Issue 26, 2015

A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents

Abstract

Reaction of porphycene isothiocyanates with primary and secondary amines leads to the formation of thiazolo[4,5-c]porphycenes, with a substantial shift in the absorption and fluorescence spectra. The conjugates show fluorescence in the near-infrared and are capable of photosensitizing the production of the cytotoxic species singlet oxygen.

Graphical abstract: A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents

Supplementary files

Article information

Article type
Communication
Submitted
13 Nov 2014
Accepted
08 Dec 2014
First published
11 Dec 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 5586-5589

Author version available

A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents

O. Planas, T. Gallavardin and S. Nonell, Chem. Commun., 2015, 51, 5586 DOI: 10.1039/C4CC09070E

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