| Literature DB >> 20340115 |
Joanna Luszczyn1, Marta E Plonska-Brzezinska, Amit Palkar, Alina T Dubis, Agneta Simionescu, Dan T Simionescu, Beata Kalska-Szostko, Krzysztof Winkler, Luis Echegoyen.
Abstract
Small carbon nano-onions (CNOs, 6-8 shells) were prepared in high yield and functionalized with carboxylic groups by chemical oxidation. After functionalization these nanostructures were soluble in aqueous solutions. 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2 tetrazolium (MTS) tests showed excellent cytocompatibility of all CNOs analyzed at 30 and 300 microg mL(-1), so these carbon nanostructures can be safely used for biological applications. The first covalent functionalization of oxidized CNOs (ox-CNOs) with biomolecules, by using biotin-avidin interactions is reported here. Multilayers were prepared on a gold surface by layer-by-layer assembly and the process was monitored by surface plasmon resonance (SPR) spectroscopy and atomic force microscopy (AFM). Covalent binding of molecules to the short amine-terminated organosulfur monolayers was assessed by Fourier transform infrared spectroscopy using total attenuated reflactance mode (FT-IR/HATR).Entities:
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Year: 2010 PMID: 20340115 DOI: 10.1002/chem.200903277
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236