Device and method for controlling electrical field
11059052 ยท 2021-07-13
Assignee
Inventors
Cpc classification
B03C5/026
PERFORMING OPERATIONS; TRANSPORTING
B03C5/005
PERFORMING OPERATIONS; TRANSPORTING
B03C5/028
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
A method for dielectrophoresis includes applying an electric field across a micro-fluidic chamber with an alternating current (AC), trapping the target particles on the at least one carrier particle, transporting the target particles from a first location in the chamber to a second location in the chamber distanced from the first location with the at least one carrier particle and dynamically controlling the trapping and the transporting based on remotely applying forces on the at least one carrier particle. The trapping is based on localized gradients of the electric field induced by the carrier particle. The applied electric field is uniform absent a carrier particle present in the micro-fluidic chamber. The micro-fluidic chamber contains an electrolyte-solution with suspended target particles and at least one carrier particle freely floating on or in the electrolyte-solution.
Claims
1. A method for dielectrophoresis (DEP), the method comprising: by an alternating current (AC) source applying an electric field across a micro-fluidic chamber with an AC, wherein the micro-fluidic chamber contains an electrolyte-solution with suspended target particles and at least one carrier particle freely floating on or in the electrolyte-solution, wherein the electric field is uniform absent said at least one carrier particle present in the micro-fluidic chamber, and wherein said at least one carrier particle induces a gradient to said electric field; by a controller: selectively trapping the target particles on the at least one carrier particle based on localized gradients of the electric field induced by the carrier particle; transporting the target particles from a first location in the micro-fluidic chamber to a second location in the micro-fluidic chamber distanced from the first location with the at least one carrier particle; and dynamically controlling the trapping and the transporting by dynamically selecting a frequency of the AC.
2. The method according to claim 1, comprising, by said controller, dynamically controlling release of said trapped target particles from said at least one carrier particle, based on said dynamic selection of said frequency of the AC.
3. The method of claim 1, wherein the trapping and the transporting are dynamically controlled based on selection of amplitude of the AC.
4. The method according to claim 1, wherein dynamically controlling the transporting is based on selecting on demand a first pre-defined frequency configured to induce self DEP (s-DEP) on the at least one carrier particle.
5. The method according to claim 1, wherein the trapping is dynamically controlled based on selection of a frequency of the AC electric field and the transporting is dynamically controlled based on an externally applied magnetic field.
6. The method according to claim 5, wherein the at least one carrier particle includes magnetic functionalization.
7. The method according to claim 6, wherein the magnetic functionalization is based on magnetic material coated on the carrier particle or a magnetic core of the carrier particle.
8. The method according to claim 1, wherein the trapping is dynamically controlled based on selection of a frequency of the AC electric field and the transporting is dynamically controlled based on an externally applied optical force.
9. The method according to claim 5, wherein the at least one carrier particle is a homogenous particle.
10. The method according to claim 1, wherein the at least one carrier particle is a symmetry broken particle.
11. The method according to claim 10, wherein the at least one carrier particle is a Janus particle.
12. The method according to claim 10, wherein the localized gradient induced is based on proximity of the particle to a conducting wall of the micro-fluidic chamber.
13. The method according to claim 10, wherein the transporting is in a direction perpendicular to the direction of the electric field.
14. The method according to claim 1, wherein the at least one carrier particle is at least one of a particle doublet, a cluster and a particle with non-spherical shape, and wherein the localized gradients induced is based on the geometric characteristics of the target particle.
15. The method according to claim 1, wherein the at least one carrier particle is functionalized with molecular biological probes.
16. The method according to claim 1, wherein dynamically controlling the trapping is based on selecting on demand a pre-defined frequency configured to induce positive DEP (p-DEP) on the target particles.
17. The method according to claim 1, wherein dynamically controlling the trapping or release is based on selecting on demand a pre-defined frequency configured to induce negative DEP (n-DEP) on the target particles.
18. The method according to claim 1, comprising: applying a first electric field defined by a first pre-defined frequency for a first pre-defined time period, wherein the first pre-defined frequency is configured to induce p-DEP on the target particles; applying a second electric field defined by a second pre-defined frequency for a second pre-defined time period subsequent to the first pre-defined time period, wherein the second pre-defined frequency is configured to induce n-DEP of any contaminants attached to the carrier; and applying a third electric field defined by a third pre-defined frequency for a third pre-defined time period subsequent to the second pre-defined time period, wherein the third pre-defined frequency is configured to induce transporting of the target particles trapped on the at least one carrier particle.
19. A device for dielectrophoresis comprising: a micro-fluidic chamber comprising: an electrolyte-solution with suspended target particles; at least one carrier particle freely floating on or in the electrolyte-solution; a first electrode and second electrode, each abutting a floor or a ceiling of the micro-fluidic chamber; an AC source applying AC on the first and second electrode, wherein the AC induces an electric field across the micro-fluidic chamber, wherein the electric field is uniform absent said at least one carrier particle present in the micro-fluidic chamber, and wherein said at least one carrier particle induces a gradient to said electric field; and controller configured to dynamically control selective trapping of the target particles by said at least one carrier particle, and transporting trapped target particles from a first location in the chamber to a second location in the chamber distanced from the first location in a direction perpendicular to the direction of the electric field, by dynamically selecting a frequency of the AC.
20. The device according to claim 19, wherein said controller is also configured to dynamically control release of said trapped target particles from said at least one carrier particle, based on said dynamic selection of said frequency of the AC.
21. The device according to claim 20, wherein the controller is configured to select on demand a first pre-defined frequency configured to induce s-DEP of the at least one carrier particle.
22. The device according to claim 19, wherein the controller is configured to dynamically control trapping based on selection of a frequency of the AC and is configured to dynamically control transporting based on an externally applied magnetic field.
23. The device according to claim 22, wherein the at least one carrier particle includes magnetic functionalization.
24. The device according to claim 19, wherein the at least one carrier particle is a homogenous particle.
25. The device according to claim 19, wherein the at least one carrier particle is a symmetry broken particle.
26. The device according to claim 25, wherein the at least one carrier particle is a Janus particle.
27. The device according to claim 25, wherein the at least one carrier particle is at least one of a particle doublet, a cluster and a particle with a non-spherical shape.
28. The device according to claim 19, wherein the at least one carrier particle is functionalized with molecular biological probes.
29. The device according to claim 19, wherein the controller is configured to select on demand a pre-defined frequency configured to induce p-DEP on the target particles.
30. The device according to claim 29, wherein the controller is configured to select on demand a pre-defined frequency configured to induce n-DEP on any contaminants.
31. The device according to claim 19, wherein the controller is configured to select on demand a pre-defined frequency configured to induce n-DEP on the target particles.
Description
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS
(1) The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
(2) Some embodiments of the invention are herein described, by way of example only, with reference to the accompanying images and drawings. With specific reference now to the images and drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of embodiments of the invention. In this regard, the description taken with the drawings makes apparent to those skilled in the art how embodiments of the invention may be practiced.
(3) In the drawings:
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DESCRIPTION OF SPECIFIC EMBODIMENTS OF THE INVENTION
(24) The present invention, in some embodiments thereof, relates to an electrical field control and, more particularly, but not exclusively, to a device and method which can trap target particles by dielectrophoresis, transport target particles by dielectrophoresis, and/or alter electric field gradient within a chamber.
(25) Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not necessarily limited in its application to the details of construction and the arrangement of the components and/or methods set forth in the following description and/or illustrated in the drawings and/or the Examples. The invention is capable of other embodiments or of being practiced or carried out in various ways.
(26) According to some embodiments of the present invention, a uniform oscillatory electric field is applied across a micro-fluidic chamber externally and frequency of the applied field is manipulated to induce desired gradients in the field adjacent to the carrier particles suspended in the chamber, e.g. between the carrier particles and an adjacent conducting wall of the micro-fluidic chamber. Optionally, the carrier particle is, for example a doublet from with two Janus particles (or other complex geometry carrier particle), and the desired gradients in the field adjacent to the carrier particles suspended in the chamber may also be formed between the two Janus particles. The latter may apply for other complex carrier geometries and the Janus particle doublet is one example. According to some embodiments of the present invention, dynamic control of frequency and amplitude of the external electric field may provide for controlling trapping and releasing of target particles with the carrier particles without relying on other physical mechanisms. In some exemplary embodiments, dynamic control of the frequency also provides for controlling transportation of the target particles with the carrier particles.
(27) In some exemplary embodiments, single polarizable particles or structures formed from multiple particles are placed in specific locations within the chamber so that the spatio-temporal distribution of the electric field is controlled by the interaction between the particles and the external electric field. In these embodiments, it is not necessary to employ dielectrophoresis or to manipulate or trap target particles.
(28) In some exemplary embodiments, the carrier particle may be symmetric and transport of the particle may be induced by an external driving force other than the electric field gradient. Optionally, adding magnetic functionalization e.g. substituting the partial metallic coating of the particles with magnetic coating or using a carrier particle with a magnetic core enables controlling transport based on an external magnetic field in conjunction with the applied electric field. Optionally, other driving forces may be applied for transport, e.g. DC electric field, pressure field, an optical driving force, or a mechanical driving force.
(29) In other exemplary embodiments, the carrier particle is a symmetry broken particle. The symmetry broken particle may have symmetry broken geometric properties, e.g. particle doublet or symmetry broken electrical properties, e.g. a Janus particle. According to some embodiments of the present invention, the symmetry broken particle is also operated as a transport vehicle. The propulsion mechanism is induced by the localized symmetry breaking and is based on either induced-charge electro-phoresis (ICEP) or self-DEP (s-DEP) depending on frequency of the externally applied electric field.
(30) Self-DEP as used herein refers to a propulsion mechanism in which the driving gradient in the electric field for mobilizing the carrier particle is self-induced by proximity of the carrier particle to a conducting channel wall. According to some exemplary embodiments, self-DEP is induced by applying an oscillatory electric field with frequency above a pre-defined critical frequency. According to some exemplary embodiments, the critical frequency depends on the electrolyte concentration and particle radius. Optionally, ICEP may be used also to free stuck particles from the substrate, after which the frequency may be increased to induce transportation by s-DEP.
(31) In some exemplary embodiments, when the symmetry broken carrier particle is a metallodielectric Janus particle, self-DEP may be distinguished from ICEP by a switching of direction of the carrier particle. Under ICEP, the carrier particle typically travels with its dielectric hemisphere forwards due to stronger ICEO around the metallic hemisphere. Field gradients beneath the metallic hemisphere typically drive the carrier particle in the direction of its metallic end. In some exemplary embodiments, a critical frequency at which a metallodielectric Janus particle switches direction represents a point just after its dipolophoretic (DIP) velocity equals zero. The term DIP velocity as used herein refers to summation of the generally opposing DEP and ICEP velocities that operate on the carrier particle at lower frequencies.
(32) Optionally, the carrier particles, e.g. symmetrical or symmetric broken particles may be functionalized with molecular probes to enhance accumulation and selective trapping via hybridization of target biomolecules.
(33) According to some exemplary embodiments there is a frequency range e.g. 100 KHz for the specific combination of 300 nm polystyrene target particles and 15 m Janus particle, that enables trapping target particles due to positive DEP (p-DEP) and also to transport the target particles based on self-DEP when symmetry broken particles are used. According to some exemplary embodiments, target particles that have been trapped due to p-DEP may be released on demand by switching frequency of the external electric field to align with a negative DEP (n-DEP) response for the target particles. The crossover frequency (COF) for the transition from p-DEP and n-DEP typically depends on the specifics of the target particle, e.g. dielectric particle, cell, or biomolecule and the solution. For example dielectric particles may commonly exhibit a single COF and shift from p-DEP to n-DEP behavior with increasing frequency. In contrast, biological cells, which are more complex entities commonly exhibit two COFs. Control of the frequency may be used for selective sorting and transport. For example if the driving frequency with the p-DEP response of the target and n-DEP of any other contaminants, only the former will adhere to the particle.
(34) In some exemplary embodiments, taking dielectric target particles that exhibit a p-DEP to n-DEP transition with increasing frequency as an example, frequencies significantly above a frequency that induces p-DEP for target particles (and below the frequency the COF frequency that shifts to a n-DEP behavior of the target particles) is applied for a defined time period to enhance trapping of the target particles and then the frequency is reduced (within a range of p-DEP) to enhance mobilization of the carrier particle while the target particles are still trapped. In some exemplary embodiments, the carrier particles tend to mobilize at a faster rate at the lower frequency range for self-DEP, e.g. frequencies around 100 KHz. In some exemplary embodiments, an applied voltage is controlled, e.g. increased to increase trapping.
(35) Optionally, even lower frequencies, e.g. DC to an order of magnitude of 10 KHz, may also be applied to trap and concentrate target particles based on a combination of DEP, electro-hydro-dynamic flow and induced-charge electro-osmotic flow (ICEO).
(36) Exemplary, target particles include colloids, polymers, metallics, biomolecules, and cells. Optionally, the device and method described herein may be applied to separation and/or cleaning and may be used as an immunoassay platform. The device and method described herein may be applied to solid carriers as well as particles that are not encapsulated within droplets.
(37) Reference is now made to
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(39) Reference is now made to
(40) Reference is now made to
(41) According to some exemplary embodiments, DEP device 300 includes one or more carrier particles 100 each of which are configured to both trap and transport target particles suspended in chamber 310 when exposed to a uniform electric field E established between first electrode 320 and second electrode 330. In some exemplary embodiments, particle 100 is a symmetry broken particle, e.g. particle doublet or Janus particle and its proximity to at least one of first electrode 320 and second electrode 330 induces a local gradient in electric field E that drives movement of the particles 100. In some exemplary embodiments, diameter of particles 100 is defined in relation to height of chamber 310 so that a desired local gradient may be established.
(42) In one exemplary embodiment, particle 100 is a Janus particle with a diameter of 15 m and height H of chamber 310 or distance between first electrode 320 and second electrode 330 may be for example 120 m. Typically movement of particle 100 due to the induced local gradient in the electric field E is along an X-Y plane. Optionally, a diameter D of chamber 310 is for example 2 mm in diameter. In some exemplary embodiments, the Janus particle may be a sphere formed from Ps with a hemisphere of the sphere coated with 10 nm Cr and then 20 nm of Au. Alternatively, the carrier particle 100 may be formed from Ps with portion of the sphere coated with 10 nm Cr and then 20 nm of Au, e.g. stripes or asymmetric portion of the sphere.
(43) According to some embodiments of the present invention controller 350 controls the trapping, transporting and releasing the target particles by adjusting frequency of AC source 340. The frequencies applied for trapping, transporting and releasing are typically defined based on properties of target particles, properties of particle 100 and properties of the solution contained in chamber 310.
(44) Alternatively, carrier particle 100 may be a replaced by homogenous particle, e.g. a sphere from Ps that is fully coated with Au and chamber 310. In some exemplary embodiments, trapping and releasing of target particles on the homogenous carrier particle may be controlled by controller 350 which alters the AC frequency of AC source 340. In some exemplary embodiments, an additional mechanism of transportation may be associated with an additional physical mechanism, e.g. magnetic force may also be controlled by controller 350 for transporting the homogenous carrier particle. Optionally, a coil for inducing a magnetic field may be associated with device 300 and may be used to magnetically drive mobilization of the homogenous particles.
(45) Reference is now made to
(46) According to some exemplary embodiments, the DEP device 301 includes a micro-fluidic chamber 311 filled with a solution that contains target particles 200. The solution may be de-ionized water or electrolyte. The solution may optionally also include other elements or contaminants from which the target particles are to be separated. Optionally, micro-fluidic chamber 311 is a reservoir that is optionally rounded. In some exemplary embodiments, chamber 311 includes a first electrode 321 and second electrode 331 both positioned on either the bottom or top slide of the chamber 311. Each of first electrode 321 and second electrode 331 are connected to an AC source 340 and controller 350 for generating a desired uniform electric field across chamber 311 and parallel to the cover slip. In some exemplary embodiments, chamber 311 may be used with a complex carrier particle 101 for trapping and transporting target particles.
(47) Reference is now made to
(48) According to some exemplary embodiments, at t=0 seconds, an electric field with first frequency defined for inducing p-DEP, e.g. 100 KHz for target particle 200 is applied across chamber 310. In some exemplary embodiments, over time the first frequency induces localized electric field gradients around particle 100 that attract target particles 200 (
(49) In some exemplary embodiments, the same frequency is maintained to mobilize Janus particle 100 via self-DEP to a desired location while target particles 200 that have been trapped remain attached to Janus particle 100. Optionally, Janus particle 100 may be mobilized from a start location 305 to a target location 355 over a plurality of seconds or minutes, e.g. 11 seconds (
(50) In some exemplary embodiments, when Janus particle 100 reaches a desired location, e.g. after a defined time period, frequency of the AC signal generating the uniform electric field is increased to a level that induces n-DEP on particles 200, e.g. frequency is increased to 2 MHz. Reaching n-DEP for target particle 200 provides for releasing target particle 200 from Janus particle 100 (
(51) Reference is now made to
(52) In some exemplary embodiments, a symmetrical carrier particle is used instead of a Janus particle. In such embodiments, selective trapping is performed by adjusting the frequencies to correspond to p-DEP for target particles and n-DEP for contaminants and mobilization to a desired release site is controlled by alternate driving forces. Optionally, the alternate driving force is a magnetic driving force that attracts a magnetic coating or core on particles 100.
(53) Reference is now made to
(54) Optionally, a frequency of the electric field is altered to a second pre-defined frequency to remove contaminants that may also be attracted to the carrier particles. Typically, the contaminants may be removed by selecting a frequency that induces n-DEP on the contaminants and p-DEP on the target particles. (block 710)
(55) Optionally, a frequency of the electric field is altered to a third pre-defined frequency to accelerate mobilization of the carrier particles together with the target particles that have been trapped. Optionally the frequency is above the critical frequency for inducing self-DEP on the carrier particles. Typically, velocity of the carrier particle tends to decrease with an increase in frequency. Optionally, higher frequencies are applied to accelerate trapping and then lower frequencies are applied to mobilize, the carrier particle together with the trapped particles using an ICEP mechanism. (block 715)
(56) Optionally, once the trapping duration is completed and/or once the carrier particle has reached a desired site, a frequency of the electric field is altered to a forth pre-defined frequency to release the target particles. Typically, the forth pre-defined frequency is a frequency that induces n-DEP on the target particles. (block 720)
(57) In some exemplary embodiments, release of the target particles facilitates detection or secondary processing of the target particles (block 725).
(58) According to some exemplary embodiments, frequencies for inducing p-DEP, n-DEP and self-DEP and time periods required to obtain a desired accumulation or reach a desired site are pre-determined based on known properties of the device, known properties of the target particles, solution and empirical data.
(59) According to some exemplary embodiments, there is provided a method of controlling spatio-temporal distribution of an electric field in a microfluidic chamber. The method comprises distributing symmetry broken structures in the microfluidic chamber, applying an electric field across the microfluidic chamber, and controlling the electric field and the locations of the structures, such that electric field gradients induced adjacent to the structures control the spatio-temporal distribution of the electric field in the microfluidic chamber.
(60) In some embodiments of the present invention the symmetry broken structures comprise symmetry broken particles. In some embodiments of the present invention the symmetry broken structures comprise multi-particle structure. In some embodiments of the present invention the symmetry broken particles comprise Janus particles.
(61) It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention, which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable sub-combination or as suitable in any other described embodiment of the invention. Certain features described in the context of various embodiments are not to be considered essential features of those embodiments, unless the embodiment is inoperative without those elements.
(62) Various embodiments and aspects of the present invention as delineated hereinabove and as claimed in the claims section below find experimental support in the following examples.
EXAMPLES
(63) Reference is now made to the following examples, which together with the above descriptions illustrate some embodiments of the invention in a non limiting fashion.
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(67) Where: .sub.cr is critical frequency for inducing self-DEP;
(68) is the molar concentration of the electrolyte; a is radius of the target particle; and D.sub.s is the diffusion coefficient of the KCl electrolyte
(69) Closed symbols in the graph stand for the frequency at which the first particle was seen to translate backwards while open symbols for the frequency at which no more particles were observed to move forward.
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(77) Although the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications and variations will be apparent to those skilled in the art. Accordingly, it is intended to embrace all such alternatives, modifications and variations that fall within the spirit and broad scope of the appended claims.