Encapsulation of cinnamon and thyme essential oils components (cinnamaldehyde and thymol) in β-cyclodextrin: Effect of interactions with water on complex stability

被引:170
|
作者
Ponce Cevallos, Peggy A. [1 ]
Buera, Maria P. [1 ]
Elizalde, Beatriz E. [1 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ind, RA-1428 Buenos Aires, DF, Argentina
关键词
beta-Cyclodextrin; Water sorption properties; Thymol; Cinnamaldehyde; Inclusion complexes; ANTIOXIDANT ACTIVITY; INCLUSION COMPLEX; CARVACROL; CRYSTAL; H-1-NMR; RELEASE;
D O I
10.1016/j.jfoodeng.2010.01.039
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Thymol and cinnamaldehyde formed inclusion complexes with beta-cyclodextrin (beta-CD) upon mixing the components in aqueous media and subsequent freeze-drying, as confirmed by differential scanning calorimetry. The samples were stored at constant relative humidities (RH) from 22% to 97%, at 25 degrees C. The release of encapsulated compounds was determined following the melting enthalpy of each guest. Water sorption isotherms for beta-CD and the complexes showed constant and low water sorption at RH <80%, then the uptake of water increased abruptly. The amount of sorbed water at each RH was smaller for the complexes than for beta-CD. The guest molecules displaced water molecules from inside the cavity of beta-CD. No thymol or cinnamaldehyde release was detected at RH <84%, and it increased abruptly from 84% RH, coincidentally with the abrupt increase of sorbed water. Water sorption significantly affects beta-CD complexes stability, which is thus governed by the shape of the water sorption isotherm. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:70 / 75
页数:6
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