Multiple micellization and dissociation transitions of thermo- and light-sensitive poly(ethylene oxide)-b-poly(ethoxytri(ethylene glycol) acrylate-co-o-nitrobenzyl acrylate) in water

被引:177
作者
Jiang, Xueguang [1 ]
Lavender, Christopher A. [1 ]
Woodcock, Jeremiah W. [1 ]
Zhao, Bin [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
D O I
10.1021/ma7028105
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This article reports on the synthesis of thermo- and light-sensitive hydrophilic block copolymers, poly(ethylene oxide)-b-poly(ethoxytri (ethylene glycol) acrylate-co-o-nitrobenzyl acrylate), and the study of their micellization/dissociation transitions in water in response to temperature changes and UV irradiation. The block copolymers with controlled molecular weights and narrow polydispersities were synthesized by atom transfer radical polymerization of a mixture of ethoxytri (ethylene glycol) acrylate and o-nitrobenzyl acrylate with a molar ratio of 100: 10 from a PEO macroinitiator. Dynamic light scattering and fluorescence spectroscopy studies showed that these copolymers were molecularly dissolved in water at lower temperatures and self-assembled into micelles with the thermosensitive block associating into the core and the PEO block forming the corona when the temperature was above the lower critical solution temperature (LCST) of the thermosensitive block. Upon UV irradiation, the o-nitrobenzyl group was cleaved and the LCST of the thermosensitive block was increased, causing the dissociation of micelles into unimers and the release of encapsulated fluorescent dye Nile Red into water. Further increasing the temperature induced the formation of micelles again and the re-encapsulation of Nile Red. The thermo-induced formation and dissociation of micelles were reversible.
引用
收藏
页码:2632 / 2643
页数:12
相关论文
共 79 条
[1]   Temperature-sensitive dendritic micelles [J].
Aathimanikandan, SV ;
Savariar, EN ;
Thayumanavan, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (42) :14922-14929
[2]   Thermo- and pH-responsive micelles of poly(acrylic acid)-block-poly(N,N-diethylacrylamide) [J].
André, X ;
Zhang, MF ;
Müller, AHE .
MACROMOLECULAR RAPID COMMUNICATIONS, 2005, 26 (07) :558-563
[3]   REDOX-ACTIVE MONOMERIC AND POLYMERIC SURFACTANTS [J].
ANTON, P ;
HEINZE, J ;
LASCHEWSKY, A .
LANGMUIR, 1993, 9 (01) :77-85
[4]   Synthesis and self-association of stimuli-responsive diblock copolymers by living cationic polymerization [J].
Aoshima, S ;
Sugihara, S ;
Shibayama, M ;
Kanaoka, S .
MACROMOLECULAR SYMPOSIA, 2004, 215 :151-163
[5]  
Aoshima S, 2000, J POLYM SCI POL CHEM, V38, P3962, DOI 10.1002/1099-0518(20001101)38:21<3962::AID-POLA130>3.0.CO
[6]  
2-9
[7]   Switching the inside and the outside of aggregates of water-soluble block copolymers with double thermoresponsivity [J].
Arotçaréna, M ;
Heise, B ;
Ishaya, S ;
Laschewsky, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (14) :3787-3793
[8]   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
[9]   Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy [J].
Bae, Y ;
Nishiyama, N ;
Fukushima, S ;
Koyama, H ;
Yasuhiro, M ;
Kataoka, K .
BIOCONJUGATE CHEMISTRY, 2005, 16 (01) :122-130
[10]   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