RESUMO
Objective.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 anin situsensor for magnetic-based modalities and increase the ability to detect diverse signals across multiple brain regions.Approach.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.Main results.We present detailed quantification of the device performance using realistic finite element simulations with signals and geometries acquired from patch-clamped neuronsin vitroand 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 × 10µm) 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.Significance.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.
