Prolonged enhanced chemiluminescence

• US 4,950,588 A
• Filed: 09/27/1988
• Issued: 08/21/1990
• Est. Priority Date: 07/10/1985
• Status: Expired due to Fees

• Current Assignee: Miles, Inc. (Bayer AG)
• Original Assignee: Molecular Diagnostics, Inc. (Medite Cancer Diagnostics, Inc.)
• Inventors: Dattagupta, Nanibhushan
• Primary Examiner(s): Spiegel, Jack
• Application Number:
  US07/250,985
• Time in Patent Office: 693 Days
• Field of Search: 435/6, 435/7, 435/28, 435/810, 436/561, 436/518, 436/544, 436/800, 436/805, 436/905
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: G01N 33/533 with fluorescent label
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

A chemiluminescence process comprising the contacting of a chemiluminescence precursor, an oxidant, an enzyme, a chemiluminescence enhancer and a nitrogen compound selected from the group consisting of ammonia and water-soluble organic amines. The reaction of such process can be used in detection of nucleic acid hybrids, antibodies, antigens and peroxidase enzymes and in producing light.

Claims

1. In a chemiluminescence process comprising the contacting of a chemiluminescence precursor, an oxidant, an enzyme, and a chemiluminescence enhancer, the improvement comprising conducting the process in the presence of a nitrogen compound selected from the group consisting of ammonia, an aromatic heterocyclic compound and a water-soluble organic amine.

2. A chemiluminescence process according to claim 1, wherein said water-soluble organic amine is selected from the group consisting of alkyl amines, polyamines, aryl amines and benzyl amines.

3. A chemiluminescence process according to claim 2, wherein said polyamines are selected from the group consisting of spermine, spermidine, putrescine, butylene-diamine.

4. A chemiluminescence process according to claim 2, wherein said alkyl amines are of the formula ##STR18## wherein X₁, X₂, X₃ are the same or different and are unsubstituted or substituted aliphatic saturated hydrocarbon radicals having 1 to 8 carbon atoms.

5. A chemiluminescence process according to claim 1, wherein said nitrogen compound is ammonia.

6. A chemiluminescence process according to claim 1, wherein said aromatic heterocyclic compound is selected from the group consisting of pyridine, azoles and thiazines.

7. A chemiluminescence process according to claim 6, wherein said azole is imidazole.

8. A chemiluminescence process according to claim 6, wherein said thiazines are selected from the group consisting of thionine and methylene blue.

9. A chemiluminescence process according to claim 1, wherein the chemiluminescense precursor is an 2,3-dihydro-1,4-phthalazinedione of the general formula ##STR19## wherein R₁ is amino and each of R₂, R₃ and R₄ is H₂ unsubstituted or substituted C₁ -C₆ -alkyl or alkenyl, hydroxyl, C₁ -C₆ -alkoxy, carboxyl or amino or R₂ is amino and each of R₁, R₃ and R₄ is H, unsubstituted or substituted C₁ -C₆ -alkyl or alkenyl, hydroxyl, C₁ -C₆ -alkoxy, carboxyl,or amino or R₁ and R₂ are together and are an amino or substituted amino derivative of a benzo-group, and each of R₃ and R₄ is H, unsubstituted or substituted C₁ -C₆ -alkyl or alkenyl, hydroxyl, C₁ -C₆ -alkoxy, carboxyl or amino.

10. A chemiluminescence process according to claim 1, wherein said chemiluminescence precursor is selected from the group consisting of luminol and isoluminol.

11. A chemiluminescence process according to claim 1, wherein the oxidant is hydrogen peroxide.

12. A chemiluminescence process probe according to claim 1, wherein said enzyme is selected from the group consisting of horseradish peroxidase, microperoxidase and lactoperoxidase.

13. A chemiluminescence process according to claim 1, wherein said enhancer is selected from the group consisting of 4-chlorophenol, 4-bromophenol, 4-iodophenol, 4-bromo-2-chlorophenol, 2,4-dichlorophenol, 3,4-dichlorophenol, 4-methylphenol, 4-tert. butylphenol, ethyl 3-(4-hydroxyphenyl)propionate, 4-benzylphenol, 4-(3'"'"'-methylcrotyl)phenol, 4-styrylphenol, 4-(2'"'"'4'"'"'-dinitrostyryl)phenol, 4-hydroxylcinnamic acid, alpha-cyano-4-hydroxycinnamic acid, 4-phenylphenol, 4-(4'"'"'-hydroxyphenyl) phenol, 2-chloro-4-phenylphenol, 4-(4'"'"'-hydroxyphenyl)benzophenone, 4-(phenylazo)phenol, 4-(2'"'"'-carboxylphenylazo) phenol, 4-phenoxyphenol, 4-(4'"'"'-hydroxyphenoxy)phenol, 4-hydroxyphenyl sulphide, 4-hydroxyphenyl disulphide, naphth-2-ol, 1-bromonaphth-2-ol, 6-bromomaphth-2-ol, 1,6-dibromonaphth-2-ol and 6-hydroxybenzothiazoles of the formula ##STR20## wherein R is H, CN or unsubstituted or substituted thiazole, and each of X₁, X₂ and X₃ is H, substituted or unsubstituted C₁ -C₆ -alkyl or alkenyl, hydroxyl, substituted hydroxyl, C₁ -C₆ -alkoxy, carboxyl, amino or substituted amino.

14. A chemiluminescence process according to claim 7, wherein said imidazole is selected from the group consisting of 1-methylimidazole, 2-methylimidazole and 4-methylimidazole.

15. A chemiluminescence process according to claim 6, wherein said azole is 1-H-tetrazole.

18. A method for detecting a nucleic acid hybrid comprising contacting in a mixture a sample suspected of containing a specific nucleic acid, hybridized with a probe, the probe comprising a nucleic acid containing a sequence complementary to the suspected specific nucleic acid in the sample, said probe linked to (a) a chemiluminesnce precursor, or (b) an enhancer or (c) an enzyme, the mixture comprising a oxidant, a nitrogen compound selected from the group consisting of ammonia, an aromatic heterocyclic compound and a water-soluble organic amine, and the remaining unlinked precursor or enhancer or enzyme, detecting the extent of light emission and relating the amount of light emission to the amount of nucleic acid hybrid, wherein the precursor, the enhancer and the enzyme are as defined in claim 1.

19. A method according to claim 18 wherein the oxidant is selected from the group consisting of a peroxide and a perborate ion.

16. A chemiluminescence assay for the determination of a peroxidase enzyme comprising contacting an unknown sample with a chemiluminescence precursor, an oxidant, a chemiluminescence enhancer and a nitrogen compound selected from the group consisting of ammonia, an aromatic heterocyclic compound and a water-soluble organic amine, determining the extent of light emission and correlating the determination of light emission to the determination of the enzyme.

17. A test kit for conducting a chemiluminescence assay comprising in containers a chemiluminescence precursor, an enzyme, an oxidant, a chemiluminescence enhancer and a nitrogen compound selected from the group consisting of ammonia, an aromatic heterocyclic compound and a water-soluble organic amine.