Improving the physical stability of freeze-dried amorphous sugar matrices by compression at several hundreds MPa

Ryo Kagotani, Kohshi Kinugawa, Mayo Nomura, Hiroyuki Imanaka, Naoyuki Ishida, Koreyoshi Imamura

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Amorphous matrices, composed of sugars, are markedly plasticized by moisture uptake, which results in physical instability. Our previous studies, in the compression pressure range ≤443 MPa, indicated that when a matrix is compressed, the amount of sorbed water at given relative humidities (RHs) decreases, whereas the glass transition temperature (Tg) remains constant. Herein, the effect of higher compression pressures than those used previously was explored to investigate the feasibility of using compression to improve the physical stability of amorphous sugar matrix against water uptake and subsequent collapse. Amorphous sugar samples were prepared by freeze-drying and then compressed at 0-665 MPa, followed by rehumidification at given RHs. The physical stability of the amorphous sugar sample was evaluated by measuring Tg and crystallization temperature (Tcry). The amounts of sorbed water, different in the interaction state, were determined using an FTIR technique. It was found that the compression at pressures of ≥443 MPa decreased the amount of sorbed water, which is a major factor in plasticization and crystallization, and thus markedly increased the Tg and Tcry relative to that for the uncompressed sample. Hence, the compression at several hundreds MPa appears to be feasible for improving the physical stability of amorphous sugar matrix.

Original languageEnglish
Pages (from-to)2187-2197
Number of pages11
JournalJournal of Pharmaceutical Sciences
Volume102
Issue number7
DOIs
Publication statusPublished - Jul 2013

Keywords

  • Amorphous sugar
  • Calorimetry (DSC)
  • Compression
  • FTIR
  • Freeze-drying
  • Glass transition temperature
  • Water sorption

ASJC Scopus subject areas

  • Pharmaceutical Science

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