High throughput, feedback-controlled electroporation microdevice for efficient molecular delivery into single cells

Patent metadata

Field	Value
Publication number	US-10927333-B2
Application number	US-201615757566-A
Country	US
Kind code	B2
Filing date	Sep 2, 2016
Priority date	Sep 4, 2015
Publication date	Feb 23, 2021
Grant date	Feb 23, 2021

Abstract

Systems and methods for cell electroporation and molecular delivery using an intelligent, feedback controlled, microscale electroporation system for transfecting single cells.

First claim

What is claimed is:

1. A system for electroporating a biological cell, the system comprising:
a microfluidic channel adapted to receive a flow of a plurality of biological cells in a buffer solution, wherein the microfluidic channel comprises a detection area;
a pair of electrodes adapted to apply an electrical field across the detection area;
a signal generator, wherein the signal generator is capable of generating a first signal, and a second signal through the electrodes, wherein the first signal is a cell detection signal and the second signal is a permeabilization signal;
a sensor, wherein the sensor is adapted to continuously monitor an impedance value of the detection area; and
a controller, wherein the controller is adapted to:
determine that a single one of the plurality of biological cells has entered the detection area by monitoring the impedance value of the detection area increasing over a baseline threshold in the presence of the first signal, and
in response to determining that the single one of the plurality of biological cells has entered the detection area, control the signal generator to generate the second signal.

2. The system of claim 1 , wherein the signal generator is capable of generating the cell detection signal and the permeabilization signal simultaneously.

3. The system of claim 1 , wherein the sensor comprises a lock-in amplifier.

4. The system of claim 1 , wherein the sensor further comprises an imaging device capable of measuring fluorescence of a cell within the detection area.

5. The system of claim 1 , wherein the microfluidic channel is adapted to hydrodynamically focus the flow of a plurality of biological cells through the detection area.

6. The system of claim 1 , wherein the system further comprises a second microfluidic channel adapted to receive a flow of buffer without cells, and wherein the second microfluidic channel comprises a second detection area.

7. The system of claim 6 , wherein the sensor is adapted to detect an impedance value of the second detection area, the impedance value of the second detection area providing a reference signal for determining that the single one of the plurality of biological cells has entered the detection area.

8. The system of claim 1 , wherein the signal generator unit is further capable of generating a third signal that is a delivery signal that causes delivery of a molecule into the single one of the plurality of cells within the detection area.

9. The system of claim 1 , wherein the controller unit is further adapted to control the signal generator to generate the second signal that has a plurality of pulse parameters selected based on the monitored impedance value of the detection area and associated data from a trapped cell experiment or a mathematical model.

10. The system of claim 8 , wherein the controller unit is further adapted to control the signal generator to:
stop generation of the second signal upon monitoring the impedance value of the detection area rising to greater than a permeabilization threshold value; and
generate the third electrical signal according to the impedance detected by the sensor.

11. The system of claim 8 , wherein the controller is further adapted to control the signal generator to dynamically adjust at least one parameter of the delivery signal based on the monitored impedance value to allow delivery of the molecule without reaching excessive changes in impedance indicative of cell death.

12. The system of claim 11 , wherein the controller is adapted to:
determine whether the impedance value of the detection area is about equal to the permeabilization threshold value,
wherein the controlling of the signal generator to adjust at least one parameter of the delivery signal to allow molecular delivery without reaching excessive changes in impedance indicative of cell death is in response to determining the impedance value of the detection area is not about equal to the permeabilization threshold value.

13. The system according to claim 11 , wherein the at least one parameter of the delivery signal is selected from the group of: electric field amplitude, pulse duration, pulse train frequency, duty cycle, and number of cycles.

14. The system of claim 8 , wherein the controller is adapted to control the signal generator to generate the third signal that has a plurality of pulse parameters selected based on the monitored impedance value of the detection area and associated data from a trapped cell experiment or a mathematical model.

15. The system of claim 8 , wherein the controller unit is adapted to control the signal generator to stop generation of the third signal in response to at least one of the following:
determining that the monitored impedance value is less than the threshold impedance indicating that that the single one of the plurality of biological cells has exited the detection area; or
determining that the monitored impedance value is equal to a viability threshold for over-exposure.

16. The system of claim 1 , wherein the flow of the plurality of biological cells is continuous.

17. The system according to claim 10 , wherein the permeabilization threshold value is determined experimentally or using a mathematical model.

18. The system according to claim 10 , wherein the permeabilization threshold value corresponds to an optimal cell permeabilization that does not cause cell death.

19. The system according to claim 1 , wherein the sensor is adapted to, upon determining that the single one of the plurality of biological cells has entered the detection area, operate at a sensing frequency range that is configured to sense a variation in impedance of the single one of the plurality of cells due to permeabilization, the sensing frequency range being about 1 KHz to about 10 KHz.

Assignees

• Univ Rutgers

Inventors

• Zahn Jeffrey
• Zheng Mingde
• Shreiber David I
• Lin Hao
• Shan Jerry W

Classifications

• B01L2200/0647

  Handling flowable solids, e.g. microscopic beads, cells, particles · CPC title

• B01L3/502715 Primary

  characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces · CPC title

• B01L2300/0645

  Electrodes · CPC title

• B01L3/502761

  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