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1.
Rev Sci Instrum ; 94(9)2023 Sep 01.
Article in English | MEDLINE | ID: mdl-37724927

ABSTRACT

Carbon nanotubes (CNTs) can be incorporated in various materials to enhance their mechanical or electrical properties. Information on their precise concentration and local distribution is difficult to access non-invasively. For example, electron microscopy studies require cutting of samples. Another way to measure the concentration of CNTs is by the magnetic susceptibility of the ferrocene present in the CNTs by the synthesis process, which can be performed on sample coupons on a vibrating sample magnetometer (VSM); VSM is a bulky laboratory instrument, and the size of the samples studied is constrained. In order to provide a technique that is fast, easy, cheap, and adaptable to the size of the samples, we have developed a benchtop device that measures the CNT concentration through an original inductive dynamic measurement of the ferrocene magnetic susceptibility. We present the method for extracting CNT concentrations and show the results obtained on cement matrices with CNT concentrations of the order of a few percent.

2.
bioRxiv ; 2023 Jul 02.
Article in English | MEDLINE | ID: mdl-37425851

ABSTRACT

Measuring fast neuronal signals is the domain of electrophysiology and magnetophysiology. While electrophysiology is much easier to perform, magnetophysiology avoids tissue-based distortions and measures a signal with directional information. At the macroscale, magnetoencephalography (MEG) is established, and at the mesoscale, visually evoked magnetic fields have been reported. At the microscale however, while benefits of recording magnetic counterparts of electric spikes would be numerous, they are also highly challenging in vivo. Here, we combine magnetic and electric recordings of neuronal action potentials in anesthetized rats using miniaturized giant magneto-resistance (GMR) sensors. We reveal the magnetic signature of action potentials of well isolated single units. The recorded magnetic signals showed a distinct waveform and considerable signal strength. This demonstration of in vivo magnetic action potentials opens a wide field of possibilities to profit from the combined power of magnetic and electric recordings and thus to significantly advance the understanding of neuronal circuits.

3.
ACS Sens ; 5(11): 3493-3500, 2020 11 25.
Article in English | MEDLINE | ID: mdl-33108725

ABSTRACT

Neuronal electrical activity is widely studied in vivo, and the ability to measure its magnetic equivalent to obtain an undisturbed signal with both amplitude and direction information leading to neuronal signal mapping would be a promising tool for neuroscience. To provide such a tool, a probe with spin-electronics-based magnetic sensors with orthogonal axes of sensitivity for two directions of measurement is realized, thanks to a local magnetization re-orientation technique induced by Joule heating. This probe is tested under in vivo measurement conditions in the brain of an anesthetized rat. To be as close as possible to neurons and to create minimal damage during the probe's insertion, the tip thickness has been drastically decreased using a silicon-on-insulator substrate. Our probes provide the ability to perform in vivo magnetic measurements on two orthogonal axes on a 25 µm thick silicon tip with a sensitivity of 1.7%/mT along one axis and 0.9%/mT along the perpendicular axis in the sensor plane, for a limit of detection at 1 kHz of 1.0 and 1.3 nT, respectively. These probes have been tested through a phantom study and during an in vivo experiment. The robustness and stability over one year are demonstrated.


Subject(s)
Biosensing Techniques , Silicon , Animals , Electronics , Magnetics , Neurons , Rats
4.
Neuron ; 95(6): 1283-1291.e4, 2017 Sep 13.
Article in English | MEDLINE | ID: mdl-28844526

ABSTRACT

Neuronal activity generates ionic flows and thereby both magnetic fields and electric potential differences, i.e., voltages. Voltage measurements are widely used but suffer from isolating and smearing properties of tissue between source and sensor, are blind to ionic flow direction, and reflect the difference between two electrodes, complicating interpretation. Magnetic field measurements could overcome these limitations but have been essentially limited to magnetoencephalography (MEG), using centimeter-sized, helium-cooled extracranial sensors. Here, we report on in vivo magnetic recordings of neuronal activity from visual cortex of cats with magnetrodes, specially developed needle-shaped probes carrying micron-sized, non-cooled magnetic sensors based on spin electronics. Event-related magnetic fields inside the neuropil were on the order of several nanoteslas, informing MEG source models and efforts for magnetic field measurements through MRI. Though the signal-to-noise ratio is still inferior to electrophysiology, this proof of concept demonstrates the potential to exploit the fundamental advantages of magnetophysiology.


Subject(s)
Magnetoencephalography/instrumentation , Magnetoencephalography/methods , Neurons/physiology , Animals , Cats , Evoked Potentials/physiology , Female , Male , Visual Cortex/physiology
5.
Sci Rep ; 6: 39330, 2016 12 19.
Article in English | MEDLINE | ID: mdl-27991562

ABSTRACT

The electrical activity of brain, heart and skeletal muscles generates magnetic fields but these are recordable only macroscopically, such as in magnetoencephalography, which is used to map neuronal activity at the brain scale. At the local scale, magnetic fields recordings are still pending because of the lack of tools that can come in contact with living tissues. Here we present bio-compatible sensors based on Giant Magneto-Resistance (GMR) spin electronics. We show on a mouse muscle in vitro, using electrophysiology and computational modeling, that this technology permits simultaneous local recordings of the magnetic fields from action potentials. The sensitivity of this type of sensor is almost size independent, allowing the miniaturization and shaping required for in vivo/vitro magnetophysiology. GMR-based technology can constitute the magnetic counterpart of microelectrodes in electrophysiology, and might represent a new fundamental tool to investigate the local sources of neuronal magnetic activity.


Subject(s)
Action Potentials , Electrophysiological Phenomena , Magnetic Fields , Magnetics/instrumentation , Muscle, Skeletal/physiology , Animals , Computer Simulation , Mice
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