Khaldun Mohammad Al Azzam
1*, Ermafatiha Muhammad
21 Pharmacy Program, Batterjee Medical College for Science and Technology (BMC), 21442 Jeddah, Kingdom of Saudi Arabia.
2 School of Chemical Sciences, Universiti Sains Malaysia (USM), 11800 Penang, Malaysia.
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.