结晶和分子间结合在卡巴马泽-聚乙烯罗立固体分散物中:关于药物含量变化的实验和分子模拟研究
Huaqi Wang1, Yajie Luan1, Mengke Li1
1State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, PR China.
International journal of pharmaceutics
|September 28, 2024
概括
在固体分散中增加卡巴马西药物含量会增强药物与药物的键,导致结晶性增加,溶解性降低和不稳定性. 这突显了药物含量在固体分散性能中的关键作用.
科学领域:
- 制药科学 制药科学
- 材料科学 材料科学 材料科学
背景情况:
- 固体分散对于药物输送至关重要.
- 药物含量显著影响固体分散性质.
研究的目的:
- 为了研究药物含量,分子间结合和碳氨酸-聚乙烯罗立固体分散中的结晶性之间的关系.
- 了解微观结构变化如何影响溶解性和稳定性.
主要方法:
- 实验性描述固体分散的情况.
- 分子模拟来分析结.
- 多项式适合量化分析.
主要成果:
- 更高的药物含量增加了药物-药物键 (10%至50%显示增加了十倍).
- 随着药物含量增加,药物辅助剂的键减少了45%.
- 药物含量增加导致卡巴马西结晶相形成,对溶解性和稳定性产生负面影响.
结论:
- 药物含量,分子间键和结晶性之间存在显著的相关性.
- 药物含量是影响卡巴马西固体分散物的性能的一个关键因素.
- 结果为优化固体分散配方提供了洞察力.
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