Sweet Polymers: Poly(2-ethyl-2-oxazoline) Glycopolymers by Reductive Amination

被引:17
|
作者
Mees, Maarten A. [1 ]
Effenberg, Christiane [2 ]
Appelhans, Dietmar [2 ]
Hoogenboom, Richard [1 ]
机构
[1] Univ Ghent, Dept Organ & Macromol Chem, Supramol Chem Grp, Krijgslaan 281 S4, B-9000 Ghent, Belgium
[2] Leibniz Inst Polymer Res Dresden, Hohe Str 6, D-01069 Dresden, Germany
关键词
RING-OPENING POLYMERIZATION; CHITIN DERIVATIVES; MOLECULAR-WEIGHT; IN-VITRO; POLY(2-OXAZOLINE)S; GLYCOPOLYPEPTIDES; POLYOXAZOLINES; ALTERNATIVES; HYDROLYSIS; AFFINITY;
D O I
10.1021/acs.biomac.6b01451
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carbohydrates are important in signaling, energy storage, and metabolism. Depending on their function, carbohydrates can be part of larger structures, such as glycoproteins, glycolipids, or other functionalities (glycoside). To this end, polymers can act as carriers of carbohydrates in so-called glycopolymers, which mimic the multivalent carbohydrate functionalities. We chose a biocompatible poly(2-ethyl-2-oxazoline) (PEtOx) as the basis for making glycopolymers. Via the partial hydrolysis of PEtOx, a copolymer of PEtOx and polyethylenimine (PEI) was obtained; the subsequent reductive amination with the linear forms of glucose and maltose yielded the glycopolymers. The ratios of PEtOx and carbohydrates were varied systematically, and the solution behaviors of the resulting glycoconjugates are discussed. Dynamic light scattering (DLS) revealed that, depending on the carbohydrate ratio, the glycopolymers were either fully water-soluble or formed agglomerates in a temperature-dependent manner. Finally, these polymers were tested for their biological availability by studying their lectin binding ability with Concanavalin A.
引用
收藏
页码:4027 / 4036
页数:10
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