通过序列纳米沉 (SNaP) 控制聚合物微粒形成的过程和配方参数
Parker K Lewis1, Nouha El Amri1, Erica E Burnham1
1Department of Chemical and Biomolecular Engineering, Tandon School of Engineering, New York University, Brooklyn 11201, United States.
概括
序列纳米沉 (SNaP) 提供了对聚合物微粒 (MP) 生产的精确控制,弥合了实验室精度和药物输送应用的工业可扩展性之间的差距.
科学领域:
- 材料科学
- 化学工程
- 制药科学
背景情况:
- 聚合物微粒 (MP) 对于延长释放药物的输送至关重要.
- 目前的制造方法难以平衡精确的尺寸控制和工业的可扩展性.
研究的目的:
- 引入和评估顺序纳米沉 (SNaP) 作为生产聚合物MP的可扩展方法.
- 调查控制MP大小和多分散性的关键过程参数.
主要方法:
- 使用聚乙烯醇 (PVA) 稳定的聚乙烯酸 (PLA) MPs的系统研究.
- 和撞击喷气混合几何体的比较.
- 对延迟时间和核心流度对粒子形成的影响的分析.
- 封装伊特拉科纳和释放特征的评估.
主要成果:
- 旋转混合表明核心组装优越,特别是在更高的度.
- 微粒组装遵循扩散有限的生长动力学.
- 在微粒大小 (1.6-3.0μm) 上实现精确控制,具有狭窄的多分散性.
- 使用不同稳定剂的多功能性和成功的药物封装 (83-85%的效率).
结论:
- SNaP是一个强大且可扩展的平台,用于生产高质量的制药微粒.
- 该方法为药物输送系统的关键质量属性提供了更好的控制.
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