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首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Model of the deposition of aerosol particles in the respiratory tract of the rat. II. hygroscopic particle deposition
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Model of the deposition of aerosol particles in the respiratory tract of the rat. II. hygroscopic particle deposition

机译:大鼠呼吸道中气溶胶颗粒沉积的模型。二。吸湿性颗粒沉积

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摘要

Background: Rats are frequently used to study the pharmacological and toxicological effects of inhaled aerosol particles. The deposition behavior of aerosol particles in airways is affected by their hygroscopic properties, which accordingly influence the results of such studies. Method: A recently published nonhygroscopic aerosol particle deposition model for rat airways was extended with equations for hygroscopic particle growth in humid air and with a model to mimic the temperature and relative humidity conditions in the rat airways transformed from the upper human airways. As there are no experimental data available for hygroscopic deposition in rat lungs, several model assumptions were made for the humidity distribution in the upper rat airways. Results: The total and regional deposition probability of salt particles in the diameter range 0.02 to 5 μm in rat lung was significantly changed by the hygroscopic properties. The maximum ratios of the total deposition of inhaled initially dry sodium chloride, cobalt chloride, and zinc sulfate particles compared with nonhygroscopic particles were 3.28, 2.44, and 2.13, respectively, and the minimum ratios 0.57, 0.63, and 0.70, respectively. The corresponding maximum (and minimum) ratios for the hygroscopic drugs histamine dihydrochloride, carbenicillin disodium, and atropine sulfate were 1.86 (0.65), 1.53 (0.70), and 1.35 (0.76), respectively. Total deposition was about 20% higher in human airways than in rat airways. The flow regime in the rat upper airways influenced total and regional deposition much less than it did in human airways. Conclusion: The hygroscopicity of salt and drug aerosol particles is an important factor in rat lung deposition.
机译:背景:大鼠经常被用来研究吸入气溶胶颗粒的药理和毒理作用。气溶胶颗粒在气道中的沉积行为受其吸湿性的影响,因此会影响此类研究的结果。方法:扩展了最近发布的大鼠气道的非吸湿性气溶胶颗粒沉积模型,该模型扩展了湿空气中吸湿性颗粒生长的方程式,并模拟了从上呼吸道转变的大鼠气道的温度和相对湿度条件。由于尚无可用于大鼠肺内吸湿性沉积的实验数据,因此针对大鼠上呼吸道的湿度分布做出了几个模型假设。结果:吸湿性显着改变了大鼠肺中直径范围为0.02至5μm的盐颗粒的总沉积和区域沉积概率。与非吸湿性颗粒相比,吸入的最初干燥的氯化钠,氯化钴和硫酸锌颗粒的总沉积最大比例分别为3.28、2.44和2.13,最小比例分别为0.57、0.63和0.70。吸湿性药物组胺二盐酸盐,羧苄青霉素二钠和硫酸阿托品的相应最大(和最小)比分别为1.86(0.65),1.53(0.70)和1.35(0.76)。人气道的总沉积量比大鼠气道高约20%。大鼠上呼吸道的血流状况对总和区域沉积的影响远不如人类呼吸道。结论:盐和药物气溶胶颗粒的吸湿性是影响大鼠肺沉积的重要因素。

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