Transition metal complexes with bidentate ligand having an imidazole ring

• US 8,168,052 B2
• Filed: 07/26/2010
• Issued: 05/01/2012
• Est. Priority Date: 11/15/1999
• Status: Expired due to Fees

• Current Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Mao, Fei, Heller, Adam
• Primary Examiner(s): Olsen, Kaj K
• Application Number:
  US12/843,607
• Publication Number:
  US 20100288634A1
• Time in Patent Office: 645 Days
• Field of Search: 204/403.1, 204/403.04, 204/403.14, 526/161, 546/2, 548/101
• US Class Current: 204/403.14
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1477 non-invasive
• CPC Class Codes: A61B 5/1486 using enzyme electrodes, e.g. with immobilised oxidase
• CPC Class Codes: C07F 15/0026 without a metal-carbon linkage
• CPC Class Codes: C07F 15/0053 without a metal-carbon linkage
• CPC Class Codes: C07F 15/025 without a metal-carbon linkage
• CPC Class Codes: C07F 15/065 without a metal-carbon linkage
• CPC Class Codes: C07F 9/005 Compounds of elements of Group 5 of the Periodic Table without metal-carbon linkages
• CPC Class Codes: C08F 8/42 Introducing metal atoms or metal-containing groups
• CPC Class Codes: C08F 8/44 Preparation of metal salts or ammonium salts
• CPC Class Codes: C09B 57/10 Metal complexes of organic compounds not being dyes in uncomplexed form
• CPC Class Codes: C12Q 1/004 mediator-assisted

Abstract

Novel transition metal complexes of iron, cobalt, ruthenium, osmium, and vanadium are described. The transition metal complexes can be used as redox mediators in enzyme based electrochemical sensors. In such instances, transition metal complexes accept electrons from, or transfer electrons to, enzymes at a high rate and also exchange electrons rapidly with the sensor. The transition metal complexes include at least one substituted or unsubstituted biimidazole ligand and may further include a second substituted or unsubstituted biimidazole ligand or a substituted or unsubstituted bipyridine or pyridylimidazole ligand. Transition metal complexes attached to polymeric backbones are also described.

Claims

1. A complex comprising:

a polymer;

at least one spacer covalently bonded to the polymer;

an analyte-responsive enzyme; and

a mediator chemically bonded to the at least one spacer,

wherein the mediator is a transition metal complex having the formula;

2. The complex of claim 1, wherein the at least one spacer comprises at least one non-cyclic functional group selected from the group consisting of —

(CR^rR^s)—

, —

O—

, —

S—

, —

C(O)O—

, —

S(O)₂NR^k—

, —

OC(O)NR^m—

, —

OC(S)NRⁿ, —

C(O)NR^t—

, —

NR^u—

, —

CR^v═

N—

O—

, —

CR^w═

NNR^x—

, and —

(SiR^yR^z)—

, and wherein R^r and R^s are independently hydrogen, chlorine, fluorine, or substituted or unsubstituted alkyl, alkoxy, alkenyl, or alkynyl, and R^k, R^m, Rⁿ, R^t, R^u, R^v, R^w, R^x, R^y, and R^z are independently hydrogen or substituted or unsubstituted alkyl.

3. The complex of claim 1, wherein the mediator forms one or more of carbon-carbon, carbon-nitrogen, carbon-silicon, carbon-oxygen, carbon-sulfur, sulfur-nitrogen, silicon-oxygen or metal-carbon covalent bonds with the spacer.

4. The complex of claim 3, wherein the spacer and the mediator forms one or more covalent linkages selected from the group consisting of amide, thioether, hydrazone, oxime, alkylamine, ester, imidazolium, pyridinium, ether, aminotriazine, triazinyl ether, urea, urethane, thiourea and sulfonamide.

5. The complex of claim 1, wherein the spacer is covalently bonded to one or more ligands of the mediator.

6. The complex of claim 5, wherein the one or more ligands comprises a substituted or unsubstituted heterocyclic nitrogen-containing moiety.

7. The complex of claim 1, wherein the metal of the mediator is osmium.

8. The complex of claim 1, wherein the polymer is crosslinked.

9. The complex of claim 8, wherein the polymer comprises one or more crosslinking agents, wherein the one or more crosslinking agents comprise at least one bifunctional, trifunctional or tetrafunctional crosslinking agent.

10. The complex of claim 9, wherein the one or more crosslinking agents comprises a pyridine-reactive or imidazole-reactive crosslinking agent.

11. The complex of claim 1, wherein the analyte-responsive enzyme is a glucose-responsive enzyme.

12. The complex of claim 11, wherein the analyte-responsive enzyme is glucose dehydrogenase (GDH) or glucose oxidase (GOx).

13. The complex of claim 1, wherein at least one ligand of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands is covalently bonded to the at least one spacer.

14. The complex of claim 1, wherein each heterocycle comprises a nitrogen-containing heterocycle that is coordinatively bound to M via a nitrogen atom of the heterocycle.

15. The complex of claim 14, wherein the nitrogen-containing heterocycle comprises a substituted or unsubstituted pyridine, a substituted or unsubstituted imidazole, a substituted or unsubstituted 2,2′

-bipyridine, a substituted or unsubstituted 2-(2-pyridyl)imidazole, or a substituted or unsubstituted 2,2′

-biimidazole.

16. The complex of claim 1, wherein at least two ligands of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands are combined to form at least one multidentate ligand.

17. The complex of claim 1, wherein at least four ligands of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands are combined to form at least two multidentate ligands.

18. The complex of claim 17, wherein the each of the at least two multidentate ligands is independently selected from substituted or unsubstituted 2,2′

-bipyridine, substituted or unsubstituted 2-(2-pyridyl)imidazole, or substituted or unsubstituted 2,2′

-biimidazole.

19. The complex of claim 1, wherein the complex has a molecular weight of at least 5000 daltons.

20. An electrochemical sensor comprising:

a working electrode and a counter electrode, wherein the working electrode comprises;

a polymer;

at least one spacer covalently bonded to the polymer;

an analyte-responsive enzyme; and

a mediator chemically bonded to the at least one spacer,

wherein the mediator is a transition metal complex having the formula;

21. The electrochemical sensor of claim 20, wherein the at least one spacer comprises at least one non-cyclic functional group selected from the group consisting of —

(CR^rR^s)—

, —

O—

, —

S—

, —

C(O)O—

, —

S(O)₂NR^k—

, —

OC(O)NR^m—

, —

OC(S)NRⁿ, —

C(O)NR^t—

, —

NR^u—

, —

CR^v═

N—

O—

, —

CR^w═

NNR^x—

, and —

(SiR^yR^z)—

, and wherein R^r and R^s are independently hydrogen, chlorine, fluorine, or substituted or unsubstituted alkyl, alkoxy, alkenyl, or alkynyl, and R^k, R^m, Rⁿ, R^t, R^u, R^v, R^w, R^x, R^y, and R^z are independently hydrogen or substituted or unsubstituted alkyl.

22. The electrochemical sensor of claim 20, wherein the mediator forms one or more of carbon-carbon, carbon-nitrogen, carbon-silicon, carbon-oxygen, carbon-sulfur, sulfur-nitrogen, silicon-oxygen or metal-carbon covalent bonds with the spacer.

23. The electrochemical sensor of claim 22, wherein the mediator forms one or more covalent linkages selected from the group consisting of amide, thioether, hydrazone, oxime, alkylamine, ester, imidazolium, pyridinium, ether, aminotriazine, triazinyl ether, urea, urethane, thiourea and sulfonamide.

24. The electrochemical sensor of claim 20, wherein the spacer is covalently bonded to one or more ligands of the mediator.

25. The electrochemical sensor of claim 24, wherein the one or more ligands comprises a substituted or unsubstituted heterocyclic nitrogen-containing moiety.

26. The electrochemical sensor of claim 20, wherein the metal of the mediator is osmium.

27. The electrochemical sensor of claim 20, wherein the polymer is crosslinked.

28. The electrochemical sensor of claim 27, wherein the polymer comprises one or more crosslinking agents, wherein the one or more crosslinking agents comprise at least one bifunctional, trifunctional or tetrafunctional crosslinking agent.

29. The electrochemical sensor of claim 28, wherein the one or more crosslinking agents comprises a pyridine-reactive or imidazole-reactive crosslinking agent.

30. The electrochemical sensor of claim 20, wherein the analyte-responsive enzyme is a glucose-responsive enzyme.

31. The electrochemical sensor of claim 30, wherein the analyte-responsive enzyme is glucose dehydrogenase (GDH) or glucose oxidase (GOx).

32. The electrochemical sensor of claim 20, wherein at least one ligand of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands is covalently bonded to the at least one spacer.

33. The electrochemical sensor of claim 20, wherein each heterocycle comprises a nitrogen-containing heterocycle that is coordinatively bound to M via a nitrogen atom of the heterocycle.

34. The electrochemical sensor of claim 33, wherein the nitrogen-containing heterocycle comprises a substituted or unsubstituted pyridine, a substituted or unsubstituted imidazole, a substituted or unsubstituted 2,2′

-bipyridine, a substituted or unsubstituted 2-(2-pyridyl)imidazole, or a substituted or unsubstituted 2,2′

-biimidazole.

35. The electrochemical sensor of claim 20, wherein at least two ligands of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands are combined to form at least one multidentate ligand.

36. The electrochemical sensor of claim 20, wherein at least four ligands of the L¹, L², L³, L⁴, L⁵, and L⁶ ligands are combined to form at least two multidentate ligands.

37. The electrochemical sensor of claim 36, wherein the each of the at least two multidentate ligands is independently selected from substituted or unsubstituted 2,2′

-bipyridine, substituted or unsubstituted 2-(2-pyridyl)imidazole, or substituted or unsubstituted 2,2′

-biimidazole.

38. The electrochemical sensor of claim 20, wherein the polymer is chemically bonded to the surface of the working electrode.

39. The electrochemical sensor of claim 20, wherein the polymer forms a sensing layer membrane on the surface of the working electrode.

40. The electrochemical sensor of claim 39, wherein the sensing layer membrane is crosslinked on top of the working electrode.

41. The electrochemical sensor of claim 40, wherein the sensing layer membrane is formed in situ on the working electrode by crosslinking the polymer on the working electrode.