Rational design of light-controllable polymer micelles

被引:90
作者
Zhao, Yue [1 ]
机构
[1] Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
关键词
polymer micelles; light-responsive material; polymer nanocarrier; block copolymers; self-assembly; BLOCK-COPOLYMER MICELLES; DRUG-DELIVERY SYSTEMS; VESICLES; AZOBENZENE; SURFACTANTS; RELEASE;
D O I
10.1002/tcr.20127
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amphiphilic block copolymer (BCP) micelles are nanocarriers that hold promise for controlled delivery applications. This account highlights our recent works on light-dissociable BCP micelles. We have designed and developed light-responsive amphiphilic BCPs whose micellar aggregates (core-shell micelles and vesicles) can be disrupted by light exposure. The basic strategy is to incorporate a chromophore into the structure of the hydrophobic block, whose photoreaction can result in a conformational or structural change that shifts the hydrophilic/hydrophobic balance toward the destabilization of the micelles. Using various chromophores including azobenzene, pyrene and nitrobenzene, we have achieved both reversible and irreversible dissociation of BCP micelles upon illumination with UV/visible or near infrared light. The demonstrated rational design principle based on light-changeable or light-switchable amphiphilicity is general and can be applied to many polymer/chromophore combinations. This opens the door to developing photocontrollable polymer nanocarriers offering control over when and where the release of loaded agents takes place.
引用
收藏
页码:286 / 294
页数:9
相关论文
共 29 条
[1]   Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change [J].
Bae, Y ;
Fukushima, S ;
Harada, A ;
Kataoka, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (38) :4640-4643
[2]   Stimuli-responsive polypeptide vesicles by conformation-specific assembly [J].
Bellomo, EG ;
Wyrsta, MD ;
Pakstis, L ;
Pochan, DJ ;
Deming, TJ .
NATURE MATERIALS, 2004, 3 (04) :244-248
[3]   Inner core segment design for drug delivery control of thermo-responsive polymeric micelles [J].
Chung, JE ;
Yokoyama, M ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :93-103
[4]  
De Mayo P., 1960, Advances in organic chemistry methods and results, V2, P367
[5]   Polymer vesicles [J].
Discher, DE ;
Eisenberg, A .
SCIENCE, 2002, 297 (5583) :967-973
[6]   Photofunctional vesicles containing prussian blue and azobenzene [J].
Einaga, Y ;
Sato, O ;
Iyoda, T ;
Fujishima, A ;
Hashimoto, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (15) :3745-3750
[7]   Brominated 7-hydroxycoumarin-4-ylmethyls: Photolabile protecting groups with biologically useful cross-sections for two photon photolysis [J].
Furuta, T ;
Wang, SSH ;
Dantzker, JL ;
Dore, TM ;
Bybee, WJ ;
Callaway, EM ;
Denk, W ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1193-1200
[8]   A new approach towards acid sensitive copolymer micelles for drug delivery [J].
Gillies, ER ;
Fréchet, JMJ .
CHEMICAL COMMUNICATIONS, 2003, (14) :1640-1641
[9]   Synthetic micelle sensitive to IR light via a two-photon process [J].
Goodwin, AP ;
Mynar, JL ;
Ma, YZ ;
Fleming, GR ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (28) :9952-9953
[10]   Supramolecular drug-delivery systems based on polymeric core-shell architectures [J].
Haag, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (03) :278-282