4.6 Article

Physical aging of hydroxypropyl methylcellulose acetate succinate via enthalpy recovery

Journal

SOFT MATTER
Volume 18, Issue 43, Pages 8331-8341

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2sm01189a

Keywords

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Funding

  1. Princeton Center for Complex Materials (PCCM) [DMR-2011750]
  2. MCIU/AEI/FEDER, UE [PID2021-123438NB-100]
  3. Basque Government (Eusko Jaurlaritza) [IT1566-22]
  4. National Natural Science Foundation of China [22011530456]

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This study investigated the physical aging behavior of HPMCAS, a commonly used polymer in ASD formulations. It was found that HPMCAS exhibited conventional physical aging behavior near the glass transition temperature, but a sub-alpha-relaxation process facilitated low-temperature physical aging when annealed well below T-g. The physical aging rate showed no significant change up to 40 K below T-g, and then exhibited a near monotonic decrease with decreasing temperature. The study provides critical insights into the link between ASD stability and physical aging of the glassy polymer matrix.
Amorphous solid dispersions (ASDs) utilize the kinetic stability of the amorphous state to stabilize drug molecules within a glassy polymer matrix. Therefore, understanding the glassy-state stability of the polymer excipient is critical to ASD design and performance. Here, we investigated the physical aging of hydroxypropyl methylcellulose acetate succinate (HPMCAS), a commonly used polymer in ASD formulations. We found that HPMCAS exhibited conventional physical aging behavior when annealed near the glass transition temperature (T-g). In this scenario, structural recovery was facilitated by alpha-relaxation dynamics. However, when annealed well below T-g, a sub-alpha-relaxation process facilitated low-temperature physical aging in HPMCAS. Nevertheless, the physical aging rate exhibited no significant change up to 40 K below T-g, below which it exhibited a near monotonic decrease with decreasing temperature. Finally, infrared spectroscopy was employed to assess any effect of physical aging on the chemical structure of HPMCAS, which is known to be susceptible to degradation at temperatures 30 K above its T-g. Our results provide critical insights necessary to understand better the link between the stability of ASDs and physical aging of the glassy polymer matrix.

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