http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15654
In vitro evaluation of quercetin-3-0-acyl esters as topical prodrugs (Articolo in rivista)
- Type
- Label
- In vitro evaluation of quercetin-3-0-acyl esters as topical prodrugs (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.ijpharm.2006.12.003 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Montenegro L.; Carbone C.; Maniscalco C.; Lambusta D.; Nicolosi G.; Ventura C.A.; Puglisi G.. (literal)
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- ISI Web of Science (WOS) (literal)
- Scopu (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Pharmaceutical Sciences, University of Catania, V.le A.Doria 6, Catania I-95125, Italy Istituto di Chimica Biomolecolare, CNR, Sezione di Catania, Via del Santuario 110, I-95028 Valverde, Catania, Italy
Pharmaco-Chemical Department, Faculty of Pharmacy, University of Messina, V.le Annunziata, Messina I-98168, Italy (literal)
- Titolo
- In vitro evaluation of quercetin-3-0-acyl esters as topical prodrugs (literal)
- Abstract
- Quercetin-3-O-acyl esters (I-VI) were synthesized and their usefulness as quercetin topical prodrugs was evaluated. Quercetin esters were
assayed to determine their water stability and solubility, their susceptibility to undergoing enzymatic hydrolysis and their permeation through
excised human skin. Quercetin ethyl (I) and hexyl (IV) esters proved poorly stable in aqueous media and they were not assayed further. Among
the derivatives tested, quercetin propyl (II) and butyl (III) esters were more water-soluble than the parent drug. Esters II, III and V were readily
hydrolyzed by human plasma and esters II and III penetrated excised human skin better than quercetin from aqueous saturated solutions. On the
basis of the results obtained, esters II and III could be regarded as promising quercetin topical prodrugs. (literal)
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