Martonen T B, Katz I, Fults K, Hickey A J
Health Effects Research Laboratory, Environmental Protection Agency, Research Triangle Park, North Carolina 27711.
Pharm Res. 1992 Dec;9(12):1634-9. doi: 10.1023/a:1015880828704.
Analytical estimates of the respirable fractions on inhaled pharmaceutical aerosols are obtained by inertial sampling techniques. The respirable fraction may be defined as that portion of the particle size distribution less than a designated diameter. The diameter size below which particles were considered respirable in these studies was 6.4 microns. In clinical practice, a variety of particle size distributions may be related to a single respirable fraction. Herein, three respirable fractions were each defined by six particle size distributions. The deposition patterns of aerosols exhibiting these particle size characteristics were examined in a mathematical model. The analytically defined respirable fractions were compared with predicted lung deposition values. Under clearly defined breathing conditions, there is a correlation between the nominal respirable fraction and deposition. However, it was concluded that the variations which occur in breathing parameters within patient populations may not allow a single analytically derived respirable fraction to be appropriate for all individual subjects.
通过惯性采样技术可获得吸入药物气雾剂可吸入部分的分析估计值。可吸入部分可定义为粒径分布中小于指定直径的那部分。在这些研究中,被认为可吸入的颗粒直径大小为6.4微米。在临床实践中,多种粒径分布可能与单一可吸入部分相关。在此,三种可吸入部分分别由六种粒径分布定义。在一个数学模型中研究了呈现这些粒径特征的气雾剂的沉积模式。将分析定义的可吸入部分与预测的肺部沉积值进行了比较。在明确界定的呼吸条件下,标称可吸入部分与沉积之间存在相关性。然而,得出的结论是,患者群体中呼吸参数的变化可能不允许单一分析得出的可吸入部分适用于所有个体受试者。