This work was supported by the Natural Sciences and Engineering Research Council of Canada, le Fonds québécois de la recherche sur la nature et les technologies of Québec via the Centre for Self-Assembled Chemical Structures (CSACS), the Cancer Research Society Inc. (Canada), and St-Jean Photochemicals (Quebec).
Communication
A New Two-Photon-Sensitive Block Copolymer Nanocarrier†
Article first published online: 2 APR 2009
DOI: 10.1002/anie.200900255
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Babin, J., Pelletier, M., Lepage, M., Allard, J.-F., Morris, D. and Zhao, Y. (2009), A New Two-Photon-Sensitive Block Copolymer Nanocarrier. Angewandte Chemie International Edition, 48: 3329–3332. doi: 10.1002/anie.200900255
- †
Publication History
- Issue published online: 15 APR 2009
- Article first published online: 2 APR 2009
- Manuscript Received: 15 JAN 2009
Funded by
- Natural Sciences and Engineering Research Council of Canada
- the Centre for Self-Assembled Chemical Structures (CSACS)
- Cancer Research Society Inc. (Canada)
- St-Jean Photochemicals (Quebec)
Keywords:
- block copolymers;
- dyes and pigments;
- micelles;
- photochemistry;
- photocontrollable release
Graphical Abstract

Easily disrupted: Micelles of a new amphiphilic block copolymer that bear coumarin groups are sensitive to near infrared light by two-photon absorption of the chromophore. Disruption of the micelles under irradiation at 794 nm results in release of both photocleaved coumarin and encapsulated nile red from the hydrophobic core of micelle into aqueous solution, which results in opposing changes in fluorescence emission intensity.
Abstract
Easily disrupted: Micelles of a new amphiphilic block copolymer that bear coumarin groups are sensitive to near infrared light by two-photon absorption of the chromophore. Disruption of the micelles under irradiation at 794 nm results in release of both photocleaved coumarin and encapsulated nile red from the hydrophobic core of micelle into aqueous solution, which results in opposing changes in fluorescence emission intensity.

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