pH-controlled association of PEG-containing terpolymers of N-isopropylacrylamide and 1-vinylimidazole

被引:22
作者
Bisht, HS
Wan, L
Mao, GZ
Oupicky, D [1 ]
机构
[1] Wayne State Univ, Dept Pharmaceut Sci, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Chem Engn & Mat Sci, Detroit, MI 48202 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
N-isopropylacrylamide; vinylimidazole; PEG;
D O I
10.1016/j.polymer.2005.06.080
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- and pH-controlled association of terpolymers of N-isopropylacrylamide (NIPA) with I-vinylimidazole (VI) and polyethylene glycol (PEG) has been investigated by light scattering and atomic force microscopy (AFM) in situ. The polymers contained 0-15 mol% VI and 0-2 mol% PEG. The phase transition temperatures (T-p) have been in the range of 32-45 degrees C and exhibited significant dependence on the pH of solution in the pH range between 5 and 8. The T-p of the polymers increased with increasing VI content and with decreasing pH, confirming major effect of VI ionization status on T-p. The presence of PEG grafts in the polymer structure had augmenting effect on the magnitude of pH-responsiveness and on the pH-independent colloidal stability of the polymer particles formed above T-p. Incorporation of VI into the polymer structure had similar, but pH-dependent effect on colloidal stabilization of the polymer particles. The size of the particles formed after the phase transition is driven by the association of the collapsed NIPA segments in the globule conformation and it decreased with decreasing pH. The phase transition temperature of the polymers could be adjusted to increase from temperatures below, to temperatures above body temperature upon decreasing pH from 7 to 6, suggesting that such polymers could provide a material platform for a variety of biomedical applications. AFM analysis in situ showed a fully reversible formation of particles in the solutions of the polymers above their T-p. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7945 / 7952
页数:8
相关论文
共 36 条
[1]   New antibody purification procedure using a thermally responsive poly(N-isopropylacrylamide)-dextran derivative conjugate [J].
Anastase-Ravion, S ;
Ding, Z ;
Pellé, A ;
Hoffman, AS ;
Letourneur, D .
JOURNAL OF CHROMATOGRAPHY B, 2001, 761 (02) :247-254
[2]   Exploitation of intracellular pH gradients in the cellular delivery of macromolecules [J].
Asokan, A ;
Cho, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (04) :903-913
[3]   Site-specific polymer-streptavidin bioconjugate for pH-controlled binding and triggered release of biotin [J].
Bulmus, V ;
Ding, ZL ;
Long, CJ ;
Stayton, PS ;
Hoffman, AS .
BIOCONJUGATE CHEMISTRY, 2000, 11 (01) :78-83
[4]   Formation, structure, and temperature behavior of polyelectrolyte complexes between ionically modified thermosensitive polymers [J].
Dautzenberg, H ;
Gao, YB ;
Hahn, M .
LANGMUIR, 2000, 16 (23) :9070-9081
[5]   Temperature control of biotin binding and release with a streptavidin-poly(N-isopropylacrylamide) site-specific conjugate [J].
Ding, ZL ;
Long, CJ ;
Hayashi, Y ;
Bulmus, EV ;
Hoffman, AS ;
Stayton, PS .
BIOCONJUGATE CHEMISTRY, 1999, 10 (03) :395-400
[6]   Size-dependent control of the binding of biotinylated proteins to streptavidin using a polymer shield [J].
Ding, ZL ;
Fong, RB ;
Long, CJ ;
Stayton, PS ;
Hoffman, AS .
NATURE, 2001, 411 (6833) :59-62
[7]   Preparation and tumor cell uptake of poly(N-isopropylacrylamide) folate conjugates [J].
Dubé, D ;
Francis, M ;
Leroux, JC ;
Winnik, FM .
BIOCONJUGATE CHEMISTRY, 2002, 13 (03) :685-692
[8]   Introducing reactive carboxyl side chains retains phase transition temperature sensitivity in N-isopropylacrylamide copolymer gels [J].
Ebara, M ;
Aoyagi, T ;
Sakai, K ;
Okano, T .
MACROMOLECULES, 2000, 33 (22) :8312-8316
[9]   Destabilization of cationic lipid vesicles by an anionic hydrophobically modified poly(N-isopropylacrylamide) copolymer:: a solid-state 31P NMR and 2H NMR study [J].
Franzin, CM ;
Macdonald, PM ;
Polozova, A ;
Winnik, FM .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1415 (01) :219-234
[10]   Copolymerization kinetics of N-isopropylacrylamide and diethylene glycol monomethylether monomethacrylate determined by online NMR spectroscopy [J].
Gramm, S ;
Komber, H ;
Schmaljohann, D .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2005, 43 (01) :142-148