Dataset Information

High Spatiotemporal Resolution ECoG Recording of Somatosensory Evoked Potentials with Flexible Micro-Electrode Arrays.

ABSTRACT: Electrocorticogram (ECoG) has great potential as a source signal, especially for clinical BMI. Until recently, ECoG electrodes were commonly used for identifying epileptogenic foci in clinical situations, and such electrodes were low-density and large. Increasing the number and density of recording channels could enable the collection of richer motor/sensory information, and may enhance the precision of decoding and increase opportunities for controlling external devices. Several reports have aimed to increase the number and density of channels. However, few studies have discussed the actual validity of high-density ECoG arrays. In this study, we developed novel high-density flexible ECoG arrays and conducted decoding analyses with monkey somatosensory evoked potentials (SEPs). Using MEMS technology, we made 96-channel Parylene electrode arrays with an inter-electrode distance of 700 ?m and recording site area of 350 ?m2. The arrays were mainly placed onto the finger representation area in the somatosensory cortex of the macaque, and partially inserted into the central sulcus. With electrical finger stimulation, we successfully recorded and visualized finger SEPs with a high spatiotemporal resolution. We conducted offline analyses in which the stimulated fingers and intensity were predicted from recorded SEPs using a support vector machine. We obtained the following results: (1) Very high accuracy (~98%) was achieved with just a short segment of data (~15 ms from stimulus onset). (2) High accuracy (~96%) was achieved even when only a single channel was used. This result indicated placement optimality for decoding. (3) Higher channel counts generally improved prediction accuracy, but the efficacy was small for predictions with feature vectors that included time-series information. These results suggest that ECoG signals with high spatiotemporal resolution could enable greater decoding precision or external device control.

SUBMITTER: Kaiju T

PROVIDER: S-EPMC5386975 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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High Spatiotemporal Resolution ECoG Recording of Somatosensory Evoked Potentials with Flexible Micro-Electrode Arrays.

Kaiju Taro T Doi Keiichi K Yokota Masashi M Watanabe Kei K Inoue Masato M Ando Hiroshi H Takahashi Kazutaka K Yoshida Fumiaki F Hirata Masayuki M Suzuki Takafumi T

Frontiers in neural circuits 20170411

Electrocorticogram (ECoG) has great potential as a source signal, especially for clinical BMI. Until recently, ECoG electrodes were commonly used for identifying epileptogenic foci in clinical situations, and such electrodes were low-density and large. Increasing the number and density of recording channels could enable the collection of richer motor/sensory information, and may enhance the precision of decoding and increase opportunities for controlling external devices. Several reports have ai ...[more]

PMID: 28442997

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Project description:Objective.Somatosensory evoked potentials (SSEPs) recorded with electrocorticography (ECoG) for central sulcus (CS) identification is a widely accepted procedure in routine intraoperative neurophysiological monitoring. Clinical practices test the short-latency SSEPs for the phase reversal over strip electrodes. However, assessments based on waveform morphology are susceptible to variations in interpretations due to the hand area's localized nature and usually require multiple electrode placements or electrode relocation. We investigated the feasibility of unsupervised delineation of the CS by using the spatiotemporal patterns of the SSEP captured with the ECoG grid.Approach. Intraoperatively, SSEPs were recorded from eight patients using ECoG grids placed over the sensorimotor cortex. Neurosurgeons blinded to the electrophysiology identified the sensory and motor gyri using neuronavigation based on sulcal anatomy. We quantified the most discriminatory time points in SSEPs temporal profile between the primary motor (M1) and somatosensory (S1) cortex using the Fisher discrimination criterion. We visualized the amplitude gradient of the SSEP over a 2D heat map to provide visual feedback for the delineation of the CS based on electrophysiology. Subsequently, we employed spectral clustering using the entire the SSEP waveform without selecting any time points and grouped ECoG channels in an unsupervised fashion.Main results.Consistently in all patients, two different time points provided almost equal discrimination between anterior and posterior channels, which vividly outlined the CS when we viewed the SSEP amplitude distribution as a spatial 2D heat map. The first discriminative time point was in proximity to the conventionally favored ∼20 ms peak (N20), and the second time point was slightly later than the markedly high ∼30 ms peak (P30). Still, the location of these time points varied noticeably across subjects. Unsupervised clustering approach separated the anterior and posterior channels with an accuracy of 96.3% based on the time derivative of the SSEP trace without the need for a subject-specific time point selection. In contrast, the raw trace resulted in an accuracy of 88.0%.Significance. We show that the unsupervised clustering of the SSEP trace assessed with subdural electrode grids can delineate the CS automatically with high precision, and the constructed heat maps can localize the motor cortex. We anticipate that the spatiotemporal patterns of SSEP fused with machine learning can serve as a useful tool to assist in surgical planning.

Project description:The number of people aged 12 years and older using illicit drugs reached 59.3 million in 2020, among which 5.2 million are cocaine users based on the national data. In order to fully understand cocaine addiction and develop effective therapies, a tool is needed to reliably measure real-time cocaine concentration and neural activity in different regions of the brain with high spatial and temporal resolution. Integrated biochemical sensing devices based upon flexible microelectrode arrays (MEA) have emerged as a powerful tool for such purposes; however, MEAs suffer from undesired biofouling and inflammatory reactions, while those with immobilized biologic sensing elements experience additional failures due to biomolecule degradation. Aptasensors are powerful tools for building highly selective sensors for analytes that have been difficult to detect. In this work, DNA aptamer-based electrochemical cocaine sensors were integrated on flexible MEAs and protected with an antifouling zwitterionic poly (sulfobetaine methacrylate) (PSB) coating, in order to prevent sensors from biofouling and degradation by the host tissue. In vitro experiments showed that without the PSB coating, both adsorption of plasma protein albumin and exposure to DNase-1 enzyme have detrimental effects on sensor performance, decreasing signal amplitude and the sensitivity of the sensors. Albumin adsorption caused a 44.4% sensitivity loss, and DNase-1 exposure for 24 hr resulted in a 57.2% sensitivity reduction. The PSB coating successfully protected sensors from albumin fouling and DNase-1 enzyme digestion. In vivo tests showed that the PSB coated MEA aptasensors can detect repeated cocaine infusions in the brain for 3 hrs after implantation without sensitivity degradation. Additionally, the same MEAs can record electrophysiological signals at different tissue depths simultaneously. This novel flexible MEA with integrated cocaine sensors can serve as a valuable tool for understanding the mechanisms of cocaine addiction, while the PSB coating technology can be generalized to improve all implantable devices suffering from biofouling and inflammatory host responses.

Dataset Information

High Spatiotemporal Resolution ECoG Recording of Somatosensory Evoked Potentials with Flexible Micro-Electrode Arrays.

Publications

High Spatiotemporal Resolution ECoG Recording of Somatosensory Evoked Potentials with Flexible Micro-Electrode Arrays.

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