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.
引用
收藏
页码:22 / 28
页数:7
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