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气道口径对雾化沙丁胺醇肺部给药的影响。

Effects of airway calibre on lung delivery of nebulised salbutamol.

作者信息

Lipworth B J, Clark D J

机构信息

Department of Clinical Pharmacology and Therapeutics, Ninewells Hospital & Medical School, University of Dundee, UK.

出版信息

Thorax. 1997 Dec;52(12):1036-9. doi: 10.1136/thx.52.12.1036.

Abstract

BACKGROUND

A study was undertaken to test the hypothesis that airway calibre may alter lung deposition and therefore lung bioavailability of inhaled drugs as a result of narrowed airways reducing peripheral drug delivery. This was evaluated using the early lung absorption profile of salbutamol over the first 30 minutes after inhalation.

METHODS

Three groups were compared: (1) 10 normal subjects with mean forced expiratory volume in one second (FEV1) 109.5% predicted and mid forced expiratory flow (FEF25-75) 103.0%, (2) 10 mild asthmatic patients with FEV1 102.0% and FEF25-75 82.6%, and (3) 10 severe asthmatic patients with FEV1 49.2% and FEF25-75 27.5% predicted. Each subject had one study visit where a single dose of nebulised salbutamol was given (40 micrograms/kg) via a Ventstream nebuliser with mouthpiece followed by mouth rinsing. Plasma salbutamol levels were measured at five, 10, 20, and 30 minutes after the end of nebulisation with calculation of maximal (Cmax) and average (Cav) concentration over 0-30 minutes. Systemic beta 2 responses (plasma potassium, tremor and heart rate) and airway responses (FEV1, FEF25-75) were measured before and 30 minutes after nebulisation.

RESULTS

For Cav over 0-30 minutes the severe asthmatic patients had a lower plasma salbutamol concentration (1.31 ng/ml) than either the normal subjects (2.40 ng/ml) or those with mild asthma (2.45 ng/ml): normal subjects versus severe asthmatics 95% CI 0.30 to 1.88, mild versus severe asthmatics 95% CI 0.07 to 2.21. Airway responses as delta FEF25-75 were lower in the severe asthmatic subjects (0.30 l/s) than in either the normal subjects (0.69 l/s) or those with mild asthma (0.74 l/s): normal subjects versus severe asthmatic subjects 95% CI 0.09 to 0.88, mild versus severe asthmatics 95% CI 0.04 to 0.93. Values for delta log tremor also showed attenuated responses in those with severe asthma (1.22 mg2/s) compared with normal subjects (2.00 mg2/s) or those with mild asthma (2.02 mg2/s): normal subjects versus those with severe asthma 95% CI -0.02 to 3.30, mild versus severe asthmatics 95% CI 0.02 to 3.30.

CONCLUSIONS

These results show that baseline airway calibre significantly alters the early lung absorption profile of salbutamol in patients with severe asthma. This may have implications in terms of optimising dose and delivery of inhaled beta 2 agonists in these patients.

摘要

背景

开展了一项研究以验证如下假设:气道管径可能会改变肺部药物沉积,进而因气道变窄减少外周药物递送而改变吸入药物的肺部生物利用度。这通过吸入沙丁胺醇后最初30分钟内的早期肺部吸收情况进行评估。

方法

比较了三组:(1)10名正常受试者,一秒用力呼气容积(FEV1)为预测值的109.5%,用力呼气中期流速(FEF25-75)为预测值的103.0%;(2)10名轻度哮喘患者,FEV1为102.0%,FEF25-75为82.6%;(3)10名重度哮喘患者,FEV1为49.2%,FEF25-75为预测值的27.5%。每位受试者进行一次研究访视,通过带有咬嘴的Ventstream雾化器给予单剂量雾化沙丁胺醇(40微克/千克),随后进行口腔冲洗。雾化结束后5分钟、10分钟、20分钟和30分钟测量血浆沙丁胺醇水平,并计算0至30分钟内的最大(Cmax)和平均(Cav)浓度。在雾化前和雾化后30分钟测量全身β2反应(血浆钾、震颤和心率)以及气道反应(FEV1、FEF25-75)。

结果

对于0至30分钟内的Cav,重度哮喘患者的血浆沙丁胺醇浓度(1.31纳克/毫升)低于正常受试者(2.40纳克/毫升)或轻度哮喘患者(2.45纳克/毫升):正常受试者与重度哮喘患者相比,95%置信区间为0.30至1.88,轻度与重度哮喘患者相比,95%置信区间为0.07至2.21。重度哮喘受试者的气道反应(以ΔFEF25-75表示)(0.30升/秒)低于正常受试者(0.69升/秒)或轻度哮喘患者(0.74升/秒):正常受试者与重度哮喘受试者相比,95%置信区间为0.09至0.88,轻度与重度哮喘患者相比,95%置信区间为0.04至0.93。与正常受试者(2.00毫克²/秒)或轻度哮喘患者(2.02毫克²/秒)相比,重度哮喘患者的Δ对数震颤值也显示反应减弱(1.22毫克²/秒):正常受试者与重度哮喘患者相比,95%置信区间为 -0.02至3.30,轻度与重度哮喘患者相比,95%置信区间为0.02至3.30。

结论

这些结果表明,基线气道管径显著改变了重度哮喘患者沙丁胺醇的早期肺部吸收情况。这可能对优化这些患者吸入β2激动剂的剂量和给药方式具有重要意义。

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