Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability

dc.contributor.authorHunt, Lee E
dc.contributor.authorBourne, Susan A
dc.contributor.authorCaira, Mino R
dc.date.accessioned2021-10-14T08:54:59Z
dc.date.available2021-10-14T08:54:59Z
dc.date.issued2020-12-31
dc.date.updated2021-01-22T15:47:14Z
dc.description.abstractThere is ongoing interest in exploiting the antioxidant activity and other medicinal properties of natural monophenolic/polyphenolic compounds, but their generally low aqueous solubility limits their applications. Numerous studies have been undertaken to solubilize such compounds via supramolecular derivatization with co-crystal formation with biocompatible coformer molecules and cyclodextrin (CD) complexation being two successful approaches. In this study, eight new crystalline products obtained by complexation between methylated cyclodextrins and the bioactive phenolic acids (ferulic, hydroferulic, caffeic, and p-coumaric acids) were investigated using thermal analysis (hot stage microscopy, thermogravimetry, differential scanning calorimetry) and X-ray diffraction. All of the complexes crystallized as ternary systems containing the host CD, a phenolic acid guest, and water. On heating each complex, the primary thermal events were dehydration and liberation of the respective phenolic acid component, the mass loss for the latter step enabling determination of the host-guest stoichiometry. Systematic examination of the X-ray crystal structures of the eight complexes enabled their classification according to the extent of inclusion of each guest molecule within the cavity of its respective CD molecule. This revealed three CD inclusion compounds with full guest encapsulation, three with partial guest inclusion, and two that belong to the rare class of ‘non-inclusion’ compounds.en_US
dc.identifierdoi: 10.3390/biom11010045
dc.identifier.apacitationHunt, L. E., Bourne, S. A., & Caira, M. R. (2020). Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability. <i>Biomolecules</i>, 11(1), http://hdl.handle.net/11427/35243en_ZA
dc.identifier.chicagocitationHunt, Lee E, Susan A Bourne, and Mino R Caira "Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability." <i>Biomolecules</i> 11, 1. (2020) http://hdl.handle.net/11427/35243en_ZA
dc.identifier.citationHunt, L.E., Bourne, S.A. & Caira, M.R. 2020. Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability. <i>Biomolecules.</i> 11(1) http://hdl.handle.net/11427/35243en_ZA
dc.identifier.ris TY - Journal Article AU - Hunt, Lee E AU - Bourne, Susan A AU - Caira, Mino R AB - There is ongoing interest in exploiting the antioxidant activity and other medicinal properties of natural monophenolic/polyphenolic compounds, but their generally low aqueous solubility limits their applications. Numerous studies have been undertaken to solubilize such compounds via supramolecular derivatization with co-crystal formation with biocompatible coformer molecules and cyclodextrin (CD) complexation being two successful approaches. In this study, eight new crystalline products obtained by complexation between methylated cyclodextrins and the bioactive phenolic acids (ferulic, hydroferulic, caffeic, and p-coumaric acids) were investigated using thermal analysis (hot stage microscopy, thermogravimetry, differential scanning calorimetry) and X-ray diffraction. All of the complexes crystallized as ternary systems containing the host CD, a phenolic acid guest, and water. On heating each complex, the primary thermal events were dehydration and liberation of the respective phenolic acid component, the mass loss for the latter step enabling determination of the host-guest stoichiometry. Systematic examination of the X-ray crystal structures of the eight complexes enabled their classification according to the extent of inclusion of each guest molecule within the cavity of its respective CD molecule. This revealed three CD inclusion compounds with full guest encapsulation, three with partial guest inclusion, and two that belong to the rare class of ‘non-inclusion’ compounds. DA - 2020-12-31 DB - OpenUCT DP - University of Cape Town IS - 1 J1 - Biomolecules LK - https://open.uct.ac.za PY - 2020 T1 - Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability TI - Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability UR - http://hdl.handle.net/11427/35243 ER - en_ZA
dc.identifier.urihttps://doi.org/10.3390/biom11010045
dc.identifier.urihttp://hdl.handle.net/11427/35243
dc.identifier.vancouvercitationHunt LE, Bourne SA, Caira MR. Inclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stability. Biomolecules. 2020;11(1) http://hdl.handle.net/11427/35243.en_ZA
dc.language.isoenen_US
dc.publisher.departmentDepartment of Chemistryen_US
dc.publisher.facultyFaculty of Scienceen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBiomoleculesen_US
dc.source.journalissue1en_US
dc.source.journalvolume11en_US
dc.source.urihttps://www.mdpi.com/journal/biomolecules
dc.titleInclusion of Hydroxycinnamic Acids in Methylated Cyclodextrins: Host-Guest Interactions and Effects on Guest Thermal Stabilityen_US
dc.typeJournal Articleen_US
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