Modulation of graft architectures for enhancing hydrophobic interaction of biomolecules with thermoresponsive polymer-grafted surfaces

被引:18
作者
Idota, Naokazu [2 ]
Kikuchi, Akihiko [1 ]
Kobayashi, Jun [2 ]
Sakai, Kiyotaka [3 ]
Okano, Teruo [2 ]
机构
[1] Tokyo Univ Sci, Dept Mat Sci & Technol, Noda, Chiba 2788510, Japan
[2] Tokyo Womens Med Univ TWIns, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[3] Waseda Univ, Dept Appl Chem, Shinjuku Ku, Tokyo 1698555, Japan
关键词
N-Isopropylacrylamide; Atom transfer radical polymerization; Initiator density; Block copolymer; Wettability; Capillary; Separation; AQUEOUS CHROMATOGRAPHY; STATIONARY PHASES; BRUSH SURFACES; TEMPERATURE; SEPARATION; MATRICES; LAYER;
D O I
10.1016/j.colsurfb.2011.10.033
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This paper describes the effects of graft architecture of poly(N-isopropylacrylamide) (PIPAAm) brush surfaces on thermoresponsive aqueous wettability changes and the temperature-dependent hydrophobic interaction of steroids in silica capillaries (I.D.: 50 mu m). PIPAAm brushes were grafted onto glass substrates by surface-initiated atom transfer radical polymerization (ATRP) that is one of the living radical polymerization techniques. Increases in the graft density and chain length of PIPAAm brushes increased the hydration of polymer brushes, resulting in the increased hydrophilic properties of the surface below the transition temperature of PIPAAm at 32 degrees C. More hydrophobic surface properties were also observed on surfaces modified with the block copolymers of IPAAm and n-butyl methacrylate (BMA) than that with IPAAm homopolymer-grafted surfaces over the transition temperature. Using PBMA-b-PIPAAm-grafted silica capillaries, the baseline separation of steroids was successfully achieved by only changing temperature. The incorporation of hydrophobic PBMA chains in grafted PIPAAm enhanced the hydrophobic interaction with testosterone above the transition temperature. The surface modification of hydrophobicity-enhanced thermoresponsive polymers is a promising method for the preparation of thermoresponsive biointerfaces that can effectively modulated their biomolecule and cell adsorption with the wide dynamic range of hydrophilic/hydrophobic property change across the transition temperature. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 101
页数:7
相关论文
共 33 条
[1]   Ultrathin poly(N-isopropylacrylamide) grafted layer on polystyrene surfaces for cell adhesion/detachment control [J].
Akiyama, Y ;
Kikuchi, A ;
Yamato, M ;
Okano, T .
LANGMUIR, 2004, 20 (13) :5506-5511
[2]   Stimuli responsive polymers for biomedical applications [J].
Alarcón, CDH ;
Pennadam, S ;
Alexander, C .
CHEMICAL SOCIETY REVIEWS, 2005, 34 (03) :276-285
[3]  
Buchholz BA, 2002, ELECTROPHORESIS, V23, P1398, DOI 10.1002/1522-2683(200205)23:10<1398::AID-ELPS1398>3.0.CO
[4]  
2-8
[5]   5-COORDINATED HIGH-SPIN COMPLEXES OF BIVALENT COBALT NICKEL AND COPPER WITH TRIS(2-DIMETHYLAMINOETHYL)AMINE [J].
CIAMPOLINI, M ;
NARDI, N .
INORGANIC CHEMISTRY, 1966, 5 (01) :41-+
[6]   Temperature-responsive cell culture surfaces enable "on-off" affinity control between cell integrins and RGDS ligands [J].
Ebara, M ;
Yamato, M ;
Aoyagi, T ;
Kikuchi, A ;
Sakai, K ;
Okano, T .
BIOMACROMOLECULES, 2004, 5 (02) :505-510
[7]   Switchable surface traps for injectable bead-based chromatography in PDMS microfluidic channels [J].
Ebara, Mitsuhiro ;
Hoffman, John M. ;
Hoffman, Allan S. ;
Stayton, Patrick S. .
LAB ON A CHIP, 2006, 6 (07) :843-848
[8]   EFFECT OF COMONOMER HYDROPHILICITY AND IONIZATION ON THE LOWER CRITICAL SOLUTION TEMPERATURE OF N-ISOPROPYLACRYLAMIDE COPOLYMERS [J].
FEIL, H ;
BAE, YH ;
FEIJEN, J ;
KIM, SW .
MACROMOLECULES, 1993, 26 (10) :2496-2500
[9]  
Hansch C., 1995, EXPLORING QSARS HYDR
[10]  
Heskins M., 1968, J Macromol Sci Chem A, V2, P1441, DOI [DOI 10.1080/10601326808051910, 10.1080/10601326808051910]