Abstract
A series of co-engineered macrolide–mannitol particles were successfully prepared using azithromycin (AZ) as a model drug. The formulation was designed to target local inflammation and bacterial colonization, via the macrolide component, while the mannitol acted as mucolytic and taste-masking agent. The engineered particles were evaluated in terms of their physico-chemical properties and aerosol performance when delivered via a novel high-payload dry powder Orbital™ inhaler device that operates via multiple inhalation manoeuvres. All formulations prepared were of suitable size for inhalation drug delivery and contained a mixture of amorphous AZ with crystalline mannitol. A co-spray dried formulation containing 200 mg of 50:50 w/w AZ: mannitol had 57.6% ± 7.6% delivery efficiency with a fine particle fraction (≤6.8 µm) of the emitted aerosol cloud being 80.4% ± 1.1%, with minimal throat deposition (5.3 ± 0.9%). Subsequently, it can be concluded that the use of this device in combination with the co-engineered macrolide–mannitol therapy may provide a means of treating bronchiectasis.
| Original language | English |
|---|---|
| Pages (from-to) | 859-865 |
| Number of pages | 7 |
| Journal | Drug Development and Industrial Pharmacy |
| Volume | 41 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2015 |
| Externally published | Yes |
Keywords
- Bronchiectasis
- dry powder inhaler
- inhalation
- macrolides
- mucolytics
- orbital
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