Duke Daniel J, Kastengren Alan L, Mason-Smith Nicholas, Chen Yang, Young Paul M, Traini Daniela, Lewis David, Edgington-Mitchell Daniel, Honnery Damon
Energy Systems Division, Argonne National Laboratory, Lemont, Illinois, USA.
X-ray Science Division, Argonne National Laboratory, Lemont, Illinois, USA.
Pharm Res. 2016 Apr;33(4):816-25. doi: 10.1007/s11095-015-1828-6. Epub 2015 Nov 12.
Drug concentration measurements in MDI sprays are typically performed using particle filtration or laser scattering. These techniques are ineffective in proximity to the nozzle, making it difficult to determine how factors such as nozzle design will affect the precipitation of co-solvent droplets in solution-based MDIs, and the final particle distribution.
In optical measurements, scattering from the constituents is difficult to separate. We present a novel technique to directly measure drug distribution. A focused x-ray beam was used to stimulate x-ray fluorescence from the bromine in a solution containing 85% HFA, 15% ethanol co-solvent, and 1 [Formula: see text] / [Formula: see text] IPBr.
Instantaneous concentration measurements were obtained with 1 ms temporal resolution and 5 [Formula: see text] spatial resolution, providing information in a region that is inaccessible to many other diagnostics. The drug remains homogeneously mixed over time, but was found to be higher at the centerline than at the periphery. This may have implications for oropharyngeal deposition in vivo.
Measurements in the dynamic, turbulent region of MDIs allow us to understand the physical links between formulation, inspiration, and geometry on final particle size and distribution. This will ultimately lead to a better understanding of how MDI design can be improved to enhance respirable fraction.
计量吸入器(MDI)喷雾剂中的药物浓度测量通常采用颗粒过滤或激光散射技术。这些技术在靠近喷嘴处无效,难以确定诸如喷嘴设计等因素如何影响基于溶液的MDIs中助溶剂液滴的沉淀以及最终的颗粒分布。
在光学测量中,成分的散射难以分离。我们提出了一种直接测量药物分布的新技术。使用聚焦的X射线束激发含有85%氢氟烷烃(HFA)、15%乙醇助溶剂和1[公式:见原文]/[公式:见原文]异丙托溴铵(IPBr)的溶液中溴的X射线荧光。
以1毫秒的时间分辨率和5[公式:见原文]的空间分辨率获得了瞬时浓度测量结果,在许多其他诊断方法无法触及的区域提供了信息。药物随时间保持均匀混合,但发现在中心线处比在外围更高。这可能对体内口咽部沉积有影响。
在MDIs的动态、湍流区域进行测量使我们能够理解配方、吸气和几何形状对最终颗粒大小和分布的物理联系。这最终将有助于更好地理解如何改进MDI设计以提高可吸入部分。