In vivo tumor targeting and spectroscopic detection with surface-enhanced Raman nanoparticle tags

被引:1915
作者
Qian, Ximei [1 ,3 ]
Peng, Xiang-Hong [4 ]
Ansari, Dominic O. [1 ,2 ,3 ]
Yin-Goen, Qiqin [5 ]
Chen, Georgia Z. [4 ]
Shin, Dong M. [4 ]
Yang, Lily [4 ,6 ]
Young, Andrew N. [5 ]
Wang, May D. [7 ,8 ]
Nie, Shuming [1 ,2 ,3 ]
机构
[1] Emory Univ, Dept Biomed Engn, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
[3] Georgia Inst Technol, Atlanta, GA 30322 USA
[4] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[5] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[6] Emory Univ, Dept Surg, Atlanta, GA 30322 USA
[7] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
[8] Georgia Inst Technol, Dept Elect & Comp Engn, Atlanta, GA 30332 USA
关键词
D O I
10.1038/nbt1377
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We describe biocompatible and nontoxic nanoparticles for in vivo tumor targeting and detection based on pegylated gold nanoparticles and surface-enhanced Raman scattering (SERS). Colloidal gold has been safely used to treat rheumatoid arthritis for 50 years, and has recently been found to amplify the efficiency of Raman scattering by 14-15 orders of magnitude. Here we show that large optical enhancements can be achieved under in vivo conditions for tumor detection in live animals. An important finding is that small-molecule Raman reporters such as organic dyes were not displaced but were stabilized by thiolmodified polyethylene glycols. These pegylated SERS nanoparticles were considerably brighter than semiconductor quantum dots with light emission in the near-infrared window. When conjugated to tumor-targeting ligands such as single-chain variable fragment (ScFv) antibodies, the conjugated nanoparticles were able to target tumor biomarkers such as epidermal growth factor receptors on human cancer cells and in xenograft tumor models.
引用
收藏
页码:83 / 90
页数:8
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