Protein repellency of well-defined, concentrated poly(2-hydroxyethyl methacrylate) brushes by the size-exclusion effect

被引:186
作者
Yoshikawa, C
Goto, A
Tsujii, Y
Fukuda, T [1 ]
Kimura, T
Yamamoto, K
Kishida, A
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[2] Kagoshima Univ, Grad Sch Sci & Engn, Dept Nanostructured & Adv Mat, Kagoshima 8900065, Japan
[3] Tokyo Med & Dent Univ, Inst Biomat & Bioengn, Chiyoda Ku, Tokyo 1010062, Japan
关键词
D O I
10.1021/ma0520242
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The adsorption of proteins on poly(2-hydroxyethyl methacrylate) (PHEMA) brushes was systematically studied by quartz crystal rnicrobalance (QCM) and fluorescence microscopy as a function of graft density and protein size. The graft density a (chains/nm(2)) ranged from 0.007 (dilute or semidilute brush regime) to 0.7 (concentrated brush regime), and the protein size ranged from 2 to 13 nm in an effective diameter. The lowest-density brush (sigma = 0.007) adsorbed all the tested four proteins, while the highest-density brush (a = 0.7) adsorbed none of them. The middle-density brush (sigma = 0.06) showed an intermediate behavior, adsorbing the smallest two proteins but effectively repelling the largest two. PHEMA cast films adsorbed a probe protein with the adsorbed amount increasing approximately proportionally to the film thickness, indicating that the adsorption mainly occurred in the bulk of the film. The noted results for the brushes support the idea of size-exclusion effect, an effect characteristic of concentrated polymer brushes, in which the graft chains are highly extended and highly oriented so that large molecules, sufficiently large compared with the distance between the nearest-neighbor graft points, are physically excluded from the entire brush layer. In this regard, the behavior of the lowest-density brush should be essentially similar to that of the cast film, as was in fact observed.
引用
收藏
页码:2284 / 2290
页数:7
相关论文
共 57 条
[1]  
Asolphi U., 1997, POLYMER, V38, P1513
[2]   THE INTERACTION OF PLASMA-PROTEINS WITH POLYMERS .1. RELATIONSHIP BETWEEN POLYMER SURFACE-ENERGY AND PROTEIN ADSORPTION-DESORPTION [J].
BASZKIN, A ;
LYMAN, DJ .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1980, 14 (04) :393-403
[3]   Atom transfer radical polymerization of 2-hydroxyethyl methacrylate [J].
Beers, KL ;
Boo, S ;
Gaynor, SG ;
Matyjaszewski, K .
MACROMOLECULES, 1999, 32 (18) :5772-5776
[4]   STRUCTURE OF HUMAN SERUM-ALBUMIN [J].
CARTER, DC ;
HE, XM .
SCIENCE, 1990, 249 (4966) :302-303
[5]   Tethered polymer chains: surface chemistry and their impact on colloidal and surface properties [J].
Currie, EPK ;
Norde, W ;
Stuart, MAC .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2003, 100 :205-265
[6]   Polymer brushes via surface-initiated polymerizations [J].
Edmondson, S ;
Osborne, VL ;
Huck, WTS .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (01) :14-22
[7]   Measurements of interbilayer forces and protein adsorption on uncharged lipid bilayers displaying poly(ethylene glycol) chains [J].
Efremova, NV ;
Bondurant, B ;
O'Brien, DF ;
Leckband, DE .
BIOCHEMISTRY, 2000, 39 (12) :3441-3451
[8]   Controlled graft polymerization of methyl methacrylate on silicon substrate by the combined use of the Langmuir-Blodgett and atom transfer radical polymerization techniques [J].
Ejaz, M ;
Yamamoto, S ;
Ohno, K ;
Tsujii, Y ;
Fukuda, T .
MACROMOLECULES, 1998, 31 (17) :5934-5936
[9]   Atom-transfer radical grafting polymerization of 2-methacryloyloxyethyl phosphorylcholine from silicon wafer surfaces [J].
Feng, W ;
Brash, J ;
Zhu, SP .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2004, 42 (12) :2931-2942
[10]  
FENG W, IN PRESS LANGMUIR