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In vivo biodistribution and highly efficient tumour targeting of carbon nanotubes in mice

Published on January 8, 2007 at 4:20 PM · No Comments

In the first experiment of its kind, investigators at the Center for Cancer Nanotechnology Excellence Focused on Therapy Response (CCNE-TR), based at Stanford University, have shown that single-walled carbon nanotubes (SWCNTs) wrapped in poly(ethylene glycol), or PEG, can successfully target tumors in living animals.

The results of this work, which was conducted by Hongjie Dai, Ph.D., and colleagues, appear in the journal Nature Nanotechnology.

The CCNE-TR team began by coating commercially available SWCNTs with PEG, a biocompatible polymer used frequently in drug delivery applications to increase circulation lifetimes and water solubility. The investigators used PEG of two different lengths, producing coated SWCNTs of 1 nanometer in diameter/100 nanometers in length or 5 nanometers in diameter/300 nanometers in length. The researchers then attached a tumor-targeting peptide known as cyclic-RGD to the end of the PEG chains. RGD, short for the arginine, glycine, and aspartic acid amino acids that make up this peptide, binds to the protein ævß3, which is found on the surface of certain types of malignant cells. Each nanotube contained multiple cyclic-RGD targeting molecules.

To track the nanotubes in living animals, the researchers also attached to the PEG chains multiple copies of a molecule, known as DOTA, that will bind to various metal ions. In this case, the investigators used the DOTA molecules to bind a radioactive isotope of copper, 64Cu, which can be imaged using positron emission tomography (PET). Stability assays showed all of these add-ons remained firmly attached to the nanotubes even after heating them to 70°C for more than one week.

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