4.2 Article

Imaging breast cancer cells and tissues using peptide-labeled fluorescent silica nanoparticles

Journal

JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
Volume 8, Issue 5, Pages 2483-2487

Publisher

AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jnn.2008.362

Keywords

fluorescent nanoparticles; RGD peptide; integrin; imaging; breast cancer

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The imaging of tumor cells and tumor tissue samples is very important for cancer detection and therapy. We have taken advantages of fluorescent silica nanoparticles (FSiNPs) coupled with a molecular recognition element that allows for effective in vitro and ex vivo imaging of tumor cells and tissues. In this study, we report on the targeting and imaging of MDA-MB-231 human breast cancer cells using arginine-glycine-aspartic acid (RGD) peptide-labeled FSiNPs. When linked with RGD peptide using the cyanogen bromide (CNBr) method, the FSiNPs exhibited high target binding to alpha(v)beta(3) integrin receptor (ABIR)-positive MDA-MB-231 breast cancer cells in vitro. Further study regarding the ex vivo imaging of tumor tissue samples was also carried out by intravenously injecting RGID peptide-labeled FSiNPs into athymic nude mice bearing the MDA-MB-231 tumors. Tissue images demonstrated that the high integrin alpha(v)beta(3) expression level of the MDA-MB-231 tumors was clearly visible due to the special targeting effects of the RGD peptide-labeled FSiNPs, and the tumor fluorescence reached maximum intensity at 1 h postinjection. Our results break new ground for using FSiNPs to optically image tumors, and may also broaden the applications of silica nanoparticles in biomedicine.

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