O'Callaghan C, Cant M, Robertson C
Department of Thoracic Medicine, Royal Children's Hospital, Melbourne, Australia.
Thorax. 1994 Oct;49(10):961-4. doi: 10.1136/thx.49.10.961.
It is common for inhaled steroids to be delivered through a large volume spacer device. Comparatively little is known about how this practice affects the dose of drug received by patients compared with drug delivered directly from a metered dose inhaler.
The amount of beclomethasone dipropionate, contained in particles of various size, available for inhalation from a 750 ml polycarbonate spacer (Volumatic) was determined by impinger measurement and high performance liquid chromatography. Three strengths of metered dose inhalers were studied (50 micrograms, 100 micrograms, and 250 micrograms/actuation). The effect of multiple actuations of beclomethasone dipropionate into a Volumatic spacer, and increasing residence times of drug within the spacer before inhalation, on the amount of drug available to the patient for inhalation was determined.
The amount of beclomethasone dipropionate in particles < 5 microns when delivered by a spacer device or directly from a metered dose inhaler was similar. The total amount of beclomethasone dipropionate available for inhalation per actuation decreased by 20 micrograms with the 50 micrograms inhaler, 48 micrograms with the 100 micrograms inhaler, and 161 micrograms with the 250 micrograms inhaler, when given via the spacer compared with delivery directly from a metered dose inhaler. There was a progressive decrease in drug available for inhalation per actuation as the number of actuations into the spacer increased, for all strengths of beclomethasone dipropionate tested. A progressive decrease in drug recovered per actuation was also seen with increasing residence times of drug within the spacer before inhalation.
Use of the spacer device significantly reduced the amount of nonrespirable beclomethasone dipropionate available for inhalation. The amount of beclomethasone dipropionate within respirable particles decreased considerably following multiple actuations into the spacer and with increasing residence times within the spacer before inhalation. When given via a spacer device beclomethasone dipropionate should be inhaled immediately after actuation and multiple actuations into the device should be avoided.
通过大容量储雾罐装置吸入类固醇是常见做法。与直接从定量吸入器给药相比,对于这种做法如何影响患者接受的药物剂量,人们了解相对较少。
通过冲击器测量和高效液相色谱法,测定了750毫升聚碳酸酯储雾罐(Volumatic)中不同大小颗粒所含的丙酸倍氯米松可供吸入的量。研究了三种剂量强度的定量吸入器(每次喷药50微克、100微克和250微克)。确定了将丙酸倍氯米松多次喷入Volumatic储雾罐以及在吸入前药物在储雾罐内停留时间增加对可供患者吸入的药物量的影响。
通过储雾罐装置给药或直接从定量吸入器给药时,直径<5微米颗粒中的丙酸倍氯米松量相似。与直接从定量吸入器给药相比,通过储雾罐给药时,每次喷药可供吸入的丙酸倍氯米松总量,50微克吸入器减少了20微克,100微克吸入器减少了48微克,250微克吸入器减少了161微克。对于所测试的所有强度的丙酸倍氯米松,随着喷入储雾罐的次数增加,每次喷药可供吸入的药物量逐渐减少。随着吸入前药物在储雾罐内停留时间的增加,每次喷药回收的药物量也逐渐减少。
使用储雾罐装置显著减少了可供吸入的不可吸入丙酸倍氯米松量。多次喷入储雾罐以及吸入前在储雾罐内停留时间增加后,可吸入颗粒中的丙酸倍氯米松量大幅减少。通过储雾罐装置给药时,丙酸倍氯米松应在喷药后立即吸入,应避免多次向装置内喷药。