Reactive Nanoparticles Derived from Polysaccharide Phenyl Carbonates

GND
1013355881
ORCID
0000-0002-0273-1996
Zugehörigkeit
Institute of Organic Chemistry and Macromolecular Chemistry, Friedrich-Schiller-University of Jena, Humboldtstr 10, 07743 Jena, Germany, martin.gericke@uni-jena.de
Gericke, Martin;
GND
1222569213
Zugehörigkeit
Department of Hematology and Medical Oncology, Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany, katja.geitel@uni-jena.de
Geitel, Katja;
GND
1301945927
Zugehörigkeit
Department of Hematology and Medical Oncology, Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany, cornelia.joerke@med.uni-jena.de
Jörke, Cornelia;
GND
124767021X
ORCID
0000-0002-6601-2456
Zugehörigkeit
Department of Hematology and Medical Oncology, Jena University Hospital, Am Klinikum 1, 07747 Jena, Germany, joachim.clement@med.uni-jena.de
Clement, Joachim H.;
GND
120056801
Zugehörigkeit
Institute of Organic Chemistry and Macromolecular Chemistry, Friedrich-Schiller-University of Jena, Humboldtstr 10, 07743 Jena, Germany, thomas.heinze@uni-jena.de
Heinze, Thomas

Polysaccharide (PS) based nanoparticles (NP) are of great interest for biomedical applications. A key challenge in this regard is the functionalization of these nanomaterials. The aim of the present work was the development of reactive PS-NP that can be coupled with an amino group containing compounds under mild aqueous conditions. A series of cellulose phenyl carbonates (CPC) and xylan phenyl carbonates (XPC) with variable degrees of substitution (DS) was obtained by homogeneous synthesis. The preparation of PS-NP by self-assembling of these hydrophobic derivatives was studied comprehensively. While CPC mostly formed macroscopic aggregates, XPC formed well-defined spherical NP with diameters around 100 to 200 nm that showed a pronounced long-term stability in water against both particle aggregation as well as cleavage of phenyl carbonate moieties. Using an amino group functionalized dye it was demonstrated that the novel XPC-NP are reactive towards amines. A simple coupling procedure was established that enables direct functionalization of the reactive NP in an aqueous dispersion. Finally, it was demonstrated that dye functionalized XPC-NP are non-cytotoxic and can be employed in advanced biomedical applications.

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