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一种新型的呼吸驱动集成涡旋间隔器装置可提高氟替卡松/沙美特罗联合用药时的相对肺部生物利用度。

A novel breath-actuated integrated vortex spacer device increases relative lung bioavailability of fluticasone/salmeterol in combination.

作者信息

Nair Arun, Clearie Karine, Menzies Daniel, Meldrum Karen, McFarlane Lesley, Lipworth Brian J

机构信息

Asthma and Allergy Research Group, Department of Medicine and Therapeutics, Ninewells Hospital and Medical School, University of Dundee, Ninewells Avenue, Dundee, Scotland, UK.

出版信息

Pulm Pharmacol Ther. 2009 Aug;22(4):305-10. doi: 10.1016/j.pupt.2009.02.001.

Abstract

BACKGROUND

Spacer devices facilitate respirable drug delivery. A novel breath-actuated antistatic spacer with integrated vortex chamber (Synchro-Breathe) device has been developed, which is compact,portable and user friendly as compared to conventional spacers which are bulky and cumbersome. The relative bioavailability to the lung of inhaled fluticasone and salmeterol combination is primarily dependent on respirable dose delivery and can be reliably quantified using adrenal suppression and early fall in serum potassium (marker of systemic beta-2 adrenoreceptor response) as surrogate markers for delivered lung dose.

AIMS AND OBJECTIVES

To compare the in vivo relative bioavailability to the lung of Hydrofluoroalkane(HFA) Seretide delivered via Synchro-Breathe (SB); an optimally prepared 750 ml large volume plastic spacer, Volumatic (VM); and conventional Evohaler pMDI (EH).

METHODS

Nineteen healthy volunteers completed the study using a randomised double blind, double dummy crossover design. Single doses of placebo or Seretide HFA 250 (total dose ex-valve: fluticasone 2000 mcg/salmeterol 200 mcg) were administered via SB, VM and EH. Overnight urinary cortisol creatinine (OUCC) and serum potassium (K) were measured at baseline and after each dose as systemic surrogates of relative respirable dose delivery for the fluticasone and salmeterol moieties, respectively.

RESULTS

Significant suppression of OUCC and K occurred from baseline with SB and VM but not EH devices(geometric mean fold suppression, 95% CI, p and arithmetic mean fall mmol/L, 95% CI, respectively); EH:1.51(0.43-1.01), p 1/4 0.06; VM: 2.52(1.57-4.04), p < 0.001; SB: 2.66(1.57-4.49), p < 0.001(equating to 33.8%,60.2% and 62.3% falls, respectively). For K, the falls for EH were 0.09(0.25 to 0.07), p 1/4 0.69; VM: 0.27(0.46 to 0.08), p 1/4 0.003; SB: 0.32(0.53 to 0.11), p 1/4 0.002 (equating to 2.2%, 6.8%, and 8.06% fall,respectively). There were no significant differences between SB and VM.

CONCLUSION

The breath-actuated Synchro-Breathe device was comparable to an optimally prepared Volumatic spacer, and resulted in commensurate improvement in relative lung bioavailability for both fluticasone and salmeterol moieties compared to pMDI.

摘要

背景

储雾罐装置有助于实现可吸入药物递送。已研发出一种新型的带有集成涡流腔的呼吸驱动抗静电储雾罐(同步呼吸)装置,与传统的笨重且使用不便的储雾罐相比,它体积小巧、便于携带且用户友好。吸入氟替卡松和沙美特罗组合药物在肺部的相对生物利用度主要取决于可吸入剂量的递送,并且可以通过肾上腺抑制和血清钾早期下降(全身β-2肾上腺素能受体反应的标志物)作为递送肺部剂量的替代标志物来可靠地进行量化。

目的

比较通过同步呼吸(SB)装置、优化制备的750毫升大容量塑料储雾罐(Volumatic,VM)以及传统的爱全乐压力定量吸入器(EH)递送的氢氟烷烃(HFA)舒利迭在体内对肺部的相对生物利用度。

方法

19名健康志愿者采用随机双盲、双模拟交叉设计完成了该研究。通过SB、VM和EH分别给予单剂量的安慰剂或舒利迭HFA 250(阀外总剂量:氟替卡松2000微克/沙美特罗200微克)。在基线以及每次给药后测量过夜尿皮质醇肌酐(OUCC)和血清钾(K),分别作为氟替卡松和沙美特罗部分相对可吸入剂量递送的全身替代指标。

结果

与基线相比,SB和VM装置导致OUCC和K显著降低,但EH装置未出现这种情况(几何平均抑制倍数,95%置信区间,p值以及算术平均下降毫摩尔/升,95%置信区间);EH:1.51(0.43 - 1.01),p = 0.06;VM:2.52(1.57 - 4.04),p < 0.001;SB:2.66(1.57 - 4.49),p < 0.001(分别相当于下降33.8%、60.2%和62.3%)。对于K,EH的下降幅度为0.09(0.25至0.07),p = 0.69;VM:0.27(0.46至0.08),p = 0.003;SB:0.32(0.53至0.11),p = 0.002(分别相当于下降2.2%、6.8%和8.06%)。SB和VM之间无显著差异。

结论

呼吸驱动的同步呼吸装置与优化制备的Volumatic储雾罐相当,并且与压力定量吸入器相比,在氟替卡松和沙美特罗部分的相对肺部生物利用度方面有相应的提高。

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