Cyclodextrins can be used in order to suitably modify the biopharmaceutical
properties of drugs. A complex of beclomethasone dipropionate/hydroxypropy
l-beta-cyclodextrin was formed as shown by the apparent solubility constant
, differential scanning calorimetry and X-ray spectroscopy. With a view to
developing a suitable formulation for pulmonary delivery of the above compl
ex, a comparative study of the drug/cyclodextrin complex, the physical mixt
ure of the drug and the cyclodextrin and the chug alone was performed as th
e in vitro aerosol deposition of the emitted close from an inhalation devic
e, the Micro-haler dry powder inhaler using the twin impinger apparatus (Eu
ropean Pharmacopoeia). The results show a significant respirable fraction f
or both the complex and drug/hydroxypropyl-beta-cyclodextrin mixtures used,
which indicates the potential of the above formulation for pulmonary deliv
ery. The results are in the following order: complex alone > micronized dru
g + cyclodextrin physical mixture much greater than micronized drug alone.