This work was supported by the National Institutes of Health (CA147837 and NS062725 to D.T.C.; CA135491 and CA112350-03 to J.M.O.; GM 081040 to J.D.M.). We acknowledge support from the Keck Imaging Center, the Center of Nanotechnology at the University of Washington, and the Seattle Children’s Research Institute Brain Tumor Endowment.
Communication
Design of Highly Emissive Polymer Dot Bioconjugates for In Vivo Tumor Targeting†
Article first published online: 4 MAR 2011
DOI: 10.1002/anie.201007461
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Wu, C., Hansen, S. J., Hou, Q., Yu, J., Zeigler, M., Jin, Y., Burnham, D. R., McNeill, J. D., Olson, J. M. and Chiu, D. T. (2011), Design of Highly Emissive Polymer Dot Bioconjugates for In Vivo Tumor Targeting. Angew. Chem. Int. Ed., 50: 3430–3434. doi: 10.1002/anie.201007461
- †
Publication History
- Issue published online: 31 MAR 2011
- Article first published online: 4 MAR 2011
- Manuscript Revised: 7 FEB 2011
- Manuscript Received: 28 NOV 2010
Funded by
- National Institutes of Health. Grant Numbers: CA147837, NS062725, CA135491, CA112350-03, GM 081040
- Keck Imaging Center
- Center of Nanotechnology at the University of Washington
- Seattle Children’s Research Institute Brain Tumor Endowment
Keywords:
- fluorescence;
- imaging agents;
- nanoparticles;
- semiconducting polymers;
- tumors

Lighting up brain tumors: Highly fluorescent nanodots that consist of semiconducting polymer blends were attached to the peptide ligand chlorotoxin. The nanodot–chlorotoxin conjugates were specifically targeted to malignant brain tumors in a transgenic mouse model, thus proving their potential as in vivo probes for clinical cancer diagnostics (see picture).

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