http://www.cnr.it/ontology/cnr/individuo/prodotto/ID39593
The inclusion complexes of hesperetin and its 7-rhamnoglucoside with (2-hydroxypropyl)-beta-cyclodextrin (Articolo in rivista)
- Type
- Label
- The inclusion complexes of hesperetin and its 7-rhamnoglucoside with (2-hydroxypropyl)-beta-cyclodextrin (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.jpba.2005.05.009 (literal)
- Alternative label
S. Tommasini, M.L. Calabrò, R. Stancanelli, P. Donato, C. Costa, S. Catania, V. Villari, P. Ficarra, R. Ficarra (2005)
The inclusion complexes of hesperetin and its 7-rhamnoglucoside with (2-hydroxypropyl)-beta-cyclodextrin
in Journal of pharmaceutical and biomedical analysis (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- S. Tommasini, M.L. Calabrò, R. Stancanelli, P. Donato, C. Costa, S. Catania, V. Villari, P. Ficarra, R. Ficarra (literal)
- Pagina inizio
- Pagina fine
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- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento Farmaco-Chimico, Facoltà di Farmacia, Università di Messina, Viale Annunziata, 98168 Messina, Italy
Medicina del Lavoro, Policlinico Universitario, Via Consolare Valeria 1, 98125 Messina, Italy
Dipartimento Farmaco-Biologico, Facoltà di Farmacia, Università di Messina, Viale Annunziata, 98168 Messina, Italy
CNR, Istituto per i Processi Chimico-Fisici, IPCF-CNR, Via La Farina 237, 98123 Messina, Italy (literal)
- Titolo
- The inclusion complexes of hesperetin and its 7-rhamnoglucoside with (2-hydroxypropyl)-beta-cyclodextrin (literal)
- Abstract
- The effect of (2-hydroxypropyl)-beta-cyclodextrin (HP-beta-CyD) on the solubility properties and spectroscopic features of hesperetin and its
7-rhamnoglucoside, hesperidin, was qualitatively and quantitatively investigated in water, by means of UVvis absorption and fluorescence
spectroscopy. The stoichiometric ratios and stability constants describing the extent of formation of the complexes have been determined by
phase-solubility measurements; in both cases type-AL diagrams have been obtained (soluble 1:1 complexes). The higher degree of interaction
showed by hesperetin may be attributed to the higher hydrophobicity and smaller size of the aglycone molecule, which therefore exhibits a
greater affinity for the CyD and fits better into the cavity. The effect of molecular encapsulation on the two flavanones antioxidant activity was
afterwards evaluated by means of different biological assays, concerned to the different mechanisms of in vivo action. The protection efficacy
was in all cases higher for the complexed drugs, with respect to the free ones; these results are of great interest for their potential usefulness
in pharmaceutics. (literal)
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