Trudell Medical International, London, Ontario, Canada.
AAPS PharmSciTech. 2010 Jun;11(2):843-51. doi: 10.1208/s12249-010-9452-6. Epub 2010 May 18.
The purpose of this study was to compare relative precision of two different abbreviated impactor measurement (AIM) systems and a traditional multi-stage cascade impactor (CI). The experimental design was chosen to provide separate estimates of variability for each impactor type. Full-resolution CIs are useful for characterizing the aerosol aerodynamic particle size distribution of orally inhaled products during development but are too cumbersome, time-consuming, and resource-intensive for other applications, such as routine quality control (QC). This article presents a proof-of-concept experiment, where two AIM systems configured to provide metrics pertinent to QC (QC-system) and human respiratory tract (HRT-system) were evaluated using a hydrofluoroalkane-albuterol pressurized metered dose inhaler. The Andersen eight-stage CI (ACI) served as the benchmark apparatus. The statistical design allowed estimation of precision with each CI configuration. Apart from one source of systematic error affecting extra-fine particle fraction from the HRT-system, no other bias was detected with either abbreviated system. The observed bias was shown to be caused by particle bounce following the displacement of surfactant by the shear force of the airflow diverging above the collection plate of the second impaction stage. A procedure was subsequently developed that eliminated this source of error, as described in the second article of this series (submitted to AAPS PharmSciTech). Measurements obtained with both abbreviated impactors were very similar in precision to the ACI for all measures of in vitro performance evaluated. Such abbreviated impactors can therefore be substituted for the ACI in certain situations, such as inhaler QC or add-on device testing.
这项研究的目的是比较两种不同的简化撞击器测量(AIM)系统和传统的多阶段级联撞击器(CI)的相对精度。实验设计选择了单独估计每种撞击器类型的可变性。全分辨率 CI 对于在开发过程中描述吸入产品的气溶胶空气动力学粒径分布非常有用,但对于其他应用(例如常规质量控制(QC))来说,它们过于繁琐、耗时且资源密集。本文提出了一个概念验证实验,其中两种配置为提供与 QC(QC 系统)和人体呼吸道(HRT 系统)相关的指标的 AIM 系统进行了评估,使用了氢氟烷烃-沙丁胺醇加压计量吸入器。Andersen 八阶段 CI(ACI)用作基准仪器。统计设计允许估计每个 CI 配置的精度。除了 HRT 系统的一个影响超细颗粒分数的系统误差源外,没有检测到其他任何与简化系统相关的偏差。观察到的偏差是由气流在第二撞击级的收集板上方分散时的剪切力使表面活性剂移位后,颗粒反弹引起的。随后开发了一种程序,如本系列的第二篇文章(提交给 AAPS PharmSciTech)所述,消除了这种误差源。对于评估的所有体外性能测量,两种简化撞击器的测量精度都与 ACI 非常相似。因此,在某些情况下,例如吸入器 QC 或附加装置测试,可以用简化撞击器代替 ACI。