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Startseite » Cyclodextrin » Sulfobutylation of Beta-Cyclodextrin Enhances the Complex Formation with Mitragynine: An NMR and Chiroptical Study

Sulfobutylation of Beta-Cyclodextrin Enhances the Complex Formation with Mitragynine: An NMR and Chiroptical Study

22. April 2022
Chemical structure and numbering of mitragynine and cyclodextrins

Chemical structure and numbering of mitragynine and cyclodextrins

Mitragynine (MTR), the main indole alkaloid of the well-known plant kratom (Mitragyna speciosa), is one of the most studied natural products nowadays, due to its remarkable biological effects. It is a partial agonist on the opioid receptors, and as such relieves pain without the well-known side-effects of the opioids applied in the clinical practice. MTR and its derivatives therefore became novel candidates for drug development. The poor aqueous solubility and low bioavailability of drugs are often improved by cyclodextrins (CyDs) as excipients through host-guest type complex formation. Among the wide variety of CyDs, sulfobutylether-beta-cyclodextrin (SBEβCyD) is frequently used and official in the European and U.S. Pharmacopoeia. Herein, the host-guest complexation of MTR with βCyD and SBEβCyD was studied using chiroptical and NMR spectroscopy. It was found by NMR measurements that MTR forms a rather weak (logβ11 = 0.8) 1:1 host-guest complex with βCyD, while the co-existence of the 2MTR∙SBEβCyD and MTR∙SBEβCyD species was deducted from 1H NMR titrations in the millimolar MTR concentration range. Sulfobutylation of βCyD significantly enhanced the affinity towards MTR. The structure of the formed inclusion complex was extensively studied by circular dichroism spectroscopy and 2D ROESY NMR. The insertion of the indole moiety was confirmed by both techniques.

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About this article: Várnai, B.; Zsila, F.; Szakács, Z.; Garádi, Z.; Malanga, M.; Béni, S. Sulfobutylation of Beta-Cyclodextrin Enhances the Complex Formation with Mitragynine: An NMR and Chiroptical Study. Int. J. Mol. Sci. 2022, 23, 3844. https://doi.org/10.3390/ijms23073844

Materials
MTR was isolated and purified by centrifugal partition chromatography (CPC) from kratom extract, and it was a generous gift from RotaChrom Ltd. (Dabas, Hungary). Native βCyD and randomly substituted SBEβCyD (DS~6.5) were the products of CycloLab Ltd. (Budapest, Hungary). D2O (99.9 atom% D) was purchased from Merck (Darmstadt, Germany), while acetic acid-d4 was obtained from Cambridge Isotope Laboratories Inc (Tewksbury, MA, USA). Other base chemicals of analytical grade were from commercial suppliers and used without further purification.

 

Tags: excipientsformulation

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