Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, 401 West Main Street, P. O. Box 843015, Richmond, Virginia, 23284, USA.
Department of Pharmaceutics, Virginia Commonwealth University, 410 North 12th Street, P.O. Box 980533, Richmond, Virginia, 23284, USA.
AAPS J. 2019 Feb 7;21(2):25. doi: 10.1208/s12248-018-0281-y.
Computational fluid dynamics (CFD) modeling offers a powerful tool for the development of drug delivery devices using a first principles approach but has been underutilized in the development of pharmaceutical inhalers. The objective of this study was to develop quantitative correlations for predicting the aerosolization behavior of a newly proposed dry powder inhaler (DPI). The dose aerosolization and containment (DAC) unit DPI utilizes inlet and outlet air orifices designed to maximize the dispersion of spray-dried powders, typically with low air volumes (~ 10 mL) and relatively low airflow rates (~ 3 L/min). Five DAC unit geometries with varying orifice outlet sizes, configurations, and protrusion distances were considered. Aerosolization experiments were performed using cascade impaction to determine mean device emitted dose (ED) and mass median aerodynamic diameter (MMAD). Concurrent CFD simulations were conducted to predict both flow field-based and particle-based dispersion parameters that captured different measures of turbulence. Strong quantitative correlations were established between multiple measures of turbulence and the experimentally observed aerosolization metrics of ED and MMAD. As expected, increasing turbulence produced increased ED with best case values reaching 85% of loaded dose. Surprisingly, decreasing turbulence produced an advantageous decrease in MMAD with values as low as approximately 1.6 μm, which is in contrast with previous studies. In conclusion, CFD provided valuable insights into the performance of the DAC unit DPI as a new device including a two-stage aerosolization process offering multiple avenues for future enhancements.
计算流体动力学(CFD)建模提供了一种强大的工具,可用于使用第一原理方法开发药物输送装置,但在开发制药吸入器方面的应用不足。本研究的目的是开发定量相关性,以预测新提出的干粉吸入器(DPI)的气溶胶化行为。剂量气溶胶化和容纳(DAC)单元 DPI 利用进口和出口空气孔设计,旨在最大限度地分散喷雾干燥粉末,通常使用低气量(约 10 mL)和相对低气流速率(约 3 L/min)。考虑了五种具有不同孔口出口尺寸、配置和突出距离的 DAC 单元几何形状。使用级联冲击进行气溶胶化实验,以确定平均装置发射剂量(ED)和质量中值空气动力学直径(MMAD)。同时进行 CFD 模拟,以预测基于流场和基于颗粒的分散参数,这些参数捕获了不同的湍流度量。在 ED 和 MMAD 的气溶胶化指标方面,建立了多种湍流度量与实验观察结果之间的强定量相关性。正如预期的那样,增加湍流会产生更高的 ED,最佳情况下可达到加载剂量的 85%。令人惊讶的是,减少湍流会导致 MMAD 有利地降低,最低值约为 1.6 μm,这与之前的研究相反。总之,CFD 为 DAC 单元 DPI 的性能提供了有价值的见解,这是一种新装置,包括两级气溶胶化过程,为未来的改进提供了多种途径。