Interactions of omeprazole and precursors with beta-cyclodextrin host molecules
authors Braga, SS; Ribeiro-Claro, P; Pillinger, M; Goncalves, IS; Fernandes, AC; Pereira, F; Romao, CC; Correia, PB; Teixeira-Dias, JJC
nationality International
journal JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY
author keywords ab initio calculations; CP MAS NMR; cyclodextrins; inclusion complexation; omeprazole
keywords COMPACT EFFECTIVE POTENTIALS; C-13 CHEMICAL-SHIFTS; EXPONENT BASIS-SETS; INCLUSION COMPLEXES; SOLID-STATE; ANTIFUNGAL TARGET; N-BUTANE; CONFORMATION; EFFICIENT; SYSTEMS
abstract beta-Cyclodextrin (beta-CD) was mixed with omeprazole and some of its precursors in aqueous or water/ethanol solutions, and the resulting crystalline products have been characterized by elemental analysis, thermogravimetry, powder X-ray diffraction (XRD), FTIR and C-13 CP MAS NMR spectroscopy. In the case of 2-chloromethyl-4-methoxy-3,5-dimethylpyridine.HCl, it was found that the solid product always consisted of pure beta-CD hydrate. On the other hand, a 2 : 1 (host-to-guest) inclusion complex was obtained between beta-CD and 2-methoxy-2-mercaptobenzimidazole. The thioether intermediate 5-methoxy-2-[(3,5-dimethyl-4-methoxy-2-pyridine)methylthio]-1H-benzimidazole and its sulfoxide derivative (omeprazole) both formed 1:1 inclusion complexes with beta-CD. Powder XRD indicates that the crystal packing of beta-CD host molecules is herringbone-type for the 2:1 complex, and channel-type for the 1:1 complexes. Ab initio calculations were carried out to investigate the host-guest interactions. It was found that the interaction with the pyridine fragment is wholly repulsive, due to the presence of several ring substituents. On the other hand, the inclusion of the benzimidazole fragment is energetically favored, but highly dependent on the orientation of the substituent methoxy group.
publisher KLUWER ACADEMIC PUBL
issn 0923-0750
year published 2003
volume 47
issue 1-2
beginning page 47
ending page 52
digital object identifier (doi) 10.1023/B:JIPH.0000003924.14479.9c
web of science category Chemistry, Multidisciplinary
subject category Chemistry
unique article identifier WOS:000186613300007
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journal impact factor 1.56
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