Synthesis and self-assembly of amphiphilic precision glycomacromolecules

被引:4
|
作者
Banger, Alexander [1 ]
Sindram, Julian [2 ]
Otten, Marius [2 ]
Kania, Jessica [1 ]
Wilms, Dimitri [1 ]
Strzelczyk, Alexander [1 ]
Miletic, Sean [3 ,4 ,5 ]
Marlovits, Thomas C. [3 ,4 ,5 ]
Karg, Matthias [2 ]
Hartmann, Laura [1 ]
机构
[1] Heinrich Heine Univ, Inst Organ & Macromol Chem, Univ Str 1, D-40225 Dusseldorf, Germany
[2] Heinrich Heine Univ, Inst Phys Chem Colloids & Nanoopt 1, Univ Str 1, D-40225 Dusseldorf, Germany
[3] Univ Med Ctr Hamburg Eppendorf UKE, Inst Struct & Syst Biol, Hamburg, Germany
[4] Ctr Struct Syst Biol CSSB, Hamburg, Germany
[5] Deutsch Elektronen Synchrotron Zentrum DESY, Hamburg, Germany
关键词
NILE RED; SURFACTANT; MICELLES; NANOSTRUCTURES; POLYMERIZATION; GLYCOPOLYMERS; COOPERATIVITY; FLUORESCENCE; ABSORPTION; VESICLES;
D O I
10.1039/d1py00422k
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We present the synthesis of so called amphiphilic glycomacromolecules (APGs) by using solid-phase polymer synthesis. Based on tailor made building blocks, monodisperse APGs with varying compositions are synthesized, introducing carbohydrate side chains and crosslinkable units at defined positions within the macromolecule. Self-assembly of the APGs is characterized via spectroscopic as well as scattering techniques and reveals structural dependencies between APG composition and self-assembly behavior such as the formation of spherical vs. worm-like micelles. Furthermore, polymerizable units within the APGs allow for fixation of the self-assembled structures. Carbohydrate presenting micelles are then evaluated as inhibitors of bacterial adhesion demonstrating their potential for biomedical applications.
引用
收藏
页码:4795 / 4802
页数:8
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