Szczurek Justyna, Rams-Baron Marzena, Knapik-Kowalczuk Justyna, Antosik Agata, Szafraniec Joanna, Jamróz Witold, Dulski Mateusz, Jachowicz Renata, Paluch Marian
Institute of Physics, University of Silesia , Uniwersytecka 4, 40-007 Katowice, Poland.
Silesian Center for Education and Interdisciplinary Research , 75 Pulku Piechoty 1A, 41-500 Chorzow, Poland.
Mol Pharm. 2017 Apr 3;14(4):1071-1081. doi: 10.1021/acs.molpharmaceut.6b01007. Epub 2017 Mar 7.
In this paper, we investigated the molecular mobility and physical stability of amorphous bicalutamide, a poorly water-soluble drug widely used in prostate cancer treatment. Our broadband dielectric spectroscopy measurements and differential scanning calorimetry studies revealed that amorphous BIC is a moderately fragile material with a strong tendency to recrystallize from the amorphous state. However, mixing the drug with polymer polyvinylpyrrolidone results in a substantial improvement of physical stability attributed to the antiplasticizing effect governed by the polymer additive. Furthermore, IR study demonstrated the existence of specific interactions between the drug and excipient. We found out that preparation of bicalutamide-polyvinylpyrrolidone mixture in a 2-1 weight ratio completely hinder material recrystallization. Moreover, we determined the time-scale of structural relaxation in the glassy state for investigated materials. Because molecular mobility is considered an important factor governing crystallization behavior, such information was used to approximate the long-term physical stability of an amorphous drug and drug-polymer systems upon their storage at room temperature. Moreover, we found that such systems have distinctly higher water solubility and dissolution rate in comparison to the pure amorphous form, indicating the genuine formulation potential of the proposed approach.
在本文中,我们研究了非晶态比卡鲁胺的分子流动性和物理稳定性,比卡鲁胺是一种广泛用于前列腺癌治疗的难溶性药物。我们的宽带介电谱测量和差示扫描量热法研究表明,非晶态比卡鲁胺是一种中度易碎材料,具有很强的从非晶态重结晶的倾向。然而,将该药物与聚合物聚乙烯吡咯烷酮混合可显著提高物理稳定性,这归因于聚合物添加剂产生的抗塑化作用。此外,红外研究证明了药物与辅料之间存在特定相互作用。我们发现,以2:1的重量比制备比卡鲁胺 - 聚乙烯吡咯烷酮混合物可完全抑制材料重结晶。此外,我们确定了所研究材料在玻璃态下的结构弛豫时间尺度。由于分子流动性被认为是控制结晶行为的一个重要因素,此类信息被用于估算非晶态药物和药物 - 聚合物体系在室温下储存时的长期物理稳定性。此外,我们发现与纯非晶态形式相比,此类体系具有明显更高的水溶性和溶解速率,表明所提出方法具有真正的制剂潜力。