Issue 44, 2014

Chemical imaging of live fibroblasts by SERS effective nanofilm


Reliable and strong surface enhanced Raman scattering (SERS) signatures of intracellular compartments in live NIH3T3 fibroblasts are collected in real time by means of SERS active thin nanofilm (30 nm) on colloidal silica (1.5 μm). Nanofilm is composed of preformed silver nanoparticles in the matrix of polyacrylic acid, protecting against heating (37 °C) in water, or culture medium or phosphate buffered saline aqueous solution. The SERS enhancement factors (EFs) of the order 108 allow single biomolecule detection in the native environment of a single live cell. Primary and secondary SERS hot spots of nanofilm are responsible for such high EFs. A slow SERS EF intensity decay occurs over a broader distance of micron silica with nanofilm, not achievable in a common core–shell model (silver nanoparticle coated with a thin silica layer). Extensive local field EFs and SERS EFs are mainly delivered by prolate silver nanoparticles (“rugby-like” shape). This is achieved if an incident field is polarized along the z-axis and the direction of incident polarization and main axis (z) are perpendicular to each other, not observable in water or on gold.

Graphical abstract: Chemical imaging of live fibroblasts by SERS effective nanofilm

Supplementary files

Article information

Article type
09 Sep 2014
03 Oct 2014
First published
07 Oct 2014
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2014,16, 24621-24634

Author version available

Chemical imaging of live fibroblasts by SERS effective nanofilm

D. Radziuk, R. Schuetz, A. Masic and H. Moehwald, Phys. Chem. Chem. Phys., 2014, 16, 24621 DOI: 10.1039/C4CP04034A

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