ATRP synthesis and association properties of temperature responsive dextran copolymers grafted with poly(N-isopropylacrylamide)

被引:29
作者
Patrizi, Maria Loreta [1 ]
Piantanida, Giovanna [2 ,3 ,4 ]
Coluzza, Carlo [2 ]
Masci, Giancarlo [1 ]
机构
[1] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dept Phys, I-00185 Rome, Italy
[3] Ist Cent Patol Libro, Chem Lab, I-00184 Rome, Italy
[4] Univ Ljubljana, Fac Chem & Chem Technol, Ljubljana 1000, Slovenia
关键词
Polysaccharides; Graft; Atom transfer radical polymerization; Thermosensitive; Poly(N-isopropylacrylamide); Nanoparticles; TRANSFER RADICAL POLYMERIZATION; AQUEOUS-SOLUTIONS; LIGHT-SCATTERING; ETHYL CELLULOSE; BLOCK; WATER; FLUORESCENCE; POLYMERS; BEHAVIOR; MEDIA;
D O I
10.1016/j.eurpolymj.2009.07.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Temperature responsive copolymers of dextran grafted with poly(N-isopropylacrylamide) (Dex-g-PNIPAAM) were prepared by atom transfer radical polymerization (ATRP) in homogeneous mild conditions without using protecting group chemistry. Dextran macroinitiator was synthesized by reaction of dextran with 2-chloropropionyl chloride at room temperature in DMF containing 2% LiCl. ATRP was carried out in DMF: water 50:50 (v/v) mixtures at room temperature with CuBr/Tris(2-dimethylaminoethyl)amine (Me6TREN) as catalyst. Several grafted copolymers with well defined number and length of low polydispersity grafted chains were prepared. Temperature induced association properties in aqueous solution were studied as a function of temperature and polymer concentration by dynamic light scattering, fluorescence spectroscopy and atomic force microscopy (AFM). LCST, ranging from 35 to 41 degrees C, was significantly affected by number and length of grafted chains. The fine tuning of LCST around body temperature is an important characteristic not obtainable by conventional radical grafting of PNIPAAM. Well defined spherical nanoparticles were formed above the LCST of PNIPAAM. Hydrodynamic diameter was in the range 73-98 nm. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2779 / 2787
页数:9
相关论文
共 46 条
[21]   The gene transfection efficiency of thermoresponsive N,N,N-trimethyl chitosan chloride-g-poly(N-isopropylacrylamide) copolymer [J].
Mao, Zhengwei ;
Ma, Lie ;
Yan, Jiang ;
Yan, Ming ;
Gao, Changyou ;
Shen, Jiacong .
BIOMATERIALS, 2007, 28 (30) :4488-4500
[22]   Atom transfer radical polymerization [J].
Matyjaszewski, K ;
Xia, JH .
CHEMICAL REVIEWS, 2001, 101 (09) :2921-2990
[23]   Graft copolymers prepared by atom transfer radical polymerization (ATRP) from cellulose [J].
Meng, Tao ;
Gao, Xia ;
Zhang, Jun ;
Yuan, Jinying ;
Zhang, Yuzhu ;
He, Jiasong .
POLYMER, 2009, 50 (02) :447-454
[24]   Dual stimuli-responsive nanogels by self-assembly of polysaccharides lightly grafted with thiol-terminated poly(N-isopropylacrylamide) chains [J].
Morinloto, Nobuyuki ;
Qiu, Xing-Ping ;
Winnik, Francoise M. ;
Akiyoshi, Kazunari .
MACROMOLECULES, 2008, 41 (16) :5985-5987
[25]   Controlled grafting of acetylated starch by atom transfer radical polymerization of MMA [J].
Nurmi, Leena ;
Holappa, Susanna ;
Mikkonen, Hannu ;
Seppala, Jukka .
EUROPEAN POLYMER JOURNAL, 2007, 43 (04) :1372-1382
[26]   Thermoresponsive artificial extracellular matrix for tissue engineering:: Hyaluronic acid bioconjugated with poly(N-isopropylacrylamide) grafts [J].
Ohya, S ;
Nakayama, Y ;
Matsuda, T .
BIOMACROMOLECULES, 2001, 2 (03) :856-863
[27]   Comb polymers prepared by ATRP from hydroxypropyl cellulose [J].
Ostmark, Emma ;
Harrisson, Simon ;
Wooley, Karen L. ;
Malmstrom, Eva E. .
BIOMACROMOLECULES, 2007, 8 (04) :1138-1148
[28]  
Park K., 1993, BIODEGRADABLE HYDROG
[29]   Synthesis and association properties of thermoresponsive and permanently cationic charged block copolymers [J].
Patrizi, Maria Loreta ;
Diociaiuti, Marco ;
Capitani, Donatella ;
Masci, Giancarlo .
POLYMER, 2009, 50 (02) :467-474
[30]  
Rizzardo E., 2000, ACS Symp. Ser, V768, P278, DOI DOI 10.1021/BK-2000-0768.CH020