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通过差示扫描量热法、介电和力学光谱研究过冷药物制剂泊沙康唑的分子动力学。

Molecular dynamics of the supercooled pharmaceutical agent posaconazole studied via differential scanning calorimetry and dielectric and mechanical spectroscopies.

机构信息

NanoBioMedical Centre, Adam Mickiewicz University , ul. Umultowska 85, 61-614 Poznan, Poland.

出版信息

Mol Pharm. 2013 Oct 7;10(10):3934-45. doi: 10.1021/mp4003915. Epub 2013 Sep 25.

DOI:10.1021/mp4003915
PMID:24010649
Abstract

This paper presents comprehensive studies on the molecular dynamics of a pharmaceutically important substance, posaconazole. In order to characterize relaxation dynamics in the supercooled liquid and glassy states, dielectric and mechanical spectroscopies were applied. Dielectric data have indicated multiple relaxation processes that appear above and below the glass transition temperature Tg (τα=100 s) of posaconazole. From the curvature of the dielectric log10(τα) versus inverse of temperature dependence, we determine so-called "fragility", being a very popular parameter for classifying the structural dynamics of supercooled liquids and polymers. From the calculations, we get m=150, which means that is one of the most fragile glass-forming liquids. In this paper, the relaxation dynamics of supercooled posaconazole extracted from the dielectric response function was also confronted with shear-mechanical relaxation. Finally, we have also presented a direct comparison of the fragility and the number of dynamically correlated molecules Nc determined from dynamic calorimetry curves and dielectric and mechanical spectroscopies, showing a clear deviation in the picture of glass-transition dynamics generated by calorimetric and spectroscopic techniques.

摘要

本文对一种具有重要药用价值的物质——泊沙康唑的分子动力学进行了全面研究。为了研究过冷液体和玻璃态的弛豫动力学,采用了介电和力学光谱法。介电数据表明,泊沙康唑的玻璃化转变温度 Tg(τα=100 s)以上和以下存在多个弛豫过程。从介电常数 log10(τα) 随温度倒数的曲率可以确定所谓的“脆性”,这是用于分类过冷液体和聚合物结构动力学的一个非常流行的参数。通过计算,我们得到 m=150,这意味着它是最脆弱的玻璃形成液体之一。在本文中,还将从介电响应函数中提取的过冷泊沙康唑的弛豫动力学与剪切力学弛豫进行了对比。最后,我们还对从动态量热曲线和介电及力学光谱法确定的脆性和动态相关分子数 Nc 进行了直接比较,表明量热法和光谱法所产生的玻璃化转变动力学图像存在明显差异。

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