Method and apparatus for high resolution physiological imaging of neurons
In accordance with disclosed embodiments, very high magnetic gradients and magnetic slew are applied to magnetizable particle imaging in order to realize high spatial resolution.
1. A method for providing an effective spatial resolution for imaging magnetizable particles for characterizing of neurons in living tissue without causing peripheral nerve stimulation, the method comprising:
introducing magnetizable particles into living tissue;
applying a magnetic gradient on the living tissue within a transition time of less than one millisecond; and
assessing a physiological status of the neurons by measuring the spatial distribution or orientation of the previously introduced magnetizable particles with a spatial resolution smaller than 500 microns,
wherein the assessment of the physiological status of the neurons is performed by measuring electromagnetic properties and/or orientation of at least one of the magnetizable particles using a sensor external to the living tissue, the sensor including at least one coil and at least one driver for imaging magnetizable particles.
2. The method of claim 1 , where the transition time is less than 250 microseconds.
3. The method of claim 1 , where the transition time is less than 100 microseconds.
4. The method of claim 1 , where the transition time is less than 50 microseconds.
5. The method of claim 1 , where the transition time is less than 10 microseconds.
6. The method of claim 1 , where a maximum magnitude of the magnetic gradient is greater than 100 milliTesla.
7. The method of claim 1 , where a maximum magnitude of the magnetic gradient is greater than 400 milliTesla.
8. The method of claim 1 , where a maximum magnetic gradient slew rate is greater than 1,000 Tesla/meter/second.
9. The method of claim 1 , where a maximum magnetic gradient slew rate is greater than 10,000 Tesla/meter/second.
10. The method of claim 1 , wherein the distribution of the neurons is input into a computational simulation.
11. The method of claim 1 , where the physiological status and distribution of the neurons is input into a computational simulation.
12. The method of claim 1 , where the orientation of at least one particle is influenced by electromagnetic fields in the vicinity of one or more neurons, wherein the orientation is sensed external to the living tissue.
13. The method of claim 1 , where the spatial resolution is sufficient to distinguish individual neurons.
14. An apparatus configured to provide an effective spatial resolution for imaging magnetizable particles for characterizing neurons in living tissue without causing peripheral nerve stimulation, the apparatus comprising:
application coils and drivers configured to apply a magnetic field to the living tissue with a transition time of less than one millisecond; and
imaging coils and drivers configured to assess a physiological status of the neurons by measuring the spatial distribution or orientation of previously introduced magnetizable particles with a spatial resolution smaller than 500 microns,
wherein the assessment of the physiological status of the neurons is performed by measuring electromagnetic properties and/or orientation of at least one of the magnetizable particles using the imaging coils and drivers that are external to the living tissue to perform imaging of magnetizable particles.
15. An apparatus configured to probe a function of one or more neurons in living tissue without causing peripheral nerve stimulation, the apparatus comprising:
application coils and drivers for applying a magnetic gradient to the living tissue with a transition time smaller than 500 microns, and
at least one sensor including detecting coils and drivers for detecting signals emitted by at least one previously introduced particle containing magnetizable material, the emitted signals depending on the function of one or more neurons.