Biocompatible graphene transistor array reads cellular signals

December 5, 2011

This combination of optical microscopy and fluorescence imaging shows a layer of biological cells covering a graphene-based transistor array (credit: Copyright TU Muenchen)

Researchers at Technische Universitaet Muenchen (TUM) and the Juelich Research Center have demonstrated, for the first time, a graphene-based transistor array that is compatible with living biological cells and capable of recording the electrical signals they generate.

Bioelectronic applications have been proposed that would place sensors or even actuators inside a person’s brain, eye, or ear to help compensate for neural damage. Pioneering research in this direction was done using the mature technology of silicon microelectronics, but in practice that approach may be a dead end: Both flexible substrates and watery biological environments pose serious problems for silicon devices; in addition, they may be too “noisy” for reliable communication with individual nerve cells.

The graphene alternative to silicon

Of the several material systems being explored as alternatives, graphene seems very well suited to bioelectronic applications. Graphene’s distinctive combination of characteristics makes it a leading contender for future biomedical applications requiring a direct interface between microelectronic devices and nerve cells or other living tissue. It offers outstanding electronic performance, is chemically stable and biologically inert, can readily be processed on flexible substrates, and should lend itself to large-scale, low-cost fabrication.

The latest results from the TUM-Juelich team confirm key performance characteristics of graphene and open the way for further advances toward determining the feasibility of graphene-based bioelectronics.

High spatial and temporal resolution

The experimental setup began with an array of 16 graphene solution-gated field-effect transistors (G-SGFETs) fabricated on copper foil by chemical vapor deposition and standard photolithographic and etching processes. “The sensing mechanism of these devices is rather simple,” says Dr. Jose Antonio Garrido, a member of the Walter Schottky Institute at TUM. “Variations of the electrical and chemical environment in the vicinity of the FET gate region will be converted into a variation of the transistor current.”

Directly on top of this array, the researchers grew a layer of biological cells similar to heart muscle. The “action potentials” of individual cells were detectable above the intrinsic electrical noise of the transistors, and could be recorded with high spatial and temporal resolution. For example, a series of spikes separated by tens of milliseconds moved across the transistor array in just the way action potentials could be expected to propagate across the cell layer. Also, when the cell layer was exposed to a higher concentration of the stress hormone norepinephrine, a corresponding increase in the frequency of spikes was recorded.

Separate experiments to determine the inherent noise level of the G-SFETs showed it to be comparable to that of ultralow-noise silicon devices. “Much of our ongoing research is focused on further improving the noise performance of graphene devices, and on optimizing the transfer of this technology to flexible substrates such as parylene and kapton, both of which are currently used for in vivo implants,” Garrido says. “We are also working to improve the spatial resolution of our recording devices.”

Meanwhile, they are working with scientists at the Paris-based Vision Institute to investigate the biocompatibility of graphene layers in cultures of retinal neuron cells, as well as within a broader European project called NEUROCARE, which aims at developing brain implants based on flexible nanocarbon devices.

Ref.: Lucas H. Hess et al., Graphene Transistor Arrays for Recording Action Potentials from Electrogenic Cells, Advanced Materials 2011, 23, 5045-5049. DOI: 10.1002/adma.201102990.