# US 12,599,337 B1 · Method and system for confirmation of microneedle-based analyte-selective sensor insertion into viable tissue via electrical interrogation

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- Number: US 12,599,337 B1
- Document ID: US12599337B1
- Status: Granted
- Kind: B1
- Application number: 16/051,398
- Filed: 2018-07-31
- Granted: 2026-04-14
- Earliest claimed: 2017-08-08
- Assignees: Biolinq Incorporated
- Applicants: Biolinq Incorporated
- Inventors: Joshua Windmiller; Jared Rylan Tangney
- Web page: https://patentgrep.com/patent/US12599337B1

## CPC

- A61B 5/685: {Microneedles}
- A61B 5/14532: {for measuring glucose, e.g. by tissue impedance measurement}
- A61B 5/14546: {for measuring analytes not otherwise provided for, e.g. ions, cytochromes}
- C12Q 1/001: {Enzyme electrodes}
- G01N 27/327: Biochemical electrodes {, e.g. electrical or mechanical details for in vitro measurements}
- G01N 27/3271: {Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood (amperometry per se G01N27/49; aspects concerning the enzyme reagent C12Q1/001)}
- G16H 40/40: for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
- A61B 5/0531: Measuring skin impedance
- A61B 2562/0295: Strip shaped analyte sensors for apparatus classified in A61B5/145 or A61B5/157
- A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D)
- C12Q: MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q)
- G16H: HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA

## Abstract

A system and method to confirm the insertion of an analyte-selective sensor comprising an array of microneedles possessing vertical extent between 200 and 2000 μm into viable tissue is disclosed herein. Mechanical insertion of an analyte-selective sensor is firstly attempted by means of an application of external force. Either during or following this routine, an electrical stimulus is applied between at least two distinct electrodes located within the said analyte-selective sensor; a resultant response is measured. This response is compared with a reference value to determine if insertion was successful. If insertion was successful, no further effort is required and the sensor can operate as intended. However, if insertion was not successful, the user can be instructed to continue to apply additional force to said sensor to achieve successful insertion or otherwise re-apply the said sensor altogether.

## Claims

### Claim 1

A method to confirm insertion, into cutaneous tissue, of an analyte-selective sensor comprising a first microneedle with a first electrode and a second microneedle with a second electrode, said method comprising:
applying, by an excitation circuit of the analyte-selective sensor and after an attempted insertion of the first and second microneedles into the cutaneous tissue, a first electrical potential to the first and second electrodes;
measuring, by a measurement circuit of the analyte-selective sensor, a resultant electrical value generated between the first and second electrodes through the cutaneous tissue;
comparing the resultant electrical value to a range of values indicative of insertion of the first and second microneedles into the cutaneous tissue; and
applying, by the excitation circuit of the analyte-selective sensor and responsive to the comparison indicating insertion of the first and second microneedles into the cutaneous tissue, a second electrical potential to the first and second electrodes,
wherein the second electrical potential is greater than the first electrical potential and is used to measure an analyte concentration within physiological fluid.

### Claim 2 (depends on 1)

The method of claim 1, wherein said analyte-selective sensor comprises an electrochemical sensor.

### Claim 3 (depends on 1)

The method of claim 1, wherein the attempted insertion is achieved by application of pressure, force velocity, or energy, to achieve a penetration of an outer surface of the cutaneous tissue.

### Claim 4 (depends on 1)

The method of claim 1, wherein each of the first and second electrodes comprises one or more of a metal, a semiconductor, and an organic surface of a defined geometry.

### Claim 5 (depends on 1)

The method of claim 1, wherein the first electrical potential is a fixed or time-varying electrical potential comprising a constant voltage, a voltage waveform, a sinusoidal signal, a frequency-dependent signal, an impulse, a constant phase signal, or a varying-phase signal.

### Claim 6 (depends on 1)

The method of claim 1, wherein the range of values comprises a range of voltage, current, resistance, conductance, capacitance, inductance, or impedance values.

### Claim 7

A method to confirm insertion, into cutaneous tissue, of a microneedle-based analyte-selective sensor, said method comprising:
applying, by an excitation circuit of the analyte-selective sensor and after an attempted insertion into the cutaneous tissue of at least two electrodes of the analyte-selective sensor, a first electrical potential to the at least two electrodes;
measuring, by a measurement circuit of the analyte-selective sensor, a resultant electrical value generated between the at least two electrodes through the cutaneous tissue;
comparing the resultant electrical value to a range of values indicative of insertion of the at least two electrodes into the cutaneous tissue; and
applying, by the excitation circuit of the analyte-selective sensor and responsive to the comparison indicating insertion of the at least two electrodes of analyte-selective sensor into the cutaneous tissue, a second electrical potential to the at least two electrodes,
wherein the second electrical potential is greater than the first electrical potential and is used to measure an analyte concentration within physiological fluid.

### Claim 8 (depends on 7)

The method of claim 7, wherein said cutaneous tissue comprises the epidermis, dermis, or hypodermis.

### Claim 9 (depends on 7)

The method of claim 7, wherein the attempted insertion is achieved by application of pressure, force velocity, or energy, to achieve a penetration of an outer surface of the cutaneous tissue.

### Claim 10 (depends on 7)

The method of claim 7, wherein each of said at least two electrodes comprises one or more of a metal, a semiconductor, and an organic surface of a defined geometry.

### Claim 11 (depends on 7)

The method of claim 7, wherein the first electrical potential is a fixed or time-varying electrical potential comprising a constant voltage, a voltage waveform, a sinusoidal signal, a frequency-dependent signal, an impulse, a constant phase signal, or a varying-phase signal.

### Claim 12 (depends on 7)

The method of claim 7, wherein the range of values comprises a range of voltage, current, resistance, conductance, capacitance, inductance, or impedance values.

### Claim 13

A method to confirm insertion, into cutaneous tissue, of an analyte-selective sensor comprising a microneedle array, said method comprising:
applying, by an excitation circuit of the analyte-selective sensor, a first electrical potential to at least two electrodes of the microneedle array following an attempted insertion of the microneedle array into the cutaneous tissue;
measuring, by a measurement circuit of the analyte-selective sensor, a resultant electrical value generated between the at least two electrodes through the cutaneous tissue;
comparing the resultant electrical value to a range of values indicative of insertion into the cutaneous tissue; and
applying, by the excitation circuit of the analyte-selective sensor and responsive to the comparison indicating insertion of the microneedle array into the cutaneous tissue, a second electrical potential to the at least two electrodes,
wherein the second electrical potential is greater than the first electrical potential and is used to measure an analyte concentration within physiological fluid.

### Claim 14 (depends on 13)

The method according to claim 13, wherein the attempted insertion is achieved by application of pressure, force velocity, or energy, to achieve a penetration of an outer surface of the cutaneous tissue.

### Claim 15 (depends on 13)

The method according to claim 13, wherein the first electrical potential is a fixed or time-varying electrical potential comprising one of a constant voltage, a voltage waveform, a sinusoidal signal, a frequency-dependent signal, an impulse, a constant phase signal, or a varying-phase signal.

### Claim 16 (depends on 13)

The method according to claim 13, wherein the range of values comprises a range of voltage, current, resistance, conductance, capacitance, inductance, or impedance values.

### Claim 17

A method of an analyte-selective sensor comprising a first microneedle with a first electrode and a second microneedle with a second electrode, said method comprising:
applying, by an excitation circuit of the analyte-selective sensor and after an attempted insertion of the first and second microneedles into cutaneous tissue of a user, a first electrical potential to the first and second electrodes;
measuring, by a measurement circuit of the analyte-selective sensor, a first resultant electrical value generated between the first and second electrodes through the cutaneous tissue;
comparing the resultant electrical value to a range of values indicative of insertion of the first and second microneedles into the cutaneous tissue;
providing, when the comparison indicates insertion of the first and second microneedles into the cutaneous tissue is not achieved, a direction to the user to apply a force to the analyte-selective sensor to attempt re-insertion of the analyte-selective sensor;
applying, by the excitation circuit of the analyte-selective sensor and after the attempted re-insertion of the first and second microneedles into the cutaneous tissue of the user, a second electrical potential to the first and second electrodes;
measuring, by the measurement circuit of the analyte-selective sensor, a second resultant electrical value generated between the first and second electrodes through the cutaneous tissue;
comparing the resultant electrical value to the range of values indicative of insertion of the first and second microneedles into the cutaneous tissue; and
applying, by the excitation circuit of the analyte-selective sensor and when the comparison indicates insertion of the first and second microneedles into the cutaneous tissue, a third electrical potential to the first and second electrodes,
wherein the third electrical potential is greater than the first electrical potential and the second electrical potential.

### Claim 18 (depends on 17)

The method of claim 17, wherein the application of the force in response to the direction is applied by a hand of the user.
