This book presents work on nanocarrier systems for pulmonary drug
delivery for use in the treatment of asthma. Using sucrose as a carrier,
liposomes were generated or dispersed in situ from proliposomes within
the medical nebulisers investigated. The Pari (air-jet) and the Omron
(vibrating-mesh) nebulisers produced large mass and lipid outputs with a
large lipid fraction deposited in the lower stage of a two-stage
impinger. The Liberty (Ultrasonic) nebuliser failed to deliver more than
6% of the lipid employed.Multilamellar liposomes were generated from
ethanol-based proliposomes. The resultant vesicles entrapped 62% of the
available salbutamol sulphate compared to only 1.23% entrapped by
liposomes made by the thin film method. Aeroneb Pro or Aeroneb Go
vibrating-mesh nebulisers generated aerosol droplets of larger volume
median diameter and narrower size distribution than the Pari (air-jet)
nebuliser. Unlike the vibrating-mesh nebulisers, the performance of the
jet nebuliser was independent of formulation. A nebuliser-dependent
significant loss of the originally entrapped drug was demonstrated. A
customised large mesh Aeroneb Pro reduced the drug losses during
nebulisation.