Glycoconjugated amphiphilic polymers via click-chemistry for the encapsulation of quantum dots

Herein, we present a strategy for the glycoconjugation of nanoparticles (NPs), with a special focus on fluorescent quantum dots (QDs), recently described by us as "preassembly" approach. Therein, prior to the encapsulation of diverse nanoparticles by an amphiphilic poly(isoprene)-b-poly(et...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 40 vom: 08. Okt., Seite 12593-600
1. Verfasser: Schmidtke, Christian (VerfasserIn)
Weitere Verfasser: Kreuziger, Anna-Marlena, Alpers, Dirk, Jacobsen, Anna, Leshch, Yevgeniy, Eggers, Robin, Kloust, Hauke, Tran, Huong, Ostermann, Johannes, Schotten, Theo, Thiem, Joachim, Thimm, Julian, Weller, Horst
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Polymers Concanavalin A 11028-71-0
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520 |a Herein, we present a strategy for the glycoconjugation of nanoparticles (NPs), with a special focus on fluorescent quantum dots (QDs), recently described by us as "preassembly" approach. Therein, prior to the encapsulation of diverse nanoparticles by an amphiphilic poly(isoprene)-b-poly(ethylene glycol) diblock copolymer (PI-b-PEG), the terminal PEG appendage was modified by covalently attaching a carbohydrate moiety using Huisgen-type click-chemistry. Successful functionalization was proven by NMR spectroscopy. The terminally glycoconjugated polymers were subsequently used for the encapsulation of QDs in a phase transfer process, which fully preserved fluorescence properties. Binding of these nanoconstructs to the lectin Concanavalin A (Con A) was studied via surface plasmon resonance (SPR). Depending on the carbohydrate moiety, namely, D-manno-heptulose, D-glucose, D-galactose, 2-deoxy-2-{[methylamino)carbonyl]amino}-D-glucopyranose ("des(nitroso)-streptozotocin"), or D-maltose, the glycoconjugated QDs showed enhanced affinity constants due to multivalent binding effects. None of the constructs showed toxicity from 0.001 to 1 μM (particle concentration) using standard WST and LDH assays on A549 cells 
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650 4 |a Research Support, Non-U.S. Gov't 
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700 1 |a Kreuziger, Anna-Marlena  |e verfasserin  |4 aut 
700 1 |a Alpers, Dirk  |e verfasserin  |4 aut 
700 1 |a Jacobsen, Anna  |e verfasserin  |4 aut 
700 1 |a Leshch, Yevgeniy  |e verfasserin  |4 aut 
700 1 |a Eggers, Robin  |e verfasserin  |4 aut 
700 1 |a Kloust, Hauke  |e verfasserin  |4 aut 
700 1 |a Tran, Huong  |e verfasserin  |4 aut 
700 1 |a Ostermann, Johannes  |e verfasserin  |4 aut 
700 1 |a Schotten, Theo  |e verfasserin  |4 aut 
700 1 |a Thiem, Joachim  |e verfasserin  |4 aut 
700 1 |a Thimm, Julian  |e verfasserin  |4 aut 
700 1 |a Weller, Horst  |e verfasserin  |4 aut 
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