Department of Pharmacognosy and Phytochemistry, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia in Katowice, ul. Jagiellonska 4, 41-200 Sosnowiec, Poland.
Institute of Physics, Faculty of Science and Technology, University of Silesia in Katowice, 75 Pułku Piechoty 1, 41-500 Chorzów, Poland.
Mol Pharm. 2022 Jan 3;19(1):80-90. doi: 10.1021/acs.molpharmaceut.1c00613. Epub 2021 Dec 1.
In this paper, several experimental techniques [X-ray diffraction, differential scanning calorimetry (DSC), thermogravimetry, Fourier transform infrared spectroscopy, and broad-band dielectric spectroscopy] have been applied to characterize the structural and thermal properties, H-bonding pattern, and molecular dynamics of amorphous bosentan (BOS) obtained by vitrification and cryomilling of the monohydrate crystalline form of this drug. Samples prepared by these two methods were found to be similar with regard to their internal structure, H-bonding scheme, and structural (α) dynamics in the supercooled liquid state. However, based on the analysis of α-relaxation times (dielectric measurements) predicted for temperatures below the glass-transition temperature (), as well as DSC thermograms, it was concluded that the cryoground sample is more aged (and probably more physically stable) compared to the vitrified one. Interestingly, such differences in physical properties turned out to be reflected in the lower intrinsic dissolution rate of BOS obtained by cryomilling (in the first 15 min of dissolution test) in comparison to the vitrified drug. Furthermore, we showed that cryogrinding of the crystalline BOS monohydrate leads to the formation of a nearly anhydrous amorphous sample. This finding, different from that reported by Megarry et al. [ 2011, 346, 1061-1064] for trehalose (TRE), was revealed on the basis of infrared and thermal measurements. Finally, two various hypotheses explaining water removal upon cryomilling have been discussed in the manuscript.
本文采用 X 射线衍射、差示扫描量热法(DSC)、热重分析、傅里叶变换红外光谱和宽频介电谱等实验技术,研究了一水合物结晶形式的药物经玻璃化和冷冻研磨后得到的无定形 bosentan(BOS)的结构和热性能、氢键模式和分子动力学。这两种方法制备的样品在其内部结构、氢键方案和过冷液体状态下的结构(α)动力学方面具有相似性。然而,基于对低于玻璃化转变温度()的温度下预测的α-松弛时间(介电测量)以及 DSC 图谱的分析,得出结论:与玻璃化样品相比,冷冻研磨样品更老化(可能更物理稳定)。有趣的是,与玻璃化样品相比,物理性质的这种差异反映在冷冻研磨 BOS 的内在溶解速率较低(在溶解试验的前 15 分钟)。此外,我们表明,冷冻研磨结晶 BOS 一水合物会导致形成几乎无水的无定形样品。与 Megarry 等人报告的 trehalose(TRE)的结果不同[2011, 346, 1061-1064],这是基于红外和热测量得出的发现。最后,本文讨论了两种不同的假设,解释了冷冻研磨时水的去除。