Silica Nanoparticles as Biological Probes
The core-shell architecture of the C dot is ideally suited to the development of multifunctional probes for biology.
In collaboration with the Baird Group here at Cornell, we have demonstrated antibody-mediated labeling with Rat Basophilic Leukemia Mast Cells using the FCeRI cell surface receptor for IgE as shown below.

In addition to labeling, we have developed a class of sensor particles based on the core-shell C Dot architecture, known as C Dot sensors.
These particles use the core dye as an internal reference, allowing quantitative concentration measurements to be performed.
By placing the sensor dye in the surface shell, the maximum possible surface area is exposed for interaction with the environment


References:
J. Choi, A. Burns, R. Williams, Z. Zhou, A. Flesken-Nikitin, W. Zipfel, U. Wiesner, A. Niktin. "Core-shell silica nanoparticles as fluorescent labels for nanomedicine" Journal of Biomedical Optics, 12(6) (2007) 064007-(1-11)
A. Burns H. Ow, U. Wiesner. "Fluorescent core-shell silica nanoparticles: towards 'Lab on a particle' architectures for nanobiotechnology" Chemical Society Reviews, 35, 2006, 1028-1042
A. Burns, P. Sengupta, T. Zedayko, B. Baird, U. Wiesner. "Core-Shell Fluorescent Silica Nanoparticles for Chemical Sensing: Towards Single Particle Laboratories" Small, 2(6) 2006, 723-726
E. Herz, A. Burns, S. Lee, P. Sengupta, D. Bonner, H. Ow, C. Liddell, B. Baird, U. Wiesner. " Fluorescent core-shell silica nanoparticles: an alternative radiative materials platform", Proceedings of the SPIE Vol. 6096: Colloidal Quantum Dots for Biomedical Applications, 2006, 1-12
H. Ow, D. Larson, M. Srivastava, B. Baird, W. Webb, U. Wiesner,"Bright and Stable Core-Shell Fluorescent Silica Nanoparticles", Nano Letters 5(1), 2005, 113-117
All images and text Copyright 2008
Wiesner Research Group - Cornell University
In vivo probes for Nanomedicine:
Further, we have begun to study the biodistribution and biocompatibility of these nanoparticles in living systems. This work has shown the particles to be non-toxic in mice, and we have demonstrated in vivo imaging of the particles both in the bloodsteram as well as within cells.
The images at right show 30nm particles in the bloodstream via multiphoton microscpy (top, red), and spontaneously endocytosed by mouse prostate carcinoma cells via TAT cell-penetrating peptides conjugated to the particle surface (bottom, red).
