LYW and BMR contributed equally to this work. This work was funded by the National Institutes of Health Nanomedicine Development Center for the Optical Control of Biological Function (PN2 EY018241) and DARPA SERS S&T Fundamental Program under LLNL Subcontract #B573237. LYW acknowledges support from a Taiwan Merit Scholarship. The authors acknowledge Somin Eunice Lee for technical insight on specific recognition of breast carcinoma cells by anti-HER-2 labeled probes and David Y. Liang for his assistance in SERS data analysis.
Communication
Bioinspired Nanocorals with Decoupled Cellular Targeting and Sensing Functionality†
Article first published online: 27 JAN 2010
DOI: 10.1002/smll.200901604
Copyright © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Wu, L. Y., Ross, B. M., Hong, S. and Lee, L. P. (2010), Bioinspired Nanocorals with Decoupled Cellular Targeting and Sensing Functionality. Small, 6: 503–507. doi: 10.1002/smll.200901604
- †
Publication History
- Issue published online: 22 FEB 2010
- Article first published online: 27 JAN 2010
- Manuscript Revised: 19 NOV 2009
- Manuscript Received: 26 AUG 2009
Funded by
- National Institutes of Health Nanomedicine Development Center for the Optical Control of Biological Function. Grant Number: PN2 EY018241
- DARPA SERS S&T Fundamental Program. Grant Number: #B573237
Keywords:
- cellular sensing;
- molecular recognition;
- nanoplasmonic probes;
- optical antennas;
- surface-enhanced Raman spectroscopy (SERS)

Nanocorals demonstrate independent cell-targeting and label-free biomolecular sensing capabilities. The highly roughened gold region of the nanocoral increases the adsorption capacity and causes a strong surface-enhanced Raman spectroscopy (SERS) signal. The polystyrene region can adsorb antibodies, allowing the nanocoral to specifically bind to receptors on the cancer cell membrane making nanocorals multifunctional nanosensors for cellular diagnostics and treatment evaluation.

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