一种用于吸入输送药理学制剂的气溶胶发生器系统。

Medical instrumentation Pub Date : 1987-06-01
A A Strong, M J Hazucha, D A Lundgren, E R Cerini
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引用次数: 0

摘要

在医疗应用中广泛使用的大多数市售气溶胶发生器产生的气溶胶的特点是质量中值直径在4-8微米范围内,粒径在0.1-10.0微米范围内。然而,治疗和诊断气溶胶的理想尺寸是大约2-4微米的质量中位数直径,小于2.0几何标准偏差;这种尺寸增加了吸入试验的可重复性,提高了药物功效。我们将市售的DeVilbiss 65型雾化器与我们实验室开发的稀释/混合室相结合。在一系列操作条件和三种支气管收缩剂(组胺、氨基酚和甲胆碱)溶液的浓度下,研究了这种气溶胶发生器系统的特性。气溶胶产生系统产生的多分散气溶胶的质量中位数直径范围为1.7-2.4微米,几何标准偏差为1.5。气溶胶发生器系统的可靠和可重复性大大提高了支气管收缩药物支气管激发试验的功率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An aerosol generator system for inhalation delivery of pharmacologic agents.

Most commercially available aerosol generators widely used in medical applications produce aerosols characterized by a large mass median diameter in the 4-8 micron range and the particle size in the 0.1-10.0 microns range. The desirable size of therapeutic and diagnostic aerosols, however, is about 2-4 microns mass median diameter, and less than 2.0 geometric standard deviation; this size increases the reproducibility of inhalation tests and enhances drug efficacy. We combined the commercially available DeVilbiss Model 65 nebulizer with a dilution/mixing chamber developed in our laboratory. The characteristics of this aerosol generator system were examined over a range of operating conditions and concentrations of solutions of three bronchoconstrictive agents--histamine, carbachol, and methacholine. The aerosol generator system produced a polydispersed aerosol with a mass median diameter range of 1.7-2.4 microns and geometric standard deviation of 1.5. The reliable and reproducible operation of the aerosol generator system greatly increases the power of bronchial challenge tests with bronchoconstrictive drugs.

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