首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Application of a droplet evaporation model to aerodynamic size measurement of drug aerosols generated by a vibrating mesh nebulizer.
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Application of a droplet evaporation model to aerodynamic size measurement of drug aerosols generated by a vibrating mesh nebulizer.

机译:液滴蒸发模型在振动筛网雾化器产生的药物气溶胶的空气动力学尺寸测量中的应用。

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BACKGROUND: Droplet evaporation has been known to bias cascade impactor measurement of aerosols generated by jet nebulizers. Previous work suggests that vibrating mesh nebulizers behave differently from jet nebulizers. Unlike jet nebulizers, vibrating mesh nebulizers do not rely on compressed air to generate droplets. However, entrained air is still required to transport the generated droplets through the cascade impactor during measurement. The mixing of the droplet and entrained air streams, and heat and mass transfer occurring downstream determines the final aerosol size distribution actually measured by the cascade impactor. This study is aimed at quantifying the effect of these factors on droplet size measurements for the case of vibrating mesh nebulizers. METHODS: A simple droplet evaporation model has been applied to investigate aerodynamic size measurement of drug aerosol droplets produced by a proprietary vibrating mesh nebulizer. The droplet size measurement system used in this study is the Next Generation Impactor (NGI) cascade impactor. Comparison of modeling results with experiment indicates that droplet evaporation remains a significant effect when sizing aerosol generated by a vibrating mesh nebulizer. RESULTS AND CONCLUSIONS: Results from the droplet evaporation model shows that the mass median aerodynamic diameter (MMAD) measured by the NGI is strongly influenced not only by the initial droplet size, but also by factors such as the temperature and humidity of entrained air, the nebulizer output rate, and the entrained air flow rate. The modeling and experimental results indicate that the influence of these variables on size measurements may be reduced significantly by refrigerating the impactor down to 5 degrees C prior to measurement. The same data also support the conclusion that for the case of nebulized drug solutions, laser diffraction spectrometry provides a meaningful droplet sizing approach, that is simpler and less susceptible to such droplet evaporation artifacts.
机译:背景技术:众所周知,液滴蒸发会偏向由喷射雾化器产生的气溶胶的级联撞击器测量。先前的工作表明,振动筛网雾化器的行为不同于喷射雾化器。与喷射雾化器不同,振动网状雾化器不依靠压缩空气来产生液滴。然而,在测量过程中仍需要夹带空气以将产生的液滴输送通过级联撞击器。液滴和夹带的空气流的混合以及下游发生的热量和质量传递决定了级联撞击器实际测量的最终气溶胶尺寸分布。这项研究旨在量化这些因素对振动筛网雾化器情况下液滴尺寸测量的影响。方法:一个简单的液滴蒸发模型已被用于研究由专用振动筛网雾化器产生的药物气溶胶液滴的空气动力学尺寸测量。本研究中使用的液滴尺寸测量系统是下一代撞击器(NGI)级联撞击器。模拟结果与实验结果的比较表明,当确定振动筛网雾化器产生的气溶胶的尺寸时,液滴蒸发仍然具有显着效果。结果与结论:液滴蒸发模型的结果表明,NGI测得的质量平均空气动力学直径(MMAD)不仅受初始液滴尺寸的影响很大,而且还受夹带空气的温度和湿度等因素的强烈影响。雾化器的输出速率,以及夹带的空气流速。建模和实验结果表明,通过在测量之前将冲击器冷冻至5摄氏度,可以显着减少这些变量对尺寸测量的影响。相同的数据也支持以下结论:对于雾化的药物溶液,激光衍射光谱法提供了一种有意义的液滴定径方法,该方法更简单且更不易受到这种液滴蒸发伪影的影响。

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