Finlay W H, Zuberbuhler P
Department of Mechanical Engineering, University of Alberta, Edmonton, Canada.
Chest. 1998 Dec;114(6):1676-80. doi: 10.1378/chest.114.6.1676.
To determine the amount of salbutamol or beclomethasone delivered from metered-dose inhalers (MDIs) in particle sizes appropriate for inhalational treatment with four common holding chambers (AeroChamber, OptiChamber, Space Chamber, E-Z Spacer) when used under simulated pediatric tidal breathing conditions.
Five devices of each type were tested with salbutamol (100 microg, Glaxo-Wellcome) and beclomethasone (50 microg, Glaxo-Wellcome) MDIs. Each device was connected to face replicas representative of 7-month-old (infant), 2-year-old (toddler), and 4-year-old (child) children and aerosol inhaled into a cascade impactor (Anderson) using a valve system and simulated tidal breathing patterns representative of children of these ages.
Amounts of drug inhaled in fine particles varied significantly between devices and ages (p < 0.01), eg, for beclomethasone, from 4 microg (infant, Space Chamber) to 8 microg (toddler, OptiChamber), and for salbutamol, from 18 to 36 microg. The AeroChamber and OptiChamber behaved quite similarly, delivering more drug in the fine particles than the other two devices, and having insignificant variations in these amounts with age (p > 0.05).
Amounts of drug inhaled in fine particles during pediatric tidal breathing from valved holding chambers are dependent on the holding chamber model, the drug used, and the breathing pattern, although dependence on the breathing pattern is relatively small for some of the devices tested.
确定在模拟小儿潮式呼吸条件下使用时,四种常见储物罐(爱全乐储物罐、奥倍达储物罐、空间储物罐、易吸宝储物罐)从定量吸入器(MDIs)中输送出的沙丁胺醇或倍氯米松的量,这些量应适合吸入治疗。
每种类型的五个装置分别用沙丁胺醇(100微克,葛兰素威康公司)和倍氯米松(50微克,葛兰素威康公司)定量吸入器进行测试。每个装置连接到代表7个月大(婴儿)、2岁(幼儿)和4岁(儿童)儿童的面部模型上,并使用阀门系统和气溶胶吸入到串联冲击器(安德森)中,模拟这些年龄段儿童的潮式呼吸模式。
细颗粒中吸入的药物量在不同装置和年龄之间有显著差异(p < 0.01),例如,对于倍氯米松,从4微克(婴儿,空间储物罐)到8微克(幼儿,奥倍达储物罐),对于沙丁胺醇,从18微克到36微克。爱全乐储物罐和奥倍达储物罐表现相当相似,在细颗粒中输送的药物比其他两种装置更多,并且这些量随年龄的变化不显著(p > 0.05)。
在小儿潮式呼吸期间,从带阀储物罐中吸入的细颗粒药物量取决于储物罐模型、所用药物和呼吸模式,尽管对于一些测试装置来说,对呼吸模式的依赖性相对较小。