Lovelace Respiratory Research Institute , Albuquerque, NM 87108, USA.
Inhal Toxicol. 2012 Jan;24(1):27-35. doi: 10.3109/08958378.2011.632787. Epub 2011 Dec 7.
The current data analysis tools in nuclear medicine have not been used to evaluate intra organ regional deposition patterns of pharmaceutical aerosols in preclinical species.
This study evaluates aerosol deposition patterns as a function of particle size in rats and mice using novel image analysis techniques.
Mice and rats were exposed to radiolabeled polydisperse aerosols at 0.5, 1.0, 3.0, and 5.0 µm MMAD followed by SPECT/CT imaging for deposition analysis. Images were quantified for both macro deposition patterns and regional deposition analysis using the LRRI-developed Onion Model.
The deposition fraction in both rats and mice was shown to increase as the particle size decreased, with greater lung deposition in rats at all particle sizes. The Onion Model indicated that the smaller particle sizes resulted in increased peripheral deposition.
These data contrast the commonly used 10% deposition fraction for all aerosols between 1.0 and 5.0 µm and indicate that lung deposition fraction in this range does change with particle size. When compared to historical data, the 1.0, 3.0, and 5.0 µm particles result in similar lung deposition fractions; however, the 0.5 µm lung deposition fraction is markedly different. This is probably caused by the current aerosols that were polydisperse to reflect current pharmaceutical aerosols, while the historical data were generated with monodisperse aerosols.
The deposition patterns of aerosols between 0.5 and 5.0 µm showed an increase in both overall and peripheral deposition as the particle size decreased. The Onion Model allows a more complex analysis of regional deposition in preclinical models.
核医学领域的当前数据分析工具尚未用于评估临床前物种中药物气溶胶在器官内的区域沉积模式。
本研究使用新的图像分析技术评估了不同粒径的气溶胶在大鼠和小鼠中的沉积模式。
用放射性标记的多分散气溶胶对小鼠和大鼠进行暴露,气溶胶的 MMAD 分别为 0.5、1.0、3.0 和 5.0 µm,随后进行 SPECT/CT 成像以进行沉积分析。使用 LRRI 开发的洋葱模型对图像进行了宏观沉积模式和区域沉积分析的定量。
结果表明,在大鼠和小鼠中,随着粒径的减小,沉积分数增加,所有粒径下大鼠的肺部沉积更多。洋葱模型表明,较小的粒径导致外周沉积增加。
这些数据与常用的 1.0 至 5.0 µm 之间所有气溶胶的 10%沉积分数形成对比,表明该粒径范围内的肺沉积分数确实随粒径而变化。与历史数据相比,1.0、3.0 和 5.0 µm 的颗粒产生相似的肺沉积分数;然而,0.5 µm 的肺沉积分数明显不同。这可能是由于当前的气溶胶是多分散的,以反映当前的药物气溶胶,而历史数据是用单分散气溶胶生成的。
0.5 至 5.0 µm 之间的气溶胶沉积模式显示,随着粒径的减小,整体和外周沉积都增加。洋葱模型允许对临床前模型中的区域沉积进行更复杂的分析。