Non-contact method for accelerating wound healing using an electromagnetic coil to induce an electric field transverse to an axis of the wound
09777265 · 2017-10-03
Assignee
Inventors
- Vish Subramaniam (Westerville, OH)
- Joseph West (Richwood, OH)
- Emily Alkandry (Columbus, OH)
- Sashwati Roy (Columbus, OH, US)
- Chandan Sen (Upper Arlington, OH, US)
- Piya Ghatak (Columbus, OH, US)
Cpc classification
C12M35/02
CHEMISTRY; METALLURGY
C12M41/46
CHEMISTRY; METALLURGY
C12N13/00
CHEMISTRY; METALLURGY
International classification
C12N13/00
CHEMISTRY; METALLURGY
A61N2/02
HUMAN NECESSITIES
Abstract
A method for accelerating the migration of cells by applying a time-varying magnetic field to induce eddy currents that promote electrotaxis (galvanotaxis) of cells. The method of the present invention accelerates the healing of wounds by electrotaxis of cells.
Claims
1. A method for controlling cell migration comprising the steps of: providing an electromagnetic coil having a first end and a second end; connecting the electromagnetic coil to a function generator; applying a time-varying voltage waveform to the electromagnetic coil; inducing a time-varying electric field around the electromagnetic coil; placing the electromagnetic coil adjacent to the location of a wound, the wound comprised of wound cells; orientating the placement of the electromagnetic coil to control the direction of the induced electric field; directing the induced electric field in a direction transverse to an axis of the wound; wherein the time-varying voltage waveform has a sharp drop at the trailing edge of the waveform and wherein the induced electric field is produced by a rapidly time-varying magnetic field; and controlling the migration of the wound cells using the induced electric field.
2. A method according to claim 1 further comprising the step of: inducing eddy currents near the location of the wound.
3. A method according to claim 1 further comprising the step of: accelerating the healing of the wound by accelerating the migration of the wound cells using the induced electric field.
4. A method according to claim 1, wherein the time-varying waveform is a sawtooth waveform.
5. A method according to claim 1, wherein the time-varying waveform is a 20 volts peak to peak, 100 Khz sawtooth waveform with a 50 ns drop off at its trailing edge.
6. A method according to claim 1, further comprising the step of: beaming an EM field from a remote source to the location of the wound.
7. A method according to claim 1, further comprising the steps of: placing a culture plate on top or on the sides of the electromagnetic coil; placing keratinocytes in the culture plate with a region between the keratinocytes devoid of keratinocytes.
8. A method according to claim 7 further comprising the steps of: taking an image of the wound after the step of inducing a time-varying electric field; and quantifying the healing potential of the induced electric field.
9. A method according to claim 1, further comprising the steps of: inducing an electric field in the direction of the surface of the wound; from below the surface of the wound; and controlling migration of cells of different types to the surface of the wound.
10. A method according to claim 1, further comprising the step of: inducing a rotating electric field in the wound.
11. A method according to claim 1, further comprising the step of: inducing a inhomogeneous electric field in the wound.
12. A method for controlling cell migration comprising the steps of: providing an electromagnetic coil having a first end and a second end; connecting the electromagnetic coil to a function generator; applying a time-varying voltage waveform to the electromagnetic coil; inducing a time-varying electric field around the electromagnetic coil; placing the electromagnetic coil adjacent to the location of a wound, the wound comprised of wound cells; orientating the placement of the electromagnetic coil to control the direction of the induced electric field; directing the induced electric field in a direction transverse to an axis of the wound; controlling the migration of the wound cells using the induced electric field; inducing an electric field in the direction of the surface of the wound; from below the surface of the wound; and controlling migration of cells of different types to the surface of the wound.
13. A method according to claim 12 further comprising the step of: inducing eddy currents near the location of the wound.
14. A method according to claim 12 further comprising the step of: accelerating the healing of the wound by accelerating the migration of the wound cells using the induced electric field.
15. A method according to claim 12, wherein the time-varying waveform is a sawtooth waveform.
16. A method according to claim 12, wherein the time-varying waveform is a 20 volts peak to peak, 100 Khz sawtooth waveform with a 50 ns drop off at its trailing edge.
17. A method according to claim 16, wherein the sawtooth waveform has a sharp drop and wherein the induced electric field is a rapidly time-varying magnetic field.
18. A method according to claim 12, further comprising the steps of: varying the characteristics of the waveform to control the migration of the wound cells.
19. A method according to claim 12, further comprising the steps of: placing a culture plate on top of the electromagnetic coil; placing keratinocytes in the culture plate with a region between the keratinocytes devoid of keratinocytes.
20. A method according to claim 19 further comprising the steps of: taking an image of the wound after the step of inducing a time-varying electric field; and quantifying the healing potential of the induced electric field.
21. A method according to claim 12, further comprising the step of: inducing a rotating electric field in the wound.
22. A method according to claim 12, further comprising the step of: inducing a inhomogeneous electric field in the wound.
23. A method according to claim 12, further comprising the step of: beaming an EM field from a remote source to the location of the wound.
24. A method according to claim 1, wherein the induced electric field has a magnitude of less than 0.7 mV/cm.
25. A method according to claim 12, wherein the induced electric field has a magnitude of less than 0.7 mV/cm.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The following detailed description of the example embodiments refers to the accompanying figures that form a part thereof. The detailed description provides explanations by way of exemplary embodiments. It is to be understood that other embodiments may be used having mechanical and electrical changes that incorporate the scope of the present invention without departing from the spirit of the invention.
(2) In addition to the features mentioned above, other aspects of the present invention will be readily apparent from the following descriptions of the drawings and exemplary embodiments, wherein like reference numerals across the several views refer to identical or equivalent features, and wherein:
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DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENT(S)
(16) The present invention relates to a method for inducing electric fields in a medium containing cells by applying time-varying magnetic fields. The method uses electromagnetic (EM) induction to induce electric fields and eddy currents in the medium and galvanotaxis of cells.
(17) Preliminary experiments have been conducted with human keratinocytes cultured in Dulbecco's Modified Eagle Medium (DMEM) to form a contiguous layer with a well-defined rectangular region devoid of cells so as to simulate a wound.
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(19) Normally, the initially vacant region is filled in as the cells grow inward to close the simulated wound (in about 6 to 8 hours) when placed in an incubator (at 37° C. with 5% CO.sub.2). In one embodiment, the culture dish with the simulated wound is placed on an electromagnetic (EM) coil (R˜22Ω, L=10 mH) situated within a fixture as shown in
(20) In one embodiment, the EM coil is driven using a function generator using a 5 Vpp, 1 Hz sawtooth wave with a sharp ˜50 ns drop to generate a rapidly time-varying magnetic field with components B.sub.r and B.sub.z. In another embodiment, a 19 Vpp, 100 kHz, sawtooth wave with a sharp ˜50 ns drop is used. By Faraday's law these temporally varying magnetic fields from the EM coil induce an electric field E.sub.θ in the medium containing the cells due to the small but non-zero electrical conductivity of the medium. This component of the induced electric field E.sub.θ has its largest component directed transverse to the axis of the simulated wound and along the axis of propagation of the healing front. At the driving frequency of 1 Hz, E.sub.θ switches direction back and forth (left and right) along the axis of the advancing healing fronts. The magnitude of E.sub.θ in one direction is larger than in the other because of the asymmetric sawtooth waveform imposed on the EM coil. In one embodiment, the cells are exposed to the electric field for 50 ns per second. The duration of this field remains 50 ns because of the characteristic of the sawtooth waveform but the overall duration can be increased by increasing the duty cycle (frequency on the function generator) from 1 Hz to 100 kHz.
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(22) Real chronic wounds are three dimensional (generally round) and not two-dimensional (or rectangular) as in the case of the assay shown in
(23) In summary, a time-varying magnetic field from an electromagnetic (EM) coil has been used to induce electric fields in a medium containing human keratinocytes and simulating a wound. In vitro measurements on a simulated wound in a contiguous layer of keratinocytes have shown that closing of the initially introduced gap can be inhibited (i.e. healing is retarded) significantly compared to control experiments where no EM field is applied. It is appreciated that directional effects due to the induced electric field causes asymmetric advancement of the wound front. By varying the characteristics of the excitation of the EM coil, and positioning of the coil relative to the wound, it is possible to accelerate wound healing. The cells remain in a contiguous layer (i.e., cells or groups of cells do not move into the gap). For example,
(24) It is possible to introduce a D.C. offset to the voltage imposed on the EM coil. However, it can be shown below that while this offset can increase the steady D.C. current in the EM coil, it does not increase E.sub.θ (because by Faraday's law, a time-varying magnetic field is necessary). For example, an offset voltage of V.sub.0 is imposed on a sinusoidally varying voltage imposed on the coil: V.sub.p=V.sub.0+V.sub.1 sin(ωt). Then, the resulting current flowing through the coil can be calculated to be (for long times):
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The induced electric field which drives eddy currents can then be approximately determined as:
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It can be seen that the offset V.sub.0 disappears. It is appreciated from the above expression for the induced electric field, that the asymmetric (in time) AC excitation of the coil should produce a time varying induced electric field and drive eddy currents that are largest in one direction.
(27) In another embodiment of the invention, a remotely placed EM source is configured to beam an EM field to induce an electric field at the wound site (e.g., remote induction scheme). In one example, a transmitting power source placed on the ceiling or wall of a hospital room beams an EM wave to a receiving coil placed in the vicinity of a wound. Alternatively it may be possible to transmit an EM wave focused on the wound such that electric fields are induced in the desired directions.
(28) While certain embodiments of the present invention are described in detail above, the scope of the invention is not to be considered limited by such disclosure, and modifications are possible without departing from the spirit of the invention as evidenced by the following claims: