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SiNAPS: An implantable active pixel sensor CMOS-probe for simultaneous large-scale neural recordings

机译:Sinaps:一种可植入的有源像素传感器CMOS探头,用于同时大规模的神经录音

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摘要

Large-scale neural recordings with high spatial and temporal accuracy are instrumental to understand how the brain works. To this end, it is of key importance to develop probes that can be conveniently scaled up to a high number of recording channels. Despite recent achievements in complementary metal-oxide semiconductor (CMOS) multi-electrode arrays probes, in current circuit architectures an increase in the number of simultaneously recording channels would significantly increase the total chip area. A promising approach for overcoming this scaling issue consists in the use of the modular Active Pixel Sensor (APS) concept, in which a small front-end circuit is located beneath each electrode. However, this approach imposes challenging constraints on the area of the in-pixel circuit, power consumption and noise. Here, we present an APS CMOS-probe technology for Simultaneous Neural recording that successfully addresses all these issues for whole-array read-outs at 25 kHz/channel from up to 1024 electrode-pixels. To assess the circuit performances, we realized in a 0.18 mu m CMOS technology an implantable single-shaft probe with a regular array of 512 electrode-pixels with a pitch of 28 mu m. Extensive bench tests showed an in-pixel gain of 45.4 +/- 0.4 dB (low pass, F-3 db = 4 kHz), an input referred noise of 73 +/- 0.67 mu V-RMS (300 Hz to 7.5 kHz) and a power consumption 6 mu W/pixel. In vivo acute recordings demonstrate that our SiNAPS CMOS-probe can sample full-band bioelectrical signals from each electrode, with the ability to resolve and discriminate activity from several packed neurons both at the spatial and temporal scale. These results pave the way to new generations of compact and scalable active single/multi-shaft brain recording systems.
机译:具有高空间和时间精度的大型神经录音是有助于了解大脑的作品。为此,开发可以方便地扩展到大量记录通道的探针是关键重要性。尽管近期在互补金属氧化物半导体(CMOS)多电极阵列探针中,但在电流电路架构中,同时记录通道的数量增加将显着增加总芯片区域。克服该缩放问题的有希望的方法包括使用模块化有源像素传感器(APS)概念,其中小前端电路位于每个电极下方。然而,这种方法对像素电路的面积,功耗和噪声施加有挑战性的限制。在这里,我们提出了一种用于同时神经记录的APS CMOS-Probe技术,该技术成功地处理了25 kHz /通道的全阵读出的所有这些问题,从多到1024个电极像素。为了评估电路性能,我们在0.18μmCMOS技术中实现了一个可植入的单轴探针,其具有512个电极像素的常规阵列,其间距为28μm。广泛的台面测试显示了45.4 +/- 0.4dB的像素增益(低通,F-3 dB = 4 kHz),输入引用噪声为73 +/-0.67μmV-rms(300Hz至7.5 kHz)和功耗& 6 mu w / pixel。在体内急性录像中表明,我们的Sinaps CMOS-探针可以从每个电极上采样全带生物电信号,其能够在空间和时间尺度上从几个填充神经元中解析和区分活性。这些结果铺平了新一代紧凑型和可伸缩的有源单轴脑记录系统的方式。

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