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Issue 34, 2018

Biocompatible crosslinked β-cyclodextrin nanoparticles as multifunctional carriers for cellular delivery

Abstract

Nanoparticle-based biomedicine has received enormous attention for theranostic applications, as these systems are expected to overcome several drawbacks of conventional therapy. Herein, effective and controlled drug delivery systems with on-demand release abilities and biocompatible properties are used as a versatile and powerful class of nanocarriers. We report the synthesis of a novel biocompatible and multifunctional material, entirely consisting of covalently crosslinked organic molecules. Specifically, β-cyclodextrin (CD) precursors were crosslinked with rigid organic linker molecules to obtain small (∼150 nm), thermally stable and highly water-dispersible nanoparticles with an accessible pore system containing β-CD rings. The nanoparticles can be covalently labeled with dye molecules to allow effective tracking in in vitro cell experiments. Rapid sugar-mediated cell-uptake kinetics were observed with HeLa cells, revealing exceptional particle uptake within only 30 minutes. Additionally, the particles could be loaded with different cargo molecules showing pH-responsive release behavior. Successful nuclei staining with Hoechst 33342 dye and effective cell killing with doxorubicin cargo molecules were demonstrated in live-cell experiments, respectively. This novel nanocarrier concept provides a promising platform for the development of controllable and highly biocompatible theranostic systems.

Graphical abstract: Biocompatible crosslinked β-cyclodextrin nanoparticles as multifunctional carriers for cellular delivery

Supplementary files

Article information

Article type
Paper
Submitted
25 Mar 2018
Accepted
14 Aug 2018
First published
16 Aug 2018

Nanoscale, 2018,10, 16284-16292

Biocompatible crosslinked β-cyclodextrin nanoparticles as multifunctional carriers for cellular delivery

S. Datz, B. Illes, D. Gößl, C. v. Schirnding, H. Engelke and T. Bein, Nanoscale, 2018, 10, 16284 DOI: 10.1039/C8NR02462F

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