Influence of the technological parameters of ultrasonic nebulisation on the nebulisation quality of alpha 1 protease inhibitor (alpha 1I)

Citation
Mp. Flament et al., Influence of the technological parameters of ultrasonic nebulisation on the nebulisation quality of alpha 1 protease inhibitor (alpha 1I), INT J PHARM, 189(2), 1999, pp. 197-204
Citations number
19
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
ISSN journal
03785173 → ACNP
Volume
189
Issue
2
Year of publication
1999
Pages
197 - 204
Database
ISI
SICI code
0378-5173(19991105)189:2<197:IOTTPO>2.0.ZU;2-O
Abstract
The principle of an ultrasonic nebuliser is based on the vibrations of a pi ezo-electric crystal driven by an alternating electrical field. These perio dical vibrations are characterised by their frequency, their amplitude and their intensity which corresponds to the energy transmitted per surface uni t. When the vibration intensity is sufficient, cavitation appears and gener ates droplets. Ventilation enables an airflow to cross the nebuliser and to expulse the aerosol droplets. For a given nebuliser, the vibration frequen cy of the piezo-electric crystal is fixed and is often in the range of 1-2. 5 MHz. In most cases, an adjustment in vibration intensity is possible by m odifying vibration amplitude. The ventilation level is adjustable. The infl uence of these two parameters on the efficiency of ultrasonic nebulisation is studied. The study was carried out with a protein solution that had to b e administered into the lungs. The solution used presented a viscosity of 1 .25 mPa and a surface tension of 53 mN/m. The integrity of the protein was checked which was submitted to different vibration conditions. Nebulisation efficiency was evaluated by determining droplet size, the percentage of dr ug nebulised and nebulisation time. An increase in vibration intensity does not modify the size of droplets emitted, but decreases nebulisation time a nd raises the quantity of protein nebulised, thus improving performance. On the other hand, an increase in ventilation increases the size of droplets emitted, decreases nebulisation time and the quantity of protein nebulised because more drug is lost on the walls of the nebuliser. High intensity ass ociated with low ventilation favours drug delivery deep into the lungs. (C) 1999 Elsevier Science B.V. All rights reserved.