Multiplexed on-chip impedance cytometry system and method

Patent metadata

Field	Value
Publication number	US-11965810-B2
Application number	US-201917280480-A
Country	US
Kind code	B2
Filing date	Sep 26, 2019
Priority date	Sep 26, 2018
Publication date	Apr 23, 2024
Grant date	Apr 23, 2024

Abstract

An exemplary method and system is disclosed that facilitate the integration of multiplexed single-cell impedance cytometry in a high throughput format, which can be deployed upstream from microfluidic sample preparation and/or downstream to microfluidic cell separation. In exemplary method and system may employ impedance-based quantification of cell electrophysiology on the same microfluidic chip (i.e., “on-chip”) to provide distinguishing phenotypic information on the sample, without the need for additional sample handling, preparation or dilution steps as would be needed for other flow cytometry techniques.

First claim

What is claimed is:

1. A method of operating a microfluidic chip, the method comprising:
flowing a sample comprising biologic or particle components in a plurality of microfluidic channels of the microfluidic chip, including an upstream microfluidic channel and a plurality of downstream microfluidic channels, wherein the upstream microfluidic channel is connected to the plurality of downstream microfluidic channels;
applying a first set of electric field across a first set of one or more electrodes located in the upstream microfluidic channel to selectively urge the biologic or particle components into one or more lanes of a plurality of lanes in a flow to continuously separate the biologic or particle components to channel inlets of the plurality of downstream microfluidic channels;
applying a second set of electric field across a second set of one or more electrodes located in at least one downstream microfluidic channel of the plurality of downstream microfluidic channels, including in a first downstream microfluidic channel; and
interrogating, via the second set of one or more electrodes, electrical responses of the separated biologic or particle components in the at least one downstream microfluidic channel, including electrical responses of the separated biologic or particle components in the first downstream microfluidic channel,
wherein the electrical responses are analyzed via impedance magnitude-based contrast and/or impedance phase-based contrast for quantification and/or analysis of the separated biologic or particle components in at least the first downstream microfluidic channel, and
wherein the applied first set of electric field continuously separates the biologic or particle components into a second downstream microfluidic channel of the plurality of downstream microfluidic channels, wherein the biologic or particle components sorted to the second downstream microfluidic channel has a different permittivity or conductivity characteristics to the biologic or particle components sorted to the first downstream microfluidic channel based on impedance characteristics of the biologic or particle components.

2. The method of claim 1 , further comprising:
quantifying impedance magnitude and/or impedance phase characteristics of the separated biologic or particle components sorted into the second downstream microfluidic channel using the second set of one or more electrodes located in the first downstream microfluidic channel; and
quantifying impedance and/or phase impedance characteristics of separated biologic or particle components sorted into a second downstream microfluidic channel using a third set of one or more electrodes located in the second downstream microfluidic channel.

3. The method of claim 1 , wherein the electrical responses of the separated biologic or particle components in the first and second downstream microfluidic channels are measured simultaneously, and wherein the acquired electrical responses are converted to a digitally encoded signal via a common amplifier circuit.

4. The method of claim 1 , wherein signals associated with the interrogated electrical responses of the separated biologic or particle components in the first and second downstream microfluidic channels are frequency-division multiplexed into a common bus, and wherein the common bus is connected to the common amplifier circuit.

5. The method of claim 1 , wherein the first and second sets of the one or more electrodes are connected to a respective signal source, where each of the respective signal source has a distinct frequency to that of the other signal sources to facilitate frequency-division multiplexing.

6. The method of claim 2 , wherein the second set of the one or more electrodes has a first set of spacings among individual electrodes of the set, and wherein the third set of one or more electrodes has a second set of spacings among individual electrodes of the set, wherein the first set of spacings is different from the second set of spacings, and
wherein a single source signal when applied to the different spacings of the first set of spacings and the second set of spacings results in the second set of electrodes generating a field having a different temporal profile of impedance in comparison to that of the third set of electrodes.

7. The method of claim 1 , further comprising:
detecting, via one or more position detection electrodes located in the first downstream microfluidic channel, presence of the separated biologic or particle components in the first microfluid channel, wherein the detected presence of the separated biologic or particle components in the first microfluid channel is used for selective interrogation, selective sampling, and/or selective multiplexing of the separated biologic or particle components in the first microfluid channel.

8. The method of claim 1 , wherein the interrogated electrical responses are measured in the first downstream microfluidic channel while the separated biologic or particle components is continuously flowing in the first downstream microfluidic channel.

9. The method of claim 1 , wherein the interrogated electrical responses are measured in the first downstream microfluidic channel while the separated biologic or particle components are at a gated position in the first downstream microfluidic channel.

10. The method of claim 1 , wherein the second set of electric field applied across the second set of one or more electrodes is similarly, or same, across multiple measurements of multiple biologic or particle components flowing through the first downstream microfluidic channel.

11. The method of claim 1 , wherein a same set of different frequencies are applied, across multiple measurements, to each of a group of multiplexed downstream microfluidic channels.

12. The method of claim 1 , wherein the second set of electric field applied across the second set of one or more electrodes is varied across multiple measurements of the multiple biologic or particle components flowing through the first downstream microfluidic channel.

13. The method of claim 1 , wherein different frequencies are swept, across multiple measurements, across each of a respective group of multiplexed downstream microfluidic channels.

14. The method of claim 1 , wherein levels of impedance or value associated therewith is determined by analog circuit configured to:
detect small time shifts in incoming signals in a differential manner via a PLL phase extractor circuit to enable noise rejection for extracting a phase signal of the measured signal associated with current flow;
averaging the phase signal; and
converting the averaged phase signal to a binary stream of the averaged phase signal.

15. The method of claim 1 , wherein the first downstream microfluidic channel has at least one region having a cross-sectional area different to the channel, wherein the cross-sectional area is sized to increase or reduce velocity of the flow through the first downstream microfluidic channel to improve sensitivity and/or signal-to-noise performance of measurements.

16. The method of claim 1 , wherein the downstream microfluidic channel includes a third microfluidic channel that splits into a plurality of parallel channels, wherein each of the plurality of parallel channels defines a second flow rate different than the flow rate of the channel feeding the plurality of parallel channels.

17. The method of claim 1 further comprising:
continuously directing the biologic or particle components via an inertial focusing structure or a deterministic lateral displacement structu

Assignees

• Univ Virginia Patent Foundation
• Swami Nathan
• Mcgrath John
• Varhue Walter
• Honrado Carlos
• Farmehini Vahid
• Liu Yi

Inventors

• Swami Nathan
• Mcgrath John
• Varhue Walter
• Honrado Carlos
• Farmehini Vahid
• Liu Yi

Classifications

• G01N15/1056 Primary

  Physics · mapped topic

• B01L3/502761 Primary

  specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads or physically stretching molecules · CPC title

• G01N15/1031

  by measuring electrical or magnetic effects · CPC title

• B01L2200/027

  for microfluidic devices · CPC title

• B01L2200/0652

  Sorting or classification of particles or molecules · CPC title