Issue 8, 2014

A facile transetherification route to polysulfone-poly(ethylene glycol) amphiphilic block copolymers with improved protein resistance

Abstract

A transetherification reaction between polysulfone (PSf) and poly(ethylene glycol) (PEG) alkoxide was proposed and explored for the preparation of polysulfone-poly(ethylene glycol) (PSf–PEG) amphiphilic block copolymers. The reaction efficiency and product structure were investigated by GPC, FTIR and 1H NMR. A bimolecular nucleophilic substitution mechanism (SN2) was proposed and verified by analyzing the linkage and terminal structures of the products. The molecular weight of copolymers determined by GPC was coincident with theoretical value. The mechanical properties of PSf–PEG were preserved by using HO–PEG–OH of high molecular weight. TGA and DSC were adopted to characterize the thermal properties of prepared copolymers. The good non-specific protein absorption resistance of PSf–PEG materials renders them desirable candidates for biomedical applications.

Graphical abstract: A facile transetherification route to polysulfone-poly(ethylene glycol) amphiphilic block copolymers with improved protein resistance

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2013
Accepted
27 Dec 2013
First published
06 Jan 2014

Polym. Chem., 2014,5, 2836-2842

A facile transetherification route to polysulfone-poly(ethylene glycol) amphiphilic block copolymers with improved protein resistance

L. Wang, J. Wang, X. Gao, Z. Liang, B. Zhu, L. Zhu and Y. Xu, Polym. Chem., 2014, 5, 2836 DOI: 10.1039/C3PY01619F

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