吡拉西坦
动力学
固态
聚合物
相变
化学
相(物质)
材料科学
化学工程
高分子化学
热力学
物理化学
有机化学
药理学
物理
医学
量子力学
工程类
作者
Fanfan Fan,Yi Lu,Shuyuan Xu,Minshan Guo,Ting Cai
标识
DOI:10.1021/acs.molpharmaceut.4c01119
摘要
and the weakest effect on the transition. Below 75 °C, the addition of 1 wt % PEG can decrease the transformation rate from Form I to Form II of PCM by a few orders of magnitude, whereas no phase transition occurs in the presence of the other investigated polymers. The inhibitory effects of the same concentration of polymers on the kinetics of the solid-solid phase transition of piracetam polymorphs are considerably greater than those on the crystallization of PCM from the amorphous phase, especially at low temperatures. We propose that the low segmental mobility of polymers enriched between the crystalline phases can considerably inhibit the nucleation and growth of the stable form at the interface during the phase transition. Our findings deepen the current understanding of the mechanisms underlying the solid-state phase transition of polymorphic drugs in the presence of polymeric excipients, providing a promising formulation approach for stabilizing the metastable pharmaceutical polymorphs.
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