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雾化器性能:AFLM研究。法国囊性纤维化防治协会

Nebulizer performance: AFLM study. Association Française de Lutte contre la Mucoviscidose.

作者信息

Faurisson F, Dessanges J F, Grimfeld A, Beaulieu R, Kitzis M D, Peytavin G, Lefebvre J P, Farinotti R, Sautegeau A

机构信息

INSERM U 13, Paris, France.

出版信息

Respiration. 1995;62 Suppl 1:13-8. doi: 10.1159/000196488.

DOI:10.1159/000196488
PMID:7792434
Abstract

This study was conducted by the AFLM order to determine the performance characteristics of 12 commercially available nebulizers (6 ultrasonic and 6 jet) used in the treatment of cystic fibrosis (CF). The nebulizers were connected to a circuit which simulated the ventilation of a CF child and CF adult, and were tested using three drug solutions: tobramycin (T), colistin (C), and amiloride (A). Nebulizer performance was evaluated according to the volume of drug solution delivered in 10 min during the simulated inspiratory phase (VI), drug granulometry (G%), drug concentration modification in the nebulizer reservoir (delta C), and percentage of efficiently aerosolized drug EA%). The ultrasonic devices delivered a significantly higher VI than the jet nebulizers (p < 0.0001) for all three study drug. Ventilation rate did not influence VI. Regarding granulometry, higher percentages of T and A were found to be contained in droplets ranging from 0.5 to 5.0 micron following ultrasonic nebulization. Drug concentration modifications were independent of the nebulizer used but were influenced by drug type; overconcentrations of T and A were observed (delta C = +10.5 +/- 18.6 and +13.4 +/- 8.9%, respectively). On average, the ultrasonic devices achieved a higher EA% than the jet nebulizers (17.3 +/- 6.7 and 9.7 +/- 9.6%, respectively). This study highlights the significant variability in performance of different nebulizer types and empahsizes the importance of accurately testing nebulizers prior to clinical use so that the most efficacious nebulizer/drug combinations may be prescribed.

摘要

美国雾化治疗学会(AFLM)开展了这项研究,以确定用于治疗囊性纤维化(CF)的12种市售雾化器(6种超声雾化器和6种喷射雾化器)的性能特征。这些雾化器连接到一个模拟CF儿童和CF成人通气的回路,并使用三种药物溶液进行测试:妥布霉素(T)、黏菌素(C)和阿米洛利(A)。根据模拟吸气阶段10分钟内输送的药物溶液体积(VI)、药物粒度(G%)、雾化器储液器中的药物浓度变化(ΔC)以及有效雾化药物的百分比(EA%)来评估雾化器性能。对于所有三种研究药物,超声设备输送的VI显著高于喷射雾化器(p < 0.0001)。通气率不影响VI。关于粒度,超声雾化后发现,粒径在0.5至5.0微米范围内的液滴中,T和A的含量百分比更高。药物浓度变化与所使用的雾化器无关,但受药物类型影响;观察到T和A出现浓度过高的情况(ΔC分别为+10.5±18.6和+13.4±8.9%)。平均而言,超声设备的EA%高于喷射雾化器(分别为17.3±6.7和9.7±9.6%)。这项研究突出了不同类型雾化器性能的显著差异,并强调了在临床使用前准确测试雾化器的重要性,以便能够开出最有效的雾化器/药物组合处方。

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Respiration. 1995;62 Suppl 1:13-8. doi: 10.1159/000196488.
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引用本文的文献

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Crit Care. 2005 Feb;9(1):R53-9. doi: 10.1186/cc3020. Epub 2005 Jan 6.
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Dose-response to salbutamol via a novel palm sized nebuliser (Aerodose Inhaler), conventional nebuliser (Pari LC Plus) and metered dose inhaler (Ventolin Evohaler) in moderate to severe asthmatics.通过一种新型手掌大小的雾化器(Aerodose吸入器)、传统雾化器(Pari LC Plus)和定量气雾剂(万托林气雾剂)对中重度哮喘患者进行沙丁胺醇的剂量反应研究。
Br J Clin Pharmacol. 2005 Jan;59(1):5-13. doi: 10.1111/j.1365-2125.2005.02168.x.
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Pulmonary drug delivery. Part II: the role of inhalant delivery devices and drug formulations in therapeutic effectiveness of aerosolized medications.
肺部给药。第二部分:吸入给药装置和药物制剂在雾化药物治疗效果中的作用。
Br J Clin Pharmacol. 2003 Dec;56(6):600-12. doi: 10.1046/j.1365-2125.2003.01893.x.
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Determination of the relative bioavailability of salbutamol to the lungs and systemic circulation following nebulization.雾化吸入后沙丁胺醇在肺部与体循环中的相对生物利用度测定。
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