Roberts Daryl L, Chambers Frank, Copley Mark, Mitchell Jolyon P
Applied Particle Principles, LLC, Hamilton, Virginia.
Inhalytic Ltd., Kent, United Kingdom.
J Aerosol Med Pulm Drug Deliv. 2020 Aug;33(4):214-229. doi: 10.1089/jamp.2019.1590. Epub 2020 Feb 26.
Determination of aerosol aerodynamic particle size distributions (APSD) from dry-powder inhalers (DPIs), following quality control procedures in the pharmacopeial compendia, requires that the flow through the measurement apparatus, comprising induction port, optional pre-separator, and cascade impactor, starts from zero on actuation of the inhaler, using a solenoid valve to apply vacuum to the apparatus exit. The target flow rate, governed by the inhaler resistance, is reached some time afterward. Understanding the behavior of the DPI design-specific flow rate-rise time curve can provide information about the kinetics of the initial powder dispersion in the inhaler and subsequent transport through the APSD measurement equipment. Accurate and precise measures of the internal volume of each component of this apparatus are required to enable reliable relationships to be established between this parameter and those defining the flow rate-rise time curve. An improved method is described that involves progressive withdrawal of an accurately known volume of air from the interior passageways of the apparatus-on-test that are closed to the outside atmosphere. This approach is applicable for determining internal volumes of components having complex internal geometries. Filling some components with water, along with volumetric or gravimetric measurement, has proven valuable for the induction port and for checking other measurements. Values of internal volume are provided for the USP (United States Pharmacopeia)/PhEur (European Pharmacopoeia) induction port, the Next-Generation Impactor (NGI™) with and without its pre-separator, and various Andersen 8-stage cascade impactor configurations with and without their pre-separators. These data are more accurate and precise, and therefore update those reported by Copley et al.
根据药典中的质量控制程序,测定来自干粉吸入器(DPI)的气溶胶空气动力学粒径分布(APSD)时,要求通过测量装置(包括进气口、可选的预分离器和级联冲击器)的气流在吸入器启动时从零开始,使用电磁阀对装置出口施加真空。之后的某个时间达到由吸入器阻力控制的目标流速。了解DPI特定设计的流速上升时间曲线的行为可以提供有关吸入器中初始粉末分散动力学以及随后通过APSD测量设备传输的信息。需要准确精确地测量该装置各组件的内部容积,以便在该参数与定义流速上升时间曲线的参数之间建立可靠的关系。本文描述了一种改进方法,该方法涉及从与外界大气隔绝的被测装置内部通道中逐步抽出准确已知体积的空气。这种方法适用于确定具有复杂内部几何形状的组件的内部容积。事实证明,向一些组件中注水并进行容量或重量测量,对于进气口和检查其他测量值很有价值。提供了美国药典(USP)/欧洲药典(PhEur)进气口、带和不带预分离器的下一代冲击器(NGI™)以及带和不带预分离器的各种安德森8级级联冲击器配置的内部容积值。这些数据更准确、精确,因此更新了科普利等人报告的数据。