A resveratrol/sulfobutylether-b-cyclodextrin inclusion complex was prepared using the freeze-drying method and characterized in solution through UV–vis spectroscopy, solubility phase studies and Job’splot methods. At the solid state it was characterized using the FTIR-ATR technique. Sulfobutylether-b-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 (Kc, 10,114 M−1). Complexation strongly increases the water solubility of resveratrol (from 0.03 mg/ml to 1.1 mg/ml, at 25◦C) and positively influences its in vitro anticancer activity which was observed on a human breast cancer cellline (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.

A characterization study of resveratrol/sulfobutylether-b-cyclodextrin inclusion complex andin vitro anticancer activity

VENUTI, Valentina;MAJOLINO, Domenico;STANCANELLI, Rosanna;TOMMASINI, Silvana;VENTURA, Cinzia Anna
2014-01-01

Abstract

A resveratrol/sulfobutylether-b-cyclodextrin inclusion complex was prepared using the freeze-drying method and characterized in solution through UV–vis spectroscopy, solubility phase studies and Job’splot methods. At the solid state it was characterized using the FTIR-ATR technique. Sulfobutylether-b-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 (Kc, 10,114 M−1). Complexation strongly increases the water solubility of resveratrol (from 0.03 mg/ml to 1.1 mg/ml, at 25◦C) and positively influences its in vitro anticancer activity which was observed on a human breast cancer cellline (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.
2014
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/2666387
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