IP Library Granted Patent US 12,507,921
Granted Patent B2
US 12,507,921 · App. 18/778,772 · Granted Dec 30, 2025

Sensor assembly of a microneedle array-based continuous analyte monitoring device

Inventors: Daniel Alonso-Soski (San Diego, CA); Alan Steven Campbell (La Mesa, CA); Jared Rylan Tangney (Encinitas, CA); Jennifer Ruth Walters Fuchs (Carlsbad, CA); Joshua Ray Windmiller (San Diego, CA)
Assignee: Biolinq Incorporated
A61B5/1473A61B5/685A61B5/14532A61B2560/0219
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Quick Facts
Patent No.
US 12,507,921
App. No.
18/778,772
Granted
Dec 30, 2025
Kind
B2
Abstract

Aspects of the current subject matter are directed to a sensor assembly of an analyte monitoring device including one or more microneedle arrays. Aspects are directed to components and architecture of a sensor assembly to implement power and processing aspects of a microneedle array-based continuous analyte monitoring device for the detection and measuring of an analyte. A source of a power-on event is determined, and the analyte monitoring device is transitioned to a mode that corresponds to the determined source. When a power-on event is determined to be a valid power-on event, the analyte monitoring device is transition to a mode that corresponds to a type of the valid power-on event.

Claims (52)

1 . A method of operating an analyte monitoring device, the method comprising:

determining, by a controller of the analyte monitoring device when the analyte monitoring device is in a first operating configuration, that at least one microneedle of a plurality of microneedles is inserted into skin of a user; and

responsive to determining the at least one microneedle is inserted into the skin of the user, transitioning, by the controller, the analyte monitoring device from the first operating configuration to a second operating configuration,

wherein a first working electrode, a second working electrode, a reference electrode, and a counter electrode are each positioned on a respective microneedle of the plurality of microneedles,

wherein the first operating configuration comprises a two-electrode electrochemical cell in which the reference electrode and the counter electrode are combined, the two-electrode electrochemical cell being configured to confirm insertion of the at least one microneedle, and

wherein the second operating configuration comprises a three-electrode electrochemical cell in which the reference electrode and the counter electrode are independent of one another, the three-electrode electrochemical cell being configured to sense a level of an analyte in the skin of the user.

2 . The method of claim 1 , wherein, in the two-electrode electrochemical cell, the reference electrode and the counter electrode are combined at a reference point that connects a counter electrode input and a reference electrode input.

3 . The method of claim 1 , wherein a first switch and a second switch are configured to transition the analyte monitoring device between the first operating configuration and the second operating configuration.

4 . The method of claim 3 , wherein the first switch is positioned between the counter electrode input and the reference electrode, and wherein the second switch is positioned at a reference electrode input.

5 . The method of claim 1 , wherein the determination of the at least one microneedle inserted into the skin of the user comprises a determination that at least one of a first current and a second current satisfy a predetermined threshold,

the first current resulting from a first bias potential applied between the first working electrode and the combined reference electrode and counter electrode, and

the second current resulting from a second bias potential applied between the second working electrode and the combined reference electrode and counter electrode.

6 . The method of claim 5 , wherein, in the second operating configuration, an operational bias potential is applied to at least one of the first working electrode and the second working electrode.

7 . The method of claim 6 , wherein the operational bias potential is greater than the first bias potential and the second bias potential.

8 . The method of claim 1 , wherein the determination of the at least one microneedle inserted into the skin of the user comprises a determination that a first current satisfies a predetermined threshold, the first current resulting from a first bias potential applied between the first working electrode and the combined reference electrode and counter electrode, and

wherein, in the second operating configuration, an operational bias potential is applied to the second working electrode.

9 . The method of claim 8 , wherein a third working electrode is positioned on a respective microneedle of the plurality of microneedles, and

wherein, in the second operating configuration, the operational bias potential is applied to the third working electrode.

10 . An analyte monitoring device comprising:

an analyte sensor comprising a plurality of microneedles configured to be inserted into skin of a user;

a first working electrode, a second working electrode, a reference electrode, and a counter electrode, each positioned on a respective microneedle of the plurality of microneedles; and

a controller configured to:

determine, when the analyte monitoring device is in a first operating configuration, that at least one microneedle of the plurality of microneedles is inserted into the skin of the user; and

responsive to the determination of the at least one microneedle inserted into the skin of the user, transition the analyte monitoring device from the first operating configuration to a second operating configuration,

wherein the first operating configuration comprises a two-electrode electrochemical cell in which the reference electrode and the counter electrode are combined, the two-electrode electrochemical cell being configured to confirm insertion of the at least one microneedle, and

wherein the second operating configuration comprises a three-electrode electrochemical cell in which the reference electrode and the counter electrode are independent of one another, the three-electrode electrochemical cell being configured to sense a level of an analyte in the skin of the user.

11 . The analyte monitoring device of claim 10 , wherein, in the two-electrode electrochemical cell, the reference electrode and the counter electrode are combined at a reference point that connects a counter electrode input and a reference electrode input.

12 . The analyte monitoring device of claim 10 , wherein a first switch and a second switch are configured to transition the analyte monitoring device between the first operating configuration and the second operating configuration.

13 . The analyte monitoring device of claim 12 , wherein the first switch is positioned between the counter electrode and the reference electrode, and wherein the second switch is positioned at a reference electrode input.

14 . The analyte monitoring device of claim 10 , wherein the determination of the at least one microneedle inserted into the skin of the user comprises a determination that at least one of a first current and a second current satisfies a predetermined threshold,

the first current resulting from a first bias potential applied between the first working electrode and the combined reference electrode and counter electrode, and

the second current resulting from a second bias potential applied between the second working electrode and the combined reference electrode and the counter electrode.

15 . The analyte monitoring device of claim 14 , wherein, in the second operating configuration, an operational bias potential is applied to at least one of the first working electrode and the second working electrode.

16 . The analyte monitoring device of claim 15 , wherein the operational bias potential is greater than the first bias potential and the second bias potential.

17 . The analyte monitoring device of claim 10 , wherein the determination of the at least one microneedle inserted into the skin of the user comprises a determination that a first current satisfies a predetermined threshold, the first current resulting from a first bias potential applied between the first working electrode and the combined reference electrode and counter electrode, and

wherein, in the second operating configuration, an operational bias potential is applied to the second working electrode.

18 . The analyte monitoring device of claim 17 , wherein a third working electrode is positioned on a respective microneedle of the plurality of microneedles, and

wherein, in the second operating configuration, the operational bias potential is applied to the third working electrode.

19 . A method of operating an analyte monitoring device, the method comprising:

measuring a first current at a first working electrode, the first current resulting from a first bias potential applied between the first working electrode and a reference point;

measuring a second current at a second working electrode, the second current resulting from a second bias potential between the second working electrode and the reference point; and

responsive to a determination that at least one of the first current and the second current satisfies a predetermined threshold, transitioning the analyte monitoring device from a two-electrode electrochemical cell in which a reference electrode and a counter electrode are combined, the two-electrode electrochemical cell being configured to confirm insertion of at least one microneedle of the analyte monitoring device in skin of a user, to a three-electrode electrochemical cell in which the reference electrode and the counter electrode are independent of one another, the three-electrode electrochemical cell being configured to sense a level of an analyte in the skin of the user, wherein the three-electrode electrochemical cell comprises an operational mode during which an operational bias potential is applied,

wherein the analyte monitoring device comprises a microneedle array comprising a plurality of microneedles,

wherein the first working electrode, the second working electrode, the reference electrode, and the counter electrode are each positioned on a respective microneedle of the plurality of microneedles.

20 . The method of claim 19 , wherein the reference electrode and the counter electrode are combined at the reference point.

21 . The method of claim 20 , wherein the reference point is disconnected to form the three-electrode electrochemical cell in the operational mode.

22 . The method of claim 19 , wherein a first switch and a second switch are configured to transition the analyte monitoring device to the three-electrode electrochemical cell from the two-electrode electrochemical cell.

23 . The method of claim 19 , wherein in the operational mode, the operational bias potential is applied to at least one of the first working electrode and the second working electrode.

24 . The method of claim 19 , wherein the analyte monitoring device further comprises a second counter electrode, the second counter electrode positioned on a respective microneedle of the microneedle array, wherein the counter electrode and the second counter electrode are shorted together.

25 . The method of claim 19 , wherein the operational bias potential is greater than the first bias potential and the second bias potential.

26 . The method of claim 19 , wherein a third working electrode is positioned on a respective microneedle of the plurality of microneedles, and

wherein in the operational mode, the operational bias potential is applied to the third working electrode.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2025
From: ALONSO-SOSKI, DANIEL; CAMPBELL, ALAN STEVEN; TANGNEY, JARED RYLAN; FUCHS, JENNIFER RUTH WALTERS; WINDMILLER, JOSHUA RAY
To: BIOLINQ INCORPORATED
Reel/Frame 070988/0391 →
Continuity (3)
Continuation 18347522 · Jul 5, 2023
Provisional Application 63358459 · Jul 5, 2022
Related Publication 20240366125A1 · Nov 7, 2024
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