Solvent influence on the phase behavior and glass transition of Amorphous Solid Dispersions

Eur J Pharm Biopharm. 2021 Jan:158:132-142. doi: 10.1016/j.ejpb.2020.11.002. Epub 2020 Nov 16.

Abstract

Understanding the long-term stability of amorphous solid dispersions (ASDs) is important for their successful approval for market. ASD stability does not only depend on the interplay between the active pharmaceutical ingredient (API) and the polymer in the final formulation but may already be disadvantageously influenced by process steps during the production (e.g. selection of inappropriate solvent for spray drying). Residual solvent can affect the API solubility in the polymer, molecular mobility (by influencing the glass-transition temperature) and induce liquid-liquid phase separation. Enhanced mobility in the ASD due to residual solvent can promote recrystallization in ASDs. The removal of residual solvent can be expensive, time-consuming, and usually requires secondary drying procedures to fulfil the regulatory requirements. The aim of this work is to predict the API solubility in polymer-solvent mixtures, solvent influence on the glass transition, and the occurrence of liquid-liquid phase separation of solvent-loaded ASDs using the thermodynamic model PC-SAFT and to experimentally validate these predictions. ASDs containing the APIs ritonavir or naproxen and the polymers poly(vinylpyrrolidone), poly (vinylpyrrolidone-co-vinyl acetate), or hydroxypropyl methylcellulose acetate succinate were spray-dried using the solvents acetone, ethanol, and dichloromethane. API solubility, sorption behavior, liquid-liquid phase separation and glass transition in the ternary API/polymer/solvent mixtures were predicted based on the binary phase behavior between API/solvent, API/polymer, and polymer/solvent and successfully validated experimentally using dynamic vapor sorption (DVS), and Raman spectroscopy. Thus, the presented methodology allows for an in-silico selection of appropriate solvent systems for solvent-based ASD preparation based on a limited amount of experimental data for binary systems only.

Keywords: Amorphous solid dispersion; Liquid-liquid phase separation; PC-SAFT; Residual solvent; Solubility; Solvent selection; Wet glass transition.

Publication types

  • Validation Study

MeSH terms

  • Chemistry, Pharmaceutical / methods
  • Computer Simulation
  • Drug Compounding / methods*
  • Drug Stability
  • Models, Chemical*
  • Polymers / chemistry*
  • Solubility
  • Solvents / chemistry*
  • Spectrum Analysis, Raman
  • Spray Drying
  • Transition Temperature
  • Vitrification*

Substances

  • Polymers
  • Solvents