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Synthesis and self-assembly of a hydrophilic, thermo-responsive poly(ethylene oxide) rnonomethyl ether-block-poly(acrylic acid)-block-poly (N-isopropylacrylamide) copolymer to form micelles for drug delivery
被引:23
作者:
He, Xiaohua
[1
]
Wu, Xiaomeng
[1
]
Gao, Chunyan
[1
]
Wang, Kai
[1
]
Lin, Shaoliang
[2
]
Huang, Wei
[1
]
Xie, Meiran
[1
]
Yan, Deyue
[1
,3
]
机构:
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
[2] E China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Adv Polymer Mat Shanghai, Shanghai 200237, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
基金:
高等学校博士学科点专项科研基金;
关键词:
Block copolymer;
Micelles;
Atom transfer radical polymerization;
Thermo-responsive;
Poly(N-isopropylacrylamide);
CROSS-LINKED MICELLES;
TRANSFER RADICAL POLYMERIZATION;
BLOCK-COPOLYMERS;
TRIBLOCK COPOLYMER;
RAFT POLYMERIZATION;
HYBRID MICELLES;
NANOPARTICLES;
RELEASE;
FABRICATION;
SWELLABILITY;
D O I:
10.1016/j.reactfunctpolym.2011.02.001
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
A hydrophilic, thermo-responsive triblock copolymer poly(ethylene oxide) monomethyl ether-block-poly(acrylic acid)-block-poly(N-isopropylacrylamide) (MPEO-b-PAA-b-PNIPAM) was synthesized by sequential atom transfer radical polymerization and hydrolysis. These polymers were characterized in detail by H-1 NMR, FT-IR and gel permeation chromatography. In aqueous solution, MPEO-b-PAA-b-PNIPAM can self-assemble into core-shell-corona micelles above a LCST of the PNIPAM block. Condensation reactions easily cross-link the PAA shells, which enhances micellar stability. Doxorubicin (DOX), a model drug, was loaded into the core of the polymeric micelles and followed a pattern of thermo-sensitive drug release in vitro in cumulative release studies. (c) 2011 Elsevier Ltd. All rights reserved.
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页码:544 / 552
页数:9
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