Light-Regulated Supramolecular Engineering of Polymeric Nanocapsules

被引:79
|
作者
Achilleos, Demetra S. [1 ,2 ]
Hatton, T. Alan [3 ]
Vamvakaki, Maria [1 ,2 ]
机构
[1] Fdn Res & Technol Hellas, Inst Elect Struct & Laser, Iraklion 71110, Crete, Greece
[2] Univ Crete, Dept Mat Sci & Technol, Iraklion 71003, Crete, Greece
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
关键词
TRANSFER RADICAL POLYMERIZATION; BLOCK-COPOLYMER; RESPONSIVE VESICLES; HOLLOW SPHERES; NANOPARTICLES; FABRICATION; SPIROPYRAN; MICROCAPSULES; MICELLES; CAPSULES;
D O I
10.1021/ja212177q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This article describes the light-driven supramolecular engineering of water-dispersible nanocapsules (NCPs). The novelty of the method lies in the utilization of an appropriate phototrigger to stimulate spherical polymer brushes, consisting of dual-responsive 2-(dimethylamino)ethyl methacrylate (DMAEMA) and light-sensitive spiropyran (SP) moieties, for the development or disruption of the NCPs in a controlled manner. The fabrication of the nanocarriers is based on the formation of H-type pi-pi interactions between merocyanine (MC) isomers within the sterically crowded environment of the polymer brushes upon UV irradiation, which enables the SP-to-MC isomerization of the photosensitive species. After HF etching of the inorganic core, dual-responsive polymeric vesicles whose walls' robustness is provided by the MC MC cross-link points are formed. Disruption of the vesicles can be achieved remotely by applying a harmless trigger such as visible-light irradiation. The hydrophilic nature of the DMAEMA comonomer facilitates the engineering of the vesicles in environmentally benign aqueous media and enables the controlled alteration of the NCPs size upon variation of the solution pH. The inherent ability of the NCPs to fluoresce in water opens new possibilities for the development of addressable nanoscale capsules for biomedical applications.
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页码:5726 / 5729
页数:4
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