Nanoprobes for intracellular and single cell surface-enhanced Raman spectroscopy (SERS)

被引:68
作者
Vitol, Elina A. [1 ,2 ,3 ]
Orynbayeva, Zulfiya [2 ,3 ,4 ]
Friedman, Gary [2 ,3 ]
Gogotsi, Yury [1 ,2 ,3 ]
机构
[1] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[2] Drexel Univ, AJ Drexel Nanotechnol Inst, Philadelphia, PA 19104 USA
[3] Drexel Univ, Dept Elect & Comp Engn, Philadelphia, PA 19104 USA
[4] Drexel Univ, Coll Med, Dept Surg, Philadelphia, PA 19102 USA
关键词
SERS; TERS; cells; nanoparticles; nanopipettes; carbon nanotubes; SCATTERING SERS; GOLD NANORODS; SILVER NANOPARTICLES; MOLECULAR-DYNAMICS; PLASMA-MEMBRANE; CANCER-CELLS; IDENTIFICATION; FLUORESCENCE; ADSORPTION; COMPONENTS;
D O I
10.1002/jrs.3100
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Surface-enhanced Raman spectroscopy (SERS) is a promising and powerful label free technique for high resolution analysis of single cells. For intracellular analysis, there is a need for SERS-active nanoprobes that are minimally invasive to cells, do not affect cell viability, and provide reproducible signals. This work reviews the state-of-the-art tools currently available for intracellular SERS. Various types of SERS probes are considered, including colloidal gold and silver nanoparticles, metallized optical fibers, and tip-enhanced Raman probes. We also discuss recently developed SERS-active nanopipettes implemented on the basis of pulled glass microcapillaries. Finally, the critical aspects of selecting an optimal SERS nanoprobe for single-cell analysis depending on a particular application are summarized. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:817 / 827
页数:11
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