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Photo-responsive reversible micelles based on azobenzene-modified poly(carbonate)s via azide–alkyne click chemistry†
Ding Hu,Yefei Li,Yile Niu,Ling Li,Jingwen He,Xiangyu Liu,Xinnian Xia,Yanbing Lu,Yuanqin Xiong,Weijian Xu
RSC Advances Pub Date : 09/05/2014 00:00:00 , DOI:10.1039/C4RA07345B
Abstract

Photo-induced reversible amphipathic copolymer PMPC-azo was click conjugated by connecting amphiphilic poly(ethylene glycol)-modified poly(carbonate)s (PEG-b-poly(MPC)) and azide-functional trifluoromethoxy-azobenzene (azo-N3). The resulting copolymer self-assembled into spherical micelles with a hydrophobic azo core stabilized by a hydrophilic PEG corona in aqueous solution. As characterized by time-resolved UV-vis spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM), these micelles showed reversible self-assembly and disassembly in aqueous solution under alternating UV and visible light irradiation. The model drug Nile Red (NR) was then successfully encapsulated into the micelles. Light-controlled release and re-encapsulation behaviors were demonstrated by fluorescence spectroscopy. The cell cytotoxicity of PMPC-azo micelles was also evidenced by MTT assay. This study provides a convenient method to construct smart nanocarriers for controlled release and re-encapsulation of hydrophobic drugs.

Graphical abstract: Photo-responsive reversible micelles based on azobenzene-modified poly(carbonate)s via azide–alkyne click chemistry
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