Pharmacokinetic and tolerability profiles of tobramycin nebuliser solution 300 mg/4 ml administered by PARI eFlow® rapid and PARI LC Plus® nebulisers in cystic fibrosis patients

被引:17
作者
Govoni, Mirco [1 ]
Poli, Gianluigi [1 ]
Acerbi, Daniela [1 ]
Santoro, Debora [1 ]
Cicirello, Helen [2 ]
Annoni, Ottavia [3 ]
Ruzicka, Jozef [4 ]
机构
[1] Chiesi Farmaceutici SpA, I-43100 Parma, Italy
[2] Chiesi Pharmaceut Inc, Rockville, MD 20850 USA
[3] CROSS Res SA, CH-6864 Arzo, Switzerland
[4] Fak Nemocn S Poliklin Bratislava Ruzinov, Bratislava 82606, Slovakia
关键词
Tobramycin; Nebulisation; Pharmacokinetics; Safety and tolerability; Cystic fibrosis; Chronic infection; Pseudomonas aeruginosa; PSEUDOMONAS-AERUGINOSA INFECTION; INHALED TOBRAMYCIN; THERAPY; BRAMITOB((R)); JET;
D O I
10.1016/j.pupt.2012.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Tobramycin nebuliser solution (TNS) is indicated for maintenance therapy in cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa (PA) infections. Adherence to recommended therapy in CF has always been a challenge and new generation nebulisers are increasingly used "off label" to reduce the time required for inhalation, potentially improving patient compliance. Methods: In this open-label, randomised, multi-centre, two-period crossover study, 27 CF patients with PA infection received TNS 300 mg/4 mL (TNS4) via the PARI eFlow (R) rapid or PARI LC Plus (R) nebuliser twice daily for 28 days in two study periods separated by a 4-week washout. The pharmacokinetic profile in plasma and sputum were determined after single and multiple dose administration on Day 1 and Day 28, respectively. Nebulisation times and general safety and tolerability profiles were evaluated throughout the study. Results: Plasma tobramycin pharmacokinetic profiles were similar for the eFlow and LC Plus nebulisers both on Day 1 and Day 28. After multiple dose administration for 28 days, the eFlow/LC Plus ratio of geometric means for plasma C-max and AUC(0-t), were 85.32 (90% CI, 61.24-118.86) and 87.44 (90% CI, 64.87-117.87), respectively. Despite the high variability, sputum tobramycin C-max and AUC(0-t) for the eFlow on Day 28 tended to be higher than for the LC Plus (90% CI for the ratio, 86.11-226.45 and 81.81-236.71), respectively. Nebulisation times were significantly shorter for the eFlow with a median time for nebulisation of 5 min in comparison to 13 min for the LC Plus. Safety data confirmed a favourable safety profile for TNS4, with the majority of the findings being related to the underlying CF disease. Conclusions: Plasma and sputum pharmacokinetic data in CF patients with chronic PA infection support comparable pulmonary delivery and safety of TNS4 administered using different nebulisers, with a significantly shorter nebulisation time for the eFlow. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:249 / 255
页数:7
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