Controllable self-assembly of an amphiphilic drug with β-cyclodextrin and α-amylase

被引:5
|
作者
Li, Shangyang
Xing, Pengyao
Zhang, Lin
Xin, Feifei
Nie, Jinhui
Wang, Hailu
Ma, Mingfang
Wu, Yurong
Hao, Aiyou [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
关键词
beta-Cyclodextrin; Vesicle; Enzyme-responsive; Complex; Drugs; VESICLES; SYSTEMS; RECOGNITION; SURFACTANT; POLYMERS; MEDIA; JANUS;
D O I
10.1016/j.colsurfa.2014.01.020
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein, we report a novel responsive assembly system consisting of an amphiphilic drug fenspiride and beta-cyclodextrin in host-guest approach. Fenspiride molecules can self-assembled into vesicles in aqueous solution. The obtained vesicles were characterized in detail by transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). Furthermore, such a vesicular structure will be destroyed upon the addition of beta-cyclodextrin due to the formation of inclusion complexes by host-guest interactions. In addition, amylase is a digestive enzyme which can catalyze the breakdown of starch into sugars. Adding a-amylase into the system could release fenspiride molecules, and trigger the self-assembly of fenspiride molecules again. It is anticipated that this research will provide widespread applications in the fields of responsive materials and biochemistry related to enzyme-responsive model system and host-guest chemistry. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
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