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Summary: Researchers have successfully printed microelectrode arrays onto gelatin candies and other soft materials. They report the technique could pave the way to creating new medical diagnostic tools.
Microelectrodes can be used for direct measurement of electrical signals in the brain or heart. These applications require soft materials, however. With existing methods, attaching electrodes to such materials poses significant challenges. A team at the Technical University of Munich (TUM) has now succeeded in printing electrodes directly onto several soft substrates.
Researchers from TUM and Forschungszentrum Jülich have successfully teamed up to perform inkjet printing onto a gummy bear. This might initially sound like scientists at play – but it may in fact point the way forward to major changes in medical diagnostics. For one thing, it was not an image or logo that Prof. Bernhard Wolfrum’s team deposited on the chewy candy, but rather a microelectrode array. These components, comprised of a large number of electrodes, can detect voltage changes resulting from activity in neurons or muscle cells, for example.
Second, gummy bears have a property that is important when using microelectrode arrays in living cells: they are soft. Microelectrode arrays have been around for a long time. In their original form, they consist of hard materials such as silicon. This results in several disadvantages when they come into contact with living cells. In the laboratory, their hardness affects the shape and organization of the cells, for example. And inside the body, the hard materials can trigger inflammation or the loss of organ functionalities.
Rapid prototyping with inkjet printers
When electrode arrays are placed on soft materials, these problems are avoided. This has sparked intensive research into these solutions. Until now, most initiatives have used traditional methods, which are time-consuming and require access to expensive specialized laboratories. “If you instead print the electrodes, you can produce a prototype relatively quickly and cheaply. The same applies if you need to rework it,” says Bernhard Wolfrum, Professor of Neuroelectronics at TUM. “Rapid prototyping of this kind enables us to work in entirely new ways.”
Wolfrum and his team work with a high-tech version of an inkjet printer. The electrodes themselves are printed with carbon-based ink. To prevent the sensors from picking up stray signals, a neutral protective layer is then added to the carbon paths.
Materials for various applications
The researchers tested the process on various substrates, including PDMS (polydimethylsiloxane) – a soft form of silicon – agarose – a substance commonly used in biology experiments – and finally various forms of gelatin, including a gummy bear that was first melted and then allowed to harden. Each of these materials has properties suitable for certain applications. For example, gelatin-coated implants can reduce unwanted reactions in living tissue.
Through experiments with cell cultures, the team was able to confirm that the sensors provide reliable measurements. With an average width of 30 micrometers, they also permit measurements on a single cell or just a few cells. This is difficult to achieve with established printing methods.
“The difficulty is in fine-tuning all of the components – both the technical set-up of the printer and the composition of the ink,” says Nouran Adly, the first author of the study. “In the case of PDMS, for example, we had to use a pre-treatment we developed just to get the ink to adhere to the surface.”
Wide range of potential applications
Printed microelectrode arrays on soft materials could be used in many different areas. They are suitable not only for rapid prototyping in research, but could also change the way patients are treated. “In the future, similar soft structures could be used to monitor nerve or heart functions in the body, for example, or even serve as a pacemaker,” says Prof. Wolfrum. At present he is working with his team to print more complex three-dimensional microelectrode arrays. They are also studying printable sensors that react selectively to chemical substances, and not only to voltage fluctuations.
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Source: Paul Hellmich – TUM Publisher: Organized by NeuroscienceNews.com. Image Source: NeuroscienceNews.com image is credited to N. Adly / TUM. Original Research: Open access research for “Printed microelectrode arrays on soft materials: from PDMS to hydrogels” by Nouran Adly, Sabrina Weidlich, Silke Seyock, Fabian Brings, Alexey Yakushenko, Andreas Offenhäusser & Bernhard Wolfrum in Flexible Electronics. Published May 24 2018. doi:10.1038/s41528-018-0027-z
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[cbtabs][cbtab title=”MLA”]TUM “Researchers Print Sensors on Gummi Candy.” NeuroscienceNews. NeuroscienceNews, 22 June 2018. <https://neurosciencenews.com/gummi-candy-sensors-9421/>.[/cbtab][cbtab title=”APA”]TUM (2018, June 22). Researchers Print Sensors on Gummi Candy. NeuroscienceNews. Retrieved June 22, 2018 from https://neurosciencenews.com/gummi-candy-sensors-9421/[/cbtab][cbtab title=”Chicago”]TUM “Researchers Print Sensors on Gummi Candy.” https://neurosciencenews.com/gummi-candy-sensors-9421/ (accessed June 22, 2018).[/cbtab][/cbtabs]
Printed microelectrode arrays on soft materials: from PDMS to hydrogels
Microelectrode arrays (MEAs) provide promising opportunities to study electrical signals in neuronal and cardiac cell networks, restore sensory function, or treat disorders of the nervous system. Nevertheless, most of the currently investigated devices rely on silicon or polymer materials, which neither physically mimic nor mechanically match the structure of living tissue, causing inflammatory response or loss of functionality. Here, we present a new method for developing soft MEAs as bioelectronic interfaces. The functional structures are directly deposited on PDMS-, agarose-, and gelatin-based substrates using ink-jet printing as a patterning tool. We demonstrate the versatility of this approach by printing high-resolution carbon MEAs on PDMS and hydrogels. The soft MEAs are used for in vitro extracellular recording of action potentials from cardiomyocyte-like HL-1 cells. Our results represent an important step toward the design of next-generation bioelectronic interfaces in a rapid prototyping approach.
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