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影响沙丁胺醇定量吸入器输送的总剂量和“可吸入”剂量的因素。

Factors affecting total and "respirable" dose delivered by a salbutamol metered dose inhaler.

作者信息

Everard M L, Devadason S G, Summers Q A, Le Souëf P N

机构信息

Perth Medical Aerosol Research Group, University Department of Paediatrics, Princess Margaret Hospital for Children, Subiaco, Western Australia.

出版信息

Thorax. 1995 Jul;50(7):746-9. doi: 10.1136/thx.50.7.746.

Abstract

BACKGROUND

Many factors contribute to the high variability of doses delivered to the lungs of patients using metered dose inhalers (MDIs). Relatively little attention has been paid to the contribution to this variability of the way in which the MDI is handled before the inhalation manoeuvre. Instruction leaflets often recommend procedures at odds with those used for in vitro testing of the device. The standard protocol for in vitro assessment of salbutamol MDIs involves shaking the MDI vigorously for 30 seconds and wasting the first two actuations. Subsequent actuations are introduced into the testing device at five second intervals. Patient instructions do not include a recommendation to waste the first two actuations and recommend a delay of one minute between actuations. A series of experiments was performed to determine whether such differences might be important.

METHODS

The total and "respirable" doses delivered by a salbutamol MDI (Ventolin, Allen & Hanburys) under various conditions were assessed with a multistage liquid impinger. The quantity of drug deposited on each stage was measured by an ultraviolet spectrophotometric method. The effect on the delivered dose of not shaking the canister, not wasting the first two doses, waiting 30 seconds between actuations, and using multiple rapid actuations was assessed by comparing the results with those obtained using the standard in vitro testing protocol.

RESULTS

Compared with a standard protocol, it was found that not shaking the MDI before use reduced the total and "respirable" dose by 25.5% and 35.7%, respectively. The dose delivered when actuating the MDI at 30 second intervals was no different from that when intervals was no different from that when intervals of five seconds were used. Two actuations separated by one second had no effect on the total dose but reduced the "respirable" dose by 15.8%, while four rapid actuations reduced the total and "respirable" doses by 8.2% and 18.2%, respectively. Storing the MDI stem down reduced the total and "respirable" dose delivered in the first actuation by 25.0% and 23.3% despite shaking the MDI before use.

CONCLUSIONS

MDIs containing drug in suspension must be shaken before use to resuspend the drug contained in the MDI, but shaking does not alter the composition of the suspension in the metering chamber and hence the dose in the first actuation remains low. Very rapid actuations can reduce the dose delivered per actuation, but salbutamol MDIs can be actuated immediately after a 10 second breath holding pause without affecting the dose delivered.

摘要

背景

多种因素导致使用定量吸入器(MDI)给患者肺部输送的剂量存在高度变异性。对于吸入操作前MDI的使用方式对这种变异性的影响,相对较少受到关注。说明书通常推荐的操作程序与用于该装置体外测试的程序不一致。沙丁胺醇MDI体外评估的标准方案包括将MDI剧烈摇晃30秒,并弃去前两次喷雾。随后的喷雾以5秒的间隔引入测试装置。患者说明书中没有包括弃去前两次喷雾的建议,而是建议两次喷雾之间间隔1分钟。进行了一系列实验以确定这些差异是否可能很重要。

方法

使用多级液体冲击器评估沙丁胺醇MDI(万托林,艾伦汉伯里公司)在各种条件下输送的总剂量和“可吸入”剂量。通过紫外分光光度法测量沉积在每个阶段的药物量。通过将结果与使用标准体外测试方案获得的结果进行比较,评估不摇晃药罐、不弃去前两剂、两次喷雾之间等待30秒以及进行多次快速喷雾对输送剂量的影响。

结果

与标准方案相比,发现使用前不摇晃MDI分别使总剂量和“可吸入”剂量降低了25.5%和35.7%。以30秒间隔喷雾MDI时输送的剂量与以5秒间隔喷雾时没有差异。间隔1秒的两次喷雾对总剂量没有影响,但使“可吸入”剂量降低了15.8%,而四次快速喷雾分别使总剂量和“可吸入”剂量降低了8.2%和18.2%。将MDI药杆向下存放,尽管使用前摇晃了MDI,但第一次喷雾时输送的总剂量和“可吸入”剂量分别降低了25.0%和23.3%。

结论

含有混悬液药物的MDI在使用前必须摇晃以重新混悬MDI中的药物,但摇晃不会改变计量室内混悬液的成分,因此第一次喷雾时的剂量仍然较低。非常快速的喷雾会减少每次喷雾输送的剂量,但沙丁胺醇MDI在屏气10秒后可立即喷雾,而不会影响输送的剂量。

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