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DNA-Based Tracers for Next Level Industrial Tracing


Für den Inhalt der Angaben zeichnet die Projektleitung verantwortlich.


Dieses von der Gebert Rüf Stiftung geförderte Projekt wird von folgenden weiteren Projektpartnern mitgetragen: Haelixa; ETH Zurich


  • Projekt-Nr: GRS-042/16 
  • Förderbeitrag: CHF 245'000 
  • Bewilligung: 24.01.2017 
  • Dauer: 06.2017 - 12.2018 
  • Handlungsfeld:  Pilotprojekte, 1998 - 2018



Tracing technologies became an essential tool for companies in a diverse range of areas, such as industrial and environmental fluid monitoring (e.g. track subsurface fluids in order to map underground geothermal/oil reservoirs), authentication and traceability of products (e.g. fuels, luxury goods). However, current tracing technologies have demonstrated major limitations due to lack of a large number of distinct "fingerprints" (uniquely detectable tracers), their cost, and toxicity.

A research team in the Functional Materials Laboratory at ETH Zurich has developed a disruptive DNA-based tracing technology, based on the use of a new class of tracers, composed of DNA sequences (the actual tracer) encapsulated within extremely small particles. The technology provides a theoretically unlimited number of unique fingerprints, absence of toxicity, and is cost-effective.

The DNA-based tracing platform can have a significant impact on society: from speeding up geothermal energy development and utilization by increasing the knowledge of the underground, to tracing and monitoring products and assets in a safer, more reliable, and less expensive manner. Now that this potential has been demonstrated at a research level, on a small scale, it is necessary to develop an industry-relevant platform, from which society can really benefit.

The proposed project aims at developing the processes required for efficient tracer manufacture and detection for large-scale, real-life applications, with focus on the use of the tracers for enhanced exploration and monitoring of underground reservoirs.

Was ist das Besondere an diesem Projekt?

The technology combines in a novel, original way the use of DNA, bio-analytics and particle technology, to generate a potent solution, capable of bringing traceability to the next level. Thanks to its significantly higher versatility and sensitivity than current tracers, and the integration of multiple functions (e.g. sensing, data storage), the technology is a promising candidate to become the new standard in the tracing industry.

However, even after years of successful research, the technology will not reach its full advantage until robust manufacturing and analytical methods
to deliver these products are developed for large scale, real life uses. Additionally, industry leaders interested in our technology, have underlined the importance of having access to fast results on-site. Without this feature, many potential users, in both the geothermal/oilfield and the anti-counterfeiting business, would be reluctant to implement the technology. At the moment, we use standard benchtop qPCR (polymerase chain reaction) machines, which only allow to obtain results within 1.5-2 hours. However, faster, portable detection solutions are nowadays available and can be integrated (after appropriate modification/optimization) in our system to achieve a ca. three-fold reduction in the analysis time. Finally, setting stringent tracer quality control requirements is essential for product/service delivery.

This project aims at filling the mentioned gaps and advancing towards technology commercialization.


In this project, we have translated a tracing technology developed at ETH into a platform ready for industrialization. An optimized big scale tracer manufacturing procedure has been established. The initial small scale, labour-intensive and time-consuming manufacturing procedure has been converted into a scalable, cost-effective approach, capable of delivering in high volumes with optimized costs. Moreover, with goal of integrating a rapid on-site tracer detection method, a systematic evaluation of commercially available portable qPCR devices has been conducted. An optimal detection procedure with the portable qPCR device of choice has been established, as well a simplified sample work-up. The individual, newly developed products and methods have been further integrated in a standardized workflow and have been tested on-site (local aquifer).


Mikutis, G., Deuber, C. A, Schmid, L., Kittilä, A., Lobsiger, N., Puddu, M., Asgeirsson, D., Grass, R. N., Saar, M. O., Stark, W. J., Silica encapsulated DNA-based tracers for aquifer characterization, submitted for publication 2018;
G. Mikutis, C. A. Mora, M. Puddu, R. N. Grass, W. J. Stark, DNA-based sensor particles enable measuring light intensity in single cells, Adv. Mater., 28(14), 2765-2770, 2015. Featured in Nature Review Materials;
M. Puddu, G. Mikutis, W. J. Stark, R. N. Grass, Submicrometer-sized thermometer particles exploiting selective nucleic acid stability, Small, 12(4), 452-456, 2015;
M. Puddu, D. Paunescu, W. J. Stark, R. N. Grass, Magnetically recoverable, thermostable, hydrophobic DNA/Silica encapsulates and their application as invisible oil tags, ACS Nano, 8, 2677-2685, 2014;
D. Paunescu, M. Puddu, J.O.B. Soellner, P.R. Stoessel, R.N. Grass, Reversible DNA encapsulation in silica to produce ROS-resistant and heat-resistant synthetic DNA ‘fossils’, Nat. Protoc., 8, 2440-2448, 2013.



Am Projekt beteiligte Personen

Letzte Aktualisierung dieser Projektdarstellung  15.01.2020