# US 2023/0264192 A1 · Microfluidic electrochemical analyte detectors

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- Number: US 2023/0264192 A1
- Document ID: US20230264192A1
- Status: Published application
- Kind: A1
- Application number: 18/006,445
- Filed: 2021-07-16
- Published: 2023-08-24
- Earliest claimed: 2020-07-23
- Assignees: Massachusetts Institute of Technology
- Applicants: Massachusetts Institute of Technology
- Inventors: Dan Wu; Joel Voldman
- Web page: https://patentgrep.com/patent/US20230264192A1

## CPC

- B01L 3/502715: {characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces}
- B01L 3/50273: {characterised by the means or forces applied to move the fluids}
- B01L 2200/0668: Trapping microscopic beads
- B01L 2300/0636: Integrated biosensor, microarrays
- B01L 2300/0645: Electrodes
- B01L 2300/0816: Cards, e.g. flat sample carriers usually with flow in two horizontal directions
- B01L 2300/0864: comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
- B01L 2300/088: Channel loops
- B01L 2400/0481: squeezing of channels or chambers
- B01L 2400/0655: pinch valves
- B01L 2400/0666: Solenoid valves
- B01L: CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE

## Abstract

Microfluidic chips containing electrochemical biosensors are described. The electrochemical biosensors include a flow layer intersected by valves of a control layer, which control the fluid flow. The flow layer includes two zones, an analyte capture zone for mixing a sample with an analyte capture element, and a detection zone for detecting the analyte. Both zones include a rotary mixer for mixing, and where needed, trapping, washing, and flowing the captured analyte. The captured analyte is detected by the sensing region of the detection zone. The microfluidic chips may be integrated into devices for automated, fast, point-of-care determination of analyte concentration.

## Claims

### Claim 1

A microfluidic chip comprising one or more electrochemical biosensors, each biosensor comprising:
a) a flow layer comprising
an analyte capture zone comprising a microfluidic rotary mixer; and
a detection zone comprising a microfluidic rotary mixer with a sensing region comprising a working electrode;
wherein the analyte capture zone is fluidically connected with the detection zone by a microfluidic channel; and
b) a control layer comprising one or more valves positioned above or below the flow layer and intersecting the analyte capture zone, the detection zone, or both,
wherein the rotary mixers are looped microfluidic channels intersected with at least one, at least two, or at least three valves.

### Claim 2 (depends on 1)

The microfluidic chip of claim 1, wherein the one or more valves of the control layer comprise a flexible membrane at intersections with the analyte capture zone, the detection zone, or both.

### Claim 3 (depends on 1)

The microfluidic chip of claim 1, wherein the one or more valves of the control layer form a rotary pump comprising at least three valves configured for sequential operability and intersecting the analyte capture zone and/or the detection zone.

### Claim 4 (depends on 3)

The microfluidic chip of claim 3, wherein the rotary pump is a peristaltic pump.

### Claim 5 (depends on 1)

The microfluidic chip of claim 1, comprising an inlet zone comprising one or more microfluidic channels fluidically connected to the analyte capture zone.

### Claim 6 (depends on 1)

The microfluidic chip of claim 1, comprising a collection zone comprising one or more microfluidic channels fluidically connected to the detection zone.

### Claim 7 (depends on 1)

The microfluidic chip of claim 1, wherein the control layer comprises one or more microfluidic valves intersecting any one of microfluidic channels fluidically connecting the inlet zone to the analyte capture zone, the analyte capture zone to the detection zone, and the detection zone to the collection zone.

### Claim 8 (depends on 1)

The microfluidic chip of claim 1, wherein the control layer is below the flow layer and the valves are pushed up into the flow layer.

### Claim 9 (depends on 1)

The microfluidic chip of claim 1, wherein the flow layer comprises microfluidic channels having a substantially circular cross-section.

### Claim 10 (depends on 1)

The microfluidic chip of claim 1, wherein the flow layer comprises microfluidic channels having a substantially angular cross-section, wherein height to width ratio of the microfluidic channels is between about 1:2 and about 1:15.

### Claim 11 (depends on 1)

The microfluidic chip of claim 1, wherein the flow layer comprises microfluidic channels having a diameter or a height between about 10 μm and 1000 μm, and length between about 5 and 100 mm.

### Claim 12 (depends on 1)

The microfluidic chip of claim 1, wherein the microfluidic rotary mixer comprises a looped microfluidic channel having a geometry selected from the group consisting of a square, a rectangular, and a triangular cross-section.

### Claim 13 (depends on 1)

The microfluidic chip of claim 1, wherein the detection zone comprises a trap region comprising a magnet, a gel, or a capture substance.

### Claim 14 (depends on 1)

The microfluidic chip of claim 1, wherein the sensing region is coated with a capture moiety.

### Claim 15 (depends on 1)

The microfluidic chip of claim 1, comprising between two and ten electrochemical biosensors.

### Claim 16 (depends on 1)

A device comprising the microfluidic chip of claim 1.

### Claim 17 (depends on 16)

The device of claim 16, comprising a microfluidic controlling module and a display means.

### Claim 18 (depends on 17)

The device of claim 17, wherein the microfluidic controlling module comprises a solenoid valve array.

### Claim 19 (depends on 1)

A method of making the microfluidic chip of claim 1 or a device comprising the microfluidic chip comprising forming the flow layer and/or the control layer using one or more methods selected from the group consisting of stereolithography, soft lithography, laser machining, micromachining, curing, bonding, three-dimensional printing, molding, micromolding, thermal setting, metal deposition, and coating.

### Claim 20 (depends on 1)

A method of measuring analyte concentration in a sample comprising applying the sample and an analyte capture element to the flow layer of the microfluidic chip of claim 1, or to a device comprising the microfluidic chip.

### Claim 21 (depends on 20)

The method of claim 20, comprising mixing the sample and the analyte capture element in the microfluidic rotary mixer of the analyte capture zone to obtain captured analyte.

### Claim 22 (depends on 20)

The method of claim 20, comprising trapping the captured analyte in a trap region of the detection zone.

### Claim 23 (depends on 22)

The method of claim 22, comprising trapping the captured analyte in a trap region of the detection zone and washing with buffer.

### Claim 24 (depends on 21)

The method of claim 21, comprising flowing the captured analyte over the sensing region to contact the one or more electrodes of the sensing region.

### Claim 25 (depends on 20)

The method of claim 20, comprising adding a substrate reagent and recording a change in current from the sensing region.

### Claim 26 (depends on 20)

The method of claim 20, wherein any one of mixing, trapping, washing, and flowing is accomplished using one or more peristaltic pumps.

### Claim 27 (depends on 20)

The method of claim 20, comprising detecting a concentration of the analyte in the sample based on a change in current from the sensing region.

### Claim 28 (depends on 20)

The method of claim 20, wherein the microfluidic chip operates with sample volumes between about 0.5 μm and 500 μL.

### Claim 29 (depends on 20)

The method of claim 20, wherein the microfluidic chip operates at flow rates between about 0.5 μL/min and 15 μL/min.

### Claim 30 (depends on 20)

The method of claim 20, wherein the valves in the microfluidic chip operate at pressures between about 5 psi and 50 psi.

### Claim 31 (depends on 20)

The method of claim 20, wherein the microfluidic chip operates at valve closure between about 50% and 95%.

### Claim 32 (depends on 20)

The method of claim 20, wherein the microfluidic chip comprises between two and ten electrochemical biosensors and is configured to measure the concentration of the same analyte with the biosensors, or the concentrations two to ten different analytes with biosensors.