Interfacial assembly of dendritic microcapsules with host-guest chemistry

被引:88
|
作者
Zheng, Yu [1 ,2 ]
Yu, Ziyi [2 ]
Parker, Richard M. [2 ]
Wu, Yuchao [1 ,2 ]
Abell, Chris [2 ]
Scherman, Oren A. [1 ,2 ]
机构
[1] Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England
[2] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
PEPTIDE AMPHIPHILE VESICLES; CROSS-LINKING; ENCAPSULATION; FABRICATION; EMULSIONS; CAPSULES; RELEASE;
D O I
10.1038/ncomms6772
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The self-assembly of nanoscale materials to form hierarchically ordered structures promises new opportunities in drug delivery, as well as magnetic materials and devices. Herein, we report a simple means to promote the self-assembly of two polymers with functional groups at a water-chloroform interface using microfluidic technology. Two polymeric layers can be assembled and disassembled at the droplet interface using the efficiency of cucurbit[8]uril (CB[8]) host-guest supramolecular chemistry. The microcapsules produced are extremely monodisperse in size and can encapsulate target molecules in a robust, well-defined manner. In addition, we exploit a dendritic copolymer architecture to trap a small hydrophilic molecule in the microcapsule skin as cargo. This demonstrates not only the ability to encapsulate small molecules but also the ability to orthogonally store both hydrophilic and hydrophobic cargos within a single microcapsule. The interfacially assembled supramolecular microcapsules can benefit from the diversity of polymeric materials, allowing for fine control over the microcapsule properties.
引用
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页数:9
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