Tag Archives: spectroscopy

Sensitive plasmon resonance and the Lycurgus Cup

It’s been a while since I’ve written about the Lycurgus Cup (my Sept. 21, 2010 posting). Dated from the 4th Century AD or CE, the cup is often cited as ancient nanotechnology due to certain optical properties made possible by the inclusion of nanoparticles so it glows green or red depending on the direction of the light.

A Feb. 14, 2013 news item on ScienceDaily features some work in the area of nanoplasmonics that was inspired by the cup,

Utilizing optical characteristics first demonstrated by the ancient Romans, researchers at the University of Illinois at Urbana-Champaign have created a novel, ultra-sensitive tool for chemical, DNA, and protein analysis.

“With this device, the nanoplasmonic spectroscopy sensing, for the first time, becomes colorimetric sensing, requiring only naked eyes or ordinary visible color photography,” explained Logan Liu, an assistant professor of electrical and computer engineering and of bioengineering at Illinois. “It can be used for chemical imaging, biomolecular imaging, and integration to portable microfluidics devices for lab-on-chip-applications. His research team’s results were featured in the cover article of the inaugural edition of Advanced Optical Materials (AOM, optical section of Advanced Materials).

The Lycurgus cup was created by the Romans in 400 A.D. Made of a dichroic glass, the famous cup exhibits different colors depending on whether or not light is passing through it; red when lit from behind and green when lit from in front. It is also the origin of inspiration for all contemporary nanoplasmonics research — the study of optical phenomena in the nanoscale vicinity of metal surfaces.

The University of Illinois College of Engineering Feb. 14, 2013 news release, which originated the news item,

“This dichroic effect was achieved by including tiny proportions of minutely ground gold and silver dust in the glass,” Liu added. “In our research, we have created a large-area high density array of a nanoscale Lycurgus cup using a transparent plastic substrate to achieve colorimetric sensing. The sensor consists of about one billion nano cups in an array with sub-wavelength opening and decorated with metal nanoparticles on side walls, having similar shape and properties as the Lycurgus cups displayed in a British museum. Liu and his team were particularly excited by the extraordinary characteristics of the material, yielding  100 times better sensitivity than any other reported nanoplasmonic device.

This image shows a model of nano cup arrays. (Credit: University of Illinois at Urbana-Champaign)

This image shows a model of nano cup arrays. (Credit: University of Illinois at Urbana-Champaign)

Here’s a little more about colorimetrics and what the researchers are trying to accomplish (from the news release; Note: A link has been removed),

Colorimetric techniques are mainly attractive because of their low cost, use of inexpensive equipment, requirement of fewer signal transduction hardware, and above all, providing simple-to-understand results. … The current design will also enable new technology development in the field of DNA/protein microarray.

“Our label-free colorimetric sensor eliminates the need of problematic fluorescence tagging of DNA/ protein molecules, and the hybridization of probe and target molecule is detected from the color change of the sensor,” stated Manas Gartia, first author of the article, “Colorimetrics: Colorimetric Plasmon Resonance Imaging Using Nano Lycurgus Cup Arrays.” “Our current sensor requires just a light source and a camera to complete the DNA sensing process. This opens the possibility for developing affordable, simple and sensitive mobile phone-based DNA microarray detector in near future. Due to its low cost, simplicity in design, and high sensitivity, we envisage the extensive use of the device for DNA microarrays, therapeutic antibody screening for drug discovery, and pathogen detection in resource poor setting.”

In addition to Gartia and Liu, the paper’s co-authors included Austin Hsiao, Anusha Pokhriyal, Sujin Seo, Gulsim Kulsharova, and Brian T. Cunningham at Illinois, and  Tiziana C. Bond, at the Meso, Micro and Nano Technologies Center at Lawrence Livermore National Laboratory, California.

The team’s article is behind a paywall and you can find a complete citation by clicking on the link to ScienceDaily news item.

All about the University of Calgary and its microscopy and imaging facility

A July 24, 2012 news item on Nanowerk features the the equipment and capabilities of …

The Calgary Microscopy and Imaging Facility (MIF) is a world-class university-wide facility housing transmission electron microscopy (TEM), scanning electron microscopy (SEM), advanced light microscopy, atomic force microscopy (AFM), including single cell force spectroscopy (SCFS), and advanced image processing for three-dimensional electron and light microscopy, directed by Professor Matthias Amrein.

Single cell force spectroscopy at the MIF has now attracted high profile research with three NanoWizard® AFM systems from JPK [Instruments], one of which is equipped with the CellHesion® module. Describing the work of the Calgary group, Professor Amrein says “While we do some work for the energy sector (to predict behaviour of nanoparticles injected into oil reservoirs) our main focus is medicine. We delve into very fundamental problems such as “how does a malaria red blood cell attach itself to a blood vessel” or “how does binding of a ligand to a cell surface receptor or contact of a crystalline surface with the plasma membrane drive lipid sorting and how will this lead to signalling” but then immediately apply it to a practical problem such as “how does contact of uric acid crystals with dendritic cells cause gout in affected joints and how can we prevent this occurrence?” We want to understand disease processes at a very fundamental level so we know how to intervene in the best possible way. For example, a chronic inflammatory disease such as gout or arteriosclerosis may be triggered by a very specific interaction of a particle (uric acid crystals, cholesterol crystals, amyloid plaque, …. ) and specific cell (dendritic cell, macrophage, T-cell, …). Understanding this interaction will lead to targeted treatment “block the interaction” rather than the non-specific dampening of inflammation such as by corticosteroids with its many well-documented side effects and limited efficacy.”

It’s always nice to get some information about activities in microscopy, etc. in Canada although I’m not sure what occasioned the news item/release.