Adsorption of fibrinogen and lysozyme on silicon grafted with poly(2-methacryloyloxyethyl phosphorylcholine) via surface-initiated atom transfer radical polymerization

被引:331
作者
Feng, W
Zhu, SP
Ishihara, K
Brash, JL
机构
[1] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L7, Canada
[2] Univ Tokyo, Sch Engn, Dept Mat Engn, Bunkyo Ku, Tokyo 1138656, Japan
关键词
D O I
10.1021/la050277i
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surfaces based on grafted poly(2-methacryloyloxyethyl phosphorylcholine) (poly(MPC)) "brushes" with a constant graft density of 0.39 chain/nm(2) and chain length from 5 to 200 monomer units were prepared by surface-initiated atom transfer radical polymerization (ATRP) on silicon wafers. The chain length and layer thickness of the poly(MPC) grafts were varied via the ratio. of MPC to sacrificial initiator. The surfaces were characterized by water contact angle, XPS, and AFM. The effect of poly(MPC) chain length on fibrinogen and lysozyme adsorption was studied in TBS buffer at pH 7.4. The adsorption of both proteins on the poly(MPC)-grafted surfaces was greatly reduced compared to the unmodified silicon. Adsorption decreased with increasing chain length of the poly(MPC) grafts. Grafts of chain length 200 (MW 59 000) gave adsorption levels of 7 and 2 ng/cm(2), respectively, for fibrinogen and lysozyme at 1 mg/mL protein concentration, corresponding to reductions of greater than 98% compared to the unmodified silicon. Adsorption experiments using mixtures of the two proteins showed that the suppression of protein adsorption on the poly(MPC)-grafted surfaces was not strongly dependent on protein size or charge.
引用
收藏
页码:5980 / 5987
页数:8
相关论文
共 63 条
[1]   PREVENTION OF PROTEIN ADSORPTION AND PLATELET-ADHESION ON SURFACES BY PEO PPO PEO TRIBLOCK COPOLYMERS [J].
AMIJI, M ;
PARK, K .
BIOMATERIALS, 1992, 13 (10) :682-692
[2]   Protein repellent polyurethane-urea surfaces by chemical grafting of hydroxyl-terminated poly(ethylene oxide): effects of protein size and charge [J].
Archambault, JG ;
Brash, JL .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2004, 33 (02) :111-120
[3]   Exploiting the current paradigm of blood-material interactions for the rational design of blood-compatible materials [J].
Brash, JL .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2000, 11 (11) :1135-1146
[4]   Biomedical surface science: Foundations to frontiers [J].
Castner, DG ;
Ratner, BD .
SURFACE SCIENCE, 2002, 500 (1-3) :28-60
[5]   BIOMEMBRANES AND NEW HEMOCOMPATIBLE MATERIALS [J].
CHAPMAN, D .
LANGMUIR, 1993, 9 (01) :39-45
[6]   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
[7]  
Furuzono T, 1999, J APPL POLYM SCI, V73, P2541, DOI 10.1002/(SICI)1097-4628(19990919)73:12<2541::AID-APP23>3.0.CO
[8]  
2-5
[9]   Polymer brushes that resist adsorption of model proteins: Design parameters [J].
Halperin, A .
LANGMUIR, 1999, 15 (07) :2525-2533
[10]   BIOMEMBRANE SURFACES AS MODELS FOR POLYMER DESIGN - THE POTENTIAL FOR HEMOCOMPATIBILITY [J].
HAYWARD, JA ;
CHAPMAN, D .
BIOMATERIALS, 1984, 5 (03) :135-142