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

被引:0
作者
Wu, Ping [1 ]
He, Xiaoxiao [1 ]
Wang, Kemin [1 ]
Tan, Weihong [1 ]
Ma, Ding [2 ]
Yang, Wanhua [2 ]
He, Chunmei [1 ]
机构
[1] Hunan Univ, Key Lab Bionanotechnol & Mol Engn Hunan Prov, State Key Lab Chemobiosensing & Chemometr, Ctr Biomed Engn, Changsha 410082, Hunan, Peoples R China
[2] Tongji Med Univ, Wuhan 430000, Peoples R China
关键词
fluorescent nanoparticles; RGD peptide; integrin; imaging; breast cancer;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:2483 / 2487
页数:5
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