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两种定量气雾剂给药的沙丁胺醇颗粒的体外吸入行为及治疗反应

In vitro inhalation behaviour and therapeutical response of salbutamol particles administered from two metered dose aerosols.

作者信息

Vidgren P, Silvasti M, Vidgren M, Paronen P, Tukiainen H, Lehti H

机构信息

Orion Pharmaceutica, Kuopio.

出版信息

Pharmazie. 1991 Jan;46(1):41-3.

PMID:1857729
Abstract

In this study the particle size, as well as the in vitro deposition and the immediate bronchodilating effect on asthmatic patients, of two salbutamol inhalation aerosol preparations (Ventoline, Glaxo, UK, and salbutamol inhalation aerosol, Orion Pharmaceutica, Finland) were compared. The in vitro deposition study was performed using the modified Sierra Andersen cascade impactor. The bronchodilating effect of inhaled aerosol doses were monitored by measuring peak expiratory flow (PEF) values. In the clinical study, the pulse and blood pressure of the patients, as well as the side effects, were also recorded. Due to the anatomy and physiology of human lungs, the accepted optimum size for inhaled drug particles is under 5 microns, and preferably under 2 microns. Over 95% of the drug particles in both aerosol preparations were under 5 microns. 30% of the salbutamol particles in the Ventoline inhalation aerosol were under 2 microns, whereas in Orion salbutamol aerosol 14% of the drug particles were under 2 microns. Respectively 23% of Ventoline and 19% of the Orion salbutamol preparation penetrated into the therapeutically most significant imitated alveolar stages of the modified cascade impactor. Both salbutamol aerosols showed a clear clinical efficacy in the bronchodilating test. In addition, no significant differences existed in the bronchodilating effect of these inhalation aerosols. In conclusion, although there seemed to be a slight difference in the particle size distribution and in the in vitro inhalation behaviour, this variation did not have any effect on the clinical response.

摘要

在本研究中,比较了两种沙丁胺醇吸入气雾剂制剂(英国葛兰素公司的万托林和芬兰奥立安制药公司的沙丁胺醇吸入气雾剂)的粒径、体外沉积情况以及对哮喘患者的即时支气管扩张作用。体外沉积研究使用改良的塞拉·安德森级联撞击器进行。通过测量呼气峰值流速(PEF)值来监测吸入气雾剂剂量的支气管扩张作用。在临床研究中,还记录了患者的脉搏、血压以及副作用。由于人类肺部的解剖结构和生理特点,吸入药物颗粒的公认最佳尺寸为5微米以下,最好是2微米以下。两种气雾剂制剂中超过95%的药物颗粒都在5微米以下。万托林吸入气雾剂中30%的沙丁胺醇颗粒在2微米以下,而在奥立安沙丁胺醇气雾剂中,14%的药物颗粒在2微米以下。万托林制剂和奥立安沙丁胺醇制剂分别有23%和19%的药物颗粒进入了改良级联撞击器中具有治疗意义的模拟肺泡阶段。两种沙丁胺醇气雾剂在支气管扩张试验中均显示出明显的临床疗效。此外,这些吸入气雾剂的支气管扩张作用没有显著差异。总之,尽管在粒径分布和体外吸入行为方面似乎存在细微差异,但这种变化对临床反应没有任何影响。

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