Light induced molecular release from vesicles based on amphiphilic linear-dendritic block copolymers

被引:45
作者
Blasco, Eva [1 ]
del Barrio, Jesus [1 ]
Sanchez-Somolinos, Carlos [2 ]
Pinol, Milagros [1 ]
Oriol, Luis [1 ]
机构
[1] Univ Zaragoza, Dept Quim Organ, Fac Ciencias, ICMA,CSIC, E-50009 Zaragoza, Spain
[2] Univ Zaragoza, ICMA, CSIC, Dept Fis Mat Condensada, E-50009 Zaragoza, Spain
关键词
DIBLOCK COPOLYMERS; CLICK CHEMISTRY; PHOTOINDUCED FUSION; FLUORESCENCE; MICELLES; BEHAVIOR; MACROMOLECULES; POLYMERSOMES;
D O I
10.1039/c2py21025h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on the synthesis and characterization of new amphiphilic linear-dendritic block copolymers (LDBCs) as well as their self-assembly in water to form polymeric vesicles. We have also investigated the encapsulation of both hydrophilic and hydrophobic fluorescent probes by these stimuli-responsive polymeric vesicles and the use of light as an external stimulus to trigger the release of the probes. The LDBCs are composed of a 2000 g mol(-1) poly(ethylene glycol) (PEG) linear segment linked to a fourth generation 2,2-di(hydroxymethyl) propionic acid (bis-MPA) based dendron with 4-isobutyloxyazobenzene units at the periphery. By tuning the chemical structure of the azobenzene moieties, a specific LDBC has been identified that forms stable vesicles in water as it is clearly revealed by TEM and Cryo-TEM images. Encapsulation of both hydrophobic and hydrophilic molecules by these vesicular self-assemblies has been investigated by fluorescence analysis as well as the release of the loaded probes triggered by low intensity UV illumination, which is related to trans-to-cis isomerisation of the azobenzene moieties. Thus, the potential of these photo-responsive vesicles as light-responsive nanocarriers is demonstrated.
引用
收藏
页码:2246 / 2254
页数:9
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