Cyclodextrin-Based Pickering Emulsion Significantly Increases 6-Gingerol Loading Through Two Different Mechanisms: Cyclodextrin Cavity and Pickering Core
文献类型: 外文期刊
第一作者: Kou, Xingran
作者: Kou, Xingran;Ke, Qinfei;Kou, Xingran;Su, Dongdong;Zhang, Jingzhi;Zhu, Jiamin;Meng, Qingran;Ke, Qinfei;Pan, Fei
作者机构:
关键词: beta-cyclodextrin; 6-gingerol; self-assembly; Pickering emulsion
期刊名称:FOODS ( 影响因子:5.1; 五年影响因子:5.6 )
ISSN:
年卷期: 2025 年 14 卷 6 期
页码:
收录情况: SCI
摘要: We previously found that host-guest interactions can drive gingerols (Gs) and cyclodextrins (CDs) together to form inclusion complexes (G/CD), which can further construct amphiphilic microcrystals and resultant Pickering emulsions through self-assembly. In this follow-up study, we explored the detailed formation processes and mechanisms of the 6-G/beta-CD inclusion complex and the resultant Pickering emulsion. The influence of the 6-G/beta-CD molar ratio on the structure, morphology, and loading capacity of the inclusion complex and resultant Pickering emulsion were investigated. The results show that the cyclodextrin-based Pickering emulsion can load 6-G in two places; one place is the cyclodextrin cavity, whose loading capacity is up to 9.28%, while the other one is the Pickering core, with its highest loading capacity at 32.31% when the 6-G/beta-CD molar ratio is 5:1. In the above case, the 6-G/beta-CD inclusion complex was found to form a unit cell with a 1:2 molar ratio and then self-assemble into amphiphilic microcrystals through cage-type arrangement structures at the oil-water interface, mainly driven by van der Waals forces and hydrogen bonds. This study is helpful in the design and preparation of CD-based high-loading carriers for bioactive compound delivery.
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