2008
DOI: 10.1007/s10847-008-9450-4
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Association of 3-O-methylquercetin with β-cyclodextrin: complex preparation, characterization and ex vivo skin permeation studies

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Cited by 17 publications
(20 citation statements)
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“…Additionally, the low gel-β release was a result of hampered caffeic acid dissociation from the CD cavity, since the complex formed with this CD was more stable than HPβCD [21]. This suggests that the sustained release was dependent on the CD ability to retain the caffeic acid in the network, as previously reported for CD-based hydrogels loaded with hydrophobic molecules [3,17,23,28].…”
Section: Biological Properties Of Gel-β and Gel-hpβsupporting
confidence: 54%
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“…Additionally, the low gel-β release was a result of hampered caffeic acid dissociation from the CD cavity, since the complex formed with this CD was more stable than HPβCD [21]. This suggests that the sustained release was dependent on the CD ability to retain the caffeic acid in the network, as previously reported for CD-based hydrogels loaded with hydrophobic molecules [3,17,23,28].…”
Section: Biological Properties Of Gel-β and Gel-hpβsupporting
confidence: 54%
“…Figure 3 present the FTIR spectra obtained from the gel-β and gel-HPβ with and without caffeic acid, and also, the network components alone (βCD, HPβCD, HPMC and caffeic acid). Both CD spectra show higher intensity on the following peaks (βCD/HPβCD): 3416/3447 cm -1 (O-H stretching), 2924 cm -1 (asymmetric vibrational stretching of C-H), 1645/1640 cm -1 (hydrogen interactions), 1157 cm -1 (C-O stretching) and 1029/1034 cm -1 (C-O-C) [3,16,17]. The HPMC spectrum showed a profile similar to the CD and the strong intensity peaks were identified: 3447 cm -1 (O-H stretching), 2924 cm -1 (asymmetric vibrational stretching of C-H), 1640 cm -1 (hydrogen interactions), 1115 and 1063 cm -1 (ether bond) [18,19].…”
Section: Physicochemical Characterization Of Gel-β and Gel-hpβmentioning
confidence: 99%
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“…Two polymers suit perfectly in this description: hydroxypropyl methylcellulose (HPMC) and chitosan (CS). The first one is a non‐ionic and hydrophilic cellulose derivative employed in several skin formulations containing phenolic compounds, such as coumestrol, formononetin and biochanin A and also, to 3‐ O MQ . Chitosan is a polymer with polycationic character.…”
Section: Introductionmentioning
confidence: 99%
“…Most of the properties of A. satureioides extracts have been attributed to the antioxidant properties of the flavonoids. In this context, a recent study, considering previously described activities indicating that the topical delivery of 3-O-methylquercetin might have therapeutic application for the treatment of Herpes Simplex Virus infections, evaluated the possibility of enhancing its aqueous solubility, and, hence, its bioavailability, through the formation of a complex with β-cyclodextrin (Schwingel et al 2008). SFE has been extensively studied as an alternative method to obtain these substances from vegetable matrices.…”
Section: Introductionmentioning
confidence: 99%