Tobramycin Inhalation Powder™:a novel drug delivery system for treating chronic Pseudomonas aeruginosa infection in cystic fibrosis


Autoria(s): Parkins, Michael D; Elborn, J Stuart
Data(s)

01/10/2011

Resumo

Lung disease in cystic fibrosis (CF) is typified by the development of chronic airways infection culminating in bronchiectasis and progression to end-stage respiratory disease. Pseudomonas aeruginosa, a ubiquitous gram-negative bacteria, is the archetypical CF pathogen and is associated with an accelerated clinical decline. The development and widespread use of chronic suppressive aerosolized antibacterial therapies, in particular Tobramycin Inhalation Solution (TIS), in CF has contributed to reduced lung function decline and improved survival. However, the requirement for the aerosolization of these agents through nebulizers has been associated with increased treatment burden, reduced quality of life and remain a barrier to broader uptake. Tobramycin Inhalation Powder (TIP™) has been developed by Novartis with the express purpose of delivering the same benefits as TIS in a time-effective manner. Administered via the T-326™ (Novartis) Inhaler in four individual 28-mg capsules, TIP can be administered in a quarter of the time of traditional nebulizers and is inherently portable. In clinical studies, TIP has been shown to be safe, result in equivalent or superior reductions in P. aeruginosa sputum density and produce similar improvements in pulmonary function. TIP offers significant advantages in time saving, portability and convenience over traditional nebulized TIS with comparable clinical outcomes for individuals with CF.

Identificador

http://pure.qub.ac.uk/portal/en/publications/tobramycin-inhalation-powder(a4110a08-1788-408c-b98e-4e09cb289cf1).html

http://dx.doi.org/10.1586/ers.11.56

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Parkins , M D & Elborn , J S 2011 , ' Tobramycin Inhalation Powder™ : a novel drug delivery system for treating chronic Pseudomonas aeruginosa infection in cystic fibrosis ' Expert review of respiratory medicine , vol 5 , no. 5 , pp. 609-22 . DOI: 10.1586/ers.11.56

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700/2740 #Pulmonary and Respiratory Medicine #/dk/atira/pure/subjectarea/asjc/2700/2723 #Immunology and Allergy #/dk/atira/pure/subjectarea/asjc/2700/2739 #Public Health, Environmental and Occupational Health
Tipo

article