were characterized using differential scanning calorimetry (DSC), fluorescence spectroscopy, X-ray photoelectron spectroscopy (XPS), as well as surface-normalized dissolution rate (SNDR) measurements.

Quaternary phase diagrams were calculated using a four-component Flory–Huggins model. It was found that the addition of water to the solvent system can lead to phase separation during the spray-drying process. A 10:90 H2O/MeOH solvent system caused a minor extent of phase separation. Phase heterogeneity in the 50 and 75% drug loading ASDs prepared from this spray solvent can be detected using DSC but not with other techniques used. The 25% drug loading system did not show phase heterogeneity in solid-state characterization but exhibited a compromised dissolution rate compared to that of the miscible ASD prepared from H2O-free solvent. This is possibly due to the formation of slow-releasing drug-rich phases upon phase separation. ASDs prepared with a 60:40 H2O/MeOH solvent mixture showed phase heterogeneity with all analytical methods used.

The surface composition of dispersion particles as measured by fluorescence spectroscopy and XPS showed good agreement, suggesting surface drug enrichment of the spray-dried ASD particles prepared from this solvent system. Calculated phase diagrams and drying trajectories were consistent with experimental observations, suggesting that small variations in solvent composition may cause significant changes in ASD phase behavior during drying. These findings should aid in spray-drying process development for ASD manufacturing and can be applied broadly to assess the risk of phase separation for spray-drying systems using mixed organic solvents or other solvent-based processes.

Download the full publication here: Water-Induced Phase Separation of Spray-Dried Amorphous Solid Dispersions

or continue reading here: Mol. Pharmaceutics 2020, More on water-Induced Phase Separation of Spray-Dried Amorphous Solid Dispersions  Publication Date:September 15, 2020, Na Li, Jonathan L. Cape, Bharat R. Mankani, Dmitry Y. Zemlyanov, Kimberly B. Shepard, Michael M. Morgen, and Lynne S. Taylor* https://doi.org/10.1021/acs.molpharmaceut.0c00798

 

Materials

Ritonavir, PVPVA-64 (Kollidon 64), pyrene, methanol, acetonitrile
Tags: excipientsformulation

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