Inhalation of tobramycin using simulated cystic fibrosis patient profiles

被引:30
|
作者
Haynes, Alfred [1 ]
Geller, David [2 ]
Weers, Jeffry [1 ]
Ament, Brian [1 ]
Pavkov, Richard [3 ]
Malcolmson, Richard [1 ]
Debonnett, Laurie [3 ]
Mastoridis, Paul [3 ]
Yadao, Anthony [3 ]
Heuerding, Silvia [4 ]
机构
[1] Novartis Pharmaceut, 150 Ind Rd, San Carlos, CA 94070 USA
[2] Florida State Univ, Coll Med, Orlando, FL USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] Novartis Pharma AG, Basel, Switzerland
关键词
dry powder inhaler; T-326; Inhaler; inspiratory flow; delivered dose; PulmoSphere; DRY POWDER INHALERS; INSPIRATORY FLOW-RATES; LUNG DEPOSITION; TREATMENT COMPLEXITY; DRUG-DELIVERY; RESISTANCE; ADULTS; INDACATEROL; VOLUNTEERS; CHALLENGES;
D O I
10.1002/ppul.23451
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IntroductionTOBI((R)) Podhaler is a capsule-based drug-device combination (tobramycin inhalation powder [TIP] 28mg capsules via unit-dose dry powder T-326 Inhaler [Podhaler]) developed for treatment of Pseudomonas aeruginosa infection in cystic fibrosis (CF). We explored how inspiratory flow profiles and mouth-throat geometries affect drug delivery with the T-326 Inhaler. MethodsInspiratory flow profiles were recorded from 38 subjects aged 6-71 who had CF and varying degrees of lung function impairment. Ten of the inspiratory flow profiles were simulated in the laboratory using a custom breath simulator to determine delivered dose (DD) from the T-326 Inhaler. In vitro total lung dose (TLDin vitro) was measured using four anatomical throat models, ranging from a child to a large adult. ResultsAerosol performance was assessed across a range of inspiratory flow profiles. Mean DD ranged from 88.8% to 97.0% of declared capsule content. TLDin vitro ranged from 54.8% to 72.4% of capsule content between the flow profile/throat options tested, and the mean TLDin vitro across the range of flow profiles and anatomical throats tested was 635%. ConclusionsOur findings indicate that the T-326 Inhaler provides reliable drug delivery at flow rates likely to be achieved by a broad spectrum of patients with CF. Importantly, forceful inhalation was not required to achieve a robust TLDin vitro. Pediatr Pulmonol. 2016;51:1159-1167. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:1159 / 1167
页数:9
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