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

Journal 2014 · IF 2.354 · 发表于 2014 年 1 月 24 日
作者: Shangyang Li,Pengyao Xing,Lin Zhang,Feifei Xin,Jinhui Nie,Hailu Wang,Mingfang Ma,Yurong Wu,Aiyou Hao
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摘要

Herein, we report a novel responsive assembly system consisting of an amphiphilic drug fenspiride and β-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 β-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 α-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.