WO2020219593A1 - Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing - Google Patents
Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing Download PDFInfo
- Publication number
- WO2020219593A1 WO2020219593A1 PCT/US2020/029387 US2020029387W WO2020219593A1 WO 2020219593 A1 WO2020219593 A1 WO 2020219593A1 US 2020029387 W US2020029387 W US 2020029387W WO 2020219593 A1 WO2020219593 A1 WO 2020219593A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- electrodes
- fluid
- electrode
- membrane
- counter
- Prior art date
Links
- 239000002245 particle Substances 0.000 title claims abstract description 173
- 239000012530 fluid Substances 0.000 claims abstract description 270
- 238000000034 method Methods 0.000 claims abstract description 268
- 239000012528 membrane Substances 0.000 claims abstract description 195
- 230000005684 electric field Effects 0.000 claims abstract description 77
- 230000003100 immobilizing effect Effects 0.000 claims abstract description 30
- 238000000576 coating method Methods 0.000 claims description 118
- 239000011248 coating agent Substances 0.000 claims description 99
- 230000002209 hydrophobic effect Effects 0.000 claims description 81
- 229920000642 polymer Polymers 0.000 claims description 38
- 229910052751 metal Inorganic materials 0.000 claims description 36
- 239000002184 metal Substances 0.000 claims description 36
- 239000004020 conductor Substances 0.000 claims description 33
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 30
- 229910021389 graphene Inorganic materials 0.000 claims description 30
- 239000000693 micelle Substances 0.000 claims description 30
- 102000004169 proteins and genes Human genes 0.000 claims description 24
- 108090000623 proteins and genes Proteins 0.000 claims description 24
- 239000003960 organic solvent Substances 0.000 claims description 21
- 239000003921 oil Substances 0.000 claims description 18
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- 241000700605 Viruses Species 0.000 claims description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 17
- 239000000919 ceramic Substances 0.000 claims description 17
- 229910044991 metal oxide Inorganic materials 0.000 claims description 17
- 150000004706 metal oxides Chemical class 0.000 claims description 17
- 239000004065 semiconductor Substances 0.000 claims description 17
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 17
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 17
- 239000012062 aqueous buffer Substances 0.000 claims description 16
- 230000000712 assembly Effects 0.000 claims description 15
- 238000000429 assembly Methods 0.000 claims description 15
- 239000002322 conducting polymer Substances 0.000 claims description 15
- 229920001940 conductive polymer Polymers 0.000 claims description 15
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 claims description 15
- 239000002502 liposome Substances 0.000 claims description 15
- 239000004094 surface-active agent Substances 0.000 claims description 15
- 238000003780 insertion Methods 0.000 claims description 8
- 230000037431 insertion Effects 0.000 claims description 8
- 239000010410 layer Substances 0.000 description 69
- 210000004027 cell Anatomy 0.000 description 60
- 239000000463 material Substances 0.000 description 38
- 238000004720 dielectrophoresis Methods 0.000 description 36
- 239000011148 porous material Substances 0.000 description 24
- 238000002161 passivation Methods 0.000 description 19
- 239000000523 sample Substances 0.000 description 16
- 239000007789 gas Substances 0.000 description 14
- 238000004520 electroporation Methods 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000005516 engineering process Methods 0.000 description 8
- 239000012777 electrically insulating material Substances 0.000 description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
- 238000005070 sampling Methods 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 102000004196 processed proteins & peptides Human genes 0.000 description 5
- 108090000765 processed proteins & peptides Proteins 0.000 description 5
- 150000003384 small molecules Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 108010043958 Peptoids Proteins 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 229910010272 inorganic material Inorganic materials 0.000 description 4
- 239000011147 inorganic material Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 230000010363 phase shift Effects 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- 230000021164 cell adhesion Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 150000001282 organosilanes Chemical class 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- -1 poly(2-hydroxyethyl methacrylate) Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000004088 simulation Methods 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000004630 atomic force microscopy Methods 0.000 description 2
- 150000001540 azides Chemical class 0.000 description 2
- 239000003124 biologic agent Substances 0.000 description 2
- 238000004113 cell culture Methods 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000002953 phosphate buffered saline Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 239000012491 analyte Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000010256 biochemical assay Methods 0.000 description 1
- 238000005842 biochemical reaction Methods 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000006143 cell culture medium Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005370 electroosmosis Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- XPBBUZJBQWWFFJ-UHFFFAOYSA-N fluorosilane Chemical compound [SiH3]F XPBBUZJBQWWFFJ-UHFFFAOYSA-N 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 230000005661 hydrophobic surface Effects 0.000 description 1
- 238000002847 impedance measurement Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 238000000520 microinjection Methods 0.000 description 1
- 239000002070 nanowire Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229960000502 poloxamer Drugs 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 210000001912 transporting cell Anatomy 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502761—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C5/00—Separating dispersed particles from liquids by electrostatic effect
- B03C5/02—Separators
- B03C5/022—Non-uniform field separators
- B03C5/026—Non-uniform field separators using open-gradient differential dielectric separation, i.e. using electrodes of special shapes for non-uniform field creation, e.g. Fluid Integrated Circuit [FIC]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C5/00—Separating dispersed particles from liquids by electrostatic effect
- B03C5/005—Dielectrophoresis, i.e. dielectric particles migrating towards the region of highest field strength
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C5/00—Separating dispersed particles from liquids by electrostatic effect
- B03C5/02—Separators
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M1/00—Apparatus for enzymology or microbiology
- C12M1/42—Apparatus for the treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M35/00—Means for application of stress for stimulating the growth of microorganisms or the generation of fermentation or metabolic products; Means for electroporation or cell fusion
- C12M35/02—Electrical or electromagnetic means, e.g. for electroporation or for cell fusion
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
- C12M47/04—Cell isolation or sorting
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/40—Concentrating samples
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/06—Fluid handling related problems
- B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
- B01L2200/0668—Trapping microscopic beads
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/06—Auxiliary integrated devices, integrated components
- B01L2300/0627—Sensor or part of a sensor is integrated
- B01L2300/0645—Electrodes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/0415—Moving fluids with specific forces or mechanical means specific forces electrical forces, e.g. electrokinetic
- B01L2400/0424—Dielectrophoretic forces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C2201/00—Details of magnetic or electrostatic separation
- B03C2201/26—Details of magnetic or electrostatic separation for use in medical or biological applications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/40—Concentrating samples
- G01N2001/4038—Concentrating samples electric methods, e.g. electromigration, electrophoresis, ionisation
Definitions
- Dielectrophoresis is an electro-physical phenomenon that occurs when an electrically neutral, but polarizable, substance, such as a biological molecule or a cell, in a non linear electric field experiences a force in the electric field gradient. This occurs because one side of the particle experiences a larger dipole force than the other due to the variation in electric field across the particle.
- the DEP force is nominally given by the following equation:
- F DEP ne m r 3 Re(f CM )V ⁇ E ⁇ 2
- r is the radius of the particle
- e m is the permittivity of the fluid
- E is the electric field
- fc M is the Clausius-Mossotti factor, a complex value that depends on the difference in permittivity between the fluid and the particle, and which determines if the DEP force will be positive or negative.
- DEP can be exploited, for example, for single-cell analyses in microfluidic -based applications.
- Using DEP in standard biochemical assays for example, by applying DEP to isolate single cells for impedance or fluorescence characterization (or any non-contact evaluation technique) has been demonstrated in fluidic environments.
- using DEP to isolate single cells for direct manipulation of the cells presents additional challenges due to, for example and not limited to, the introduction of a probing tool for local manipulation of the cells in a fluidic and non-linear electric field environment. Therefore, there is a need for a novel system and technological platform that can employ DEP to isolate single cells for direct manipulation in a fluidic and non-linear electric field environment.
- an apparatus configured for immobilization of a particle.
- the apparatus includes a membrane for separating a fluid from a compartment; one or more electrodes disposed proximate to the membrane; a counter-electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non linear electric field across the one or more electrodes and the counter-electrode; and a power source for providing an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field for immobilizing a particle suspended in the fluid that flows between the one or more electrodes and the counter electrode.
- AC alternating current
- a method for operating an apparatus for immobilization of a particle includes providing a power source;
- a membrane configured for separating a fluid from a compartment; providing one or more electrodes disposed proximate to the membrane; providing a counter-electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode; supplying, via the power source, an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field; and immobilizing, via a
- dielectrophoretic force generated by the oscillating non-linear electric field a particle suspended in the fluid that flows between the one or more electrodes and the counter-electrode.
- an apparatus configured for immobilization of a particle.
- the apparatus includes one or more electrodes and a counter-electrode configured for generating a non-linear electric field for immobilizing a particle suspended in a fluid that flows between the one or more electrodes and the counter-electrode; and a membrane disposed proximate a surface of the one or more electrodes, the surface of the one or more electrodes distal the counter-electrode, wherein the membrane is configured for separating the fluid from a compartment, and has an opening configured to allow for insertion of a sharp member disposed in the compartment.
- a method for operating an apparatus for immobilization of a particle includes providing a power source;
- a method for operating an apparatus for immobilization of a particle includes providing a power source;
- the method also includes providing a counter-electrode.
- the method also includes providing a third electrode disposed proximate the surface of the membrane.
- Figures 1A-1D show schematic views of an apparatus configured for immobilization of a particle, in accordance with various embodiments.
- Figures 2A-2D show schematic illustrations of an apparatus configured for immobilization of a particle, in accordance with various embodiments.
- Figures 3A-3D show schematic illustrations of an apparatus configured for interrogation of a particle, in accordance with various embodiments.
- Figure 4 shows a schematic illustration of an apparatus configured for location manipulation of a particle, in accordance with various embodiments.
- Figures 5A-5D are various schematic views of the apparatus 400 configured for location manipulation of a particle, in accordance with various embodiments.
- Figures 6A-6D illustrate various configurations of an apparatus configured for immobilization of a particle, in accordance with various embodiments.
- Figures 7A-7C show schematic illustrations of various configurations of an apparatus configured for immobilization of a plurality of particles, in accordance with various
- Figure 8 is a graphical diagram displaying simulation results for an apparatus for immobilization of a particle, in accordance with various embodiments.
- Figure 9 is a three-dimensional chart showing results of an analysis for an apparatus for immobilization of a particle, in accordance with various embodiments.
- Figure 10 is a flow chart for an example method of operating an apparatus for immobilization of a particle, in accordance with various embodiments.
- Figure 11 is a flow chart for an example method of operating an apparatus for immobilization of a particle, in accordance with various embodiments.
- Figure 12 is a flow chart for an example method of operating an apparatus for immobilization of a particle, in accordance with various embodiments.
- the term“particle” refers to an object or a group of objects that individually or together have a physical property.
- the particle has a composition that can include mixtures, including, but not limited to living cells, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, surfactant assemblies or their combination.
- the particle can be an individual, or a plurality of, cell (or cells), virus (or viruses), bacterium or bacteria, or any organism(s), alive or dead.
- the particle can be free floating in a fluid, e.g., suspended in the fluid, can be adherent, can change shape, can merge, can split apart, etc.
- the term“pore” refers to an opening between two regions.
- the term“payload” includes any chemical compound, polymer, biological macromolecule, or combination.
- the term“signal” includes any electrical events, such as variations in voltage, current, frequency, phase, or duration that may comprise DC, AC, or a superposition of frequency components.
- the term“interference” refers to any electromagnetic disturbance that interrupts, obstructs, or otherwise degrades or limits the effective transmission or readout of a signal or signal component.
- the term“membrane” refers to any partition or physical barrier separating two regions.
- the term“interrogation” refers to activities such as, for example, material sampling, physical probing, sensing, payload delivery, interaction, physical touching, capillary wicking, and/or insertion.
- the disclosure generally relates to an apparatus for local manipulation of neutral particles or biological molecules in a fluidic and non-linear electric field environment and various (e.g., microfluidics) applications thereof.
- the disclosure relates to an apparatus for dielectrophoresis-based (DEP-based) immobilization of biological objects, single cells or groups of cells in proximity to a compartment (or cavity) for local manipulation of the molecules or cells.
- DEP-based dielectrophoresis-based
- the compartment or cavity can be filled with one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the compartment can contain a fluid within the compartment that is immiscible with a fluid outside the compartment.
- the compartment can contain a non-aqueous fluid or microelectronics incompatible with an aqueous environment.
- the disclosure relates to an apparatus for local manipulation of an individual object or cell across a compartment via an interface with Micro-Electro-Mechanical System (MEMS) based structures and/or probing tools and/or electrodes for Nanopore Electroporation (NEP) applications.
- MEMS Micro-Electro-Mechanical System
- NEP Nanopore Electroporation
- Suitable applications based on the technology disclosed herein includes in- situ biological interrogation, cellular engineering, single cell genomics, electrochemical and physical interrogation of biological samples (e.g., patch clamp or atomic force microscopy (AFM)), droplet microfluidics (e.g., sampling or microinjection of droplet fluid), and any other suitable applications.
- AFM atomic force microscopy
- Suitable applications that the technology can be applied to include interrogation of discrete biologies, e.g., interrogation or probing of cells, living cells, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, surfactant assemblies or their combination, etc.
- the technology disclosed herein relates to coupling aqueous microfluidic environments with structures that can be in non-aqueous environments, e.g. electronics that can be in a non-conductive fluid or processes which can use hydrophobic solvents.
- the disclosed technology can offer local manipulation of isolated particles in a fluidic environment at scale, while allowing access from a compartment that contains sensitive MEMS components or electronics is disclosed. This can be done by coupling MEMS processes with microfluidic processes to allow for high-throughput processing and interrogation of suspended particles (the term particle or particles may refer to“biological object, objects or cells” and non-biological objects).
- the technology described herein relates to a high-throughput, DEP-based particle immobilization (trapping) apparatus that pins and immobilizes one or more particles in a fluid that flows adjacent to a membrane that separates the fluid from a compartment (isolated compartment or cavity) that contains electronic components, including MEMS structures.
- a membrane openings also refer to herein as“pores” or“micropores”
- the openings can be used for providing access to one or more particles suspended in the fluid to be individually interfaced and/or interacted with individual MEMS/electrical structures residing across the membrane in the compartment.
- the membrane can also be designed to maintain a stable liquid/gas interface or liquid-liquid interface between two immiscible fluids using fluid dynamic strategies that include, but are not limited to, surface patterning via hydrophobic or hydrophilic coatings, and/or pressure control of both fluid media on either side of the membrane.
- This interface can also be controlled to intentionally move fluid into or out of the cavity via modulation of surface energy via electrostatics, by pressurizing or depressurizing the cavity, or by changing the size or shape of the pore (e.g. by inserting a hollow microneedle into the pore to decrease the effective capillary radius).
- the apparatus includes a membrane for separating a fluid, for example, in a microfluidic channel, from a compartment.
- the apparatus also includes one or more electrodes disposed on the membrane away from the compartment and a counter-electrode having a dissimilar surface area than the one or more electrodes.
- the one or more electrodes and the counter electrode also referred to herein as“DEP electrodes” are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode.
- the apparatus also includes an electrical input and output source for providing and sensing a signal across the one or more electrodes and/or the counter-electrode.
- the signal is an AC voltage for generating an oscillating non-linear electric field for immobilizing a particle suspended in the fluid that flows between the one or more electrodes and the counter-electrode.
- the membrane has an opening through which to allow for mechanical manipulation of the particle that is immobilized.
- the mechanical manipulation includes probing the particle with a sharp member configured to enter across the membrane from the compartment.
- the sharp member is a MEMS structure or a Nano-Electro-Mechanical System (NEMS) structure.
- the sharp member is a needle, a pillar or a hollow tube.
- the disclosed technology relates to an apparatus having a microfluidics membrane hybrid architecture that is tailored for optimum interrogation of discrete objects (e.g., discrete globular objects) suspended in a fluid medium.
- the globular objects can be spatially confined using DEP in proximity to the membrane, including a porous membrane.
- the pores in the membrane are geometrically and chemically optimized/tailored to prevent fluid exchange across the membrane.
- Applications of the apparatus can include interrogating discrete biological systems within a fluidic environment by an external probe.
- the technology related to the microfluidics membrane hybrid architecture described herein can be integrated into a larger device architecture via typical MEMS fabrication methods.
- the external probe can be fabricated, via MEMS fabrication methods, and disposed in the compartment.
- the apparatus includes an array of electrodes (or the array of one or more electrodes, e.g., a pair of electrodes, a set of three electrodes, a set of four electrodes, and so on) co-localized with pores (e.g., opening 125, 225a-d, etc.), allowing access to trapped particles from a cavity.
- the pores are made to be hydrophobic by a chemical treatment coating the interior walls of the pores.
- the edge surface of the pores on either side of the membrane and/or pore interior are coated/chemically functionalized with a range of material classes including, for example, any small molecule, proteins, peptides, peptoids, polymers, or inorganic materials listed above in any suitable combination. Some examples of surface chemistries and their functionalities are included herein.
- coatings of the interior of the pore and/or one side of the membrane can include a hydrophobic material, such as a hydrophobic organosilane, e.g. a fluorosilane, in order to prevent leakage of aqueous solution through the pore.
- a surface can be coated to discourage cell adhesion, using a chemical such as for example, but not limited to, a poloxamer or poly(2-hydroxyethyl methacrylate) or any suitable protein blocking solution, such as for example, bovine serum albumin, in order to prevent nonspecific cell adhesion away from trapping sites, for example, approximate the opening or pore.
- a chemical such as for example, but not limited to, a poloxamer or poly(2-hydroxyethyl methacrylate) or any suitable protein blocking solution, such as for example, bovine serum albumin
- surface coatings may include, for example, biological or organic materials, such as proteins, peptides, polymers, hydrocarbon chains of varying lengths, any combination of which can be used for preventing cell adhesion as well as payload/analyte adhesion prevention.
- such surface coatings may be used for preventing molecular payload adhesion, particularly with respect to molecular payload that is disposed on a sharp member or needle.
- a coating on one side of the membrane with a hydrophilic material such as hyaluronic acid, titanium oxide, polyethylene glycol, etc. in order to ensure efficient wetting of those surfaces and prevent outflow flow of hydrophobic material from the opening.
- any combination of the aforementioned approaches can be employed in order to separate hydrophobic and hydrophilic fluids in separate openings, pores, or cavities.
- the various implementations disclosed herein represent a unique capability for high- volume trapping of biological objects and/or cells for characterization, sampling, payload delivery, or modification via techniques, such as, for example, electrochemical, impedometric, optical methods, and MEMS-based cellular manipulation in a fluidic environment.
- physical and material properties and parameters such as, for example, the size and hydrophobicity of the pore (or opening), size of the electrode, conductivity of the fluid medium, and operating frequency of the electrodes can be optimized based on the application and the biological objects or cells to be interrogated.
- the apparatus can be configured for selective release of cells after
- the apparatus can also be optimized by exploiting the dielectrophoretic (DEP) force.
- DEP dielectrophoretic
- the DEP force generated is proportional to the square of the field gradient according to the DEP equation described above, a highly non-linear electric field can be generated across the one or more electrodes and the counter-electrode.
- AC alternating current
- a confined highly non-linear electric field can be generated to act on a biological object or cell, and immobilize it in the trapping area.
- the DEP force can be tuned to trap the object between the electrodes at the opening.
- the wall of the opening in the electrode is coated with a hydrophobic material
- the contact angle of the coated inner wall of the opening can relate to the capillary pressure of the fluid via the following equation: where r is the radius of the opening, y is the surface tension (approximately 72.75 mN/m for water and air) and Q is the contact angle.
- a contact angle 0 of above 90 represents a hydrophobic material while a contact angle below 90 represents a hydrophilic material.
- the capillary pressure for an air-water interface reaches 40-60 kPa with a relatively large opening of about 4 pm or 5 pm.
- a hydrophobic coating on the inner wall of the opening can prevent fluid from flowing through the opening from the aqueous side into an air-filled compartment that can contain MEMS or other electronic components.
- the same principle holds for other types of fluid phase separation across the membrane, depending on whether the aqueous or non-aqueous side of the membrane is at higher or lower pressure the pore can be patterned with a hydrophobic or hydrophilic surface treatment respectively.
- the apparatus having one or more electrodes and a counter-electrode arranged in such a way to produce a nonlinear electric field can be configured to trap, immobilize or confine a biological object or a cell in a fluid and to be probed, via an opening, by a MEMS structure that resides in the compartment without compromising any fluid exposure to the sensitive electronic components.
- the apparatus has one or more electrodes and a counter-electrode that are of the same or substantially similar size can be configured to generate a highly non-linear electric field in order to trap, immobilize or confine a biological object or a cell in a fluid and to be probed, via an opening, by a MEMS structure that resides in the compartment without compromising any fluid exposure to the sensitive electronic components.
- each of the trapping sites e.g., an opening or a pore
- additional electrodes can be configured for impedance sensing in the presence of an object, for example, a particle or a cell.
- the method of manufacturing the apparatus is scalable, and thus allowed for parallel immobilization and interrogation of biological objects or cells at clinically relevant quantities.
- Figures 1A-1D show schematic views of an apparatus for immobilization of a particle, according to various implementations as disclosed herein.
- Figure 1A shows a schematic top view of an example apparatus 100, in accordance with various embodiments.
- the apparatus 100 includes an opening 125 (also referred to herein as“pore”), a plurality of electrodes 120 and one or more interconnects 130.
- the plurality of electrodes 120 as illustrated, can include a plurality of individual disparate electrode surface areas formed in an array or a grid.
- the electrode 120 is illustrated as a ring or circular electrode, the electrode 120 can be a pair of electrodes 620a, 620b, 620c, 620d, 720 as shown and described with respect to Figures 6A-6D and 7A-7C, or any number of sets of electrodes disposed proximate the opening 125, in accordance with various embodiments. Accordingly, the physical, chemical, material parameters as described further below with respect to the electrode 120 can be applicable to any of the pair of electrodes 620a, 620b, 620c, 620d, 720 as shown and described with respect to Figures 6A-6D and 7A-7C.
- the electrode 120 has a thickness between about 1 nm to about 50 pm. In various implementations, the electrode 120 has a thickness between about 10 nm to about 5 pm, about 10 nm to about 10 pm about 10 nm to about 5 pm, about 100 nm to about 4 pm, about 300 nm to about 3 pm, about 400 nm to about 5 pm, about 500 nm to about 5 pm, inclusive of any thickness ranges therebetween.
- the electrode 120 includes at least one of a transparent conducting material or a doped semiconducting material with sufficient electrochemical stability.
- the transparent conducting material includes indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- each of the plurality of electrodes 120 (referring to an array of electrodes 120) has an opening 125.
- some of the plurality of electrodes 120 have an opening 125 and some electrodes 120 do not have an opening 125.
- the electrodes 120 that have an opening 125 and the electrodes 120 that do not have an opening 125 are strategically arranged based on the application of the apparatus 100.
- the opening 125 has a size (also referred to herein as a diameter if circular or a lateral dimension if any non-circular geometry) between about 0.1 nm to about 1 mm. In various implementations, the opening 125 has a size between about 1 nm to about 100 nm, about 100 nm to about 1 pm, about 1 pm to about 10 pm, about 100 nm to about 25 pm, about 1 pm to about 100 pm, or about 1 pm to about 50 pm, inclusive of any size ranges therebetween.
- the electrodes 120 in the plurality of electrodes 120 have an electrode-to-electrode separation distance between two adjacent electrodes from about 1 pm to about 5 mm, from about 1 pm to about 1 mm, from about 10 pm to about 500 pm, or from about 10 pm to about 1 mm, inclusive of any separation distance ranges therebetween.
- the electrode 120 and the one or more interconnects 130 include the same material.
- the one or more interconnects 130 includes at least one of a transparent conducting material or a doped semiconducting material with sufficient electrochemical stability.
- the transparent conducting material includes indium tin oxide, metal nanowire mesh, graphene, a doped graphene, a conducting polymer, a thin metal layer, an atomic-layer metal film, or any other suitable transparent conductor.
- FIG. 1C shows a cross-sectional view (orthogonal to the view of Figure IB) of the apparatus 100, according to various implementations.
- the apparatus 100 includes the plurality of electrodes 120 and a counter-electrode 140.
- each electrode 120 in the plurality of electrodes 120 can be a pair of electrodes 620a, 620b, 620c, 620d, 720 as shown and described with respect to Figures 6A-6D and 7A-7C, or any number of sets of electrodes disposed proximate the opening 125.
- each electrode 120 in the plurality of electrodes 120 can be a pair of electrodes 620a, 620b, 620c, 620d, 720 as shown and described with respect to Figures 6A-6D and 7A-7C, or any number of sets of electrodes disposed proximate the opening 125.
- the counter-electrode 140 is a plane electrode that spans across a portion, a substantial portion, almost an entirety, or an entirety of the apparatus 100.
- the counter-electrode 140 can be bigger than each of the plurality of electrodes 120.
- the counter-electrode 140 can have a surface area that is bigger than a surface area of each of the individual electrodes 120.
- the ratio of the surface area between the counter-electrode 140 and an electrode 120 can be about 1:1, 1.1:1, 2:1, 5: 1, 10:1, 50:1, 100:1, 1 million: 1, or any suitable ratios therebetween.
- the electrode 120 and the counter-electrode 140 have the same or substantially similar in size. In various implementations, the electrode 120 and the counter-electrode 140 are disposed on the same plane.
- the plurality of electrodes 120 and the counter-electrode 140 are configured to receive a fluid (indicated as parallel arrows in Figure 1C) that flows in a channel 160 between the plurality of electrodes 120 and the counter-electrode 140.
- the fluid that flows in the channel 160 can include, for example, but not limited to, an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the fluid flows in the channel 160 at a flow rate between 0 to 10 mL/s.
- the fluid is static and, therefore, has minimal to no flow rate.
- the fluid flows from about 0.001 ml ,/s to about 0.1 mL/s, about 0.01 mL/s to about lmL/s, or about 0.1 mL/s to about 10 mL/s, inclusive of any flow rate ranges therebetween.
- Figure ID shows a zoomed-in cross-sectional view of one of the plurality of electrodes 120 of the apparatus 100.
- the apparatus 100 includes a membrane 110, the electrode 120, an interconnect 130, and a passivation layer 150.
- the membrane 110 includes an electrically insulating material.
- the membrane 110 includes an electrically insulating material, including, but not limited to silicon nitride, silicon oxide, a metal oxide, a carbide (such as, for example, SiCOH), a ceramic (such as, for example, alumina), and a polymer.
- the membrane 110 includes an electrically conducting material, such as a metal or a doped semiconductor material.
- the membrane 110 can be a single layer or a composite layer having a multilayer stack that includes any of the aforementioned materials.
- the wall forming the channel 160 comprises a channel material that can include, for example but not limited to, silicon, glass, plastic, or various elastomers such as, for example, poly(dimethyl siloxane) (PDMS), which can be used as structural materials for the fluidic layer.
- the channel 160 has dimensions from about 1 nm to about 1 cm, from about 100 nm to about 100 mm, from about 200 nm to about 1 mm, or from about 200 nm to about 500 pm, inclusive of any dimensions therebetween.
- the height of the channel 160 is set by the particle size being probed and in order to avoid clogging should be at least twice the diameter of the particle.
- the membrane 110 has a thickness between about 10 nm to about 1 cm. In various implementations, the membrane has a thickness between about 10 nm to about 5 mm, between about 10 nm to about 1 mm, between about 10 nm to about 100 pm, about 50 nm to about 10 pm, about 50 nm to about 5 pm, about 100 nm to about 10 pm, about 100 nm to about 5 pm, or about 100 nm to about 2 pm, inclusive of any thickness ranges therebetween. In various implementations, the membrane 110 or any layer of material comprising the membrane can be patterned.
- the particle 165 can have a size between about 1 nm to about 1 mm. In various implementations, the particle 165 can have a size between about 10 nm to about 500 pm, about 50 nm to about 200 pm, about 200 nm to about 100 pm, about 300 nm to about 50 pm, about 100 nm to about 200 pm, about 100 nm to about 100 pm, or about 200 nm to about 50 pm, inclusive of any size ranges therebetween.
- the sharp member 185 is configured to move within the opening 125, and move through the membrane 110, the electrode 120, and the passivation layer 150.
- the opening 125 allows for mechanical manipulation of the particle 165 that is immobilized.
- the mechanical manipulation includes probing, inserting, penetrating, electroporating, sensing, depositing material, sampling material, or otherwise manipulating the particle 165 with the sharp member 185 configured to enter across the membrane 110, the electrode 120, and/or the passivation layer 150.
- the mechanical manipulation is conducted by the sharp member 185.
- the compartment 180 includes a MEMS structure or a NEMS structure, including the sharp member 185.
- the sharp member 185 can be configured to operate as a third electrode in the form of a probe across the membrane 110.
- This third electrode probe may be biased with a DC or AC signal for sensing or actuation, for instance with a pulsed DC signal for Nanopore Electroporation (NEP) applications or with a low-power AC signal of a separate frequency for the purpose of measuring impedance.
- the DEP electrodes themselves may also carry a separate superposed AC or DC signal chosen to be easily isolated from the DEP signal via downstream filtering.
- the hydrophobic coating or hydrophilic coating are disposed (or deposited) on wall of the membrane 110 and/or the electrode 120 to prevent the fluid from entering into the compartment.
- the coating is chemically and covalently attached to the relevant surfaces.
- the hydrophobic coating can include a variety of classes such as azides, organosilanes, or fluorocarbons.
- the hydrophilic coating can include a range of material classes including any small molecule, proteins, peptides, peptoids, polymers, or inorganic materials.
- the wall of the opening 125 has a combination of patterned hydrophilic and hydrophobic coatings.
- the hydrophobic coating has a contact angle between about 95° and about 165°. In various implementations, the hydrophobic coating has a contact angle between about 100° and about 165°, about 105° and about 165°, about 110° and about 165°, about 120° and about 165°, about 95° and about 150°, about 95° and about 140°, or about 95° and about 130°, inclusive of any contact angle ranges therebetween.
- the hydrophilic coating has a contact angle between about 20° and about 80°. In various implementations, the hydrophilic coating has a contact angle between about 25° and about 80°, about 30° and about 80°, about 35° and about 80°, about 40° and about 80°, about 20° and about 70°, about 20° and about 60°, or about 20° and about 50°, inclusive of any contact angle ranges therebetween.
- a power source (not shown) can be electrically connected to the plurality of electrodes 120 and the counter-electrode 140 to provide an alternating current (AC) across the plurality of electrodes 120 and the counter-electrode 140 to generate an oscillating non-linear electric field for immobilizing (or trapping) the particle 165 suspended in the fluid that flows between the plurality of electrodes 120 and the counter electrode 140.
- an in-plane electric field with multiple electrodes can be applied to induce a local field minimum for alternate DEP field.
- one or more AC or DC signals may be superposed on the DEP actuation signal for applications including impedance sensing, electrowetting, or electroporation.
- the AC across the plurality of electrodes 120 (electrode 120 if a single electrode or a pair of electrodes, such as 620a, 620b, 620c, 620d, 720) and the counter-electrode 140 is supplied at a voltage between about 1 mV and about 300 V.
- the AC across the plurality of electrodes 120 and the counter-electrode 140 is supplied at a voltage between about 5 mV and about 50 V between about 5 mV and about 20 V, about 250 mV and about 5 V, about 500 mV and about 50 V, about 750 mV and about 50 V, about 1 V and about 50 V, about 5 V and about 50 V, about 10 V and about 50 V, about 250 mV and about 40 V, about 250 mV and about 30 V, about 250 mV and about 20 V, about 250 mV and about 10 V, about 250 mV and about 8 V, about 250 mV and about 6 V about 250 mV and about 5 V, about 500 mV and about 5 V, or about 1 V and about 5 V, inclusive of any voltage ranges therebetween.
- the AC across the plurality of electrodes 120 (electrode 120 if a single electrode) and the counter-electrode 140 is supplied at a voltage between about 1 mV and about 20 V, between about 1 mV and about 10 V, between about 1 mV and about 8V, between about 1 mV and about 6 V, between about 1 mV and about 5 V, between about 1 mV and about 4 V, between about 1 mV and about 3 V, between about 1 mV and about 2 V, between about 1 mV and about 1 V, between about 1 mV and about 750 mV, between about 1 mV and about 500 mV, between about 1 mV and about 250 mV, between about 1 mV and about 200 mV, between about 1 mV and about 150 mV, between about 1 mV and about 100 mV, between about 1 mV and about 50 mV, inclusive of any ranges therebetween.
- the AC across the plurality of electrodes 120 (electrode 120 if a single electrode or a pair of electrodes, such as 620a, 620b, 620c, 620d, 720) and the counter-electrode 140 is supplied at an oscillating frequency between about 1 Hz and about 1 THz.
- the AC across the plurality of electrodes 120 and the counter- electrode 140 is supplied at an oscillating frequency between about 10 Hz and about 100 GHz, about 10 Hz and about 10 GHz, about 100 Hz and about 10 GHz, about 1 kHz and about 1 GHz, about 10 kHz and about 1 GHz, about 100 kHz and about 1 GHz, about 500 kHz and about 1 GHz, about 1 MHz and about 1 GHz, about 10 MHz and about 1 GHz, about 100 MHz and about 1 GHz, about 10 kHz and about 500 MHz, about 10 kHz and about 100 MHz, about 10 kHz and about 50 MHz, about 10 kHz and about 30 MHz, about 10 kHz and about 20 MHz, about 10 kHz and about 10 MHz, about 100 kHz and about 10 MHz, or about 500 kHz and about 10 MHz, or about 1 MHz and about 10 MHz, inclusive of any frequency ranges therebetween.
- a direct current (DC) is applied across the plurality of electrodes 120 (electrode 120 if a single electrode or a pair of electrodes, such as 620a, 620b, 620c, 620d, 720) and the counter-electrode 140.
- the DC and AC can be superimposed when applied a current across the plurality of electrodes 120 (electrode 120 if a single electrode or a pair of electrodes, such as 620a, 620b, 620c, 620d, 720) and the counter electrode 140.
- the plurality of electrodes 120 and the counter-electrode 140 can be individually addressed, addressed in groups, or electrically short-circuited (e.g., shorted) together.
- each in the pair of electrodes, such as 620a, 620b, 620c, 620d, 720 can be individually addressed, addressed in groups, or electrically short- circuited (e.g., shorted) together.
- the AC can be supplied to each of the plurality of electrodes 120 and the counter-electrode 140 individually, or in groups.
- the plurality of electrodes 120 and the counter-electrode 140 can be shorted for some of the plurality of electrodes 120 and the counter-electrode 140, and not the other electrodes 120 in the plurality of electrodes 120 and the counter-electrode 140.
- any combination or configuration of arrangements between the plurality of electrodes 120 and the counter-electrode 140 can be implemented for the apparatus 100.
- Figures 2A-2D show schematic illustrations of an apparatus configured for immobilization of a particle, in accordance with various embodiments.
- Figures 2A-2D illustrate various structural configurations of an apparatus, where the configurations illustrate, for example, but not limited to, specific layer arrangements, placement and type of coatings, such as hydrophobic or hydrophilic coatings.
- the configurations shown in Figures 2A, 2B, 2C, and 2D are non-limiting examples, and thus, any desired structural configurations in addition to the illustrations can be employed to perform immobilization and/or interrogation of a particle, in accordance with various embodiments.
- Figure 2A illustrates a cross-sectional view of an apparatus 200a, in accordance with various embodiments.
- the apparatus 200a includes a membrane 210a, a metal layer 230al, a passivation layer 250a, and another metal layer 230a2 that are stacked on one another, and includes an opening 225a.
- the apparatus 200a also includes a coating 270al disposed on the exposed surface of the membrane 210a and a coating 270a2 disposed on the inside of the wall (inner wall) of the opening 225a, in accordance with various embodiments.
- the coating 270al and the coating 270a2 are the same coating.
- the coatings 270al and 270a2 can include the same pattern or different patterns.
- FIG. 2B illustrates a cross-sectional view of an apparatus 200b, in accordance with various embodiments.
- the apparatus 200b includes a membrane 210b, a metal layer 230bl, a passivation layer 250b, and another metal layer 230b2 that are stacked on one another, and includes an opening 225b.
- the apparatus 200b includes a coating 270b 1 disposed on the exposed surface of the membrane 210b and a coating 270b2 disposed on the inside of the wall of the opening 225b, in accordance with various embodiments.
- the coating 270b 1 and the coating 270a2 are different coatings.
- the coatings 270b 1 and 270b2 can include the same pattern or different patterns.
- FIG. 2C illustrates a cross-sectional view of an apparatus 200c, in accordance with various embodiments.
- the apparatus 200c includes a membrane 210c, a metal layer 230c 1, a passivation layer 250c, and another metal layer 230c2 that are stacked on one another, and includes an opening 225c.
- the apparatus 200c includes a coating 270c disposed on the inside of the wall of the opening 225b, and does not include a coating on the exposed surface of the membrane 210c, in accordance with various embodiments.
- the coating 270c can include a pattern.
- the membranes 210a, 210b, and 210c can be the same or substantially similar to the membrane 110 as described with respect to Figure ID, unless stated otherwise, and therefore, will not be described in full detail.
- the membranes 210a, 210b, and 210c can be the same or substantially similar to the membrane 110 as described with respect to Figure ID, unless stated otherwise, and therefore, will not be described in full detail.
- the membranes 210a, 210b, and 210c can include an electrically insulating material.
- the membranes 210a, 210b, and 210c can include an electrically insulating material, including, but not limited to silicon nitride, silicon oxide, a metal oxide, a carbide (such as, for example, SiCOH), a ceramic, such as, alumina, and a polymer.
- the membranes 210a, 210b, and 210c can include an electrically conducting material, such as a metal or a doped semiconductor material.
- the membranes 210a, 210b, and 210c can be a single layer or a composite layer having a multilayer stack that includes any of the aforementioned materials.
- the membranes 210a, 210b, and 210c can have a thickness between about 10 nm to about 1 cm. In various implementations, the membranes 210a, 210b, and 210c can have a thickness between about 10 nm to about 5 mm, between about 10 nm to about 1 mm, between about 10 nm to about 100 pm, about 50 nm to about 10 pm, about 50 nm to about 5 pm, about 100 nm to about 10 pm, about 100 nm to about 5 pm, or about 100 nm to about 2 pm, inclusive of any thickness ranges therebetween.
- the metal layers 230al, 230a2, 230b 1, 230b2, 230c 1, and 230c2 can be the same or substantially similar to the electrode(s) 120 and/or interconnect 130 as described with respect to Figures 1A-1D, unless stated otherwise, and therefore, will not be described in full detail.
- the metal layers 230al, 230bl, and 230c 1 can be an electrode layer that can include for example, the electrode 120 or the electrodes 620a, 620b, 620c, 620d, 720).
- the metal layers 230al, 230bl, and 230cl can be the interconnect layers 130 or 730.
- the metal layers 230a2, 230b2, and 230c2 can be the interconnect layers 130 or 730, or an electrode layer that can be configured to use with a sharp member (e.g., 185, 385a-d, etc.), for sensing (as a sensing electrode), as an NEP electrode, or as a metal shielding electrode.
- a sharp member e.g., 185, 385a-d, etc.
- the passivation layers 250a, 250b, and 250c can be the same or substantially similar to the passivation layer 150 as described with respect to Figure ID, unless stated otherwise, and therefore, will not be described in full detail.
- the coatings 270al, 270a2, 270bl, 270b2, and 270c can be the same or substantially similar to the coating as described with respect to Figure ID, unless stated otherwise, and therefore, will not be described in full detail.
- each the coatings 270al, 270a2, 270bl, 270b2, and 270c can be a hydrophobic coating or a hydrophilic coating.
- the hydrophobic coating or hydrophilic coating are disposed (or deposited) on the exposed surface of each of the membranes 210a and 210b, and/or on the inside of the wall (inner wall) of the openings 225a, 225b, and 225c to prevent a fluid from entering across the respective openings 225a, 225b, and 225c.
- the coatings 270al, 270a2, 270b 1, 270b2, and 270c are chemically and covalently attached to the relevant surfaces.
- the hydrophobic coating can include a variety of classes such as azides, organosilanes, or fluorocarbons.
- the hydrophilic coating can include a range of material classes including any small molecule, proteins, peptides, peptoids, polymers, or inorganic materials.
- the wall of each of the openings 225a, 225b, and 225c has a combination of patterned hydrophilic and hydrophobic coatings.
- the hydrophobic coating of each the coatings 270al, 270a2, 270b 1, 270b2, and 270c can have a contact angle between about 95° and about 165°.
- the hydrophobic coating has a contact angle between about 100° and about 165°, about 105° and about 165°, about 110° and about 165°, about 120° and about 165°, about 95° and about 150°, about 95° and about 140°, or about 95° and about 130°, inclusive of any contact angle ranges therebetween.
- the hydrophilic coating of each the coatings 270al is hydrophilic
- 270a2, 270bl, 270b2, and 270c can have a contact angle between about 20° and about 80°.
- the hydrophilic coating has a contact angle between about 25° and about 80°, about 30° and about 80°, about 35° and about 80°, about 40° and about 80°, about 20° and about 70°, about 20° and about 60°, or about 20° and about 50°, inclusive of any contact angle ranges therebetween.
- Figure 2D illustrates a cross-sectional view of an apparatus 200d, in accordance with various embodiments.
- the apparatus 200d can be the same or substantially similar to one of the apparatuses 200a, 200b, 200c, or 100.
- the apparatus 200d can include any of the layers or any combination of the layers as shown to be included in the apparatuses 200a, 200b, 200c, or 100.
- the apparatus 200d is depicted as having a channel 260d on one side and a compartment 280d on the other side.
- the channel 260d can be the same or substantially similar to the channel 260 as described with respect to Figures 1C and ID, unless stated otherwise, and therefore, will not be described in full detail.
- the compartment 280d can be the same or substantially similar to the compartment 180 as described with respect to Figure ID, unless stated otherwise, and therefore, will not be described in full detail.
- the compartment 280d is formed in a material 205d that includes, for example, an electrically insulating material, including, but not limited to silicon nitride, silicon oxide, glass, a metal oxide, a carbide (such as, for example, SiCOH), a ceramic, such as, alumina, a polymer including plastic and various elastomers, such as poly(dimethyl siloxane) (PDMS), or any material that can be used as a structural material.
- an electrically insulating material including, but not limited to silicon nitride, silicon oxide, glass, a metal oxide, a carbide (such as, for example, SiCOH), a ceramic, such as, alumina, a polymer including plastic and various elastomers, such as poly(dimethyl siloxane) (PDMS), or any material that can be used as a structural material.
- an electrically insulating material including, but not limited to silicon nitride, silicon oxide, glass, a metal oxide,
- the apparatus includes an opening 225d.
- the opening 225d can be the same or substantially similar to one of the openings 225a, 225b, and 225c.
- the opening 225d can include a coating disposed thereon that is the same or substantially similar to the coating on the inner wall of the openings 225a, 225b, and 225c, unless stated otherwise, and therefore, will not be described in full detail.
- the compartment 280d also includes an electrode layer 290d and a via 298d disposed in the electrode layer 290d, in accordance with various embodiments.
- the electrode layer 290d can be configured to actuate a sharp member, such as the sharp member 185 as described with respect to Figure ID.
- the via 298d can be configured to pump a fluid in or out of the compartment 280d.
- the fluid can include for example, but limited to, aqueous solution, aqueous solution containing biological or chemical reagents, organic solvents, mineral oil, fluorinated oil, air, mixed gases for cell culture (e.g. 5% C02), inert gas, and the like.
- the apparatus 200d can include one or more coatings disposed on the surface and/or on the inside of the inner wall of the opening 225d.
- the coatings on the surface and on the inside of the opening 225d can be the same or different.
- the coating on the surface and the coating on the inside of the opening 225d can include the same pattern or different patterns.
- Figures 3A-3D show schematic illustrations 300a, 300b, 300c, and 300d, respectively, of an apparatus configured for interrogation of a particle, in accordance with various embodiments.
- the configurations shown in Figures 3A, 3B, 3C, and 3D are non-limiting examples, and thus, any desired structural configurations in addition to the illustrations can be utilized to perform immobilization and/or interrogation of a particle, in accordance with various embodiments.
- the illustrations 300a, 300b, 300c, and 300d include a membrane 310, a metal layer 330, and a passivation layer 350.
- the illustrations 300a, 300b, 300c, and 300d include an opening 325 across a channel 360 and a compartment 380.
- the illustrations 300a, 300b, 300c, and 300d also include a particle 365 having an inner portion 363 (e.g., nucleus or inner component) trapped, disposed, or otherwise immobilized approximate the opening 325.
- the particle 365 is immobilized and ready for probing or interrogation.
- the membranes 310 can be the same or substantially similar to the membranes 110, 210a, 210b, or 210c as described with respect to Figures ID, 2A, 2B, and 2C, unless stated otherwise, and therefore, will not be described in full detail.
- the metal layer 330 can be the same or substantially similar to the electrode(s) 120 and/or interconnect 130, or any of the metal layers 230al, 230a2, 230bl, 230b2, 230cl, and 230c2 as described with respect to Figures 1A-1D, 2A- 2C, unless stated otherwise, and therefore, will not be described in full detail.
- the passivation layer 350 can be the same or substantially similar to the passivation layers 150, 250a, 250b, or 250c as described with respect to Figures ID, 2A, 2B, and 2C, unless stated otherwise, and therefore, will not be described in full detail.
- the opening 325 can be the same or substantially similar to one of the openings 125, 225a, 225b, 225c, or 225d as described with respect to Figures ID, 2A, 2B, 2C, and 2D, unless stated otherwise, and therefore, will not be described in full detail.
- the opening 325 may include a coating disposed thereon that is the same or substantially similar to the coating on the inner wall of the openings 125, 225a, 225b, or 225c as described with respect to Figures ID, 2A, 2B, and 2C, unless stated otherwise, and therefore, will not be described in full detail.
- the channel 360 can be the same or substantially similar to the channels 160 or 260d as described with respect to Figures 1C, ID, and 2D, unless stated otherwise, and therefore, will not be described in full detail.
- the compartment 380 can be the same or substantially similar to the compartments 180 or 280d as described with respect to Figure ID and 2D, unless stated otherwise, and therefore, will not be described in full detail.
- each of the illustrations 300a, 300b, 300c, and 300d includes sharp members 385a, 385b, 385c, and 385d, respectively.
- Figure 3A shows the sharp member 385a having a sharp tip.
- Figure 3B shows the sharp member 385b having a hollow inner portion 383b and a coated tip 388b.
- Figure 3C shows the sharp member 385c having a coating 388c disposed on its sharp tip.
- Figure 3D shows the sharp member 385d having a hollow inner portion 383d and a coating 388d disposed on its tip.
- each of the sharp members 385 is configured to move within the opening 325, and move through the membrane 310, the metal layer 330, and the passivation layer 350.
- the opening 325 allows for mechanical manipulation of the particle 365 that is immobilized.
- the mechanical manipulation includes probing, inserting, penetrating, electroporating, sensing, depositing material, sampling material, or otherwise manipulating the particle 365 with the sharp members 385 configured to enter across the membrane 310, the metal layer 330, and/or the passivation layer 350.
- the mechanical manipulation is conducted by any of the sharp members 385.
- the sharp members 385 can be any of needle, a pillar, a hollow tube, nano-needle or a micro-needle having a length between about 10 nm to about 50 pm.
- the inner portions 383b and 383d can have an inner diameter from about 200 nm to about 100 pm, from about 10 nm to about 10 pm, or from about 1 nm to 1 pm.
- each of the sharp members 385 can be manufactured or fabricated via MEMS or NEMS methods, in accordance with various embodiments.
- each of the sharp members 385 can be configured to operate as a third electrode in the form of a probe across the membrane 310.
- This third electrode probe may be biased with a DC or AC signal for sensing or actuation, for instance with a pulsed DC signal for Nanopore Electroporation (NEP) applications or with a low-power AC signal of a separate frequency for the purpose of measuring impedance.
- the DEP electrodes themselves may also carry a separate superposed AC or DC signal chosen to be easily isolated from the DEP signal via downstream filtering.
- a means of signal decoupling between the nanopore electroporation (NEP) signal and DEP signal may be implemented by physical shielding with materials, or careful signal control.
- the sharp members 385 can enter from the compartment 380 where each of the sharp members 385 resides before its movement, e.g., before actuation of the sharp members 385 along the longitudinal axis, e.g., vertically upward. Additional details are provided with respect to Figure ID and further details will be provided with respect to Figure 4.
- FIG. 4 shows a schematic illustration of an apparatus 400 configured for location manipulation of a particle, in accordance with various embodiments.
- the apparatus 400 can be the same or substantially similar to one of the apparatuses 100, 200a, 200b, 200c, or 200d as described with respect to Figures 1A-1D, 2A-2D.
- the apparatus 400 includes a membrane 410, a metal layer 430, a passivation layer 150, and an opening 425.
- the illustration shown in Figure 4 also includes a counter-electrode 440, a channel 460, and a compartment 480.
- the illustration also includes a particle 465 having an inner portion 463 (e.g., nucleus or inner component) trapped, disposed, or otherwise immobilized approximate the opening 425.
- an inner portion 463 e.g., nucleus or inner component
- the channel 460 and the compartment 480 can each include a fluid.
- the fluid includes one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the channel 460 can include a fluid (e.g., a first fluid) that is immiscible with a fluid (e.g., a second fluid) included in the compartment 480, or vice versa.
- the fluid in the channel 460 can be a hydrophobic fluid while the fluid in the compartment 480 can be a hydrophilic fluid, or vice versa.
- the channel 460 can be configured to contain an aqueous solution, such as phosphate -buffered saline (PBS) or cell culture media, for the purpose of transporting cells or conducting biochemical reactions and the compartment 480 is configured to contain air or inert gas, in order to isolate sensitive electrical components from the aqueous solution of the channel 460.
- PBS phosphate -buffered saline
- the compartment 480 is configured to contain air or inert gas, in order to isolate sensitive electrical components from the aqueous solution of the channel 460.
- the channel 460 can be configured to contain an aqueous solution and the compartment 480 is configured to contain an organic solvent or oil, or vice versa, for a variety of purposes including for example, to protect electrical components that are sensitive to corrosion or electrolysis, for a chemical reaction that can use an organic solvent, or to sample small molecules.
- the channel 460 and the compartment 480 can be configured to contain dissimilar aqueous solutions in each chamber, for example, configuring the channel 460 to contain a solution carrying a suspension of cells and the compartment 480 to contain another solution with dissolved genetic material for delivering to captured cells via nanopore electroporation (NEP).
- NEP nanopore electroporation
- the compartment 480 is formed in a material 405 that includes, for example, an electrically insulating material, including, but not limited to silicon nitride, silicon oxide, glass, a metal oxide, a carbide (such as, for example, SiCOH), a ceramic, such as, alumina, a polymer including plastic and various elastomers, such as poly(dimethyl siloxane) (PDMS), or any material that can be used as a structural material.
- the compartment 480 also includes an electrode layer 490 and a via 498 disposed in the electrode layer 490, in accordance with various embodiments.
- the via 498 can be configured to pump a fluid in or out of the compartment 480.
- the fluid can include for example, but limited to, aqueous solution, aqueous solution containing biological or chemical reagents, organic solvents, mineral oil, fluorinated oil, air, mixed gases for cell culture (e.g. 5% C02), inert gas, and the like.
- the compartment 480 also includes a substrate platform 495 on which a sharp member 485 is affixed.
- the substrate platform 495 is configured to move against the electrode layer 490, via any suitable mechanism (e.g., via electrostatic force) as disclosed in various embodiments of this disclosure.
- the substrate platform 495 can be configured to actuate to move up and down so as to move the sharp member 485, whereby the actuation enables the sharp member 485 to probe, insert, or interrogate the particle 465 and/or its inner portion 463.
- Figures 5A-5D are various schematic views of the apparatus 400 configured for location manipulation of a particle, in accordance with various embodiments.
- Figure 5A shows a cross-sectional view of the apparatus 400 and
- Figure 5B shows another view of the apparatus 400 to the view of Figure 5A.
- Figures 5C and 5D show a zoomed-in perspective view and a zoomed-in cross-sectional view of the base of the sharp member 485 that is affixed to the substrate platform 495.
- the sharp member 485 is a hollow structure with an inner hollow (interior) portion 483.
- Figures 5C and 5D show a wicking structure 496 disposed within the substrate platform 495 and connected to an inlet 486 of the sharp member 485 to provide fluidic communication between the inner portion 483 and the interior of the compartment 480.
- the combination of the wicking structure 496 and the inlet 486 is configured for a controlled fluidic communication that enables a controlled flow, such as, for example, but not limited to, electro- osmotic flow, electro-kinetic flow, capillary flow, or any other suitable flow or wicking mechanisms.
- the wicking mechanisms can be used to supply any payload or payload mixture via the hollow portion 483 of the sharp member 485 and into the trapped or immobilized particle 465.
- the hollow sharp member 485 can be configured to allow for particle penetration and electroporation via a fluid wicking path (e.g., a path through which the fluid is absorbed) from the substrate platform that resides within the compartment 480.
- the compartment 480 can be filled with any suitable payload fluid, fluid mixture, or an inert non-polar liquid.
- the payload may be delivered to any region of the particle 465, for example, to specific portion of a cell, such as a nucleus.
- Figures 6A-6D illustrate various configurations of an apparatus configured for immobilization of a particle, in accordance with various embodiments.
- Figures 6A, 6B, and 6D illustrate non-limiting example electrode configurations for controlling an electric field across a given electrode pair.
- Figure 6C illustrates a non-limiting example of an electrode configuration for controlling an electric field across an electrode pair and a ring counter-electrode.
- FIG. 6A is an illustration of an electrode configuration 600a showing a top view of a pair of electrodes 620a that are disposed across an opening 625a.
- each of the electrodes 620a has a flat tip that generates straight electric field line between the two opposing flat tips from each of the electrodes 620a.
- the layout shown in Figure 6A is constructed to trap or immobilize a particle approximate the opening 625a using the electric field lines generated across the two flat tips near the opening 625 a.
- the two tips of the electrodes 620 concentrate the electric field along the opening 625a.
- a passivation material 650a for example, to limit the stray electric field lines, to limit corrosion of electrodes or electrolysis, or to prevent electrical current flow in the bulk fluid.
- FIG. 6B is an illustration of an electrode configuration 600b showing a top view of a pair of electrodes 620b that are disposed across an opening 625b.
- each of the electrodes 620b has a sharp tip that generates focused electric field lines between the two opposing sharp tips from each of the electrodes 620b.
- the layout shown in Figure 6B is constructed to trap or immobilize a particle approximate the opening 625b using a more focused electric field generated across the two sharp tips near the opening 625b.
- the electric field lines generated between the two sharp tips of the electrodes 620b are nonlinear and focused at the sharp tips.
- a passivation material 650b for example, to limit the stray electric field lines, to limit corrosion of electrodes or electrolysis, or to prevent electrical current flow in the bulk fluid.
- FIG. 6C is an illustration of an electrode configuration 600c showing a pair of electrodes similar to those shown in Figure 6A, as well as a ring electrode 622c.
- each of the electrodes 620c is connected to buried interconnects 630c, which is separated from the ring electrode 622c by a layer of dielectric material 650c, similar to the configuration shown in Figure 1C.
- the pair of electrodes 620c are configured to function similarly to the electrodes 620a and 620b, shown in Figures 6A and 6B, i.e., to generate a concentrated electric field localized around an opening 625c.
- the ring electrode 622c is configured as a common ground for the two electrodes 620c, confining the in-plane stray electric field to the area around the trapping site, i.e., the opening 625c.
- surface areas outside of the electrodes 620c, ring electrode 622c, and the opening 625c are covered with a passivation material 650c, for example, to limit the stray electric field lines, to limit corrosion of electrodes or electrolysis, or to prevent electrical current flow in the bulk fluid.
- FIG. 6D is an illustration of an electrode configuration showing a cross-sectional view of an example electrode configuration 600d, in accordance with various embodiments.
- the electrode configuration 600d includes a pair of electrodes 620d and a passivation (dielectric) material 650d that are disposed on a membrane 610d and across an opening 625 d.
- passivation (dielectric) material 650d that are disposed on a membrane 610d and across an opening 625 d.
- FIGS 7A-7C show schematic illustrations of various example configurations of an apparatus configured for immobilization of a plurality of particles, in accordance with various embodiments.
- the apparatus includes an insulation layer 750, electrodes 720, interconnects 730, and a dielectric layer 752 that are stacked on top of each other and are disposed on a membrane 710.
- the insulation layer 750 includes a window 704 in the insulation layer 750 that exposes a top surface portion of each of the electrodes 720.
- FIG. 7A shows a perspective view of an example electrode configuration 700a of an apparatus having an array of electrodes for immobilizing and/or interrogation, in accordance with various embodiments.
- the configuration 700a includes a plurality of pairs of electrodes 720 that are disposed across each of a plurality of openings 725.
- the configuration 700a also includes a plurality of interconnects 730 that are configured for interconnecting various electrodes 720.
- the interconnects 730 are disposed in the same layer as the electrodes 720.
- FIG. 7B shows a perspective view of another example electrode configuration 700b of an apparatus having an array of electrodes for immobilizing and/or interrogation, in accordance with various embodiments.
- the configuration 700b includes a plurality of pairs of electrodes 720 that are disposed across each of a plurality of openings 725.
- the configuration 700a also includes a plurality of interconnects 730 that are configured for interconnecting various electrodes 720.
- the interconnects 730 are disposed on a different layer as the electrodes 720, as shown in Figure 7B.
- Figure 7C shows a cross-sectional view 700c of the electrode configuration 700b.
- the cross-section along the lines A-A’ of the apparatus shows how the electrodes 720 are interfaced with the interconnects 730, which are disposed within the dielectric layer 752.
- the dielectric layer 752 is disposed below the electrodes 720.
- the interconnects 730 is embedded in the dielectric layer 752 and interfaced with the electrodes 720 vertically.
- each electrode in the pair of electrodes 620a, 620b, 620c, 620d, and 720 can be operated out of phase at a phase shift of about 180 degrees with respect to the other electrode in each pair of electrodes.
- the phase shift can be 360 degrees/number of electrodes, for example, a phase shift of 120 degrees if it is a three- electrode configuration, or a phase shift of 90 degrees for a 4-electrode configuration, that is being used for trapping or immobilizing.
- FIG 8 is a graphical diagram 800 displaying simulation results for an apparatus for immobilization of a particle (not shown).
- an AC field is supplied across a plurality of electrodes 820 and a counter-electrode 840.
- a DEP force on the order of tens to hundreds of nanonewtons (nN) is generated across the plurality of electrodes 820 and the counter-electrode 840.
- the generated DEP can trap or immobilize a particle (or a cell), for example, against a fluid velocity up to centimeters per second (cm/s).
- the simulation in the graphical diagram 800 shown in Figure 8 is generated using a simulation software program, to illustrate electric field lines 824 with a maximum field of 70 kV/m in a simulated 5 V oscillating at 1 MHz across the plurality of electrodes 820 and the counter-electrode 840.
- Figure 9 is a three-dimensional chart 900 showing results of an analysis for an apparatus for immobilization of a particle.
- the capillary backpressure in Pascal
- the capillary pressure equation described above in the case of a water-air interface.
- negative values shown in the chart 900 correspond to pressure in the direction of the fluid, e.g., away from the compartment, for example, that houses MEMS components.
- FIG 10 is a flow chart for an example method S100 of operating an apparatus for immobilization of a particle, according to an illustrative implementation.
- the method S100 includes providing a power source at step SI 10.
- the method S100 also includes providing a membrane configured for separating a fluid from a compartment at step S120.
- the method S100 also includes providing one or more electrodes disposed proximate to the membrane at step S130.
- the one or more electrodes is disposed proximate to a surface of the membrane, the surface distal to the compartment.
- the one or more electrodes is disposed proximate to a surface of the membrane, the surface proximate to the compartment.
- the method S100 also includes providing a counter-electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode at step S140.
- the method S100 includes supplying, via the power source, an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field at step S150.
- the method S100 also includes immobilizing, via a dielectrophoretic (DEP) force generated by the oscillating non-linear electric field, a particle suspended in the fluid that flows between the one or more electrodes and the counter-electrode at step S160.
- the method S100 optionally includes probing, via an opening in the membrane, the particle with a sharp member configured to enter across the membrane from the compartment at step S170.
- the sharp member includes a MEMS structure or a NEMS structure.
- the method optionally includes manipulating, via the opening, the particle that is immobilized. In various implementations, the method optionally includes inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- the membrane includes at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- the membrane has a thickness between about 10 nm to about 1 cm. In various implementations, the membrane has a thickness between about 100 nm to about 10 pm.
- the opening has a size between about 10 nm to about 50 pm. In various implementations, the opening has a size between about 1 pm to about 5 pm.
- a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- the hydrophobic coating has a contact angle between about 95° and about 165°.
- the hydrophilic coating has a contact angle between about 20° and about 80°.
- the first surface is smaller than the second surface.
- the one or more electrodes includes a plurality of individual disparate one or more electrodes surface areas formed in an array.
- the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V. In various implementations, the AC across the one or more electrodes and the counter electrode is supplied at a voltage between about 1 mV and about 20 V.
- the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz. In various implementations, the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- the one or more electrodes includes at least one of a transparent conducting material or a doped semiconducting material.
- the transparent conducting material includes indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- the one or more electrodes has a thickness between about 1 nm to about 50 pm. In various implementations, the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- the fluid includes one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the fluid is a first fluid
- the compartment comprises a second fluid that is immiscible with the first fluid.
- the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- the particle has a size between about 1 nm to about 1 mm.
- the particle includes one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- a feedback control mechanism can be configured via impedance sensing to allow for optimization of cell capture in an automated workflow.
- a particle trapping event can be detected via impedance sensing using a superposed sensing frequency that is filtered by capacitance measurement of the particle (e.g., by measuring capacitance of the membrane of a cell). This frequency can then be isolated from the driving dielectrophoretic (DEP) frequency by a filter circuit and the magnitude and phase information at this frequency is correlated with the expected effect of a trapped particle.
- DEP dielectrophoretic
- the DEP electrodes can be turned off, thereby allowing the flow to dispose of the particle. Then the trapping procedure can be reattempted.
- a real-time optimization can be carried out by recirculating flow until a sufficient percentage of particles (or cells) are captured at the probing sites, adjusting the signal voltage and flow rate accordingly.
- the procedure is similar, but a third electrode is present in a MEMS probe that is inserted into the cell interior through the pore, allowing for a direct impedance measurement from the interior of the cell.
- the compartment e.g., the cavity region
- the compartment is conductive to allow for an electrical signal to be applied to the fluid contents contained within.
- This cavity is separated by a membrane from the fluid flowing region with a pore or plurality of pores and accompanying DEP electrodes spatially overlaid with each pore in the same fashion as previous embodiments. Particles of any type including living cells, and/or vesicles may be trapped and electroporated via the signal applied to the fluid contents of the cavity transmitted through the membrane pore in order to allow the addressed electroporation of cell arrays.
- This embodiment also can include a counter-electrode on the top of the fluid flow region.
- a means of signal decoupling between the nanopore electroporation (NEP) signal and DEP signal may be implemented by physical shielding with materials, or careful signal control.
- the NEP cavity (previously the MEMS cavity) can be configured with a fluid input channel that can supply any payload or payload mixture to the cavity for subsequent NEP delivery into a DEP trapped particle.
- These fluid input channels may be multiplexed (e.g., combined, redirected, etc.) in an array coming from multiple sources with different payload compositions or may be configured to supply one type of payload composition.
- a single array of these NEP - DEP (probing) sites can be sectored on a chip to include sectors with a multiplexed configuration and/or a single source configuration on one chip.
- the hollow probe e.g., a sharp member
- a fluid wicking path e.g., a path through which the fluid is absorbed
- the MEMS cavity is filled with a uniform payload fluid mixture.
- the MEMS cavity is filled with an inert non-polar liquid and the fluid wicking path up through the inside of the hollow probe to its tip is filled with a polar liquid and payload mixture.
- this hollow probe may be actuated and inserted at any depth within the DEP trapped particle after which a signal is applied to the probe for electroporation and payload delivery.
- the payload may be delivered to any region of the particle and in the cases of a cell or the nucleus.
- the hollow probe may be configured to receive a signal that allows for the variable sorption or desorption of payload solution within its interior with high volumetric precision in order to allow for physical volumetric injection or sampling of fluid at different regions within a particle, cell, or vesicle for example.
- FIG 11 is a flow chart for an example method S200 of operating an apparatus for immobilization of a particle, according to an illustrative implementation.
- the method S200 includes providing a power source at step S210.
- the method S200 also includes providing one or more electrodes and a counter-electrode configured for generating a non-linear electric field for immobilizing a particle suspended in a fluid that flows between the one or more electrodes and the counter-electrode at step S220.
- the method S200 also includes providing a membrane disposed proximate a surface of the one or more electrodes, the surface of the one or more electrodes distal the counter-electrode, wherein the membrane is configured for separating the fluid from a compartment, and has an opening configured to allow for insertion of a sharp member disposed in the compartment at step S230.
- the method S200 also includes supplying, via the power source, an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field at step S240.
- the method S200 also includes immobilizing, via a dielectrophoretic force generated by the oscillating non-linear electric field, a particle suspended in the first fluid at step S250.
- the method S200 optionally includes probing, via an opening in the membrane, the particle with a sharp member configured to enter across the membrane from the compartment at step S260.
- the sharp member includes a MEMS structure or a NEMS structure.
- the method optionally includes manipulating, via the opening, the particle that is immobilized. In various implementations, the method optionally includes inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- the membrane includes at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- the membrane has a thickness between about 10 nm to about 1 cm. In various implementations, the membrane has a thickness between about 100 nm to about 10 pm.
- the opening has a size between about 10 nm to about 50 pm. In various implementations, the opening has a size between about 1 pm to about 5 pm.
- a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- the hydrophobic coating has a contact angle between about 95° and about 165°.
- the hydrophilic coating has a contact angle between about 20° and about 80°.
- the first surface is smaller than the second surface.
- the one or more electrodes includes a plurality of individual disparate electrode surface areas formed in an array.
- the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V. In various implementations, the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz. In various implementations, the AC across the one or more electrodes and the counter electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- the one or more electrodes includes at least one of a transparent conducting material or a doped semiconducting material.
- the transparent conducting material includes indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- the one or more electrodes has a thickness between about 1 nm to about 50 pm. In various implementations, the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- the fluid includes one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the fluid is a first fluid
- the compartment comprises a second fluid that is immiscible with the first fluid.
- the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- the particle has a size between about 1 nm to about 1 mm.
- the particle includes one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- FIG 12 is a flow chart for an example method S300 of operating an apparatus for immobilization of a particle, in accordance with various embodiments.
- the method S300 includes providing a power source at step S310.
- the method S300 also includes providing a membrane configured for separating a fluid from a compartment at step S320.
- the method S300 also includes providing a pair of electrodes disposed proximate a surface of the membrane, wherein the pair of electrodes is configured to generate a non-linear electric field across the electrodes at step S330.
- the method S300 also includes supplying, via the power source, an alternating current (AC) across the electrodes, thereby generating an oscillating non linear electric field at step S340.
- the method S300 also includes immobilizing, via a dielectrophoretic force generated by the oscillating non-linear electric field, a particle suspended in the fluid that flows between the electrodes at step S350.
- the method S300 optionally includes probing, via an opening in the membrane, the particle with a sharp member configured to enter across the membrane from the compartment at step S360.
- the sharp member includes a MEMS structure or a NEMS structure.
- the method optionally includes providing a counter electrode. In various implementations, the method optionally includes providing a third electrode disposed proximate the surface of the membrane. In various implementations, the third electrode is a ring electrode. In various implementations, the method optionally includes manipulating, via the opening, the particle that is immobilized. In various implementations, the method optionally includes inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- each of the pair of electrodes comprises a sharp tip or flat tip.
- the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- the membrane has a thickness between about 10 nm to about 1 cm. In various implementations, the membrane has a thickness between about 100 nm to about 10 pm.
- the opening has a size between about 10 nm to about 50 pm. In various implementations, the opening has a size between about 1 pm to about 5 pm.
- a wall of the opening has a hydrophobic coating or a hydrophilic coating. In various implementations, the hydrophobic coating has a contact angle between about 95° and about 165°. In various implementations, the hydrophilic coating has a contact angle between about 20° and about 80°.
- the first surface is smaller than the second surface.
- the membrane includes a plurality of electrode pairs formed in an array.
- the AC across the pair of electrodes and the counter electrode is supplied at a voltage between about 1 mV and about 300 V.
- the AC across the pair of electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- the AC across the pair of electrodes and the counter electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz. In various implementations, the AC across the pair of electrodes and the counter-electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- one electrode of the pair of electrodes includes at least one of a transparent conducting material or a doped semiconducting material.
- the transparent conducting material includes indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- the pair of electrodes has a thickness between about 1 nm to about 50 pm. In various implementations, the pair of electrodes has a thickness between about 10 nm to about 5 pm.
- the fluid includes one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- the fluid is a first fluid
- the compartment comprises a second fluid that is immiscible with the first fluid.
- the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 1 An apparatus comprising a membrane for separating a fluid from a compartment; one or more electrodes disposed proximate to the membrane; a counter electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode; and a power source for providing an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field for immobilizing a particle suspended in the fluid that flows between the one or more electrodes and the counter-electrode.
- AC alternating current
- EMBODIMENT 2 The apparatus of embodiment 1, wherein the membrane comprises an opening.
- EMBODIMENT 3 The apparatus of embodiment 2, wherein the opening allows for mechanical manipulation of the particle that is immobilized and the mechanical manipulation includes probing the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 4 The apparatus of any preceding embodiment, wherein the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- EMBODIMENT 5 The apparatus of any preceding embodiment, wherein the membrane has a thickness between about 10 nm to about 1 cm.
- EMBODIMENT 6 The apparatus of any preceding embodiment, wherein the membrane has a thickness between about 100 nm to about 10 pm.
- EMBODIMENT 7 The apparatus of embodiment 2, wherein the opening has a size between about 10 nm to about 50 pm.
- EMBODIMENT 8 The apparatus of any preceding embodiment, wherein the opening has a size between about 1 pm to about 5 pm.
- EMBODIMENT 9 The apparatus of any preceding embodiment, wherein a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- EMBODIMENT 10 The apparatus of embodiment 9, wherein the hydrophobic coating has a contact angle between about 95° and about 165°.
- EMBODIMENT 11 The apparatus of any preceding embodiment, wherein the hydrophilic coating has a contact angle between about 20° and about 80°.
- EMBODIMENT 12 The apparatus of any preceding embodiment, wherein a surface area of the one or more electrodes is smaller than a surface area of the counter-electrode.
- EMBODIMENT 13 The apparatus of any preceding embodiment, wherein the one or more electrodes comprises a plurality of individual disparate electrode surface areas formed in an array.
- EMBODIMENT 14 The apparatus of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V.
- EMBODIMENT 15 The apparatus of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- EMBODIMENT 16 The apparatus of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz.
- EMBODIMENT 17 The apparatus of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- EMBODIMENT 18 The apparatus of any preceding embodiment, wherein the one or more electrodes comprises at least one of a transparent conducting material or a doped semiconducting material.
- EMBODIMENT 20 The apparatus of any preceding embodiment, wherein the one or more electrodes has a thickness between about 1 nm to about 50 pm.
- EMBODIMENT 21 The apparatus of any preceding embodiment, wherein the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- EMBODIMENT 22 The apparatus of any preceding embodiment, wherein the fluid comprises one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid, or a gas.
- EMBODIMENT 23 The apparatus of any preceding embodiment, wherein the particle has a size between about 1 nm to about 1 mm.
- EMBODIMENT 24 The apparatus of any preceding embodiment, wherein the particle comprises one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- EMBODIMENT 25 The apparatus of any preceding embodiment, wherein the compartment comprises a Micro-Electro-Mechanical System (MEMS) structure or a Nano- Electro-Mechanical System (NEMS) structure.
- MEMS Micro-Electro-Mechanical System
- NEMS Nano- Electro-Mechanical System
- EMBODIMENT 26 A method for operating an apparatus comprising providing a power source; providing a membrane configured for separating a fluid from a compartment; providing one or more electrodes disposed proximate to the membrane; providing a counter- electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode; supplying, via the power source, an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field; and immobilizing, via a dielectrophoretic force generated by the oscillating non-linear electric field, a particle suspended in the fluid that flows between the one or more electrodes and the counter electrode.
- AC alternating current
- EMBODIMENT 27 The method of embodiment 26, wherein the membrane comprises an opening.
- EMBODIMENT 28 The method of any preceding embodiment, further comprising manipulating, via the opening, the particle that is immobilized.
- EMBODIMENT 29 The method of any preceding embodiment, further comprising probing, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 30 The method of any preceding embodiment, further comprising inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 32 The method of any preceding embodiment, wherein the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- EMBODIMENT 33 The method of any preceding embodiment, wherein the membrane has a thickness between about 10 nm to about 1 cm.
- EMBODIMENT 34 The method of any preceding embodiment, wherein the membrane has a thickness between about 100 nm to about 10 pm.
- EMBODIMENT 36 The method of any preceding embodiment, wherein the opening has a size between about 1 pm to about 5 pm.
- EMBODIMENT 37 The method of any preceding embodiment, wherein a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- EMBODIMENT 38 The method of embodiment 37, wherein the hydrophobic coating has a contact angle between about 95° and about 165°.
- EMBODIMENT 39 The method of any preceding embodiment, wherein the hydrophilic coating has a contact angle between about 20° and about 80°.
- EMBODIMENT 40 The method of any preceding embodiment, wherein a surface area of the one or more electrodes is smaller than a surface area of the counter-electrode.
- EMBODIMENT 41 The method of any preceding embodiment, wherein the one or more electrodes comprises a plurality of individual disparate electrode surface areas formed in an array.
- EMBODIMENT 42 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V.
- EMBODIMENT 43 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- EMBODIMENT 46 The method of any preceding embodiment, wherein the one or more electrodes comprises at least one of a transparent conducting material or a doped semiconducting material.
- EMBODIMENT 47 The method of any preceding embodiment, wherein the transparent conducting material comprises indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- EMBODIMENT 48 The method of any preceding embodiment, wherein the one or more electrodes has a thickness between about 1 nm to about 50 pm.
- EMBODIMENT 49 The method of any preceding embodiment, wherein the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- EMBODIMENT 50 The method of any preceding embodiment, wherein the fluid comprises one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid or a gas.
- EMBODIMENT 51 The method of any preceding embodiment, wherein the particle has a size between about 1 nm to about 1 mm.
- EMBODIMENT 52 The method of any preceding embodiment, wherein the particle comprises one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- EMBODIMENT 53 An apparatus comprising one or more electrodes and a counter electrode configured for generating a non-linear electric field for immobilizing a particle suspended in a fluid that flows between the one or more electrodes and the counter-electrode; and a membrane disposed proximate a surface of the one or more electrodes, the surface of the one or more electrodes distal the counter-electrode, wherein the membrane is configured for separating the fluid from a compartment, and has an opening configured to allow for insertion of a sharp member disposed in the compartment.
- EMBODIMENT 54 The apparatus of embodiment 53, wherein the sharp member is a Micro-Electro-Mechanical System (MEMS) structure or a Nano-Electro-Mechanical System (NEMS) structure.
- MEMS Micro-Electro-Mechanical System
- NEMS Nano-Electro-Mechanical System
- EMBODIMENT 55 The apparatus of any preceding embodiment, wherein the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- EMBODIMENT 56 The apparatus of any preceding embodiment, wherein the membrane has a thickness between about 10 nm to about 1 cm.
- EMBODIMENT 57 The apparatus of any preceding embodiment, wherein the membrane has a thickness between about 100 nm to about 10 pm.
- EMBODIMENT 58 The apparatus of any preceding embodiment, wherein the opening has a size between about 10 nm to about 50 pm.
- EMBODIMENT 59 The apparatus of any preceding embodiment, wherein the opening has a size between about 1 pm to about 5 pm.
- EMBODIMENT 60 The apparatus of any preceding embodiment, wherein a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- EMBODIMENT 61 The apparatus of embodiment 60, wherein the hydrophobic coating has a contact angle between about 95° and about 165°.
- EMBODIMENT 62 The apparatus of any preceding embodiment, wherein the hydrophilic coating has a contact angle between about 20° and about 80°.
- EMBODIMENT 63 The apparatus of any preceding embodiment, wherein a surface area of the one or more electrodes is smaller than a surface area of the counter-electrode.
- EMBODIMENT 64 The apparatus of any preceding embodiment, wherein the one or more electrodes comprises a plurality of individual disparate electrode surface areas formed in an array.
- EMBODIMENT 65 The apparatus of any preceding embodiment, further comprising a power source for supplying an alternating current (AC) across the one or more electrodes and the counter-electrode.
- AC alternating current
- EMBODIMENT 66 The apparatus of embodiment 65, wherein the AC is supplied at a voltage between about 1 mV and about 300 V.
- EMBODIMENT 67 The apparatus of any preceding embodiment, wherein the AC is supplied at a voltage between about 1 mV and about 20 V.
- EMBODIMENT 68 The apparatus of any preceding embodiment, wherein the AC is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz.
- EMBODIMENT 69 The apparatus of any preceding embodiment, wherein the AC is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- EMBODIMENT 70 The apparatus of any preceding embodiment, wherein the one or more electrodes comprises at least one of a transparent conducting material or a doped semiconducting material.
- EMBODIMENT 71 The apparatus of embodiment 70, wherein the transparent conducting material comprises indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- EMBODIMENT 72 The apparatus of any preceding embodiment, wherein the one or more electrodes has a thickness between about 1 nm to about 50 pm.
- EMBODIMENT 73 The apparatus of any preceding embodiment, wherein the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- EMBODIMENT 75 The apparatus of any preceding embodiment, wherein the particle has a size between about 1 nm to about 1 mm.
- EMBODIMENT 76 The apparatus of any preceding embodiment, wherein the particle comprises one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- EMBODIMENT 77 A method for operating an apparatus comprising providing a power source; providing one or more electrodes and a counter-electrode configured for generating a non-linear electric field for immobilizing a particle suspended in a fluid that flows between the one or more electrodes and the counter-electrode; providing a membrane disposed proximate a surface of the one or more electrodes, the surface of the one or more electrodes distal the counter-electrode, wherein the membrane is configured for separating the fluid from a compartment, and has an opening configured to allow for insertion of a sharp member disposed in the compartment; supplying, via the power source, an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field; and immobilizing, via a dielectrophoretic force generated by the oscillating non-linear electric field, a particle suspended in the fluid.
- AC alternating current
- EMBODIMENT 78 The method of embodiment 77, wherein the membrane comprises an opening.
- EMBODIMENT 80 The method of any preceding embodiment, further comprising probing, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 81 The method of any preceding embodiment, further comprising inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 82 The method of embodiment 81, wherein the sharp member comprises a Micro-Electro-Mechanical System (MEMS) structure or a Nano-Electro-Mechanical System (NEMS) structure.
- MEMS Micro-Electro-Mechanical System
- NEMS Nano-Electro-Mechanical System
- EMBODIMENT 83 The method of any preceding embodiment, wherein the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- EMBODIMENT 84 The method of any preceding embodiment, wherein the membrane has a thickness between about 10 nm to about 1 cm.
- EMBODIMENT 85 The method of any preceding embodiment, wherein the membrane has a thickness between about 100 nm to about 10 pm.
- EMBODIMENT 86 The method of any preceding embodiment, wherein the opening has a size between about 10 nm to about 50 pm.
- EMBODIMENT 87 The method of any preceding embodiment, wherein the opening has a size between about 1 pm to about 5 pm.
- EMBODIMENT 88 The method of any preceding embodiment, wherein a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- EMBODIMENT 89 The method of embodiment 88, wherein the hydrophobic coating has a contact angle between about 95° and about 165°.
- EMBODIMENT 90 The method of any preceding embodiment, wherein the hydrophilic coating has a contact angle between about 20° and about 80°.
- EMBODIMENT 91 The method of any preceding embodiment, wherein a surface area of the one or more electrodes is smaller than a surface area of the counter-electrode.
- EMBODIMENT 92 The method of any preceding embodiment, wherein the one or more electrodes comprises a plurality of individual disparate electrode surface areas formed in an array.
- EMBODIMENT 93 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V.
- EMBODIMENT 94 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- EMBODIMENT 95 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz.
- EMBODIMENT 96 The method of any preceding embodiment, wherein the AC across the one or more electrodes and the counter-electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- EMBODIMENT 97 The method of any preceding embodiment, wherein the one or more electrodes comprises at least one of a transparent conducting material or a doped semiconducting material.
- EMBODIMENT 98 The method of embodiment 97, wherein the transparent conducting material comprises indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- EMBODIMENT 99 The method of any preceding embodiment, wherein the one or more electrodes has a thickness between about 1 nm to about 50 pm.
- EMBODIMENT 100 The method of any preceding embodiment, wherein the one or more electrodes has a thickness between about 10 nm to about 5 pm.
- EMBODIMENT 101 The method of any preceding embodiment, wherein the fluid comprises one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid or a gas.
- EMBODIMENT 102 The method of embodiment 101, wherein the fluid is a first fluid, the compartment further comprises a second fluid, wherein the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 103 The method of any preceding embodiment, wherein the first fluid and the second fluid are immiscible.
- EMBODIMENT 104 The method of any preceding embodiment, wherein the particle has a size between about 1 nm to about 1 mm.
- EMBODIMENT 105 The method of any preceding embodiment, wherein the particle comprises one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- EMBODIMENT 106 The apparatus of any preceding embodiment, wherein the fluid is a first fluid, the compartment comprises a second fluid that is immiscible with the first fluid.
- EMBODIMENT 107 The method of any preceding embodiment, wherein the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 108 The method of any preceding embodiment, wherein the fluid is a first fluid, the compartment comprises a second fluid that is immiscible with the first fluid.
- EMBODIMENT 109 The method of embodiment 108, wherein the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 110 The apparatus of any preceding embodiment, wherein the fluid is a first fluid, the compartment comprises a second fluid that is immiscible with the first fluid.
- EMBODIMENT 111 The apparatus of embodiment 110, wherein the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 112. A method for operating an apparatus comprising providing a power source; providing a membrane configured for separating a fluid from a compartment; providing a pair of electrodes disposed proximate a surface of the membrane, wherein the pair of electrodes is configured to generate a non-linear electric field across the electrodes; supplying, via the power source, an alternating current (AC) across the electrodes, thereby generating an oscillating non-linear electric field; and immobilizing, via a dielectrophoretic force generated by the oscillating non-linear electric field, a particle suspended in the fluid that flows between the electrodes.
- AC alternating current
- EMBODIMENT 113 The method of emboidment 112, further comprising providing a counter-electrode, wherein the membrane comprises an opening.
- EMBODIMENT 114 The method of any preceding embodiment, further comprising providing a third electrode disposed proximate the surface of the membrane.
- EMBODIMENT 115 The method of any preceding embodiment, further comprising probing, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 116 The method of any preceding embodiment, further comprising: inserting, via the opening, the particle with a sharp member configured to enter across the membrane from the compartment.
- EMBODIMENT 117 The method of any preceding embodiment, wherein each of the pair of electrodes comprises a sharp tip or flat tip, or the third electrode is a ring electrode.
- EMBODIMENT 118 The method of any preceding embodiment, wherein the sharp member comprises a Micro-Electro-Mechanical System (MEMS) structure or a Nano-Electro- Mechanical System (NEMS) structure.
- MEMS Micro-Electro-Mechanical System
- NEMS Nano-Electro- Mechanical System
- EMBODIMENT 119 The method of any preceding embodiment, wherein the membrane comprises at least one of silicon nitride, silicon oxide, a metal oxide, a carbide, a ceramic, alumina, or a polymer.
- EMBODIMENT 120 The method of any preceding embodiment, wherein the membrane has a thickness between about 10 nm to about 1 cm.
- EMBODIMENT 121 The method of any preceding embodiment, wherein the membrane has a thickness between about 100 nm to about 10 pm.
- EMBODIMENT 122 The method of any preceding embodiment, wherein the opening has a size between about 10 nm to about 50 pm.
- EMBODIMENT 123 The method of any preceding embodiment, wherein the opening has a size between about 1 pm to about 5 pm.
- EMBODIMENT 124 The method of any preceding embodiment, wherein a wall of the opening has a hydrophobic coating or a hydrophilic coating.
- EMBODIMENT 125 The method of any preceding embodiment, wherein the hydrophobic coating has a contact angle between about 95° and about 165°.
- EMBODIMENT 126 The method of any preceding embodiment, wherein the hydrophilic coating has a contact angle between about 20° and about 80°.
- EMBODIMENT 127 The method of any preceding embodiment, wherein the opening is disposed between the pair of electrodes.
- EMBODIMENT 128 The method of any preceding embodiment, wherein the membrane comprises a plurality of electrode pairs formed in an array and a plurality of openings, wherein each of the openings is disposed between each of the plurality of electrode pairs.
- EMBODIMENT 129 The method of any preceding embodiment, wherein the AC across the pair of electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 300 V.
- EMBODIMENT 130 The method of any preceding embodiment, wherein the AC across the pair of electrodes and the counter-electrode is supplied at a voltage between about 1 mV and about 20 V.
- EMBODIMENT 131 The method of any preceding embodiment, wherein the AC across the pair of electrodes and the counter-electrode is supplied at an oscillating frequency of between about 10 Hz and about 10 GHz.
- EMBODIMENT 132 The method of any preceding embodiment, wherein the AC across the pair of electrodes and the counter-electrode is supplied at an oscillating frequency of between about 1 kHz and about 1 GHz.
- EMBODIMENT 133 The method of any preceding embodiment, wherein one electrode of the pair of electrodes comprises at least one of a transparent conducting material or a doped semiconducting material.
- EMBODIMENT 134 The method of embodiment 133, wherein the transparent conducting material comprises indium tin oxide, graphene, doped graphene, a conducting polymer, or a thin metal layer.
- EMBODIMENT 135. The method of any preceding embodiment, wherein the pair of electrodes has a thickness between about 1 nm to about 50 pm.
- EMBODIMENT 136 The method of any preceding embodiment, wherein the pair of electrodes has a thickness between about 10 nm to about 5 pm.
- EMBODIMENT 137 The method of any preceding embodiment, wherein the fluid comprises one of an aqueous fluid, an aqueous buffer, an organic solvent, a hydrophobic fluid or a gas.
- EMBODIMENT 138 The method of any preceding embodiment, wherein the particle has a size between about 1 nm to about 1 mm.
- EMBODIMENT 139 The method of any preceding embodiment, wherein the particle comprises one of a biological organism, a biological structure, a cell, a living cell, viruses, oil droplets, liposomes, micelles, reverse micelles, protein aggregates, polymers, or surfactant assemblies.
- EMBODIMENT 140 The method of any preceding embodiment, wherein the fluid is a first fluid, the compartment comprises a second fluid that is immiscible with the first fluid.
- EMBODIMENT 141 The method of embodiment 140, wherein the first fluid is a hydrophobic fluid and the second fluid is a hydrophilic fluid, or vice versa.
- EMBODIMENT 142 The apparatus of any preceding embodiment, wherein the one or more electrodes is disposed proximate to a surface of the membrane, the surface distal to the compartment.
- EMBODIMENT 143 The apparatus of any preceding embodiment, wherein the one or more electrodes is disposed proximate to a surface of the membrane, the surface proximate to the compartment.
- EMBODIMENT 144 The method of embodiment 26, wherein the one or more electrodes is disposed proximate to a surface of the membrane, the surface distal to the compartment.
- EMBODIMENT 145 The method of embodiment 26, wherein the one or more electrodes is disposed proximate to a surface of the membrane, the surface proximate to the compartment.
- references to“or” may be construed as inclusive so that any terms described using “or” may indicate any of a single, more than one, and all of the described terms.
- the labels “first,”“second,”“third,” and so forth are not necessarily meant to indicate an ordering and are generally used merely to distinguish between like or similar items or elements.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Sustainable Development (AREA)
- Analytical Chemistry (AREA)
- Clinical Laboratory Science (AREA)
- Electrochemistry (AREA)
- Cell Biology (AREA)
- Hematology (AREA)
- Dispersion Chemistry (AREA)
- Fluid Mechanics (AREA)
- Electromagnetism (AREA)
- Microelectronics & Electronic Packaging (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Medicinal Chemistry (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Electrostatic Separation (AREA)
Abstract
Description
Claims
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17/605,558 US20220280943A1 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
KR1020217037449A KR102677639B1 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of particles close to cavities for interfacing |
KR1020247020315A KR20240097974A (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
CN202080030859.0A CN113811394A (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of particles proximate to a cavity for an interface |
JP2021563055A JP7404396B2 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of particles in close proximity to cavities for interfacing |
CA3137731A CA3137731A1 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
AU2020263374A AU2020263374B2 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
EP20794867.0A EP3959018A4 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
SG11202111508YA SG11202111508YA (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
IL287333A IL287333A (en) | 2019-04-23 | 2021-10-17 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
JP2023209795A JP2024041757A (en) | 2019-04-23 | 2023-12-13 | Dielectrophoretic immobilization of particle in proximity to cavity for interfacing |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962837646P | 2019-04-23 | 2019-04-23 | |
US62/837,646 | 2019-04-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2020219593A1 true WO2020219593A1 (en) | 2020-10-29 |
Family
ID=72941838
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2020/029387 WO2020219593A1 (en) | 2019-04-23 | 2020-04-22 | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing |
Country Status (11)
Country | Link |
---|---|
US (1) | US20220280943A1 (en) |
EP (1) | EP3959018A4 (en) |
JP (2) | JP7404396B2 (en) |
KR (2) | KR20240097974A (en) |
CN (1) | CN113811394A (en) |
AU (1) | AU2020263374B2 (en) |
CA (1) | CA3137731A1 (en) |
IL (1) | IL287333A (en) |
SG (1) | SG11202111508YA (en) |
TW (1) | TW202106869A (en) |
WO (1) | WO2020219593A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023160777A1 (en) * | 2022-02-23 | 2023-08-31 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V. | Device and method for manipulating biological cells and method of manufacturing the device |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20210346844A1 (en) * | 2020-05-05 | 2021-11-11 | Massachusetts Institute Of Technology | Electrokinetic-Based Concentrator Device and Method |
WO2024073585A2 (en) * | 2022-09-30 | 2024-04-04 | Mekonos, Inc. | Systems and methods for single-cell trapping via dielectrophoresis |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050266478A1 (en) * | 2002-01-24 | 2005-12-01 | Mingxian Huang | Biochips including ion transport detecting structures and methods of use |
US20100224493A1 (en) * | 2009-03-09 | 2010-09-09 | Virginia Tech Intellectual Properties, Inc. | Devices and methods for contactless dielectrophoresis for cell or particle manipulation |
US20160033378A1 (en) * | 2014-06-12 | 2016-02-04 | Wafergen, Inc. | Single cell capture with polymer capture films |
WO2018080325A1 (en) * | 2016-10-31 | 2018-05-03 | Mekonos Limited | Improved sensing for automated biological cell injection |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7244349B2 (en) * | 1997-12-17 | 2007-07-17 | Molecular Devices Corporation | Multiaperture sample positioning and analysis system |
WO2002059598A1 (en) * | 2001-01-26 | 2002-08-01 | Cytion S.A. | Method and apparatus for the precise positioning of cells and other small objects |
WO2002077259A2 (en) * | 2001-03-24 | 2002-10-03 | Aviva Biosciences Corporation | Biochips including ion transport detecting structures and methods of use |
WO2002103354A1 (en) * | 2001-06-20 | 2002-12-27 | Sophion Bioscience A/S | An apparatus and method for determining and/or monitoring electrophysiological properties of ion channels |
CN1729285A (en) * | 2001-06-29 | 2006-02-01 | 里兰·斯坦福初级大学董事会 | Artificial synapse chip interface for electronic prosthetic retina |
US6887362B2 (en) | 2002-02-06 | 2005-05-03 | Nanogen, Inc. | Dielectrophoretic separation and immunoassay methods on active electronic matrix devices |
AU2003234323A1 (en) * | 2002-05-03 | 2003-11-17 | The Regents Of The University Of California | Fast electrical lysis of cells and rapid collection of the contents thereof using capillary electrophoresis |
AU2003278461A1 (en) * | 2002-10-16 | 2004-05-04 | Cellectricon Ab | Nanoelectrodes and nanotips for recording transmembrane currents in a plurality of cells |
US7105081B2 (en) * | 2002-12-20 | 2006-09-12 | Board Of Regents, The University Of Texas System | Methods and apparatus for electrosmear analysis |
US7112433B2 (en) * | 2003-04-24 | 2006-09-26 | Hewlett-Packard Development Company, L.P. | Electrical analysis of biological membranes |
US9562837B2 (en) * | 2006-05-11 | 2017-02-07 | Raindance Technologies, Inc. | Systems for handling microfludic droplets |
ITMI20061063A1 (en) * | 2006-05-31 | 2007-12-01 | Mindseeds Lab S R L | METRODO AND PE SYSTEM RLA SELECTION AND MODIFICATION OF SINGLE CELLS AND THEIR SMALL AGGREGATES |
JP2011104487A (en) | 2009-11-13 | 2011-06-02 | Tosoh Corp | Apparatus for treating fine particle |
US9146227B2 (en) * | 2010-12-30 | 2015-09-29 | Molecular Devices, Llc | Planar patch clamp devices and methods for fabrication and use |
US9387488B2 (en) * | 2012-11-13 | 2016-07-12 | Academia Sinica | Molecular entrapment and enrichment |
CN104789468B (en) | 2014-07-22 | 2017-10-20 | 奥克莱流体公司 | Particle screen selecting device |
-
2020
- 2020-04-22 AU AU2020263374A patent/AU2020263374B2/en active Active
- 2020-04-22 WO PCT/US2020/029387 patent/WO2020219593A1/en unknown
- 2020-04-22 JP JP2021563055A patent/JP7404396B2/en active Active
- 2020-04-22 CA CA3137731A patent/CA3137731A1/en active Pending
- 2020-04-22 EP EP20794867.0A patent/EP3959018A4/en active Pending
- 2020-04-22 US US17/605,558 patent/US20220280943A1/en active Pending
- 2020-04-22 KR KR1020247020315A patent/KR20240097974A/en not_active Application Discontinuation
- 2020-04-22 KR KR1020217037449A patent/KR102677639B1/en active IP Right Grant
- 2020-04-22 SG SG11202111508YA patent/SG11202111508YA/en unknown
- 2020-04-22 CN CN202080030859.0A patent/CN113811394A/en active Pending
- 2020-04-23 TW TW109113700A patent/TW202106869A/en unknown
-
2021
- 2021-10-17 IL IL287333A patent/IL287333A/en unknown
-
2023
- 2023-12-13 JP JP2023209795A patent/JP2024041757A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050266478A1 (en) * | 2002-01-24 | 2005-12-01 | Mingxian Huang | Biochips including ion transport detecting structures and methods of use |
US20100224493A1 (en) * | 2009-03-09 | 2010-09-09 | Virginia Tech Intellectual Properties, Inc. | Devices and methods for contactless dielectrophoresis for cell or particle manipulation |
US20160033378A1 (en) * | 2014-06-12 | 2016-02-04 | Wafergen, Inc. | Single cell capture with polymer capture films |
WO2018080325A1 (en) * | 2016-10-31 | 2018-05-03 | Mekonos Limited | Improved sensing for automated biological cell injection |
Non-Patent Citations (1)
Title |
---|
See also references of EP3959018A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023160777A1 (en) * | 2022-02-23 | 2023-08-31 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V. | Device and method for manipulating biological cells and method of manufacturing the device |
Also Published As
Publication number | Publication date |
---|---|
AU2020263374A1 (en) | 2021-11-04 |
KR20240097974A (en) | 2024-06-27 |
EP3959018A1 (en) | 2022-03-02 |
KR20210153683A (en) | 2021-12-17 |
US20220280943A1 (en) | 2022-09-08 |
CA3137731A1 (en) | 2020-10-29 |
SG11202111508YA (en) | 2021-11-29 |
AU2020263374B2 (en) | 2023-05-11 |
JP2024041757A (en) | 2024-03-27 |
KR102677639B1 (en) | 2024-06-24 |
CN113811394A (en) | 2021-12-17 |
TW202106869A (en) | 2021-02-16 |
JP2022530064A (en) | 2022-06-27 |
EP3959018A4 (en) | 2022-06-15 |
JP7404396B2 (en) | 2023-12-25 |
IL287333A (en) | 2021-12-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2020263374B2 (en) | Dielectrophoretic immobilization of a particle in proximity to a cavity for interfacing | |
US9995668B2 (en) | Apparatus for manipulating, modifying and characterizing particles in a micro channel | |
CA2485099C (en) | Apparatus including ion transport detecting structures and methods of use | |
US20130146459A1 (en) | Multiphase non-linear electrokinetic devices | |
US20020036139A1 (en) | Method and apparatus for programmable fluidic processing | |
US20080286750A1 (en) | Apparatus including ion transport detecting structures and methods of use | |
JP2005513455A (en) | Dielectric gate for injecting and controlling fluids | |
JP2004503361A (en) | Apparatus and method for fluid injection | |
WO2006027757A2 (en) | Microfluidic device using a collinear electric field | |
EP2928606B1 (en) | Manipulation of objects in microfluidic devices using external electrodes | |
US20110259742A1 (en) | Droplet Based Miniaturized Device With On-Demand Droplet-Trapping, -Fusion, And -Releasing | |
JP2005515058A (en) | Wallless channel for fluid path assignment and restriction | |
US8821702B2 (en) | Devices and methods for electroosmotic transport of non-polar solvents | |
US20220305491A1 (en) | Scalable systems and methods for automated biosystem engineering | |
TW202436615A (en) | Systems and methods for single-cell trapping via dielectrophoresis | |
WO2024073585A2 (en) | Systems and methods for single-cell trapping via dielectrophoresis | |
Lee | Fundamental studies of AC/DC electrokinetic phenomena for the realization of microchip capillary electrophoresis for single-cell analysis | |
Rezaei Nejad | Development of techniques for rapid isolation and separation of particles in digital microfluidics |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 20794867 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 3137731 Country of ref document: CA |
|
ENP | Entry into the national phase |
Ref document number: 2021563055 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2020263374 Country of ref document: AU Date of ref document: 20200422 Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 20217037449 Country of ref document: KR Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 2020794867 Country of ref document: EP Effective date: 20211123 |