Sliver type autonomous biosensors

• US 20040180391A1
• Filed: 10/10/2003
• Published: 09/16/2004
• Est. Priority Date: 10/11/2002
• Status: Abandoned Application

• Current Assignee: Case Western Reserve University
• Original Assignee: Case Western Reserve University
• Inventors: Yang, Jian, Rozakis, George, Gratzl, Miklos, Tohda, Koji
• Application Number:
  US10/683,315
• Publication Number:
  US 20040180391A1
• Time in Patent Office: Days
• US Class Current: 435/14
• CPC Class Codes: A61B 5/14528 invasively
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14539 for measuring pH
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61B 5/14865 invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors
• CPC Class Codes: A61B 5/686 Permanently implanted devices, e.g. pacemakers, other stimulators, biochips A61B5/6861 takes precedence
• CPC Class Codes: C12Q 1/001 Enzyme electrodes

Abstract

In vivo or in vitro monitoring of chemical and biochemical species (e.g., pH, or glucose levels) in the interstitial fluid of patients or in a sample of a fluid to be analyzed is provided by a probe (10, 70, 210, 270). For in vivo monitoring, the probe is readily inserted by a minimally invasive method. Optical or electrochemical sensing methods are employed to detect a physical or chemical change, such as pH, color, electrical potential, electric current, or the like, which is indicative of the concentration of the species or chemical property to be detected. Visual observation by the patient may be sufficient to monitor certain biochemicals (e.g., glucose) with this approach. A CAP membrane allows high enzyme loadings, and thus enables use of microminiature probes, and/or diagnosis of low levels of the analyte(s), with sufficient signal-to-noise ratio and low background current.

Claims

1. A sensor probe for detection of an analyte in solution the probe comprising:

a sensing element which exhibits a detectable change in response to the analyte, the sensing element including;

an immobilized optical sensing system comprising;

an enzyme capable of catalyzing a reaction of the analyte to form a reaction product,

an ionophore which extracts an ion from the reaction product, and

a chromoionophore sensitive to the ion which exhibits a detectable color change in response to the ion.

2. The sensor probe of claim 1, wherein the analyte is selected from the group consisting of glucose, lactate, oxygen, galactose, urea, creatinin, pH, K⁺, and Na⁺.

3. The sensor probe of claim 2, wherein the analyte includes glucose and the enzyme includes at least one of glucose oxidase and glucose dehydrogenase.

4. The sensor probe of claim 1, wherein the chromoionophore is a hydrogen ion selective chromoionophore.

5. The sensor probe of claim 4, wherein the chromoionophore is selected from the group consisting of:

chromoionophore I (9-(diethylamino)-5-(octadecanoylimino)-5H-benzo[a]phenoxazine);

chromoionophore II (9-dimethylamino-5-[4-(16-butyl-2,14-dioxo-3,15 ioxaeicosyl)phenylimino]benzo[a]phenoxazine);

chromionophore III, (9-(diethylamino)-5-[(2-octyldecyl)imino]benzo[a]phenoxazine;

chromoionophore IV (5-octadecanoyloxy-2-(4-nitrophenylazo)phenol);

chromoionophore V (9-(diethylamino)-5-(2-naphthoylimino)-5H-benzo[a]phenoxazine);

chromoionophore VI (4′

,5′

-dibromofluorescein octadecyl ester);

chromoionophore XI (fluorescein octadecyl ester; and

combinations thereof.

6. The sensor probe of claim 5, werein the chromoionophore includes (9-(dimethylamino)-5-[(2-octadecyl)imino]benzo[a]phenoxazine.

7. The sensor probe of claim 1, wherein the ionophore is selected from the group consisting of:

a) sodium ionophores, selected from the group consisting of;

bis [(12-crown-4)methyl]2-dodecyl-2-methylmalonate;

N,N′

, N″

-triheptyl-N,N′

,N″

-trimethyl-4,4′

4″

-propylidynetris(3-oxabutyramide);

N,N′

-dibenzyl-N,N′

-diphenyl-1,2-phenylenedioxydiacetamide;

N,N,N′

,N′

-tetracyclohexyl-1,2-phenylenedioxydiacetamide;

4-octadecanoyloxymethyl-N,N,N′

,N′

-tetracyclohexyl-1,2-phenylenedioxydiacetamide);

2,3;

11,12-didecalino-16-crown-5), bis(benzo-15-crown-5);

b) potassium ionophores selected from the group consisting of;

bis[(benzo-15-crown-5)-4′

-methyl]pimelate;

2-dodecyl-2-methyl-1,3-propanedil bis[N-{5′

-nitro(benzo-15-crown-5)-4′

-yl]carbamate];

c) calcium ionophores selected from the group consisting of;

(−

)-(R,R)-N,N′

-bis-[11-(ethoxycarbonyl)undecyl]-N,N′

-4,5-tetramethyl-3,6-dioxaoctane-diamide;

N,N,N′

,N′

-tetracyclohexyl-3-oxapentanediamide;

N,N-dicyclohexyl-N′

,N′

-dioctadecyl-3-oxapentanediamide);

10,19-bis[(octadecylcarbamoyl)methoxyacetyl]-1,4,7,13,16-pentaoxa-10,19-diazacycloheneicosane);

and combinations thereof.

8. The sensor probe of claim 1, wherein the sensing element further includes a lipophilic anion.

9. The sensor probe of claim 8, wherein the lipophilic anion is selected from the group consisting of:

potassium tetrakis(4-chlorophenyl)borate;

sodium tetrakis [3,5-bis(1,1,3,3,3-hexafluoro-2-methoxy-2-propyl)phenyl]borate;

sodium tetrakis [3,5-bis(trifluoromethyl)phenyl]borate;

sodium tetrakis(4-fluorophenyl)borate; and

combinations thereof.

10. The sensor probe of claim 1, wherein the probe includes at least two sensing elements for sensing at least two of the group consisting of glucose, lactate, oxygen, galactose, urea, creatinin, pH, K⁺, and Na⁺.

11. The sensor probe of claim 1, further including at least one reference element which does not exhibit a color change in response to the analyte.

12. The sensor probe of claim 1, wherein the enzyme is immobilized on a polymeric material, the polymeric material including at least one of cellulose acetate, cellulose acetate phthalate, and bovine albumin/glutaraldehyde.

13. The sensor probe of claim 12, wherein the polymeric material includes cellulose acetate phthalate.

14. The sensor probe of claim 12, wherein the ionophore and chromoionophore are immobilized on a second polymeric material.

15. The sensor probe of claim 1, wherein the sensor probe includes a membrane having a multilayer structure.

16. The sensor probe of claim 15, wherein at least one layer of the membrane is a negatively charged membrane which reduces efflux of gluconic acid from the sensor probe, thereby improving glucose sensitivity.

17. The sensor probe of claim 15, wherein at least one layer of the membrane includes at least one of an anti-infection agent and an antihistamine.

18. The sensor probe of claim 15, wherein at least one layer of the membrane includes further including a biocompatible material.

19. The sensor probe of claim 18, wherein at least one layer includes one or more of heparin and chitosan.

20. The sensor probe of claim 15, wherein the biocompatible membrane includes polyurethane.

21. The sensor probe of claim 1, wherein the sensing element comprises a capsule, the immobilized optical sensing system being contained within the capsule.

22. The sensor probe of claim 1, wherein the optical sensing system is immobilized on beads.

23. The sensor probe of claim 22, wherein the enzyme is immobilized on a first set of the beads and the ionophore and chromoionophore are immobilized on a second set of the beads.

24. The sensor probe of claim 22, wherein the beads are formed from at least one of at least one of cellulose acetate (CA), cellulose acetate phthalate (CAP), poly(vinyl chloride), and octadecyl silica gel (ODS silica gel).

25. The sensor probe of claim 22, wherein the beads have an average diameter of less than 10 micrometers.

26. The sensor probe of claim 21, wherein a negatively charged hydrophilic gel is disposed in the capsule.

27. The sensor probe of claim 26, wherein the negatively charged hydrophilic gel is selected from the group consisting of polyvinyl sulfate and polystyrenesulfonate.

28. The sensor probe of claim 1, wherein the optical sensing system provides a maximum color change at a pH of about 5.0 to 7.5.

29. The sensor probe of claim 1, further comprising:

a plurality of sensing elements, each of the sensing elements providing a maximum color change at a pH which differs from other sensing elements.

30. A sensing system comprising the sensor probe of claim 1 and a detector for detecting the color change.

31. The sensing system of claim 31, wherein the detector is capable of detecting a color change of the optical sensing element when the sensor probe is in the skin of a subject, and the detector is external to the skin.

32. The sensing system of claim 31, wherein the detector includes at least one of a watch or pager-type color CCD camera and a spectrometer.

33. A sensor probe comprising:

a plurality of sensing elements capable of simultaneous detection of analytes in a fluid, including;

a first sensing element which detects a first analyte selected from the group consisting of glucose, lactate, oxygen, galactose, urea, creatinin, pH, K⁺, and Na⁺;

a second sensing element which detects a second analyte different from the first analyte, selected from the group consisting of glucose, lactate, oxygen, galactose, urea, creatinin, pH, K⁺, and Na⁺.

34. The sensor probe of claim 33, further including a reference element for providing a reference color for comparison with a color change of at least one of the first and second sensing elements.

35. The sensor probe of claim 33, wherein the sensing elements each include a capsule, each capsule including a support material on which a system responsive to the analyte is immobilized.

36. The sensor probe of claim 33, wherein the first sensing element includes an enzyme which is specific for the first analyte, the enzyme catalyzing a reaction of the analyte to produce a detectable product.

37. The sensor probe of claim 36, wherein the enzyme is immobilized on a support material which includes cellulose acetate phthalate.

38. The sensor probe of claim 37, wherein the support material includes beads.

39. The sensor probe of claim 36, wherein the first sensing element further includes a dye system which exhibits a color change in response to the detectable product.

40. The sensor probe of claim 39, wherein the color change is reversible in response to a decrease in the analyte concentration.

41. The sensor probe of claim 39, wherein the dye system includes one or more of the group consisting of:

congo red, neutral red, phenol red, methyl red, lacmoid, tetrabromophenolphthalein, α

-naphtholphenol, 2-nitrophenyl octyl ether, dibenzyl ether, dioctyl phthalate, and chromoionophores.

42. The sensor probe of claim 41, wherein the dye includes a chromoionophore and the dye system further includes at least one of a lipophilic anion and an ionophore.

43. The sensor probe of claim 41, wherein the enzyme is carried by a first support material and the dye is carried by a second support material.

44. The sensor probe of claim 43, wherein the first support material includes at least one of cellulose acetate and cellulose acetate phthalate.

45. The sensor probe of claim 33, further including at least one additional sensing element, the at least one additional sensing element being selected from the group consisting of:

a sensing element which includes a reference material which does not exhibit a color change in response to the presence of the analyte;

a sensing element which includes an inactive enzyme;

a sensing element which includes a second enzyme which is specific for the analyte;

a sensing element which includes a third enzyme which is specific for a second analyte; and

a sensing element which includes a material which changes color in response to a concentration of the analyte which is higher than the concentration of the analyte for the first sensing element.

46. The sensor probe of claim 33, the first sensing element further including a metal electrode which responds to a concentration of the analyte.

47. The sensor probe of claim 46, further including an inductive coupling mechanism for supplying power to the sensor probe.

48. A sensor probe for detection of an analyte in solution the probe comprising:

a sensing element which exhibits a detectable change in response to the analyte, the sensing element including;

an immobilized optical sensing system comprising;

an enzyme capable of catalyzing a reaction of the analyte to from a reaction product, the enzyme being immobilized on a first support material which includes cellulose acetate phthalate; and

a dye system which exhibits a color change in response to the reaction product, the dye being supported on a second support material.

49. The sensor probe of claim 48, wherein the first support material and enzyme form a first layer and the second support material and dye system form a second layer.

50. The sensor probe of claim 49, wherein the first and second support materials comprise beads.

51. The sensor probe of claim 49, wherein the sensing element includes a capsule.

52. The sensor probe of claim 48, wherein the dye system includes:

an ionophore which extracts an ion from the reaction product, and

a chromoionophore sensitive to the ion which exhibits a detectable color change in response to the ion.

53. A method of forming a sensing element comprising:

immobilizing an enzyme on a first support material; and

immobilizing a dye system on a second support material.

54. The method of claim 53, wherein the step of immobilizing the enzyme includes:

contacting a first set of polymer beads with a mixture which includes the enzyme and a solvent.

55. The method of claim 53, further including:

contacting a second set of polymer beads with a mixture which includes the dye system.

56. The method of claim 54, further including:

forming the polymer beads, including;

spraying droplets of a solution of the polymer in a solvent into a gaseous flow, the solvent evaporating from the droplets in the gaseous flow to form the polymer beads; and

collecting the polymer beads in a vessel positioned to intercept the gaseous flow carrying the beads.

57. The method of claim 53, wherein the dye system exhibits a reversible color change.

58. A method of detecting an analyte in a fluid comprising:

positioning a sensor probe in the fluid, the sensor probe including;

a sensing element which exhibits a detectable change in response to the analyte, the sensing element including;

an immobilized optical sensing system comprising;

an enzyme capable of catalyzing a reaction of the analyte to from a reaction product,

an ionophore which extracts an ion from the reaction product, and

a chromoionophore sensitive to the ion which exhibits a detectable color change in response to the ion; and

detecting the color change with a detection system.

59. The method of claim 58, further including:

implanting the sensor probe into a person'"'"'s eye.

60. The method of claim 58, further including:

mounting the sensor on a contact lens.

61. The method of claim 58, further including:

mounting the detection system to the person'"'"'s glasses.

62. The method of claim 58, further including:

simultaneously detecting multiple analytes continuously and simultaneously.

63. The method of claim 58, wherein the step of detecting the color change includes:

comparing a shape of a spectrum of the color received by the detector with at least one calibration spectrum.