通过分子动态模拟对无形固体分散的物理稳定机制的定量分析
Hao Zhong1, Tianshu Lu1,2, Ruifeng Wang1
1State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, 999078, Macau, China.
The AAPS journal
|December 5, 2024
概括
API的分子流动性决定了无形固体分散 (ASD) 的稳定性. 超过临界药物负载值 (C*) 会引发不稳定性,由相互作用能量和扩散系数波动表明,有助于配方开发.
科学领域:
- 制药科学 制药科学
- 材料科学 材料科学 材料科学
- 计算化学计算化学
背景情况:
- 无形固体分散物 (ASDs) 增强难溶性药物的可溶性.
- 了解ASD物理稳定机制至关重要,但有限.
- 预测最大稳定的药物负载需要机械学的洞察力.
研究的目的:
- 调查控制ASD物理稳定的机制.
- 为预测最大稳定的药物负载提出量化值.
- 使用分子动力学模拟来理解机械学.
主要方法:
- 使用PVP,PVPVA64,纳素和乙氨基制定了18种不同的ASD.
- 采用分子动力学 (MD) 模拟来分析ASD行为.
- 综合动力学,热力学和前晶体分析.
主要成果:
- API分子流动性是ASD稳定性的主要决定因素.
- 高聚合物度通过结构约束和粘度限制了API的流动性.
- 确定了一个关键的药物负载值 (C*),超过这个值会发生不稳定.
- 相互作用能量和扩散系数的急剧波动预测ASD的稳定性.
- 使用搜索策略确定了潜在的前晶体遗址.
结论:
- MD模拟为预测ASD稳定性提供了基础.
- 定量值可以指导难溶药物的配方开发.
- 了解分子移动性和关键值可以提高ASD设计.
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