差示扫描量热法
多态性(计算机科学)
无定形固体
地塞米松
衍射
研磨
材料科学
化学工程
化学
结晶学
复合材料
工程类
热力学
物理
医学
内科学
生物化学
光学
基因
基因型
作者
Paulo F. M. de Oliveira,Jean‐François Willart,Juergen Siepmann,F. Siepmann,Marc Descamps
标识
DOI:10.1021/acs.cgd.7b01664
摘要
This study aims to investigate the polymorphism, physical stability, and amorphization possibilities of dexamethasone (DEX) drug. Milling was found to be an advantageous mean to prepare amorphous DEX nonchemically degraded. It appears to be a very useful process that allowed generating crystalline polymorphic transformation, either from the milling induced amorphous sample or from a mechanically damaged polymorphic form. The paper illustrates the interest of milling as a complementary tool to screen crystal polymorphism and to determine the relative stability of polymorphs when the decision is difficult. Physical characterizations were mainly carried out using X-ray diffraction and differential scanning calorimetry.
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