Different authors have demonstrated the inclusion of miconazole in cyclodex
trins (CD). Miconazole can be included in the CD cavity both in the neutral
and in the ionized form. The present study tries to understand which fragm
ent of the miconazole molecule is involved in the inclusion. Austin Model 1
approximate molecular orbital calculations have been performed on several
complexes between beta -cyclodextrin (beta CD) or gamma -cyclodextrin (gamm
a CD) and miconazole in the ionized and the non-ionized forms of the two R
and S enantiomers in three different orientations. We observed that beta CD
is a good vehicle to transport miconazole which can be very easily release
d. The complexation energy between miconazole and beta CD is not very high
but the entropic factor has a great incidence on the stability of the forme
d complex. The inclusion of the dichlorobenzene-CH2-O- and of the imidazole
part of the S isomer gives rise to the most probable complex in acidic con
ditions (ionized miconazole). Nevertheless, the inclusion should be conside
red as a dynamic process in which different parts of the molecule could be
alternatively included in beta CD. The present work demonstrates the high c
apability of deformation of beta CD which could easily accommodate several
types of ligand. By opposite, the cycle extension in gamma CD leads to a mo
re rigid vehicle with regards to miconazole. (C) 2001 Elsevier Science B.V.
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