Host-guest Inclusion Complexes between Mitiglinide and the NaturallyOccurring Cyclodextrins α, β, and γ: A Theoretical Approach
Khaldun Mohammad Al Azzam, Ermafatiha Muhammad
Advanced Pharmaceutical Bulletin · 2015
doi:10.15171/apb.2015.040 (opens in a new tab)
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Abstract
Purpose: The present study is aimed to study the host-guest inclusion complexation of the naturally occurring cyclodextrins (CDs), namely; (a-CD,b-CD, and g-CD) with mitiglinide (MIT). Methods: Host-guest inclusion complexation was simulated using semi-empirical PM3 method. Results: The obtained results clearly indicate that the complexes formed are energetically favored in the presence of y-CD (Ecomp = -17.884 kcal/mol) of the optimal configurations of (1:1) MIT/y-CD inclusion complexes. Moreover, the results obtained reveal that the formation of more stable MIT/y-CD complex compared to MIT/a-CD or MIT/b-CD complexes is primarily due to differences in intermolecular hydrogen bonding. Conclusion: The present theoretical results may be informative to scientists who are devoting themselves to developing effective methods for enhancing the drug solubility.
Abstract licence: CC BY
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