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A characterization study of resveratrol/sulfobutyl ether-β-cyclodextrin inclusion complex and in vitro anticancer activity
被引:107
|作者:
Venuti, Valentina
[1
]
Cannava, Carmela
[2
]
Cristiano, Maria Chiara
[3
]
Fresta, Massimo
[3
]
Majolino, Domenico
[1
]
Paolino, Donatella
[3
]
Stancanelli, Rosanna
[2
]
Tommasini, Silvana
[2
]
Ventura, Cinzia Anna
[2
]
机构:
[1] Univ Messina, Dipartimento Fis & Sci Terra, I-98166 Messina, Italy
[2] Univ Messina, Dipartimento Sci Farmaco & Prodotti Salute, I-98168 Messina, Italy
[3] Magna Graecia Univ Catanzaro, Dipartimento Sci Salute, I-88100 Catanzaro, Italy
关键词:
Resveratrol;
Sulfobutylether-beta-cyclodextrin;
FTIR-ATR;
Job's plot;
Anticancer activity;
KAPPA-B ACTIVATION;
FTIR-ATR;
PHYSICOCHEMICAL CHARACTERIZATION;
VIBRATIONAL PROPERTIES;
SOLUBILITY;
D O I:
10.1016/j.colsurfb.2013.11.025
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
A resveratrol/sulfobutylether-beta-cyclodextrin inclusion complex was prepared using the freeze-drying method and characterized in solution through UV-vis spectroscopy, solubility phase studies and Job's plot methods. At the solid state it was characterized using the FTIR-ATR technique. Sulfobutylether-beta-cyclodextrin has a high affinity for the drug, and forms an inclusion complex with a 1:1 molar ratio both in solution and as a solid sample. It also has a high stability constant (K-c, 10,114M(-1)). Complexation strongly increases the water solubility of resveratrol (from 0.03 mg/ml to 1.1 mg/ml, at 25 degrees C) and positively influences its in vitro anticancer activity which was observed on a human breast cancer cell line (MCF-7). In solid phase, FTIR-ATR revealed itself as being a useful technique in elucidating the complexation mechanism, which it did by emphasizing the functional groups involved in the activation of non-covalent "host-guest" interactions. (C) 2013 Elsevier B.V. All rights reserved.
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页码:22 / 28
页数:7
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