Background - The advent of novel treatments such as aerosolized amilor
ide are potentially useful additions to the therapeutic options availa
ble for the treatment of cystic fibrosis. Unfortunately, amiloride and
other aerosolized drug such as antibiotics are generally administered
via jet nebulisers which are time consuming to use, and thus limit th
e acceptance and efficacy of these forms of treatment. In vitro experi
ments were performed in order to determine whether amiloride could be
administered in dry powder form using a Turbohaler. Methods - Amilorid
e was micronised and loaded into 200 mu g Turbohalers. The dose delive
red per actuation and particle size distribution of the generated aero
sol were assessed using a flow of 60 l/min through the Turbohaler. The
dose of amiloride delivered was measured by collecting the aerosol on
a filter and the quantity of drug was assayed by an ultraviolet spect
rophotometric method. The particle size distribution was assessed usin
g a Malvern MasterSizer laser particle sizer and compared with that ge
nerated by a commercially available 200 mu g budesonide Turbohaler. Re
sults - The mean (SD) dose delivered per actuation was 246.3 (40.4) mu
g. The volume median diameter of the amiloride aerosol was 3.80 (0.68
) mu m compared with 3.07 (1.47) mu m for budesonide. Conclusions - Th
ese results suggest that therapeutic doses of micronised amiloride cou
ld be delivered effectively and conveniently as a dry powder aerosol u
sing a Turbohaler.