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Effect of Water on Molecular Mobility and Physical Stability of Amorphous Pharmaceuticals

机译:水对非晶态药物分子迁移率和物理稳定性的影响

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摘要

We investigated the influence of sorbed water concentration on the molecular mobility and crystallization behavior in a model amorphous drug and a solid dispersion. The temperature scaling (T-g/T) allowed us to simultaneously evaluate the effects of water content and temperature on the relaxation time. In the supercooled dispersions, once scaled, the relaxation times of the systems with different water content overlapped. Thus, the observed increase in mobility could be explained by the "plasticization" effect of water. This effect also explained the decrease in crystallization onset temperature brought about by water. That is, plasticization is the underlying mechanism governing the observed increase in mobility and physical instability in the supercooled state. Similar results were observed in the glassy drug substance. A single linear relationship was observed between crystallization time (time for 0.5% crystallization) and T-g/T in both dry and water containing systems. Since fragility is unaffected by modest amounts of water, much like crystallization time, the mobility in the glass is expected to scale with T-g.
机译:我们研究了在模型无定形药物和固体分散体中吸附水浓度对分子迁移率和结晶行为的影响。温度换算(T-g / T)使我们能够同时评估水含量和温度对弛豫时间的影响。在过冷的分散体中,一旦结垢,具有不同水含量的系统的弛豫时间就会重叠。因此,观察到的迁移率增加可以通过水的“增塑”效应来解释。该效果还解释了由水引起的结晶起始温度的降低。即,塑化是控制在过冷状态下观察到的迁移率和物理不稳定性增加的基本机制。在玻璃状药物中观察到了相似的结果。在干燥和含水体系中,结晶时间(0.5%结晶时间)与T-g / T之间观察到单一线性关系。由于脆性不受少量水的影响,就像结晶时间一样,因此玻璃中的迁移率预计会随T-g的增加而增加。

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