Analyte sensor with extended range of detection

• US 9,649,056 B2
• Filed: 12/29/2012
• Issued: 05/16/2017
• Est. Priority Date: 12/29/2011
• Status: Active Grant

• Current Assignee: Optica, Inc.
• Original Assignee: Optica, Inc.
• Inventors: Rebec, Mihailo V.
• Primary Examiner(s): Winakur, Eric
• Assistant Examiner(s): Fardanesh, Marjan
• Application Number:
  US13/731,007
• Publication Number:
  US 20130172699A1
• Time in Patent Office: 1,599 Days
• CPC Class Codes: A61B 2560/0233 Optical standards
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence

Abstract

Embodiments provide sensors, such as implantable sensors, and methods of producing such sensors. An implantable sensor may include a base, one or more chambers, and one or more sensor reagents. A membrane may be coupled to the chambers over the sensor reagents. The implantable sensor may be at least partially implanted into the dermis of an animal. One or more of the sensor reagents may emit light or exhibit a color change in response to the presence of a target analyte or reaction product thereof. The response may be detected and analyzed by the user or by a reader device to determine the target analyte concentration.

Claims

1. An analyte sensor, comprising:

a base configured to be retained at least partially in a subject'"'"'s dermis, wherein the base is solid and impermeable, and having a thickness, an upper surface and an opposite lower surface, a first end, and an opposite second end, the base defining a first chamber disposed therein, the first chamber extending partially through the thickness of the base; and

a first and a second analysis region coupled to the base, the first analysis region comprising a first analyte reagent system and the second analysis region comprising a second analyte reagent system,

wherein the first and the second analysis regions have contiguous first and second detection ranges, respectively, for a target analyte, and substantially coextensive ranges of response, the first and second analysis regions configured to exhibit different responses within said coextensive ranges upon exposure to a given concentration of the target analyte and the first analyte reagent system disposed in the first chamber.

2. The analyte sensor of claim 1, further comprising one or more membranes coupled to the base, the one or more membranes being permeable to a target analyte.

3. The analyte sensor of claim 2, wherein the one or more membranes includes a first membrane portion and a second membrane portion, wherein the permeability of the first membrane portion to the target analyte is greater than the permeability of the second membrane portion to the target analyte.

4. The analyte sensor of claim 1, the base further defining a second chamber disposed therein, the second chamber extending partially through the thickness of the base, the second analyte reagent system disposed in the second chamber.

5. The analyte sensor of claim 1, the second analyte reagent system disposed in the first chamber.

6. The analyte sensor of claim 1, wherein the first and second analyte reagent systems are configured to exhibit corresponding first and second colors upon exposure to the given concentration of the analyte, said first and second colors being different colors.

7. The analyte sensor of claim 6, wherein at least one of the first and second colors is a color in the infrared range.

8. The analyte sensor of claim 1, wherein the first analyte reagent system and the second analyte reagent system have different chemical compositions.

9. The analyte sensor of claim 1, wherein the analyte sensor has a total thickness of 30-90 μ

m.

10. The analyte sensor of claim 1, wherein the analyte sensor has total thickness of 10 um-1 mm.

11. The analyte sensor of claim 1, wherein the analyte sensor has a total thickness of 50 μ

m or less.

12. The analyte sensor of claim 1, wherein the analyte sensor is configured to be retained in the dermis of a subject for at least one minute.

13. The analyte sensor of claim 1, wherein the analyte sensor is configured to be retained within the dermis of a subject for at least one month.

14. The analyte sensor of claim 1, wherein the base comprises a polymer material and TiO₂.

15. The analyte sensor of claim 14, wherein the polymer material comprises a polyimide.

16. The analyte sensor of claim 1, wherein each of the first and the second analyte reagent systems includes at least one detection reagent and at least one indicator.

17. The analyte sensor of claim 16, further including a plurality of beads coupled to the base, wherein one or more of the detection reagent and the indicator are immobilized on the beads.

18. The analyte sensor of claim 17, the base further defining a second chamber therein, wherein one or more reagents of the first reagent system are deposited onto a first group of the beads and one or more reagents of the second reagent system are deposited onto a second group of the beads, and the beads are positioned within at least one of the first and second chambers.

19. The analyte sensor of claim 18, wherein the first and second groups of beads are disposed within one of the first and second chambers.

20. The analyte sensor of claim 16, wherein the detection reagent is configured to interact with the target analyte to cause a change in pH, and the indicator includes a pH sensitive dye configured to produce a color change in response to the change in pH.

21. The analyte sensor of claim 16, wherein the indicator includes two or more of a lipophilic anion, a chromoionophore, and an ionophore, and the detection reagent includes an enzyme.

22. The analyte sensor of claim 13, wherein a first portion of the analyte sensor is configured to be retained within the dermis of a subject and a second portion of the analyte sensor is configured to be retained externally or within the epidermis of the subject.

23. The analyte sensor of claim 1, wherein the base comprises a reflective material.

24. The analyte sensor of claim 16, wherein the detection reagent comprises glucose oxidase.

25. The analyte sensor of claim 1, wherein the analyte sensor further comprises a first component coupled to at least the first and second analysis regions, the first component configured to provide a first gradient between the first and second analysis regions.

26. The analyte sensor of claim 25, wherein the first component is a membrane or gel layer and the first gradient is a permeability gradient resulting from variations in pore size, thickness, hydrophobicity, or reagent content of the first component.

27. The analyte sensor of claim 25, wherein the analyte sensor further comprises a second component coupled to at least the first and second analysis regions, the second component configured to provide a second gradient that extends transverse to the first gradient.

28. The analyte sensor of claim 27, wherein the second component is a membrane or gel layer and the second gradient is a result of variations in pore size, thickness, hydrophobicity, or reagent content of the second component.

29. The analyte sensor of claim 27, wherein the analyte sensor has a second permeability gradient that extends transverse to the first permeability gradient, the second permeability gradient formed by variations in reagent content or buffering systems among the first and second analyte reagent systems.

30. The analyte sensor of claim 1, the analyte sensor further comprising a third analysis region, the first, second, and third analysis regions having substantially coextensive ranges of response.

31. The analyte sensor of claim 30, wherein the third analysis region has a third detection range that overlaps the second detection range, the third analysis region configured to detect the target analyte.

32. The analyte sensor of claim 30, wherein the third analysis region is configured to detect a second analyte.