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首页> 外文期刊>Molecular pharmaceutics >Predicting Crystallization of Amorphous Drugs with Terahertz Spectroscopy
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Predicting Crystallization of Amorphous Drugs with Terahertz Spectroscopy

机译:太赫兹光谱法预测非晶态药物的结晶

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There is a controversy about the extent to which the primary and secondary dielectric relaxations influence the crystallization of amorphous organic compounds below the glass transition temperature. Recent studies also point to the importance of fast molecular dynamics on picosecond-to-nanosecond time scales with respect to the glass stability. In the present study we provide terahertz spectroscopy evidence on the crystallization of amorphous naproxen well below its glass transition temperature and confirm the direct role of Johari-Goldstein (JG) secondary relaxation as a facilitator of the crystallization. We determine the onset temperature T beta above which the JG relaxation contributes to the fast molecular dynamics and analytically quantify the level of this contribution. We then show there is a strong correlation between the increase in the fast molecular dynamics and onset of crystallization in several chosen amorphous drugs. We believe that this technique has immediate applications to quantify the stability of amorphous drug materials.
机译:在玻璃化转变温度以下,主要和次要介电弛豫影响非晶态有机化合物结晶的程度存在争议。最近的研究还指出,就玻璃稳定性而言,皮秒至纳秒级时间尺度上快速分子动力学的重要性。在本研究中,我们提供了太赫兹光谱证据,证明非晶态萘普生的结晶度远低于其玻璃化转变温度,并证实了Johari-Goldstein(JG)二次弛豫作为结晶促进剂的直接作用。我们确定起始温度T beta,高于此温度,JG弛豫有助于快速的分子动力学,并分析量化该贡献的水平。然后,我们表明在几种选定的无定形药物中,快速分子动力学的增加与结晶的开始之间有很强的相关性。我们认为,该技术可立即用于量化无定形药物材料的稳定性。

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