Polysulfone based amphiphilic graft copolymers by click chemistry as bioinert membranes

被引:37
|
作者
Yilmaz, Gorkem [2 ]
Toiserkani, Hojjat [2 ]
Demirkol, Dilek Odaci [1 ]
Sakarya, Serhan [3 ]
Timur, Suna [1 ]
Torun, Lokman [4 ]
Yagci, Yusuf [2 ]
机构
[1] Ege Univ, Fac Sci, Dept Biochem, TR-35100 Izmir, Turkey
[2] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
[3] Adnan Menderes Univ, Sch Med, Dept Infect Dis & Clin Microbiol, TR-09100 Aydin, Turkey
[4] TUBITAK Marmara Res Ctr, Inst Chem, TR-41470 Gebze, Kocaeli, Turkey
关键词
Amphiphilic graft copolymer; Click chemistry; Polysulfone; Hydrophilic segments; Poly(ethylene glycol); Bio-inertness; SURFACE MODIFICATION; ULTRAFILTRATION MEMBRANES; PROTEIN ADSORPTION; MOLECULAR BRUSHES; BLOCK-COPOLYMERS; RADICAL POLYMERIZATION; COMBINATION; POLYMERS; FUNCTIONALIZATION; POLYSTYRENE;
D O I
10.1016/j.msec.2011.03.010
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A series of well-defined amphiphilic graft copolymers with hydrophobic polysulfone (PSU) as backbones and hydrophilic poly( ethylene glycol) (PEG) as side chains were synthesized and characterized. For this purpose, PSUs were converted to azido-functionalized polymers by successive chloromethylation and azidation processes to give clickable PSUs. Then, the (omega-hydroxyl function of the commercially available PEG-OH was converted into propargyl functionality by simple esterification process. Ultimately, the alkyne functionalized PEO was successfully grafted onto the PSUs by click chemistry. The final polymers and intermediates at various stages were characterized by H-1 NMR, FT-IR, and GPC techniques. The bioinert character of PEG grafted PSU was confirmed by static protein adsorption and prokaryotic and eukaryotic cell adhesion studies, and compared to that of unmodified PSU. (C) 2011 Elsevier By. All rights reserved.
引用
收藏
页码:1091 / 1097
页数:7
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