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Eur Respir J 2003; 22:263-267
Copyright ©ERS Journals Ltd 2003


Peripheral deposition of {alpha}1-protease inhibitor using commercial inhalation devices

P. Brand1, H. Beckmann2, M. Maas Enriquez2, T. Meyer3, B. Müllinger3, K. Sommerer3, N. Weber1, T. Weuthen3 and G. Scheuch3

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, {alpha}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 {alpha}1-proteinase inhibitor ({alpha}1-PI) deficiency are at risk of developing lung emphysema. To prevent the development of this disease, {alpha}1-PI replacement therapy via inhalation may be a more convenient and effective therapy than the intravenous administration of the drug.

In order to optimise this treatment approach, lung deposition of inhaled radiolabelled {alpha}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 {alpha}1-PI deficiency and mild-to-severe chronic obstructive pulmonary disease.

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 {alpha}1-PI. This time was shortest for the AKITA® system (18–24 min) and significantly higher for the PARI-LC Star® (44 min) and the HaloLite® (100 min).

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.




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