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On the correlation of output rate and aerodynamic characteristics in vibrating-mesh-based aqueous aerosol delivery

Authors :
Nina Oesterheld
Thomas Schmehl
Marie-Christine Knuedeler
Moritz Beck-Broichsitter
Werner Seeger
Source :
International Journal of Pharmaceutics. 461:34-37
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Aerosolization of aqueous formulations is of special interest for inhalative drug delivery, where an adequate nebulizer performance represents a prerequisite for improving pulmonary therapy. The present study investigated the interplay of output rate and aerodynamic characteristics of different excipient-based formulations and its impact on the atomization process by vibrating-mesh technology (i.e. eFlow®rapid). Output rate and aerodynamic characteristics were manipulated by both dynamic viscosity and conductivity of the applied formulation. Supplementation with sucrose and sodium chloride caused a decline (down to ∼0.2 g/min) and elevation (up to ∼1.0 g/min) of the nebulizer output rate, respectively. However, both excipients were capable of decreasing the aerodynamic diameter of produced aerosol droplets from >7.0 μm to values of ≤5.0 μm. Thus, the correlation of output rate and aerodynamic characteristics resulted in linear fits of opposite slopes (R2 > 0.85). Finally, the overall number of delivered aerosol droplets per time was almost constant for sucrose (≤1 × 108 droplets/s), while for sodium chloride a concentration-dependent increase was observed (up to ∼3 × 108 droplets/s). Overall, the current findings illustrated the influence of formulation parameters on the aerosolization process performed by vibrating-mesh technology. Moreover, concentration and charge distribution of aerosol populations supposedly modify the final characteristics of the delivered aerosols.

Details

ISSN :
03785173
Volume :
461
Database :
OpenAIRE
Journal :
International Journal of Pharmaceutics
Accession number :
edsair.doi.dedup.....bdf452d4041b2e18df1591d3a0db7e56
Full Text :
https://doi.org/10.1016/j.ijpharm.2013.11.036