Electrophysiological investigation of intact retina with soft printed organic neural interface

Objective. Understanding how the retina converts a natural image or an electrically stimulated one into neural firing patterns is the focus of on-going research activities. Ex vivo, the retina can be readily investigated using multi electrode arrays. However, multi electrode array recording and stimulation from an intact retina (in the eye) has been so far insufficient. Approach. In the present study, we report new soft carbon electrode arrays suitable for recording and stimulating neural activity in an intact retina. Screen-printing of carbon ink on 20 µm polyurethane (PU) film was used to realize electrode arrays with electrodes as small as 40 µm in diameter. Passivation was achieved with a holey membrane, realized using laser drilling in a thin (50 µm) PU film. Plasma polymerized EDOT was used to coat the electrode array to improve the electrode specific capacitance. Chick retinas, embryonic stage day 13, both ex-planted and intact inside an enucleated eye, were used. Main results. A novel fabrication process based on printed carbon electrodes was developed and yielded high capacitance electrodes on a soft substrate. Ex vivo electrical recording of retina activity with carbon electrodes is demonstrated. With the addition of organic photo-capacitors, simultaneous photo-electrical stimulation and electrical recording was achieved. Finally, electrical activity recordings from an intact chick retina (inside enucleated eyes) were demonstrated. Both photosensitive retinal ganglion cell responses and spontaneous retina waves were recorded and their features analyzed. Significance. Results of this study demonstrated soft electrode arrays with unique properties, suitable for simultaneous recording and photo-electrical stimulation of the retina at high fidelity. This novel electrode technology opens up new frontiers in the study of neural tissue in vivo.

Self-assembled multifunctional neural probes for precise integration of optogenetics and electrophysiology

Optogenetics combined with electrical recording has emerged as a powerful tool for investigating causal relationships between neural circuit activity and function. However, the size of optogenetically manipulated tissue is typically 1-2 orders of magnitude larger than that can be electrically recorded, rendering difficulty for assigning functional roles of recorded neurons. Here we report a viral vector-delivery optrode (VVD-optrode) system for precise integration of optogenetics and electrophysiology in the brain. Our system consists of flexible microelectrode filaments and fiber optics that are simultaneously self-assembled in a nanoliter-scale, viral vector-delivery polymer carrier. The highly localized delivery and neuronal expression of opsin genes at microelectrode-tissue interfaces ensure high spatial congruence between optogenetically manipulated and electrically recorded neuronal populations. We demonstrate that this multifunctional system is capable of optogenetic manipulation and electrical recording of spatially defined neuronal populations for three months, allowing precise and long-term studies of neural circuit functions.

A Closed-Loop Optogenetic Platform

Neuromodulation is an established treatment for numerous neurological conditions, but to expand the therapeutic scope there is a need to improve the spatial, temporal and cell-type specificity of stimulation. Optogenetics is a promising area of current research, enabling optical stimulation of genetically-defined cell types without interfering with concurrent electrical recording for closed-loop control of neural activity. We are developing an open-source system to provide a platform for closed-loop optogenetic neuromodulation, incorporating custom integrated circuitry for recording and stimulation, real-time closed-loop algorithms running on a microcontroller and experimental control via a PC interface. We include commercial components to validate performance, with the ultimate aim of translating this approach to humans. In the meantime our system is flexible and expandable for use in a variety of preclinical neuroscientific applications. The platform consists of a Controlling Abnormal Network Dynamics using Optogenetics (CANDO) Control System (CS) that interfaces with up to four CANDO headstages responsible for electrical recording and optical stimulation through custom CANDO LED optrodes. Control of the hardware, inbuilt algorithms and data acquisition is enabled via the CANDO GUI (Graphical User Interface). Here we describe the design and implementation of this system, and demonstrate how it can be used to modulate neuronal oscillations in vitro and in vivo.

Electrode pooling can boost the yield of extracellular recordings with switchable silicon probes

State-of-the-art silicon probes for electrical recording from neurons have thousands of recording sites. However, due to volume limitations there are typically many fewer wires carrying signals off the probe, which restricts the number of channels that can be recorded simultaneously. To overcome this fundamental constraint, we propose a method called electrode pooling that uses a single wire to serve many recording sites through a set of controllable switches. Here we present the framework behind this method and an experimental strategy to support it. We then demonstrate its feasibility by implementing electrode pooling on the Neuropixels 1.0 electrode array and characterizing its effect on signal and noise. Finally we use simulations to explore the conditions under which electrode pooling saves wires without compromising the content of the recordings. We make recommendations on the design of future devices to take advantage of this strategy.

Nanoimprinted conducting nanopillar arrays made of MWCNT/polymer nanocomposites: a study by electrochemical impedance spectroscopy

Conducting vertical nanopillar arrays can serve as three-dimensional nanostructured electrodes with improved electrical recording and electrochemical sensing performance in bio-electronics applications.

Sound recording and the operatic canon

This chapter considers three moments in the long relationship between sound recording and operatic canon. In the first, around 1902, the American Victor Talking Machine Company used the acoustically-recorded voice of the tenor Enrico Caruso to help “canonize” (or lend respectability to) what was then a very new form of entertainment. In the second, in the 1920s, Victor and its rival Columbia exploited the new techniques of electrical recording to make recordings of Wagner, and these and other recordings were marketed as part of a larger canon of classical-music “Masterpieces.” In the third, around 1952, newcomer EMI used tape and LP technology to produce one of the first large bodies of complete opera recordings, many of them featuring the soprano Maria Callas and an expanded Italian canon, from Pergolesi to Menotti. This chapter is paired with Hugo Shirley’s “Opera on film and the canon.”

Assessing the Complexity of Human Ventricular Anatomy: Computational Placement of Mapping Catheters in Perfusion- Fixed Human Hearts

Human ventricular cardiac anatomy is extremely complex. Access to the ventricular chambers are often necessary for both mapping and treating ventricular arrhythmias. To date, electrophysiologists who perform these catheter ablations typically rely on fluoroscopy and the patient specific electroanatomical maps they generate so to begin to navigate through these complex functional anatomies. However, limited mapping resolutions do not provide often required insights relative to actual anatomical barriers. Hence, such discordances can lead to larger induced lesion sizes and ultimately, poorer patient outcomes. Here we describe both unique anatomic studies and the development of 3D computational models and assessment strategies for investigating human ventricular anatomies as they relate to arrhythmogenic mapping and therapies. A diverse range of fixed human anatomies were used to study and predict relative distances from an inter-chamber. placed balloon catheter to both true endocardial and epicardial surfaces. This work can be used to inform mapping and ablation catheter designs so to determine and optimize the placements of mapping electrodes to ensure both accurate electrical recording and applied ablations.