Absorption kinetics after inhalation of fluticasone propionate via the Diskhaler®, Diskus® and metered-dose inhaler in healthy volunteers

被引:25
作者
Brindley, C
Falcoz, C
Mackie, AE
Bye, A
机构
[1] Glaxo Wellcome Res & Dev, Clin Pharmacol, Greenford, Middx, England
[2] Quintiles Scotland Ltd, Drug Metab & Pharmacokinet, Edinburgh, Midlothian, Scotland
[3] Eli Lilly & Co, Lilly Res Ctr Ltd, Windlesham GU20 6PH, Surrey, England
关键词
D O I
10.2165/00003088-200039001-00001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The aim of this analysis was to assess the rate and extent of systemic availability of inhaled fluticasone propionate (FP) from 2 dry powder systems (Diskhaler(R) and Diskus(R)) and a metered-dose inhaler (MDI) by deconvolution analysis. Methods: The inhalation devices were evaluated in 3 separate studies with identical protocols. 12 healthy male volunteers were randomised to receive FP given as a 1000 mug inhaled dose and 250 mug by intravenous infusion according to a double-blind double-dummy crossover design. The bioavailability of FP after inhalation represents absorption of the drug from the lungs, since the bioavailability of the swallowed portion of the inhaled dose is negligible. Results: When corrected for the bioavailability (of EP) achieved by each inhalation device, the rate of absorption of FP over the first 2 hours was rapid from all devices. The mean time for absorption of 50% of the bioavailable dose was 1.6, 2.4, and 2.2 hours for the Diskhaler(R), Diskus(R) and MDI, respectively. Thereafter, absorption from each device was prolonged, with approximately 10% of the dose remaining in the lungs 12 hours after inhalation. Conclusion: Irrespective of the inhalation device used, the prolonged absorption of FP into the systemic circulation indicates a long residence time in the lungs.
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页码:1 / 8
页数:8
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