|
|
||||||||
1-protease inhibitor using commercial inhalation devices
1 Clinical Research Group "Aerosols in Medicine" of the GSF-Institute for Inhalation Biology and the Asklepios Clinic for Respiratory Medicine, 2 Bayer Vital GmbH, Leverkusen and 3 Inamed-Intelligent Aerosol Medicine GmbH, Gauting, Germany
CORRESPONDENCE: P. Brand, GSF-Institute for Inhalation Biology, Robert-Koch-Allee 29, D-82131, Gauting, Germany. Fax: 49 8989323711. E-mail: brand@inamed.de
Keywords: Inhalation, inhalation devices,
1-protease inhibitor, replacement therapy
Received: December 19, 2002
Accepted March 14, 2003
This study was supported by Bayer Corporation, Research Triangle Park, NC, USA.
Patients with hereditary
In order to optimise this treatment approach, lung deposition of inhaled radiolabelled
The time required to deposit 50 mg of the Prolastin® (5% solution) in the lung periphery was used as a measure for the efficiency of delivery. The time was calculated from measurements of total and peripheral lung deposition of the radiolabelled
The higher efficiency of drug delivery using the AKITA® system is due to the fact that this device controls breathing patterns, which are optimised for each patient individually.
1-proteinase inhibitor (
1-PI) deficiency are at risk of developing lung emphysema. To prevent the development of this disease,
1-PI replacement therapy via inhalation may be a more convenient and effective therapy than the intravenous administration of the drug.
1-PI (Prolastin®) was studied using four different commercial inhalation devices (PARI-LC Star®, HaloLite®, and AKITA® system in combination with LC Star® and Sidestream®) in six patients with
1-PI deficiency and mild-to-severe chronic obstructive pulmonary disease.
1-PI. This time was shortest for the AKITA® system (1824 min) and significantly higher for the PARI-LC Star® (44 min) and the HaloLite® (100 min).
This article has been cited by other articles:
![]() |
M. Griese, P. Latzin, M. Kappler, K. Weckerle, T. Heinzlmaier, T. Bernhardt, and D. Hartl {alpha}1-Antitrypsin inhalation reduces airway inflammation in cystic fibrosis patients Eur. Respir. J., February 1, 2007; 29(2): 240 - 250. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |