Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, United States of America.
Wisconsin Institute for Translational Neuroengineering (WITNe), University of Wisconsin-Madison, Madison, WI, 53706, United States of America.
J Neural Eng. 2022 Jul 1;19(4). doi: 10.1088/1741-2552/ac7907.
Methods for the detection of neural signals involve a compromise between invasiveness, spatiotemporal resolution, and the number of neurons or brain regions recorded. Electrode-based probes provide excellent response but usually require transcranial wiring and capture activity from limited neuronal populations. Noninvasive methods such as electroencephalography and magnetoencephalography offer fast readouts of field potentials or biomagnetic signals, respectively, but have spatial constraints that prohibit recording from single neurons. A cell-sized device that enhances neurogenic magnetic fields can be used as ansensor for magnetic-based modalities and increase the ability to detect diverse signals across multiple brain regions.We designed and modeled a device capable of forming a tight electromagnetic junction with single neurons, thereby transducing changes in cellular potential to magnetic field perturbations by driving current through a nanofabricated inductor element.We present detailed quantification of the device performance using realistic finite element simulations with signals and geometries acquired from patch-clamped neuronsand demonstrate the capability of the device to produce magnetic signals readable via existing modalities. We compare the magnetic output of the device to intrinsic neuronal magnetic fields (NMFs) and show that the transduced magnetic field intensity from a single neuron is more than three-fold higher at its peak (1.62 nT vs 0.51 nT). Importantly, we report on a large spatial enhancement of the transduced magnetic field output within a typical voxel (40 × 40 × 10m) over 250 times higher than the intrinsic NMF strength (0.64 nT vs 2.5 pT). We use this framework to perform optimizations of device performance based on nanofabrication constraints and material choices.Our quantifications institute a foundation for synthesizing and applying electromagnetic sensors for detecting brain activity and can serve as a general method for quantifying recording devices at the single cell level.
方法的检测神经信号涉及之间的折衷的侵略性,时空分辨率,和数量的神经元或大脑记录的地区。基于电极的探头提供了极好的反应,但通常需要经颅布线和捕获活动从有限的神经元群体。非侵入性的方法,如脑电图和脑磁图提供快速读数的场电位或生物磁信号,分别,但有空间限制,禁止从单一神经元的记录。一个细胞大小的设备,可以增强神经磁场可以作为传感器的磁模态,并增加能力来检测不同的信号在多个大脑区域。我们设计和建模一个设备能够形成一个紧密的电磁结与单个神经元,从而转导变化的细胞电位的磁场扰动通过驱动电流通过一个纳米制造感应器元素。我们提出了详细的量化的设备性能使用现实的有限元模拟与信号和几何形状获得从膜片钳神经元和演示设备的能力,产生可读的磁场信号通过现有的模式。我们比较的磁输出的设备到内在神经元的磁场(nmfs)和显示的转导磁场强度从一个单一的神经元是超过三倍以上在其峰值(1.62 毫特斯拉对 0.51 毫特斯拉)。重要的是,我们报告的一个大的空间增强的转导磁场输出在一个典型的体素(40 × 40 × 10 米)超过 250 倍高于内在 nmfs 强度(0.64 毫特斯拉对 2.5 皮特斯拉)。我们使用这个框架来执行优化的设备性能的基础上,纳米制造的限制和材料的选择。我们的量化研究所合成和应用电磁传感器检测脑活动的基础,并可以作为一种通用的方法来量化记录设备在单细胞水平。