Feddah M R, Davies N M, Gipps E M, Brown K F
Faculty of Pharmacy, The University of Sydney, New South Wales, Australia.
J Aerosol Med. 2001 Winter;14(4):477-85. doi: 10.1089/08942680152744686.
Respiratory spacer devices are used mainly with pressurized metered dose inhalers, especially those containing corticosteroids, to assist with patient coordination and reduce oropharyngeal side effects. This investigation examines the influence of different spacer devices on the delivered fine particle mass (aerodynamic diameter of <3.3 microm and <4.7 microm) of the corticosteroid beclomethasone dipropionate, which approximates the respirable dose. The Anderson Mark II Cascade Impactor was used to characterise the deposition of single doses of beclomethasone dipropionate from several metered-dose inhalers. Following actuation of one single dose the amount of beclomethasone dipropionate deposited on each stage of the impactor was quantified using reverse phase high-performance liquid chromatography and ultraviolet detection. The fine particle mass smaller than 4.7 microm for Respocort delivered by the Sanner and Fisonair spacer devices was 77.7% and 41.3% higher (p < 0.04), respectively, than the metered-dose inhaler alone, while the Breathatech spacer delivered 21.4% lower (p < 0.01). The fine particle mass of Becotide delivered by the Sanner, Fisonair, Nebuhaler, and Volumatic spacer devices were 81%, 42.4%, 46.9%, and 32.8% higher (p < 0.008), respectively, than be metered dose inhaler alone. The fine particle mass for Becloforte delivered by the Sanner, Fisonair, and Volumatic spacer devices was 82.8%, 36.9%, and 48.0% higher (p < 0.009) than that delivered by metered dose inhaler alone. This study suggests that there are significant differences in the fine particle mass of beclomethasone dipropionate delivered by respiratory spacer devices when used in conjunction with commercially available metered dose inhalers of this drug.
呼吸储雾器主要与压力定量吸入器配合使用,尤其是那些含有皮质类固醇的吸入器,以帮助患者协调使用并减少口咽副作用。本研究考察了不同储雾器对皮质类固醇丙酸倍氯米松可吸入剂量(空气动力学直径<3.3微米和<4.7微米)的影响。使用安德森Mark II 级联撞击器来表征几种定量吸入器单次剂量的丙酸倍氯米松的沉积情况。单次给药后,使用反相高效液相色谱法和紫外检测法定量撞击器各阶段上沉积的丙酸倍氯米松量。使用Sanner和Fisonair储雾器时,Respocort递送的小于4.7微米的细颗粒量分别比单独使用定量吸入器时高77.7%和41.3%(p<0.04),而Breathatech储雾器递送的细颗粒量则低21.4%(p<0.01)。使用Sanner、Fisonair、Nebuhaler和Volumatic储雾器时,Becotide递送的细颗粒量分别比单独使用定量吸入器时高81%、42.4%、46.9%和32.8%(p<0.008)。使用Sanner、Fisonair和Volumatic储雾器时,Becloforte递送的细颗粒量分别比单独使用定量吸入器时高82.8%、36.9%和48.0%(p<0.009)。本研究表明,当呼吸储雾器与该药物的市售定量吸入器联合使用时,丙酸倍氯米松的细颗粒量存在显著差异。