Kothari Khushboo, Ragoonanan Vishard, Suryanarayanan Raj
†Department of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota 55445, United States.
Mol Pharm. 2015 May 4;12(5):1477-84. doi: 10.1021/mp500800c. Epub 2015 Apr 20.
We investigated the influence of polymer concentration (2.5-20% w/w) on the molecular mobility and the physical stability in solid dispersions of nifedipine (NIF) with polyvinylpyrrolidone (PVP). With an increase in polymer concentration, the α-relaxation times measured by broadband dielectric spectroscopy were longer, which reflects a decrease in molecular mobility. In the supercooled state, at a given temperature (between 55 and 75 °C), the relaxation time increased linearly as a function of polymer concentration (2.5-20% w/w). The temperature dependence of the relaxation time indicated that the fragility of the dispersion, and by extension the mechanism by which the polymer influences the relaxation time, was independent of polymer concentration. The time for NIF crystallization also increased as a function of polymer concentration. Therefore, by using molecular mobility as a predictor, a model was built to predict NIF crystallization from the dispersions in the supercooled state. The predicted crystallization times were in excellent agreement with the experimental data.
我们研究了聚合物浓度(2.5 - 20% w/w)对硝苯地平(NIF)与聚乙烯吡咯烷酮(PVP)固体分散体中分子流动性和物理稳定性的影响。随着聚合物浓度的增加,通过宽带介电谱测量的α - 弛豫时间变长,这反映了分子流动性的降低。在过冷状态下,在给定温度(55至75°C之间),弛豫时间随聚合物浓度(2.5 - 20% w/w)呈线性增加。弛豫时间的温度依赖性表明,分散体的脆性以及聚合物影响弛豫时间的机制与聚合物浓度无关。NIF结晶时间也随聚合物浓度增加。因此,以分子流动性作为预测指标,建立了一个模型来预测过冷状态下分散体中NIF的结晶情况。预测的结晶时间与实验数据高度吻合。