IP Library Granted Patent US 12685467
Granted Patent B2
US 12685467 · App. 18/740,853 · Granted Jul 21, 2026

Analyte sensor and method for manufacturing an analyte sensor

Inventors: Kirill Sliozberg (Mannheim, DE); Alexander Steck (Hirschberg, DE)
Assignee: Roche Diabetes Care, Inc.
A61B5/14865A61B2562/125
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Quick Facts
Patent No.
US 12685467
App. No.
18/740,853
Granted
Jul 21, 2026
Kind
B2
Abstract

The disclosure relates to an analyte sensor comprising a substrate, at least one working electrode, at least one second electrode and a membrane, wherein the membrane is located on top of the second electrode, and the second electrode has at least one first silver layer and at least one second silver layer which partially overlap with one another and have the same composition. The first and second silver layers intersect with one another to form a + or a T shape design. The sensor includes at least one exposed area of the first silver layer disposed on the exterior of the sensor to provide for direct contact with body fluid when implanted. The disclosure further relates to a process for manufacturing an analyte sensor.

Claims (35)

1 . An analyte sensor comprising

a substrate comprising a first side and a second side;

at least one working electrode positioned on the first side of the substrate, the at least one working electrode comprising at least one electrically conductive material;

at least one second electrode positioned on the second side of the substrate, the at least one second electrode comprising at least one first silver layer and at least one second silver layer, wherein the at least one second silver layer partially overlaps with the at least one first silver layer, wherein the at least one first and second silver layers comprise the same composition; and

a membrane comprising a polymer composition which comprises a hydrophobic polymer, wherein the membrane is located on top of the at least one second electrode,

wherein the analyte sensor comprises at least one exposed area of the at least one first silver layer, said at least one exposed area being disposed on an exterior of the analyte sensor and configured to be in direct contact with body fluid when the analyte sensor is implanted in a user.

2 . The analyte sensor according to claim 1 , wherein the at least one first silver layer intersects with the at least one second silver layer to form a + shape design.

3 . The analyte sensor according to claim 1 , wherein the at least one first silver layer intersects with the at least one second silver layer to form a T shape design.

4 . The analyte sensor according to claim 1 , wherein the at least one first silver layer intersects with the at least one second silver layer to form an X shape design.

5 . The analyte sensor according to claim 1 , wherein the analyte sensor is an implantable sensor.

6 . The analyte sensor according to claim 1 , wherein the at least one second electrode is selected from the group consisting of a counter electrode, a reference electrode and a combined counter/reference electrode.

7 . The analyte sensor according to claim 1 , wherein the first side and the second side of the substrate are positioned opposite each other.

8 . The analyte sensor according to claim 1 , wherein the at least one second electrode comprises Ag and/or AgCl.

9 . The analyte sensor according to claim 1 wherein each of the at least one first and second silver layers comprises in the range from 50 to 99 wt.-% of Ag, in the range from 0 to 30 wt.-% of AgCl and in the range from 1 to 20 wt.-% of a binder based on dry layer weight percentages of a total weight of the respective silver layer.

10 . The analyte sensor according to claim 1 wherein each of the at least one first and second silver layers comprises in the range from greater than 0 to less than 59 wt.-% of Ag, in the range from 40 to 99 wt.-% of AgCl, and in the range from 1 to 20 wt.-% of a binder based on dry layer weight percentages of a total weight of the respective silver layer.

11 . The analyte sensor according to claim 1 , wherein the at least one second electrode comprises AgCl having a load in the range from 20 μg to 150 μg.

12 . The analyte sensor according to claim 1 , wherein the analyte sensor comprises two of the exposed areas.

13 . The analyte sensor according to claim 1 , wherein the at least one second silver layer is disposed only on an interior of the analyte sensor and is not disposed on the exterior of the analyte sensor and is not configured to be in direct contact with body fluid when the analyte sensor is implanted in a user.

14 . An analyte sensor system comprising

the analyte sensor according to claim 1 ; and

an electronics unit, the electronics unit being configured to be electronically connected to the analyte sensor.

15 . A method for manufacturing an analyte sensor, the method comprising the steps:

a) providing a raw substrate which comprises a first side and a second side;

b) preparing a working electrode region on the first side of the raw substrate, the preparing of the working electrode region comprising the steps:

b1) applying an electrically conductive material to the first side of the raw substrate,

b2) applying a sensing material at least partially on the electrically conductive material;

c) preparing a second electrode region on the second side of the raw substrate, the preparing of the second electrode region comprising the steps:

c1) applying a first silver composition to form a first silver composition region which is essentially continuous on the second side of the raw substrate,

c2) applying a second silver composition as a plurality of separated second silver composition regions on the second side of the raw substrate, wherein the second silver composition has the same composition as the first silver composition and wherein the second silver composition is applied over the first silver composition such that the second silver composition regions partially overlap with the first silver composition region or the first silver composition is applied over the second silver composition so that the first silver composition region partially overlaps with the second silver composition regions;

d) applying a polymer composition on top of the second electrode region, to obtain a membrane, wherein the polymer composition comprises a hydrophobic polymer; and

e) cutting the raw substrate, the working electrode region, the second electrode region and the membrane, wherein only the first silver composition region of the second electrode region is cut such that the first silver composition region comprises at least one exposed area configured to be in direct contact with body fluid when the analyte sensor is implanted in a user.

16 . The method according to claim 15 , wherein in the regions in which the second silver composition partially overlaps with the first silver composition, the first silver composition region intersects with the second silver composition regions to form a + shape design at each intersection.

17 . The method according to claim 15 , wherein in the regions in which the second silver composition partially overlaps with the first silver composition, the first silver composition region intersects with the second silver composition regions to form a T shape design at each intersection.

18 . The method according to claim 15 , wherein in the regions in which the second silver composition partially overlaps with the first silver composition, the first silver composition region intersects with the second silver composition regions to form an X shape design at each intersection.

19 . The method according to any one of claims 15 to 18 , wherein the cutting in step e) comprises cutting such that a plurality of the exposed areas of the first silver composition region are formed.