Preparation and structural characterization of different amylose-flavor molecular inclusion complexes
文献类型: 外文期刊
作者: Feng, Tao 1 ; Wang, Hui 1 ; Wang, Ke 1 ; Liu, Yi 1 ; Rong, Zhiwei 1 ; Ye, Ran 2 ; Zhuang, Haining 3 ; Xu, Zhimin 4 ; Sun, Mi 1 ;
作者机构: 1.Shanghai Inst Technol, Sch Perfume & Aroma Technol, 100 Hai Quan Rd, Shanghai 201418, Peoples R China
2.Roha USA, St Louis, MO USA
3.Shanghai Acad Agr Sci, Inst Edible Fungi, Natl Engn Res Ctr Edible Fungi, Shanghai, Peoples R China
4.Louisiana State Univ, Ctr Agr, Sch Nutr & Food Sci, Baton Rouge, LA 70803 USA
关键词: Aliphatic alcohols;Amylose;Complexes;Flavor molecules;Naphthol
期刊名称:STARCH-STARKE ( 影响因子:2.741; 五年影响因子:3.112 )
ISSN: 0038-9056
年卷期: 2018 年 70 卷 1-2 期
页码:
收录情况: SCI
摘要: Flavor microencapsulation has been widely used in foods, medicines, cosmetics, and other fields. The use of amylose-based complexes is receiving increasing attention because they are biodegradable, non-toxic, and biocompatible, and these complexes provide a new way to develop and impart flavors. In this study, with the aim of investigating the properties of amylose-flavor complexes, linear aliphatic alcohols (C-6-C-9) and the aromatic alcohol naphthol were used to prepare inclusion complexes by the sealed heating method in yields ranging from 45 to 50%. In addition, scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) were utilized to investigate the structural characteristics of these inclusion complexes, and it was found that the amylose-n-heptanol inclusion complex was most stable. Furthermore, nuclear magnetic resonance (NMR) spectroscopy revealed that V-type crystals existed in the amylose-flavor complexes. Moreover, TGA showed that all amylose-flavor inclusion complexes have excellent thermal stability. The encapsulation efficiency of the complexes increased with decreasing chain length, but the encapsulation efficiency of the complexes with the aromatic alcohol naphthol was lower than that of the complexes with some linear alcohols. This indicated that the stereoscopic confirmation of -naphthol may influence the complexes being formed.
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