Novel luminescent metal chelates and methods for their detection

• US 20040161737A1
• Filed: 02/14/2003
• Published: 08/19/2004
• Est. Priority Date: 02/14/2003
• Status: Abandoned Application

• Current Assignee: Agilent Technologies, Inc.
• Original Assignee: Agilent Technologies, Inc.
• Inventors: Yang, Dan-Hui D., Mauze, Ganapati R.
• Application Number:
  US10/366,885
• Publication Number:
  US 20040161737A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: C07F 15/0026 without a metal-carbon linkage
• CPC Class Codes: C07F 15/0053 without a metal-carbon linkage

Abstract

The invention provides electrochemiluminescent metal chelates and methods for using these chelates in chemical and biological assays, particularly immunoassays and microarray assays.

Claims

1. A chemical compound having one of the following formulas:

MLP₂(B_u), ML₂P(B_u)

where M is selected from the group consisting of ruthenium and osmium, P is a polydentate ligand of M selected from the group consisting of substituted bipyridines, non-substituted bipyridines, substituted phenathrolines, non-substituted phenanthrolines, and any combinations thereof, and L is a ligand of M wherein L is selected from the following;

2. A chemical compound having the formula:

ML₃(B_u)

where M is selected from the group consisting of ruthenium and osmium and L is a polydentate ligand of M wherein L is selected from the following;

3. A method of detecting the presence of a substance of interest in a sample, comprising the steps of:

a) contacting the sample and a chemical compound, the chemical compound having one of the following formulas;

MLP₂(B_u), ML₂P(B_u)

where M is selected from the group consisting of ruthenium and osmium, P is a polydentate ligand of M selected from the group consisting of substituted bipyridines, non-substituted bipyridines, substituted phenathrolines, non-substituted phenanthrolines, and any combinations thereof, and L is a ligand of M wherein L is selected from the following;

wherein R₁, R₂, R₃, R₄ and R₅ could be H, alkyl, aryl, with any alkyl and aryl group having substituents selected from the moieties consisting of amino (NH₂), thiol (SH), and carboxyl (COOH) groups, either individually or any combination thereof, including multiple or no substituents of each group, for binding with chemicals and biomolecules of interest; and

X is carbon or nitrogen and B_u is a substance that is attached the complex through P, L, or both;

b) inducing the chemical compound to electrochemiluminesce by exposing the chemical compound to electrochemical energy; and

c) detecting emitted electrochemiluminescence and thereby detecting the substance of interest.

4. The method of claim 3 further comprising the addition of one or more additional chemical compounds.

5. The method of claim 3 further comprising the step of selecting B_u from the group consisting of whole cells, viruses, subcellular particles, receptors, proteins, antibodies, lipoproteins, glycoproteins, peptides, nucleic acids, polysaccharides, lipopolysaccharides, lipids, fatty acids, cellular metabolites, hormones, pharmacological agents, tranquilizers, barbiturates, alkaloids, steroids, vitamins, amino acids, sugars, mimics of these substances, fragments of these substances, combinations of these substances, combinations of fragments of these substances, and combinations containing these substances and fragments thereof.

6. The method of claim 3 further comprising the step of detecting the presence of a substance of interest and B_u is a compound capable of specifically binding to said substance of interest or B_u can compete with said substance of interest in a specific binding assay.

7. The method of claim 3, wherein B_u is a compound of biological origin or a compound having biological activity.

8. The method of claim 3, wherein B_u is an antibody or fragment thereof.

9. The method of claim 3, wherein B_u is a receptor or fragment thereof.

10. The method claim 3, wherein B_u is a nucleic acid.

11. The method of claim 3, wherein B_u is a substance that can specifically bind with another substance.

12. The method of claim 3, wherein B_u is attached to the complex via covalent bonds.

13. The method of claim 3 further comprising the step of binding B_u to the metal-containing compound prior to conducting an assay.

14. The method of claim 3 further comprising the step of binding B_u to the metal-containing compound during the process of conducting an assay.

15. The method of claim 3 further comprising the step of performing the assay in solution.

16. The method of claim 3 further comprising the step of binding the substance of interest to a surface.

17. The method of claim 16 further comprising the step of including the surface in a microarray assay system.

18. A method of detecting the presence of a substance of interest in a sample, comprising the steps of:

a) contacting the sample and a chemical compound, the chemical compound having the formula;

ML₃(B_u)

where M is selected from the group consisting of ruthenium and osmium and L is a polydentate ligand of M wherein L is selected from the following;

wherein R₁, R₂, R₃, R₄ and R₅ could be H, alkyl, aryl, with any alkyl and aryl group having substituents selected from the moieties consisting of amino (NH₂), thiol (SH), and carboxyl (COOH) groups, either individually or any combination thereof, including multiple substituents of each group wherein at least one of said substituents is present;

for binding with chemicals and biomolecules of interest;

X is selected from the group consisting of carbon and nitrogen; and

B_u is a substance that is attached to the complex through L;

b) inducing the chemical compound to electrochemiluminesce by exposing the chemical compound to electrochemical energy; and

c) detecting emitted electrochemiluminescence and thereby detecting the substance of interest.

19. The method of claim 18 further comprising the step of adding one or more additional chemical compounds.

20. The method of claim 18 further comprising the step of selecting B_u from the group consisting of whole cells, viruses, subcellular particles, receptors, proteins, antibodies, lipoproteins, glycoproteins, peptides, nucleic acids, polysaccharides, lipopolysaccharides, lipids, fatty acids, cellular metabolites, hormones, pharmacological agents, tranquilizers, barbiturates, alkaloids, steroids, vitamins, amino acids, sugars, mimics of these substances, fragments of these substances, combinations of these substances, combinations of fragments of these substances, and combinations containing these substances and fragments thereof.

21. The method of claim 18 further comprising the step of detecting the presence of a substance of interest and B_u is a compound capable of specifically binding to said substance of interest or B_u can compete with said substance of interest in a specific binding assay.

22. The method of claim 18, wherein B_u is a compound of biological origin or a compound having biological activity.

23. The method of claim 18, wherein B_u is an antibody or fragment thereof.

24. The method of claim 18, wherein B_u is a receptor or fragment thereof.

25. The method claim 18, wherein B_u is a nucleic acid.

26. The method of claim 18, wherein B_u is a substance that can specifically bind with another substance.

27. The method of claim 18, wherein B_u is attached to the complex via covalent bonds.

28. The method of claim 18 further comprising the step of binding B_u to the metal-containing compound prior to conducting an assay.

29. The method of claim 18 further comprising the step of binding B_u to the metal-containing compound during the process of conducting an assay.

30. The method of claim 18 further comprising the step of performing the assay in solution.

31. The method of claim 18 further comprising the step of binding the substance of interest to a surface.

32. The method of claim 31 further comprising the step of including the surface in a microarray assay system.