Abstract
Polymer-based biomedical electronics provide a tunable platform to interact with nervous tissue both in vitro and in vivo. Ultimately, the ability to control functional properties of neural interfaces may provide important advantages to study the nervous system or to restore function in patients with neurodegenerative disorders. Liquid crystal elastomers (LCEs) are a class of smart materials that reversibly change shape when exposed to a variety of stimuli. Our interest in LCEs is based on leveraging this shape change to deploy electrode sites beyond the tissue regions exhibiting inflammation associated with chronic implantation. As a first step, we demonstrate that LCEs are cellular compatible materials that can be used as substrates for fabricating microelectrode arrays (MEAs) capable of recording single unit activity in vitro. Extracts from LCEs are non-cytotoxic (>70% normalized percent viability), as determined in accordance to ISO protocol 10993-5 using fibroblasts and primary murine cortical neurons. LCEs are also not functionally neurotoxic as determined by exposing cortical neurons cultured on conventional microelectrode arrays to LCE extract for 48 h. Microelectrode arrays fabricated on LCEs are stable, as determined by electrochemical impedance spectroscopy. Examination of the impedance and phase at 1 kHz, a frequency associated with single unit recording, showed results well within range of electrophysiological recordings over 30 days of monitoring in phosphate-buffered saline (PBS). Moreover, the LCE arrays are shown to support viable cortical neuronal cultures over 27 days in vitro and to enable recording of prominent extracellular biopotentials comparable to those achieved with conventional commercially-available microelectrode arrays.
Highlights
Neural interfaces allow for communication with nervous tissue both in vitro and in vivo
We evaluate the functional neurotoxicity of Liquid crystal elastomers (LCEs) materials in vitro using primary neuronal networks cultured on commercially available planar microelectrode arrays
To investigate the use of LCEs as substrate materials for neural interfaces, we examine the cytotoxicity, functional neurotoxicity, and manufacturability of microelectrodes on LCEs
Summary
Neural interfaces allow for communication with nervous tissue both in vitro and in vivo. The use of polymers for in vitro neural interfaces has proven advantageous and gained traction over the past years [3,4,5,6] This includes the fabrication of mechanically flexible planar MEAs to reduce the tissue-interface mechanical mismatch [7] or using polymer actuators to allow for advanced interface control in the case of cell compartmentalization [8]. The reliability of such neural interfaces is compromised, in part, by the body’s own foreign body response (FBR), leading to localized astrogliosis and fibrotic encapsulation of the device [10] These factors may lead to accelerated mechanical/electrical device failure and/or loss of neurons at the site of implantation [11,12]. While conventional implantable microelectrode arrays are comprised of inherently stiff materials, flexible polymer substrates have gained interest for their potential in mitigating the mechanical mismatch at the tissue–device interface and reduce FBR-induced encapsulation [13,14]
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